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First-line induction chemotherapy with high-dose methotrexate versus teniposide in patients with newly diagnosed primary central nervous system lymphoma: a retrospective, multicenter cohort study

Abstract

Background

This study aimed to compare the efficacy and safety of high-dose methotrexate (HD-MTX) versus teniposide (TEN) in patients with newly diagnosed immunocompetent primary central nervous system lymphomas (PCNSLs).

Methods

The study included immunocompetent, adult patients with newly diagnosed PCNSL at 22 centers in China from 2007 to 2016. The patients received HD-MTX or TEN as first-line induction therapy. The objective response rate, progression-free survival, and overall survival were analyzed for each patient cohort.

Results

A total of 96 patients were eligible: 62 received HD-MTX, while 34 received teniposide. The overall response rate was 73.2% and 72.7% in the MTX and the TEN cohorts, respectively (P = 0.627). The median progression-free survival was 28.4 months [95% confidence interval (CI): 13.7–51.2] in the MTX cohort and 24.3 months (95% CI: 16.6–32.1) in the TEN cohort (P = 0.75). The median overall survival was 31 months (95% CI: 26.8–35.2) in the MTX cohort and 32 months (95% CI: 27.6–36.4) in the TEN cohort (P = 0.77). The incidence of any grade of coagulopathy/deep-vein thrombosis and gastrointestinal disorders was significantly higher in the MTX cohort than in the TEN cohort; no significant difference was found in the incidence of other adverse events between the two cohorts.

Conclusions

This was the first multicenter study using TEN as the main agent compared with HD-MTX in newly diagnosed primary CNS lymphoma. The TEN-based regimen was non-inferior to the HD-MTX-based regimen with similar overall responses.

Classification of evidence

This study provided Class III evidence that the teniposide-based regimen was non-inferior to high-dose methotrexate − based regimen with similar overall responses and long-time survival in immunocompetent patients with PCNSL.

Peer Review reports

Background

Primary central nervous system lymphoma (PCNSL) accounts for 2%–3% of all non-Hodgkin’s lymphoma cases with increasing incidence, particularly for elderly patients [1]. The standard therapeutic regimens for newly diagnosed PCNSL have not been well defined. Most regimens of induction chemotherapy include drugs that cross the blood–brain barrier (BBB) in conventional doses. High-dose methotrexate (HD-MTX)-based regimen is now considered the standard treatment regimen [2]. However, HD-MTX treatment − associated overall survival (OS) was less than 20%–35% [3, 4]. Even combined with cytarabine, temozolomide, etoposide, the 5-year OS rate (30% -50%) of HD-MTX based scheme is still unsatisfactory [2, 5,6,7,8] and more severe hematological toxicity. For these reasons, the development of more effective and less toxic novel therapeutic regimens for PCNSL is of great clinical importance.

High doses of intravenous methotrexate are necessary (≥ 3.5 g/m2) to overcome the BBB [5, 9,10,11,12], but the problem associated with it is the toxicity it causes. The median age at diagnosis of PCNSL is 60–65 years in China. Among them, a significant portion of elderly patients aged 70 or older cannot tolerate HD-MTX, and other equivalent drugs or treatment options for those patients are currently lacking. Many water-soluble drugs have been proven ineffective in PCNSL because of their poor ability to penetrate the BBB [13]. Teniposide, as a highly fat-soluble topoisomerase II–trapping agent, is a potent and broad-spectrum antitumor drug [14,15,16,17]. Teniposide showed anti-lymphoma ability together with other drugs, such as methotrexate, fotemustine, and dexamethasone in a small number of cases [15, 18, 19]. In a comparative study, researchers analyzed the efficacy and safety of flumustine, teniposide, and dexamethasone in patients with central nervous system lymphoma (CNSL). The results showed that 8 patients with PCNSL had an overall response rate of 88%, whereas 8 patients with secondary CNSL had an overall response rate of 63%. This study suggested that a teniposide-based regimen might be an effective treatment for CNSL [11]. A phase II clinical trial found high response rates in patients with PCNSL treated with MTX, teniposide, carmustine, and methylprednisolone after radiotherapy [14]. A clinical study in China found that, compared with HD-MTX alone, HD-MTX combined with teniposide was more effective in treating PCNSL and could effectively control tumor progression, prolong survival, and improve prognosis [15]. An early clinical study at our center confirmed that teniposide with or without rituximab was well tolerated and effective in patients with PCNSL, with a high response rate and promising long-term survival [20]. Although the efficacy of teniposide-based regimens in patients with PCNSL has been demonstrated, the efficacy and safety of teniposide versus HD-MTX have not been reported.

