Skip to main content
Download PDF

Detection of disseminated tumor cells in bone marrow predict late recurrences in operable breast cancer patients

BMC Cancer volume 19, Article number: 1131 (2019) Cite this article

Abstract

Background

Operable breast cancer patients may experience late recurrences because of reactivation of dormant tumor cells within the bone marrow (BM). Identification of patients who would benefit from extended therapy is therefore needed.

Methods

BM samples obtained pre- and post-surgery were previously analysed for presence of disseminated tumor cells (DTC) by a multimarker mRNA quantitative reverse-transcription PCR assay. Updated survival analyses were performed on all patient data (n = 191) and in a subgroup of patients alive and recurrence-free after 5 years (n = 156). DTC data were compared to the mitotic activity index (MAI) of the primary tumors. Median follow-up time was 15.3 years.

Results

Among the 191 patients, 49 (25.65%) experienced systemic relapse, 24 (49%) within 5–18 years after surgery. MAI and pre- and post-operative DTC status had significant prognostic value based on Kaplan–Meier analyses and multiple Cox regression in the overall patient cohort. With exclusion of patients who relapsed or died within 5 years from surgery, only pre-operative DTC detection was an independent prognostic marker of late recurrences. High MAI (≥10) did not predict late recurrences or disease-specific mortality.

Conclusion

Pre-operative DTC detection, but not MAI status, predicts late recurrences in operable breast cancer.

Peer Review reports

Background

Breast cancer patients are at risk of developing disease relapse decades after curative treatment because of the presence of minimal residual disease [1]. Minimal residual disease is caused by spread of invasive tumor cells from the primary tumor through the circulation to distant sites [2, 3]. Once in circulation, interaction with platelets seems to contribute to circulating tumor cell (CTC) survival as well as enhanced extravasation, especially to the bone microenvironment [4,5,6]. In breast cancer, tumor cells often migrate to the bone marrow (BM) where these disseminated tumor cells (DTCs) can survive for years by entering a dormant state. This is a prolonged quiescent state, in which tumor cells are present, but disease progression is not clinically manifested. Two mechanisms are believed to maintain tumor cell dormancy: single-cell dormancy and/or micrometastatic dormancy [7]. Single-cell dormancy, or cellular dormancy, is characterised by a state in which the tumor cells are non-proliferative and thus assumed to be resistant to traditional chemotherapeutics targeting proliferating cells [7]. In contrast, the micrometastatic dormancy model, which is supposed to be linked to more aggressive breast cancer, involves slowly proliferating tumor cells that are counterbalanced by cell death from impaired vascularisation or immunesurveillance, which prevents tumor growth [7]. However, dormant DTC survival in the BM depends on pro-survival signals from the microenvironment, as well as on development of complex immune evasion mechanisms in which interference with major histocompatibility complex–mediated antigen presentation seems to be important [8,9,10,11]. Breast cancer recurrence after a long asymptomatic period, even more than 20 years after the initial diagnosis, is believed to arise from an interruption of this dormant DTC state, possibly initiated by microenvironmental factors in the colonised tissue [12]. Thus, accurate identification of breast cancer patients at risk for late recurrences is needed to identify candidates for extended therapy and improve survival. Unfortunately, few studies report sufficiently long follow-up of breast cancer patients.

The prognostic relevance of DTC detection has been demonstrated by us and others [13,14,15,16,17,18], but only one other study has investigated the clinical significance of DTC detection for prediction of late recurrences by including long-term follow-up data [19]. For this reason, we evaluated the capacity of DTC detection prior to and after surgery to predict long-term outcome in 191 operable, prospectively recruited breast cancer patients in comparison to other well-established prognostic markers such as mitotic activity index (MAI) and lymph node status in a retrospective analysis [14,15,16]. To our knowledge, this study involves the longest follow-up reported in breast cancer studies investigating the clinical significance of DTC detection.

Methods

Patient cohort

The patients (n = 191) included in this study were consecutively recruited during the years 1998–2000. All patients had non-metastatic (M0) breast cancer, and the median age was 56 years (range 25–86 years). BM samples (20 ml in heparin) were drawn unilaterally from the posterior iliac crest under general anaesthesia immediately prior to surgery (BM1, n = 191) as well as 3 weeks (BM2) and/or 6 months (BM3) after surgery (n = 154) [16]. In addition, BM aspirates were obtained from 26 healthy women included as a control group. Written informed consent was obtained from all participants, and the project was approved by the Regional Committee for Medical and Health Research Ethics.

With regard to the treatment, all patients were treated according to the national guidelines in Norway at this time as previously described in Farmen et al., 2008 [20]. In brief, the patients either underwent a modified radical mastectomy or lumpectomy with breast-conserving surgery. Patients operated by lumpectomy received additional treatment in terms of radiotherapy to the breast. Level I or II axillary lymph node (LN) dissection was performed on all patients. Adjuvant combination therapy, including either CMF (cyclophosphamide, metotrexate and 5-fluorouracil) or FEC (5-fluorouracil, epirubicin and cyclophosphamide), was given to all high risk patients. In addition, 20 mg tamoxifen was given daily for 5 years to high-risk patients having a positive or uncertain hormone receptor status [20].

Patient follow-up data were collected from medical records at the hospital and from the patients` primary physicians. Information on time of death was obtained from the hospital records, which is updated based on information from the National Registry in Norway. The last follow-up was registered in August 2016, and the median follow-up time was 15.3 years (range 0.06–18.15 years). Early recurrence was defined as relapse within 5 years, and late recurrence was defined as relapse occurring more than 5 years after the initial surgery.

mRNA marker analyses in BM samples

BM lysates were prepared from buffy coat, and total RNA was isolated and transcribed to cDNA followed by amplification of a multimarker panel consisting of keratin 19 (KRT19), mammaglobin (hMAM) and TWIST1 mRNA in a LightCycler 480 (Roche Applied Science) instrument as previously described [14,15,16, 20]. After data analysis, a BM sample was considered to have presence of DTCs when at least one of the mRNA markers (i.e., KRT19, hMAM or TWIST1) exceeded the highest mRNA level in BM samples from the control group (n = 26), which was used as a threshold for normal expression [15, 16].

Assessment of MAI in primary tumors

The assessment of MAI was performed by a trained technician at × 400 magnification by systematic counting of well-defined mitoses in haematoxylin and eosin–stained slides of the primary tumor according to the Multicenter Mammary Carcinoma Project protocol [21,22,23], and as previously described in Gilje et al. [24]. The resulting total number of mitoses in the 10 fields of vision was defined as the MAI, and dichotomised as being < 10 or ≥ 10 where low MAI (< 10) indicates a favourable prognosis and a high MAI (≥10) a worse prognosis [25].

Statistical analyses

All statistical analyses were performed in SPSS version 24.0 (www.spss.com) and R version 3.3.3, with a two-sided p value ≤0.05 considered as statistically significant. Multiple testing were not corrected for, and missing data were excluded from all analyses. Fisher’s exact test were used to test for any relations between the multimarker BM expression and various endpoints. Kaplan–Meier estimates of clinical outcome were determined from primary surgery to A) systemic disease recurrence (systemic recurrence-free survival); B) death related to progression of breast cancer (breast cancer–specific survival); and C) death from any cause (overall survival). In this respect, pre-operative DTC status refers to DTC detection in BM samples obtained prior to surgery (BM1), while post-operative DTC status refers to DTC detection in BM samples obtained 3 weeks (BM2) and/or 6 months (BM3) after surgery. In addition, long-term survival was analysed separately by including only patients who were recurrence-free and alive 5 years (n = 156) after surgery and subtracting 5 years from their survival times.

Univariable Cox regression was performed to evaluate whether pre-operative DTC status, post-operative DTC status, pre- and post-operative DTC status, LN status, tumor size, tumor grade, age, oestrogen receptor (ER) status, progesterone receptor (PR) status, adjuvant therapy and MAI status were associated with systemic recurrence-free- and breast cancer–specific survival. Multivariable Cox regression was also performed to evaluate which of the listed risk factors independently could predict reduced systemic recurrence-free survival and breast cancer–specific survival. Pre- and post-operative DTC status could be entered into the same model, because they were not significantly associated. The multivariable analyses were performed using both forward and backward selection of covariates into the Wald model. However, only data from the backward selection is presented. A 95% confidence interval (CI) and a maximum of 50 iterations were used in these analyses.

Results

DTC detection and proliferation in operable breast cancer patients with long-term follow-up

In this study, 49/191 (26%) early-stage breast cancer patients experienced systemic relapse during a median follow-up of 15.3 years (range 0.1–18.2 years). Of these, 25 (51%) patients relapsed within 0–5 years after primary tumor resection, 9 (18%) patients relapsed between 5 and 10 years, and 15 (31%) relapsed after more than 10 years from their breast cancer surgery. Furthermore, 38/191 (19.9%) patients died from breast cancer during follow-up, compared to 37 (19.4%) patients who died from causes other than breast cancer.

Regarding BM assessments, 30/191 (15.7%) patients were DTC-positive in pre-operative BM samples, while 23/154 (14.9%) patients (missing data from 37 patients) were DTC-positive in post-operative BM samples. Of interest, 16/30 (53.3%) pre-operative DTC-positive patients relapsed compared to 33/161 (20.5%) DTC-negative patients (p < 0.001). Moreover, among the 16 relapsed pre-operative DTC-positive patients, 9 (30%) relapsed within 5 years while 7 (23.3%) relapsed within 5–18 years after their breast cancer surgery. When looking at death reports, 17 (56.7%) of the 30 pre-operative DTC-positive patients died from their disease compared to 58 (36%) of 161 DTC-negative patients (p = 0.042). In contrast, nine pre-operative DTC-positive patients had no reported disease relapse after > 15 years of follow-up. Of the 23 post-operative DTC-positive patients, 11 (47.8%) relapsed compared to 29/131 (22.1%) DTC-negative patients (p = 0.018). Four (36.4%) post-operative DTC-positive patients relapsed 5–18 years after surgery, and three of them died of breast cancer. Comparison of clinicopathological parameters and DTC status in BM before primary surgery is shown in Table 1.

Table 1 Comparison of the clinicopathological parameters of the operable breast cancer patients (n = 191) according to DTC status in bone marrow before primary surgery
Full size table

Counting of mitoses in the primary tumors for assessment of the MAI score was possible only for 179 of the 191 included patients. Among these, 60 had high MAI (≥10), indicating high proliferation in the primary tumor. Of these patients, 21 (35%) relapsed, 19 of them within the first 5 years from the diagnosis, and 20 (33%) patients died because of breast cancer.

Survival analysis

Kaplan–Meier analyses revealed that patients with DTCs present in their BM prior to surgery had significantly shorter systemic recurrence-free- (p < 0.001) and breast cancer–specific survival (p < 0.001) compared to DTC-negative patients (Fig. 1a and b). This pattern was also seen for overall survival (p = 0.013; Additional file 1: Figure S1-A). In addition, stratification of the data for adjuvant treatment demonstrated a significantly reduced systemic recurrence-free survival among the DTC-positive patients receiving adjuvant treatment (p = 0.001).

Fig. 1
figure 1

Survival analyses according to presence of disseminated tumor cells (DTCs) in bone marrow (BM) samples obtained prior to surgery (a and b) and 3 weeks and/or 6 months after surgery (c and d) from 191 operable breast cancer patients with a median follow-up of 15.3 years

Full size image

Investigations of the prognostic relevance of persistent DTCs in BM, by analyses of BM samples obtained 3 weeks and/or 6 months after primary surgery demonstrated that DTC status after surgery was a prognostic marker for both systemic recurrence-free- (p = 0.001) and breast cancer–specific survival (p = 0.002) after a median 15.3 years of follow-up (Fig. 1c and d). Furthermore, persistent DTCs in BM were associated with significantly reduced overall survival (p = 0.001; Additional file 1: Figure S1-B). Regarding primary tumor MAI status, a high MAI count was also a significant predictor of shorter systemic recurrence-free-survival (p = 0.018; Fig. 2a), breast cancer–specific survival (p < 0.001; Fig. 2b) and overall survival (p=0.026; Additional file 2: Figure S2-A). These survival curves show, however, that most disease recurrences and breast cancer–related deaths in patients with high MAI occured within the first 5 years from the primary surgery (Fig. 2a and b).