In this retrospective multicenter study, we compared the efficacy and safety of TEN and HD-MTX with or without rituximab as first-line chemotherapy in patients with newly diagnosed PCNSL. We aimed to provide a new regimen of simple drugs as a candidate choice other than HD-MTX.

Methods

Study design and patients

This was a retrospective multicenter study of immunocompetent adults with newly diagnosed PCNSL at 22 centers in China from 2007 to 2016. The inclusion criteria were as follows: patients ≥ 18 years older; immunocompetent patients; patients with newly diagnosed PCNSL confirmed by histology or cytology from cerebrospinal fluid (CSF); patients with no previous cytotoxic treatment; patients with no evidence of extra-CNS involvement; patients receiving either high-dose methotrexate (HD-MTX) (MTX cohort: high-dose methotrexate-based regimen treatment, 3–3.5 g/m2 methotrexate daily on day 1 every 14 days, with or without rituximab 375 mg/m2 on day 0) or teniposide (TEN cohort: teniposide-based regimen treatment, 60 mg/m2 teniposide daily on days 1–5 every 21 days, with or without rituximab 375 mg/m2 on day 0) as the first-line induction therapy. The major exclusion criteria were concomitant immunosuppression, including positive human immunodeficiency virus serology; no assessment of chemotherapy, and no long-term survival result. All clinical management decisions and response evaluations were independently performed by the patients’ treating physicians. The study was approved by the local institutional ethic committee. As our study involved only a retrospective review of previous clinical data, the requirement for informed consent was waived.

The demographic data and clinical features of all patients were obtained retrospectively from the medical records. The clinical variables included age at diagnosis, sex, ethnicity, height, weight, body surface area, Eastern Cooperative Oncology Group (ECOG) performance score, year of diagnosis, symptoms at diagnosis, presence/absence of B symptoms, result of pathology, International Extranodal Lymphoma Study Group (IELSG) score of primary CNS lymphoma, lactate dehydrogenase (LDH), protein level of CSF, sites of intracranial lesions, comorbidities (hypertension, coronary disease, diabetes, hyperlipidemia, viral hepatitis B, etc.), induction regimen and its toxicity, inclusion of rituximab, number of cycles, response (complete response, CR; partial response, PR; stable disease, SD; progressive disease, PD), use/type/timing of stem cell transplantation, use of radiotherapy, progression-free survival (PFS), OS, and cause of death.

The purpose of this study was to compare the efficacy and safety of a teniposide-based regimen with a high-dose methotrexate-based regimen in patients with newly diagnosed primary CNS lymphoma. The outcomes were objective response rate [including complete response rate and overall response rate (ORR) after induction chemo/immunotherapy], PFS, and OS. The OS was calculated from the time of diagnosis to death of any cause or, for the patients alive, to the date of the last follow-up, whereas PFS was the time from diagnosis to the time of relapse or progression or death from any cause. The International PCNSL Collaborative Group Response Criteria [21] was used for response assessment. Our study also analyzed the toxicity of patients in these 2 cohorts 1 month after chemotherapy. The toxicities of MTX and TEN cohorts were assessed with the Common Terminology Criteria for Adverse Events version 4.0.

Statistical analysis

The baseline (pretreatment) and treatment variables were collected, along with dates of first progression, last follow-up, and death. The normally distributed variables were expressed as mean ± standard deviation (SD), and the skewed or unknown distributed variables were displayed as the median and interquartile range (IQR). The categorical variables were presented as count (percentage). The univariate analyses (UVA) for OS were performed using each of the pretreatment variables evaluated. The survival analyses were performed regardless of the duration or type of therapy received. PFS and OS rates were estimated using the Kaplan–Meier method, and differences were assessed with the log-rank (Mantel–Cox) test. Variables with a P value < 0.05 on UVA were included in the stepwise multivariate Cox proportional-hazards model. Hazard ratios (HRs) and their 95% confidence intervals (CIs) were calculated. The Cox proportional-hazards model was recalculated with the addition of an induction regimen as a variable to evaluate the impact of the induction regimen. Kaplan–Meier survival curves were generated. Analyses were done with IBM SPSS software (version 20·0). The differences in categorical data were calculated using the chi-square or Fisher’s exact test with significance defined as P ≤ 0.05. All P values were two tailed.