Fig. 2
figure 2

Kaplan–Meier survival estimates according to high (MAI ≥ 10) or low (MAI < 10) proliferation measured by the mitotic activity index (MAI) in tissue from operable breast cancer patients. a and b) MAI status in all patients (n = 191) with median 15.3 years of follow-up. c and d) MAI status in patients (n = 144) who did not experience disease recurrence or died during the first 5 years after surgery. In this case, the first 5 years were subtracted from all survival times prior to analysis

Full size image

Univariable and multivariable Cox regression analyses were performed to estimate the prognostic impact of DTC and MAI status, as well as of other clinicopathological parameters. Univariable Cox regression clearly showed that a positive DTC status prior to surgery was a significant risk factor for both reduced systemic recurrence-free survival and breast cancer–specific survial (Additional file 3: Table S1). Furthermore, persistence of DTCs after surgery also resulted in a high risk for systemic and breast cancer–specific recurrence, but the highest risk was observed for breast cancer patients with a positive DTC status both prior to and after surgery (HR = 6.93 and 8.34, respectively). MAI status was also a significant risk factor for reduced systemic recurrence-free and breast cancer–specific survival. Among other clinicopathological parameters, LN status, tumor size, grade, and age were also significant predictors of shorter survival (Additional file 3: Table S1). Multivariable Cox regression demonstrated that both pre-operative and post-operative DTC status were independent predictors of systemic recurrence-free survival and breast cancer–specific survival respectively (Table 2). Moreover, MAI score was also an independent prognostic marker of systemic recurrence-free survival and breast cancer–specific survival, with a median follow-up of 15.3 years. LN-status was, on the other hand, not a significant risk factor in the models, probably because of an association with one of the other covariates.

Table 2 Multivariable Cox regression of systemic recurrence-free survival and breast cancer–specific survival in operable breast cancer patients (n = 191) according to pre-operative DTC status after median 15.3 years of follow-up
Full size table

Survival analysis in patients who were alive and recurrence-free after 5 years from surgery

To further explore whether DTC detection can predict late disease recurrences, we excluded patients who relapsed or died within 5 years from their primary surgery and subtracted 5 years from all follow-up times from the survival analyses. A total of 156 long-term breast cancer survivors then remained in the models. Of these, 20/156 had DTCs prior to surgery, while 15/127 patients (missing data from 29 patients) had DTCs detected after surgery. Kaplan–Meier analyses showed pre-operative DTC status to be a significant predictor of late recurrences with regard to systemic recurrence-free- (p = 0.004) and breast cancer–specific survival (p = 0.022) (Fig. 3a and b). Stratification further revealed that pre-operative DTC status predicted late systemic recurrences in ER-positive patients (p = 0.007), pN+ patients (p = 0.008), patients with larger tumor size (p < 0.001), and patients over age 55 years (p = 0.027) (data not shown). For breast cancer–specific survival, pre-operative DTC status was a prognostic factor only for pN+ patients (p = 0.006). Post-operative DTC status, on the other hand, was a significant predictor only of reduced breast cancer–specific survival (p = 0.037) and not of systemic recurrence-free survival (Fig. 3c and d). Stratification also revealed that post-operative DTC status predicted late breast cancer–specific deaths in patients with pN+ disease (p = 0.006) and not in patients with high age or a positive ER status (data not shown). Of interest, Kaplan–Meier analyses of MAI status revealed that patients with a high MAI actually had significantly longer systemic recurrence-free survival than those with low MAI (p = 0.046; Fig. 2c).

Fig. 3
figure 3

Survival analyses according to disseminated tumor cell (DTC) detection in bone marrow (BM) samples obtained prior to surgery (a and b, n = 156) and 3 weeks and/or 6 months after surgery (c and d, n = 126) from operable breast cancer patients who did not experience disease recurrence or died during the first 5 years after surgery. Median follow-up was 15.3 years, but the first 5 years were subtracted from all survival times prior to analysis

Full size image

Univariable Cox regression analysis confirmed pre-operative DTC status as a significant predictor of both shorter systemic recurrence-free- (HR = 3.38, p = 0.007) and breast cancer–specific survival (HR = 3.67, p = 0.034) after exclusion of early relapses and deaths. In contrast, neither post-operative DTC status nor MAI status was a significant predictor of systemic recurrence-free survival or breast cancer–specific survival. Multivariable Cox analyses further confirmed these data by showing that only pre-operative DTC status was an independent predictor of late systemic and breast cancer–specific recurrences (Table 3). High MAI, on the other hand, was independently associated with longer recurrence-free survival in this analysis restricted to late events (HR = 0.22, p = 0.043).

Table 3 Multivariable Cox regression of systemic recurrence-free survival and breast cancer-specific survival demonstrate that pre-operative DTC status is an independent prognostic factor for prediction of late recurrences (> 5 years) in operable breast cancer patients (n = 155). Median follow-up was 15.3 years
Full size table

Discussion

We and others have previously shown that detection of DTCs in BM samples from operable breast cancer patients is associated with adverse clinical outcomes [14,15,16, 20, 26, 27]. In this study, we revisited DTC detection data from a previously described cohort, and have now collected extended long-term patient follow-up data. In addition to analysis of all data, we restricted some analyses to include only patients who were alive and recurrence-free after 5 years from surgery. A prognostic impact of DTC detection, but not MAI, could be demonstrated with regard to prediction of late disease relapse.

About 20% of clinically disease-free breast cancer patients experience disease recurrence 7–25 years after their initial diagnosis, even after mastectomy [28, 29]. In this respect, the average recurrence risk has been calculated at 4.3% per year between 5 and 12 years after postoperative adjuvant therapy [29], while the relapse risk between 10 and 20 years is about 1.5% per year [28, 29]. Although the biology behind the late recurrences in breast cancer patients is still not clearly defined, evidence indicates that BM is a common homing target for tumor cells in many types of carcinoma before they re-circulate into other distant sites [30, 31]. However, for tumor cells to survive in the BM, this microenvironment needs to be permissive for them (the metastatic niche model) [32]. To facilitate this permissiveness, the primary tumor and secondary sites seem to communicate through exosomes and direct organ tropism, modulate immune evasion, and support mesenchymal-to-epithelial transition, thus contributing to enhanced metastasis by influencing the fate of DTCs (reviewed in [33,34,35]). Following arrival at the BM, cellular and molecular cross-talk between the DTCs and the microenvironment further directs the DTCs into various native BM niches that also promote cell survival and dormancy [36, 37]. Recently autophagy has also been revealed as a critical mechanism for both the survival and outgrowth of the DTCs [38]. In addition to this, a large proportion of DTCs display stem cell–like features, which confer resistance to cytostatic therapy and contribute to enhanced cell survival [39]. When considering that all these factors contribute to survival of latent/dormant DTCs it reveals the molecular complexity of breast cancer, which further challenges both the choice and the success of adjuvant treatment for long-term survival.

To our knowledge, our study has the longest median follow-up reported in an analysis of DTCs in breast cancer. Only one other study has analysed the prognostic value of DTC status with regard to relatively long follow-up. In that study, 189/350 (54%) patients, of whom 31% were DTC-positive, relapsed during a median 12.5 years of follow-up [17]. This is comparable to 33% of the DTC-positive patients relapsing in our study. However, in their study, DTC detection was a significant independent prognostic factor for prediction of early relapses occurring 0–5 years from surgery and not for late relapses (> 5 years from surgery) [17], in contrast to our findings.

We show that the presence of DTCs in BM before surgery is a significant predictor of late recurrences and thus reduced systemic recurrence-free and breast cancer–specific survival in operable breast cancer patients. Stratification further demonstrated that pre-operative DTC status was particularly predictive of reduced survival in postmenopausal women (p = 0.027), patients with ER-positive disease (p = 0.007), lymph node involvement (p = 0.008), and large tumors (p < 0.001) by the log-rank test. Hence, our results support the fact that ER-positive patients are at particular risk of experiencing late recurrences, and extended endocrine therapy from 5 to 10 years is now recommended for this patient group [40]. A recent report from the International Breast Cancer Study Group, in which the hazard rates of breast cancer recurrence were estimated from 4105 breast cancer patients and 24 years of follow-up, also showed that the hazard for experiencing late relapse remains elevated and fairly stable beyond 10 years in ER-positive patients [41]. Other studies also support this conclusion (reviewed in [36, 42, 43]). However, because the ER-positive patient group is heterogeneous, differences have further been demonstrated between pre- and post-menopausal women based on molecular characteristics. In this respect, it has been specified that most cases of late recurrences arise in postmenopausal ER-positive women aged 60 years or older [42, 44]. Nevertheless, our study did not confirm ER-status as an independent prognostic factor, in contrast to pre-operative DTC status.

Previously, we and others have shown that both MAI scoring and DTC detection give independent prognostic information in operable breast cancer patients [24]. Because proliferation is a key driver for cancer progression, and substantial variability in Ki67 scoring is well known to occur [45], we wanted to extend our study to include investigations of MAI as a marker for prediction of late recurrences. High proliferation is associated with a more aggressive disease, so one prediction would be a higher relapse rate among these patients, as well as more frequent systemic disease and thus a positive DTC status. Our data support a significant association between high MAI score and relapse (Fig. 3) but no significant association between high MAI and DTC positivity (data not shown). This finding is probably because patients with high proliferation in the primary tumor largely seem to experience early disease relapse, within 5 years from diagnosis, in contrast to DTC-positive patients, who experience both early and late relapses [13]. Proliferation as a marker for prediction of early relapse has also been shown in other studies [46, 47]. Moreover, several molecular multi-gene assays including proliferation markers, among other markers (such as Mammaprint [48], Oncotype Dx Recurrence Score [49], Genomic Grade Index [50], Prosigna PAM50 Risk of Recurrence Score [51], Breast Cancer Index [52] and EndoPredict [53]) also support this. These assays were developed originally to give an overall risk assessment of recurrence by providing prognostic information not contained in the clinicopathological parameters. However, with a few exceptions, these multi-gene assays provide prognostic information restricted only to the first 5 years after the diagnosis (reviewed in [54]). This situation illustrates the challenges of accurate classification of primary breast tumors for prediction of late recurrences and suggests that DTC assessment may supplement primary tumor diagnostics in prognostic stratification. A few studies comparing the risk assessment by multi-gene assays and presence of DTCs in the bone marrow of operable breast cancer patients also support this as they did not find any association between them [55, 56]. On the contrary, another study did show that DTC detection was associated with a high Oncotype DX recurrence score [57]. Further studies are warranted.

Characterisation of DTCs and CTCs has revealed a challenge in current adjuvant treatment: the choice of targeted/adjuvant therapy in almost every solid cancer is largely based on an initial tissue biopsy obtained from the primary tumor. However, primary tumor characteristics do not necessarily reflect the characteristics of the metastasising DTCs and CTCs due to tumor cell heterogeneity and acquired evolutionary changes in the DTCs/CTCs during treatment. This has been demonstrated in several breast cancer studies, especially with regard to HER2 and ER status [58,59,60,61]. HER2-positive DTCs/CTCs have been detected in patients with an apparently HER2-negative primary tumor, resulting in patients who in fact are eligible for HER2-based treatment [62, 63]. The same has been shown for ER status [60, 61, 64, 65]. DTCs and CTCs may be ER-negative and PR-negative despite originating from a hormone receptor–positive tumor, possibly explaining the failure of endocrine therapy in a subset of ER-positive patients and vice versa. To overcome the issue of tumor cell heterogeneity, it has in the recent years been much focus on detection of circulating cell-free tumor DNA (ctDNA) from plasma of cancer patients. ctDNA is extracellular DNA that may originate from apoptotic and necrotic tumor cells in the primary tumor, metastatic lesions, or CTCs/DTCs in the circulation. In this respect, the ctDNA pool should be representative of the total tumor burden in an individual cancer patient, and several studies have shown both a prognostic and a predictive value of ctDNA detection in breast cancer patients (e.g. [66, 67]). Because ctDNA analysis is easily performed, without the need for enrichment and isolation of rare cancer cells, it is likely to be the preferred option for genotyping and monitoring of treatment response in the future. Further investigations are, however, needed to elucidate whether ctDNA assessment can predict late recurrences of breast cancer similarly to or better than DTC detection. Nevertheless, analyses of CTCs and DTCs provide a unique opportunity for in-depth assessment of viable metastasising tumor cells and their interaction with the tumor microenvironment, providing access to information that cannot be revealed using ctDNA.

Conclusion

Our data show that the presence of DTCs prior to surgery is an independent predictor of late disease recurrences and thus reduced systemic recurrence-free- and breast cancer–specific survival after a median 15.3 years of follow-up. In contrast, persistence of DTCs after surgery is a significant predictor only of late breast cancer recurrences. Proliferation, on the other hand, seems best to predict early relapse. Because the ultimate goal of all clinical research is to improve patient outcomes, further molecular characterisation of the DTCs and microenvironmental factors influencing on survival of dormant DTCs as well as dormancy exit mechanisms is required to better identify breast cancer patients at high risk of developing late disease relapse and thus in need of extended therapy.