Results

Comparison of clinical characteristics of patients in HD-MTX and teniposide cohorts

Full survival data were available for 96 eligible patients from 22 centers in China. Of these, 62 patients received treatment with MTX monotherapy with or without rituximab (MTX cohort), and 34 patients received teniposide monotherapy with or without rituximab (TEN cohort). The proportion of patients whose tissue samples were obtained by stereotactic biopsy in the MTX cohort was significantly lower than that in the TEN cohort (29.5% vs 50.0%,), while the proportion of patients whose tissue samples were obtained by surgical partial resection was significantly higher than that in the TEN cohort (70.5% vs 50.0%) (P = 0.047). No significant differences were found in age, sex, ECOG performance status, IELSG risk, LDH level, CSF cytology, lymphoma categories, comorbidities, and the combination of MTX/TEN with rituximab and radiotherapy between the 2 cohorts (Table 1). The median age of the whole cohort was 55 years (range, 22–74 years), with 51.5 years in the TEN cohort (range, 22–74 years) and 58 years in the MTX cohort (range, 23–74 years) (P = 0.655). The ratio was 1.13:1 in all patients, with no difference between the two cohorts. Nearly half of the patients had poor performance status (ECOG PS ≥ 2). More than 95% patients in both cohorts had B-cell lymphoma, and most of them had diffuse large B-cell lymphoma. Most patients were diagnosed by stereotactic or surgical biopsy, and only one patient in the MTX cohort was diagnosed by cytology from CSF. The comorbidities in two groups were similar, including hypertension, coronary disease, diabetes, hyperlipidemia, viral hepatitis B. In MTX group, there was one patient with depressive state, one patient cured gastric cancer, and one patient with hysterectomy. In TEN group, there was 1 patient with a mass on kidney without pathological diagnosis and 1 patient with hysterectomy. Less than half of the patients in both cohorts received MTX or teniposide with rituximab as the first-line induction therapy, and nearly half of the patients received radiotherapy as a consolidation therapy after MTX or teniposide.

Table 1 Patients’ characteristics and distribution of lymphoma categories in the two treatment cohorts

Comparison of response rates in patients treated with MTX and TEN

The response rate was 90.3% in the MTX cohort and 97.1% in the TEN cohort. The median follow-up duration was 44 months (range, 1–81 months) in the MTX cohort and 39 months (range, 2–61 months) in the TEN cohort. The ORR was 73.2% and 72.7% in the MTX and TEN cohorts (P = 0.627). The complete response rate in the MTX cohort was higher than that in the TEN cohort, with no statistically significant difference (P = 0.182). According to the IELSG score, no difference in overall responses was found among three levels (P = 0.467). Four patients in the MTX cohort and 1 patient in the TEN cohort received autologous hematopoietic stem cell transplantation (ASCT) after the methotrexate and teniposide induction therapy. It might partially explain the higher complete response rate in the MTX cohort. None of the enrolled patients underwent allogeneic hematopoietic stem cell transplantation. Of all 89 patients who received at least 1 dose of first-line chemotherapy and fulfilled all eligibility criteria, 2 (3.6%) died during first-line therapy in the MTX cohort. The causes of death were cerebral bleeding (n = 1, 1.8%) and acute toxic effect (n = 1, 1.8%) (Table 2).

Table 2 Response rates by induction therapy in both treatment cohorts

Comparison of PFS and OS in the MTX and TEN cohorts

During follow-up, the median PFS was 28.4 months (95% CI: 13.7–51.2) in the MTX cohort and 24.3 months (95% CI: 16.6–32.1) in the TEN cohort (P = 0.75; Fig. 1A), with a 3-year PFS of 48.7% and 34.1%. The median OS was 31 months (95% CI: 26.8–35.2) in the MTX cohort and 32 months (95% CI: 27.6–36.4) in the TEN cohort (P = 0.77; Fig. 1B), with a 3-year OS of 41.9% and 41.7%, respectively. A total of 42 events were reported in the MTX cohort (relapse after responsive or stable disease in 25 patients, death while relapse-free in 2 patients, death while early progressive disease in 2 patients, death due to tumor progression in 12 patients, and death for unknown reason in 1 patient), and 33 events in the TEN cohort (relapse after responsive or stable disease in 17 patients, death while relapse-free in 2 patients, death while early progressive disease in 1 patient, death due to tumor in 13 patients, and death for unknown reason in 1 patient).