Availability of data and materials

The underlying datasets will be made available upon request to Dr. Kjersti Tjensvoll after approval from the regional ethical committee.

Abbreviations

BM:

Bone marrow

CTC:

Circulating tumor cells

DTC:

Disseminated tumor cells

ER:

estrogen receptor

HR:

Hazard ratio

MAI:

Mitotic acitivity index

References

  1. Karrison TG, Ferguson DJ, Meier P. Dormancy of mammary carcinoma after mastectomy. J Natl Cancer Inst. 1999;91(1):80–5.

    CAS  PubMed  Article  Google Scholar 

  2. Mego M, Mani SA, Cristofanilli M. Molecular mechanisms of metastasis in breast cancer--clinical applications. Nat Rev Clin Oncol. 2010;7(12):693–701.

    CAS  PubMed  Article  Google Scholar 

  3. Pantel K, Hayes DF. Disseminated breast tumour cells: biological and clinical meaning. Nat Rev Clin Oncol. 2017.

  4. Leblanc R, Peyruchaud O. Metastasis: new functional implications of platelets and megakaryocytes. Blood. 2016;128(1):24–31.

    CAS  PubMed  Article  Google Scholar 

  5. Labelle M, Begum S, Hynes RO. Direct signaling between platelets and cancer cells induces an epithelial-mesenchymal-like transition and promotes metastasis. Cancer Cell. 2011;20(5):576–90.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  6. Bakewell SJ, Nestor P, Prasad S, Tomasson MH, Dowland N, Mehrotra M, Scarborough R, Kanter J, Abe K, Phillips D, et al. Platelet and osteoclast beta3 integrins are critical for bone metastasis. Proc Natl Acad Sci U S A. 2003;100(24):14205–10.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  7. Aguirre-Ghiso JA. Models, mechanisms and clinical evidence for cancer dormancy. Nat Rev Cancer. 2007;7(11):834–46.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  8. Aptsiauri N, Cabrera T, Mendez R, Garcia-Lora A, Ruiz-Cabello F, Garrido F. Role of altered expression of HLA class I molecules in cancer progression. Adv Exp Med Biol. 2007;601:123–31.

    PubMed  Article  Google Scholar 

  9. Ghajar CM, Peinado H, Mori H, Matei IR, Evason KJ, Brazier H, Almeida D, Koller A, Hajjar KA, Stainier DY, et al. The perivascular niche regulates breast tumour dormancy. Nat Cell Biol. 2013;15(7):807–17.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  10. Yoneda T. Cellular and molecular basis of preferential metastasis of breast cancer to bone. J Orthopaedic Sci. 2000;5(1):75–81.

    CAS  Article  Google Scholar 

  11. Wang H, Yu C, Gao X, Welte T, Muscarella AM, Tian L, Zhao H, Zhao Z, Du S, Tao J, et al. The osteogenic niche promotes early-stage bone colonization of disseminated breast cancer cells. Cancer Cell. 2015;27(2):193–210.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  12. Schmidt-Kittler O, Ragg T, Daskalakis A, Granzow M, Ahr A, Blankenstein TJ, Kaufmann M, Diebold J, Arnholdt H, Muller P, et al. From latent disseminated cells to overt metastasis: genetic analysis of systemic breast cancer progression. Proc Natl Acad Sci U S A. 2003;100(13):7737–42.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  13. Braun S, Vogl FD, Naume B, Janni W, Osborne MP, Coombes RC, Schlimok G, Diel IJ, Gerber B, Gebauer G, et al. A pooled analysis of bone marrow micrometastasis in breast cancer. N Engl J Med. 2005;353(8):793–802.

    CAS  PubMed  Article  Google Scholar 

  14. Tjensvoll K, Gilje B, Oltedal S, Shammas FV, Kvaloy JT, Heikkila R, Nordgard O. A small subgroup of operable breast cancer patients with poor prognosis identified by quantitative real-time RT-PCR detection of mammaglobin a and trefoil factor 1 mRNA expression in bone marrow. Breast Cancer Res Treat. 2009;116(2):329–38.

    CAS  PubMed  Article  Google Scholar 

  15. Tjensvoll K, Oltedal S, Farmen RK, Shammas FV, Heikkila R, Kvaloy JT, Gilje B, Smaaland R, Nordgard O. Disseminated tumor cells in bone marrow assessed by TWIST1, cytokeratin 19, and Mammaglobin a mRNA predict clinical outcome in operable breast Cancer patients. Clin Breast Cancer. 2010;10(5):378–84.

    CAS  PubMed  Article  Google Scholar 

  16. Tjensvoll K, Oltedal S, Heikkila R, Kvaloy JT, Gilje B, Reuben JM, Smaaland R, Nordgard O. Persistent tumor cells in bone marrow of non-metastatic breast cancer patients after primary surgery are associated with inferior outcome. BMC Cancer. 2012;12:190.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  17. Mansi JL, Gogas H, Bliss JM, Gazet JC, Berger U, Coombes RC. Outcome of primary-breast-cancer patients with micrometastases: a long-term follow-up study. Lancet (London, England). 1999;354(9174):197–202.

    CAS  Article  Google Scholar 

  18. Janni W, Vogl FD, Wiedswang G, Synnestvedt M, Fehm T, Jückstock J, Borgen E, Rack B, Braun S, Sommer H, et al. Persistence of disseminated tumor cells in the bone marrow of breast Cancer patients predicts increased risk for relapse--a European pooled analysis. Clin Cancer Res. 2011;17(9):2967–76.

    PubMed  Article  Google Scholar 

  19. Mansi JL, Gogas H, Bliss JM, Gazet JC, Berger U, Coombes RC. Outcome of primary-breast-cancer patients with micrometastases: a long-term follow-up study. Lancet (London, England). 1999;354(9174):195–200.

    Article  Google Scholar 

  20. Farmen RK, Nordgard O, Gilje B, Shammas FV, Kvaloy JT, Oltedal S, Heikkila R. Bone marrow cytokeratin 19 mRNA level is an independent predictor of relapse-free survival in operable breast cancer patients. Breast Cancer Res Treat. 2008;108(2):251–8.

    CAS  PubMed  Article  Google Scholar 

  21. van Diest PJ, Baak JP, Matze-Cok P, Wisse-Brekelmans EC, van Galen CM, Kurver PH, Bellot SM, Fijnheer J, van Gorp LH, Kwee WS, et al. Reproducibility of mitosis counting in 2,469 breast cancer specimens: results from the multicenter morphometric mammary carcinoma project. Hum Pathol. 1992;23(6):603–7.

    PubMed  Article  Google Scholar 

  22. Baak JP, van Diest PJ, Benraadt T, Matze-Cok E, Brugghe J, Schuurmans LT, Littooy JJ. The Multi-Center Morphometric Mammary Carcinoma Project (MMMCP) in The Netherlands: value of morphometrically assessed proliferation and differentiation. J Cellular Biochem Suppl. 1993;17g:220–5.

    CAS  Article  Google Scholar 

  23. Gudlaugsson E, Skaland I, Janssen EA, van Diest PJ, Voorhorst FJ, Kjellevold K, Zur Hausen A, Baak JP. Prospective multicenter comparison of proliferation and other prognostic factors in lymph node negative lobular invasive breast cancer. Breast Cancer Res Treat. 2010;121(1):35–40.

    CAS  PubMed  Article  Google Scholar 

  24. Gilje B, Nordgard O, Tjensvoll K, Janssen EA, Soiland H, Smaaland R, Baak JP. Mitotic activity and bone marrow micrometastases have independent prognostic value in node positive breast cancer patients. Breast Cancer Res Treat. 2011;128(1):137–46.

    PubMed  Article  Google Scholar 

  25. Baak JP, van Diest PJ, Voorhorst FJ, van der Wall E, Beex LV, Vermorken JB, Janssen EA. Prospective multicenter validation of the independent prognostic value of the mitotic activity index in lymph node-negative breast cancer patients younger than 55 years. J Clin Oncol. 2005;23(25):5993–6001.

    PubMed  Article  Google Scholar 

  26. Domschke C, Diel IJ, Englert S, Kalteisen S, Mayer L, Rom J, Heil J, Sohn C, Schuetz F. Prognostic value of disseminated tumor cells in the bone marrow of patients with operable primary breast cancer: a long-term follow-up study. Ann Surg Oncol. 2013;20(6):1865–71.

    PubMed  Article  Google Scholar 

  27. Hartkopf AD BS, Taran F-A, Harbeck N, von Au A, Naume B, Pierga J-Y, Hoffmann O, Beckmann MW, Rydén L, Fehm T, Aft R, Montserrat S, Walter V, Rack B, Schuetz F, Borgen E, Ta M-H, Bittner A-K, Fasching P, Fernö M, Krawczyk N, Weilbaecher K, Margelí M, Hahn M, Jueckstock J, Domschke C, Bidard F-C, Kasimir-Bauer S, Schoenfisch B, Kurt AG, Wallwiener M, Gebauer G, Wallwiener D, Janni W, Pantel K.: International pooled analysis of the prognostic impact of disseminated tumor cells from the bone marrow in early breast cancer: Results from the PADDY study [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX Philadelphia (PA): AACR; Cancer Res 2019, 79(4 Suppl):abstract nr GS5-07.

  28. Demicheli R, Abbattista A, Miceli R, Valagussa P, Bonadonna G. Time distribution of the recurrence risk for breast cancer patients undergoing mastectomy: further support about the concept of tumor dormancy. Breast Cancer Res Treat. 1996;41(2):177–85.

    CAS  PubMed  Article  Google Scholar 

  29. Saphner T, Tormey DC, Gray R. Annual hazard rates of recurrence for breast cancer after primary therapy. J Clin Oncol. 1996;14(10):2738–46.

    CAS  PubMed  Article  Google Scholar 

  30. Pantel K, Brakenhoff RH: Dissecting the metastatic cascade. Nat Rev Cancer. 2004;4(6):448–56.

    CAS  PubMed  Article  Google Scholar 

  31. Pantel K, Brakenhoff RH, Brandt B. Detection, clinical relevance and specific biological properties of disseminating tumour cells. Nat Rev Cancer. 2008;8(5):329–40.

    CAS  PubMed  Article  Google Scholar 

  32. Psaila B, Lyden D. The metastatic niche: adapting the foreign soil. Nat Rev Cancer. 2009;9(4):285–93.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  33. Quail DF, Joyce JA. Microenvironmental regulation of tumor progression and metastasis. Nat Med. 2013;19(11):1423–37.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  34. Kaplan RN, Riba RD, Zacharoulis S, Bramley AH, Vincent L, Costa C, MacDonald DD, Jin DK, Shido K, Kerns SA, et al. VEGFR1-positive haematopoietic bone marrow progenitors initiate the pre-metastatic niche. Nature. 2005;438(7069):820–7.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  35. Cheng Q, Chang JT, Gwin WR, Zhu J, Ambs S, Geradts J, Lyerly HK. A signature of epithelial-mesenchymal plasticity and stromal activation in primary tumor modulates late recurrence in breast cancer independent of disease subtype. Breast Cancer Res. 2014;16(4):407.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  36. Gomis RR, Gawrzak S. Tumor cell dormancy. Mol Oncol. 2016.

  37. Psaila B, Kaplan RN, Port ER, Lyden D. Priming the ‘soil’ for breast cancer metastasis: the pre-metastatic niche. Breast Dis. 2006;26:65–74.

    CAS  PubMed  Article  Google Scholar 

  38. Vera-Ramirez L, Vodnala SK, Nini R, Hunter KW, Green JE. Autophagy promotes the survival of dormant breast cancer cells and metastatic tumour recurrence. Nat Commun. 2018;9(1):1944.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  39. Balic M, Lin H, Young L, Hawes D, Giuliano A, McNamara G, Datar RH, Cote RJ. Most early disseminated cancer cells detected in bone marrow of breast cancer patients have a putative breast cancer stem cell phenotype. Clin Cancer Res. 2006;12(19):5615–21.

    CAS  PubMed  Article  Google Scholar 

  40. Davies C, Pan H, Godwin J, Gray R, Arriagada R, Raina V, Abraham M, Medeiros Alencar VH, Badran A, Bonfill X, et al. Long-term effects of continuing adjuvant tamoxifen to 10 years versus stopping at 5 years after diagnosis of oestrogen receptor-positive breast cancer: ATLAS, a randomised trial. Lancet (London, England). 2013;381(9869):805–16.