Fig. 1
figure 1

Comparison of progression-free survival and overall survival in the two cohorts. Progression-free (A) and overall (B) survival of patients treated with HD-MTX or teniposide. MTX, high-dose methotrexate; TEN, teniposide

Cox regression analysis of prognostic factors for PFS and OS

The univariate analysis found that age, ECOG, IELSG risk, rituximab, and radiotherapy were not significantly associated with PFS. The multivariate analysis found radiotherapy was significantly associated with PFS (HR 0.40, 95% CI, 0.20–0.80, P = 0.009).

The univariate and multivariate analyses found that age, ECOG, rituximab, and radiotherapy were not significantly associated with OS. However, the IELSG risk was significantly associated with a worse OS in univariate and multivariate analyses (low vs intermediate, P = 0.003; low vs high, P = 0.002) (Table 3).

Table 3 Univariate and multivariate analyses for progression-free survival and overall survival

Comparing the incidence of adverse events in the MTX and TEN cohorts

Table 4 summarizes all hematological and non-hematological toxic effects that occurred during first-line chemotherapy. The prevalence of hematological toxic effects in the two cohorts was similar. The coagulopathy or DVT was more common in the MTX cohort: 13.5% with grade 1 and 1.9% with grade 5 in the MTX cohort versus 0 in the TEN cohort. The gastrointestinal toxic effects increased in the TEN cohort, but all were of grade 1–2. Acute neurotoxicity was reported in two patients (1 grade 4 and 1 grade 5, 3.8%) in the MTX cohort compared with one patient (grade 1–2, 3%) in the TEN cohort (P = 0.832).

Table 4 Toxic effects in each cohort

The most common adverse reactions during treatment in patients in the MTX and TEN cohorts included neutropenia, thrombocytopenia, anemia, febrile neutropenia/infections, hepatotoxicity, nephrotoxicity, coagulopathy/DVT, gastrointestinal, mucositis, and acute neurotoxicity. In the MTX cohort, common grade 4 adverse events included neutropenia (19.2%), thrombocytopenia (13.5%), anemia (19.2%), febrile neutropenia/infections (1.9%), mucositis (1.9%), and acute neurotoxicity (1.9%). Common grade 5 adverse events included febrile neutropenia/infections (1.9%), coagulopathy/DVT (1.9%), and acute neurotoxicity (1.9%). In the TEN cohort, the most common grade 4 adverse events included neutropenia (24.2%), thrombocytopenia (9.1%), anemia (3%), and febrile neutropenia/infections (6.1%). Grade 5 febrile neutropenia/infections occurred in only 1 (3%) patient (Table 4).

Discussion

PCNSL has posed a major challenge to physicians for decades, especially in elderly patients. This study was novel in using TEN as the main agent compared with high-dose MTX in PCNSL. This study showed that PFS and OS were similar in both treatment cohorts. Our study found that the response rate was 90.3% in the MTX cohort and 97.1% in the TEN cohort. No significant differences were observed in median PFS (28.4 months vs 24.3 months) and median OS (31 months vs 32 months) between MTX and TEN cohorts. The results of an open, randomized, phase 2 trial showed that patients with PCNSL treated with methotrexate and methotrexate plus cytarabine had an ORR of 40% and 69%, respectively [5]. A retrospective study found that patients with PCNSL treated with HD-MTX or HD-MTX/rituximab achieved CR rates of 36% and 73% and PFS rates of 4.5 months and 26.7 months, respectively. The median OS was 16.3 months in the HD-MTX cohort and was not yet reached in the HD-MTX/R cohort [23]. In a multicenter single-arm trial, the 2-year PFS was 37.3% and the OS was 47.0% after high-dose methotrexate-based immuno-chemotherapy in elderly patients with PCNSL [3]. Our study was similar to previous studies in terms of PFS and OS, with an advantage in terms of ORR [5, 23, 24]. The TEN-based regimen was non-inferior to the high-dose MTX-based regimen as the first-line therapy for patients with newly diagnosed PCNSL. Our data indicated that TEN was an effective agent in PCNSL. The findings provided another choice for patients with newly diagnosed PCNS instead of high-dose MTX. Although only IELSG risk was associated with OS, radiotherapy as a consolidation therapy improved the PFS.