    CAS  Article  Google Scholar 

  41. Colleoni M, Sun Z, Price KN, Karlsson P, Forbes JF, Thurlimann B, Gianni L, Castiglione M, Gelber RD, Coates AS, et al. Annual Hazard rates of recurrence for breast Cancer during 24 years of follow-up: results from the international breast Cancer study group trials I to V. J Clin Oncol. 2016;34(9):927–35.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  42. Esserman LJ, Moore DH, Tsing PJ, Chu PW, Yau C, Ozanne E, Chung RE, Tandon VJ, Park JW, Baehner FL, et al. Biologic markers determine both the risk and the timing of recurrence in breast cancer. Breast Cancer Res Treat. 2011;129(2):607–16.

    PubMed  PubMed Central  Article  Google Scholar 

  43. Jatoi I, Anderson WF, Jeong JH, Redmond CK. Breast cancer adjuvant therapy: time to consider its time-dependent effects. J Clin Oncol. 2011;29(17):2301–4.

    PubMed  PubMed Central  Article  Google Scholar 

  44. Yamashita H, Ogiya A, Shien T, Horimoto Y, Masuda N, Inao T, Osako T, Takahashi M, Endo Y, Hosoda M, et al. Clinicopathological factors predicting early and late distant recurrence in estrogen receptor-positive, HER2-negative breast cancer. Breast cancer (Tokyo, Japan). 2016;23(6):830–43.

    Article  Google Scholar 

  45. Polley MY, Leung SC, McShane LM, Gao D, Hugh JC, Mastropasqua MG, Viale G, Zabaglo LA, Penault-Llorca F, Bartlett JM, et al. An international Ki67 reproducibility study. J Natl Cancer Inst. 2013;105(24):1897–906.

    PubMed  PubMed Central  Article  Google Scholar 

  46. Inwald EC, Klinkhammer-Schalke M, Hofstadter F, Zeman F, Koller M, Gerstenhauer M, Ortmann O. Ki-67 is a prognostic parameter in breast cancer patients: results of a large population-based cohort of a cancer registry. Breast Cancer Res Treat. 2013;139(2):539–52.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  47. Bianchini G, Pusztai L, Karn T, Iwamoto T, Rody A, Kelly C, Muller V, Schmidt S, Qi Y, Holtrich U, et al. Proliferation and estrogen signaling can distinguish patients at risk for early versus late relapse among estrogen receptor positive breast cancers. Breast Cancer Res. 2013;15(5):R86.

    PubMed  PubMed Central  Article  Google Scholar 

  48. van de Vijver MJ, He YD, van't Veer LJ, Dai H, Hart AA, Voskuil DW, Schreiber GJ, Peterse JL, Roberts C, Marton MJ, et al. A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med. 2002;347(25):1999–2009.

    PubMed  Article  Google Scholar 

  49. Paik S, Shak S, Tang G, Kim C, Baker J, Cronin M, Baehner FL, Walker MG, Watson D, Park T, et al. A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer. N Engl J Med. 2004;351(27):2817–26.

    CAS  PubMed  Article  Google Scholar 

  50. Metzger Filho O, Ignatiadis M, Sotiriou C. Genomic grade index: an important tool for assessing breast cancer tumor grade and prognosis. Crit Rev Oncol Hematol. 2011;77(1):20–9.

    PubMed  Article  Google Scholar 

  51. Dowsett M, Sestak I, Lopez-Knowles E, Sidhu K, Dunbier AK, Cowens JW, Ferree S, Storhoff J, Schaper C, Cuzick J. Comparison of PAM50 risk of recurrence score with oncotype DX and IHC4 for predicting risk of distant recurrence after endocrine therapy. J Clin Oncol. 2013;31(22):2783–90.

    PubMed  Article  Google Scholar 

  52. Zhang Y, Schnabel CA, Schroeder BE, Jerevall PL, Jankowitz RC, Fornander T, Stal O, Brufsky AM, Sgroi D, Erlander MG. Breast cancer index identifies early-stage estrogen receptor-positive breast cancer patients at risk for early- and late-distant recurrence. Clin Cancer Res. 2013;19(15):4196–205.

    CAS  PubMed  Article  Google Scholar 

  53. Dubsky P, Filipits M, Jakesz R, Rudas M, Singer CF, Greil R, Dietze O, Luisser I, Klug E, Sedivy R, et al. EndoPredict improves the prognostic classification derived from common clinical guidelines in ER-positive, HER2-negative early breast cancer. Ann Oncol. 2013;24(3):640–7.

    CAS  PubMed  Article  Google Scholar 

  54. Sestak I, Cuzick J. Markers for the identification of late breast cancer recurrence. Breast Cancer Res. 2015;17:10.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  55. Aktas B, Bankfalvi A, Heubner M, Kimmig R, Kasimir-Bauer S. Evaluation and correlation of risk recurrence in early breast cancer assessed by Oncotype DX((R)), clinicopathological markers and tumor cell dissemination in the blood and bone marrow. Mol Clin Oncol. 2013;1(6):1049–54.

    PubMed  PubMed Central  Article  Google Scholar 

  56. Walter VP, Taran FA, Wallwiener M, Walter C, Grischke EM, Wallwiener D, Brucker SY, Hartkopf AD. A high-risk 70-gene signature is not associated with the detection of tumor cell dissemination to the bone marrow. Breast Cancer Res Treat. 2018;169(2):305–9.

    CAS  PubMed  Article  Google Scholar 

  57. Hartkopf AD, Wallwiener M, Kommoss S, Taran FA, Brucker SY. Detection of disseminated tumor cells from the bone marrow of patients with early breast cancer is associated with high 21-gene recurrence score. Breast Cancer Res Treat. 2016;156(1):91–5.

    CAS  PubMed  Article  Google Scholar 

  58. Solomayer EF, Becker S, Pergola-Becker G, Bachmann R, Kramer B, Vogel U, Neubauer H, Wallwiener D, Huober J, Fehm TN. Comparison of HER2 status between primary tumor and disseminated tumor cells in primary breast cancer patients. Breast Cancer Res Treat. 2006;98(2):179–84.

    CAS  PubMed  Article  Google Scholar 

  59. Krawczyk N, Banys M, Neubauer H, Solomayer EF, Gall C, Hahn M, Becker S, Bachmann R, Wallwiener D, Fehm T. HER2 status on persistent disseminated tumor cells after adjuvant therapy may differ from initial HER2 status on primary tumor. Anticancer Res. 2009;29(10):4019–24.

    PubMed  Google Scholar 

  60. Fehm T, Krawczyk N, Solomayer EF, Becker-Pergola G, Durr-Storzer S, Neubauer H, Seeger H, Staebler A, Wallwiener D, Becker S. ERalpha-status of disseminated tumour cells in bone marrow of primary breast cancer patients. Breast Cancer Res. 2008;10(5):R76.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  61. Jager BA, Finkenzeller C, Bock C, Majunke L, Jueckstock JK, Andergassen U, Neugebauer JK, Pestka A, Friedl TW, Jeschke U, et al. Estrogen receptor and HER2 status on disseminated tumor cells and primary tumor in patients with early breast Cancer. Transl Oncol. 2015;8(6):509–16.

    PubMed  PubMed Central  Article  Google Scholar 

  62. Meng S, Tripathy D, Shete S, Ashfaq R, Haley B, Perkins S, Beitsch P, Khan A, Euhus D, Osborne C, et al. HER-2 gene amplification can be acquired as breast cancer progresses. Proc Natl Acad Sci U S A. 2004;101(25):9393–8.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  63. Rack B, Juckstock J, Gunthner-Biller M, Andergassen U, Neugebauer J, Hepp P, Schoberth A, Mayr D, Zwingers T, Schindlbeck C, et al. Trastuzumab clears HER2/neu-positive isolated tumor cells from bone marrow in primary breast cancer patients. Arch Gynecol Obstet. 2012;285(2):485–92.

    CAS  PubMed  Article  Google Scholar 

  64. Aktas B, Muller V, Tewes M, Zeitz J, Kasimir-Bauer S, Loehberg CR, Rack B, Schneeweiss A, Fehm T. Comparison of estrogen and progesterone receptor status of circulating tumor cells and the primary tumor in metastatic breast cancer patients. Gynecol Oncol. 2011;122(2):356–60.

    CAS  PubMed  Article  Google Scholar 

  65. Banys M, Krawczyk N, Becker S, Jakubowska J, Staebler A, Wallwiener D, Fehm T, Rothmund R. The influence of removal of primary tumor on incidence and phenotype of circulating tumor cells in primary breast cancer. Breast Cancer Res Treat. 2012;132(1):121–9.

    PubMed  Article  Google Scholar 

  66. Garcia-Murillas I, Schiavon G, Weigelt B, Ng C, Hrebien S, Cutts RJ, Cheang M, Osin P, Nerurkar A, Kozarewa I, et al. Mutation tracking in circulating tumor DNA predicts relapse in early breast cancer. Sci Transl Med. 2015;7(302):302ra133.

    PubMed  Article  Google Scholar 

  67. Dawson SJ, Tsui DW, Murtaza M, Biggs H, Rueda OM, Chin SF, Dunning MJ, Gale D, Forshew T, Mahler-Araujo B, et al. Analysis of circulating tumor DNA to monitor metastatic breast cancer. N Engl J Med. 2013;368(13):1199–209.

    CAS  PubMed  Article  Google Scholar 

Download references

Acknowledgements

Thanks to Jan Terje Kvaløy, at the University of Stavanger, for statistical advice.

Funding

This study was partly financed by the Norwegian Cancer Society. The funding body did not influence or have any role in the design of the study, analysis, interpretation of data or manuscript preparation.

Author information

Authors and Affiliations

  1. Department of Haematology and Oncology, Stavanger University Hospital, N-4011, Stavanger, Norway

    Kjersti Tjensvoll, Oddmund Nordgård, Maren Skjæveland, Satu Oltedal & Bjørnar Gilje

  2. Laboratory for Molecular Biology, Stavanger University Hospital, N-4011, Stavanger, Norway

    Kjersti Tjensvoll, Oddmund Nordgård, Satu Oltedal & Emiel A. M. Janssen

  3. Department of Pathology, Stavanger University Hospital, N-4011, Stavanger, Norway

    Emiel A. M. Janssen

Authors
  1. Kjersti Tjensvoll
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Oddmund Nordgård
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Maren Skjæveland
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Satu Oltedal
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Emiel A. M. Janssen
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Bjørnar Gilje
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

KT participated in the study design, performed all real-time PCR analyses, performed statistical analyses, interpreted the results, and drafted the manuscript. ON participated in the study design and coordination of the study, interpretation of the results, statistical analyses, and manuscript preparation. MS participated in collection of the clinical follow-up data and manuscript preparation. SO performed all DNA purification and reverse transcription and contributed to manuscript preparation. EAMJ completed all MAI analyses and participated in manuscript preparation. BG is the group leader and participated in patient recruitments, BM sample collection, clinical follow-up data collection, interpretation of the results, and manuscript preparation. All authors have read and approved the manuscript.

Corresponding author

Correspondence to Kjersti Tjensvoll.

Ethics declarations

Ethics approval and consent to participate

The project was approved by the Regional Committee for Medical and Health Research Ethics West (Reference number REK 127.97) and performed in accordance with the Declaration of Helsinki. Writtten informed consent was obtained from all the participants in this study.

Consent for publication

Not applicable.

Competing interests

We declare that none of the authors have any competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1 Figure S1

: Kaplan–Meier overall survival estimates according to presence of disseminated tumour cells (DTCs) in bone marrow (BM) samples from operable breast cancer patients before as well as after (3 weeks and/or 6 months) surgery. A) and B) DTC status in all patients (n = 191), median 15.3 years follow-up. C) and D) DTC status in patients (n = 156) who did not experience disease recurrence or died during the first 5 years after surgery, and where the first 5 years were subtracted from all survival times prior to analysis.

Additional file 2 Figure S2

: Overall survival estimates according to high (MAI ≥ 10) or low (MAI < 10) proliferation measured by the mitotic activity index (MAI) in tissue from operable breast cancer patients. A) MAI status in all patients (n = 191), median 15.3 years of follow-up. B) MAI status in patients (n = 156) who did not relapse or die during the first 5 years after surgery, and where the first 5 years were subtracted from all survival times prior to analysis.

Additional file 3 Table S1

: Risk factors for reduced systemic recurrence-free- and breast cancer–specific survival in operable breast cancer patients (n = 191) with a median 15.3 years of follow-up revealed by univariable Cox regression.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Tjensvoll, K., Nordgård, O., Skjæveland, M. et al. Detection of disseminated tumor cells in bone marrow predict late recurrences in operable breast cancer patients. BMC Cancer 19, 1131 (2019). https://doi.org/10.1186/s12885-019-6268-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12885-019-6268-y

Keywords

  • Disseminated tumor cell
  • DTC
  • Dormancy
  • Breast cancer
  • Proliferation
  • Mitotic activity index
  • Late recurrence

BMC Cancer

ISSN: 1471-2407

Contact us