TEN was used as a main drug in our study for several reasons. It is lipophilic to cross the BB and is eliminated at a slow rate [17]. Several clinical trials showed that primary or metastatic lymphomas of the brain responded to TEN [15, 18, 25]. However, besides TEN, other drugs were also used in most clinical trials, such as fotemustine and methotrexate. Wu et al. [25] reported an ORR rate of 88% in 24 patients treated with teniposide plus fotemustine and dexamethasone, versus 84% in 25 patients treated with high-dose MTX plus cytarabine. In the European Organization for Research and Treatment of Cancer Lymphoma Group phase II trial, 52 patients with PCNSL received teniposide, methotrexate, carmustine, and methylprednisolone combined with radiotherapy; the ORR was 81%, and the 3-year OS was 58% [18]. Therefore, assessing how much TEN contributed to the therapeutic efficacy of PCNSL was extremely difficult. Performing a controlled trial to investigate the efficacy and safety of TEN as the main drug of the regimen compared with high-dose MTX was necessary. In this study, we selected high-dose MTX as the control; the median PFS and OS of patients were 28.4 and 31 months, respectively, consistent with the previous findings [5, 12, 23]. Although no significant differences were found in either ORR or long-term survival rates between both cohorts, our findings suggested that TEN was an effective treatment option for patients with newly diagnosed PCNSL.

Although the combination of HD-MTX-based chemotherapy followed by consolidative WBRT is still commonly used, the role of whole-brain radiotherapy after induction chemotherapy is controversial. G-PCNSL-SG-1 [9], a phase III, randomized, non-inferiority trial showed no statistically significant improvement in PFS with WBRT in patients with newly diagnosed PCNSL who achieved CR after HD-MTX chemotherapy (median PFS 18.3 vs 11.9 months, P = 0.14), but omitting WBRT might not be associated with inferior OS (median OS 32.4 vs 37.1 months, HR 1.06). A similar result was obtained in another retrospective research of 103 patients with PCNSL [26]. However, delayed neurotoxicity limited the acceptance of consolidative WBRT as a standard therapy, particularly in patients aged more than 60 years [27]. In a multicenter phase II trial, R-MPV (rituximab, HD-MTX, procarbazine, and vincristine) combined with consolidated reduced-dose WBRT and cytarabine was associated with high response rates, long-term disease control, and minimal neurotoxicity [6]. However, whether chemotherapy or low-dose WBRT contributed to the underlying cause of these results was unclear. To answer this question, the ongoing RTOG 11–14 trial (NCT05011045.) was conducted to explore the impact of consolidative WBRT. In our study, deferred WBRT improved PFS, but not OS. This could be clinically relevant in terms of lower incidence of neurotoxicity.

Whether intravenous rituximab accumulated sufficiently in the CNS to exert an effect was debatable. Holdhoff et al. [23] reported a CR rate of 36% in the HD-MTX cohort and 73% in the HD-MTX/rituximab cohort, with a median PFS of 4.5 months in the HD-MTX cohort and 26.7 months in the HD-MTX/rituximab cohort. The IELSG32 trial showed that the addition of thiotepa and rituximab to high-dose antimetabolites significantly improved ORR, PFS, and OS [28]. However, in a meta-analysis of randomized controlled trials, rituximab in combination with methotrexate-based chemotherapy did not improve OS in immunocompetent patients with newly diagnosed PCNSL [29, 30]. Therefore, the use of rituximab in PCNSL remains a controversial issue, and whether it has a positive impact on patient outcomes remains uncertain. According to the conflicting results in the literature, adding rituximab to treatment protocols of PCNSL (MTX, TEN, MBVP, etc.…) is still debatable. In our study, the addition of rituximab to HD-MTX or teniposide did not cause any significant difference in PFS and OS between the two cohorts of patients.

Nearly half of the patients with PCNSL are aged > 60 years, with 1 tenth of these aged ≥ 80 years [31]. Despite higher methotrexate relative dose intensity (MTX-RDI > 0.75 or not) [32], severe nephrotoxicity caused by MTX cannot be ignored. Whether elderly patients with PCNSL need to receive the same doses of MTX as younger patients remains uncertain [33]. However, no appropriate alternative choice is available for patients with newly diagnosed PCNSL. The data of our study indicated that the toxicity was acceptable and similar between HD-MTX and TEN cohorts. Although no severe renal damage occurred in the HD-MTX cohort, nephrotoxicity remained a concern in the real-life practice.

Our study had a few limitations. It had intrinsic limitations given that it was a retrospective analysis. Also, the radiology review was not done in a blinded manner. Although the survival in the MTX cohort was similar to the published findings [23], the time interval in this study was nearly 10 years, and rituximab was added more recently. Our retrospective analysis included all patients who had received at least 1 cycle of treatment irrespective of their baseline performance status. More than 40% of patients in both cohorts had an ECOG score of 3–4, which was a known prognostic factor in PCNSL [22, 34, 35]. The trial protocol allowed each participating institution to choose whether to administer high-dose chemotherapy followed by ASCT or whole-brain radiotherapy to patients after induction chemotherapy, which might impair comparability between the two cohorts. Finally, as our study is a retrospective, multicenter study, there is an imbalance in the decision of using MTX or teniposide among different research centers due to differences in policies or the experience of clinician.

In conclusion, the findings of this study indicated that TEN was well tolerated and effective in patients with PCNSL and could be used as an alternative to HD-MTX in patients who could not afford the risk of side effects. These findings should be confirmed in a prospective, randomized, controlled trial. In addition, further large-sample studies with longer follow-up are required to investigate the regimen of TEN combined with other drugs.

Availability of data and materials

All data generated or analysed during this study are included in this published article.

Abbreviations

ASCT:

Autologous hematopoietic stem cell transplantation

BBB:

Blood–brain barrier

BSA:

Body surface area

CI:

Confidence interval

CNS:

Central nervous system

CR:

Complete response

CSF:

Cerebrospinal fluid

DVT:

Deep-vein thrombosis

ECOG:

Eastern Cooperative Oncology Group

EORTC:

European Organization for Research and Treatment of Cancer Lymphoma Group

HD-MTX:

High-dose methotrexate

HR:

Hazard ratio

IELSG:

International Extranodal Lymphoma Study Group

LDH:

Lactate dehydrogenase

MTX:

Methotrexate

OS:

Overall survival

PCNSL:

Primary central nervous system lymphoma

PFS:

Progression-free survival

PD:

Progressive disease

PR:

Partial response

SCT:

Stem cell transplantation

SD:

Stable disease

TEN:

Teniposide

UVA:

Univariate analyses

WBRT:

Whole-brain radiotherapy

References

  1. Villano JL, Koshy M, Shaikh H, Dolecek TA, McCarthy BJ. Age, gender, and racial differences in incidence and survival in primary CNS lymphoma. Br J Cancer. 2011;105:1414–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Ferreri AJ, Reni M, Foppoli M, Martelli M, Pangalis GA, Frezzato M, et al. High-dose cytarabine plus high-dose methotrexate versus high-dose methotrexate alone in patients with primary CNS lymphoma: a randomised phase 2 trial. Lancet. 2009;374:1512–20.

    Article  CAS  PubMed  Google Scholar 

  3. Zeremski V, Koehler M, Fischer T, Schalk E. Characteristics and outcome of patients with primary CNS lymphoma in a “real-life” setting compared to a clinical trial. Ann Hematol. 2016;95:793–9.

    Article  CAS  PubMed  Google Scholar 

  4. Batchelor TT. Primary central nervous system lymphoma. Hematology Am Soc Hematol Educ Program. 2016;2016:379–85.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Rubenstein JL, Hsi ED, Johnson JL, Jung SH, Nakashima MO, Grant B, et al. Intensive chemotherapy and immunotherapy in patients with newly diagnosed primary CNS lymphoma: CALGB 50202 (Alliance 50202). J Clin Oncol. 2013;31:3061–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Morris PG, Correa DD, Yahalom J, Raizer JJ, Schiff D, Grant B, et al. Rituximab, methotrexate, procarbazine, and vincristine followed by consolidation reduced-dose whole-brain radiotherapy and cytarabine in newly diagnosed primary CNS lymphoma: final results and long-term outcome. J Clin Oncol. 2013;31:3971–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Houillier C, Ghesquieres H, Chabrot C, Soussain C, Ahle G, Choquet S, et al. Rituximab, methotrexate, procarbazine, vincristine and intensified cytarabine consolidation for primary central nervous system lymphoma (PCNSL) in the elderly: a LOC network study. J Neurooncol. 2017;133:315–20.

    Article  CAS  PubMed  Google Scholar 

  8. Mappa S, Marturano E, Licata G, Frezzato M, Frungillo N, Ilariucci F, et al. Salvage chemoimmunotherapy with rituximab, ifosfamide and etoposide (R-IE regimen) in patients with primary CNS lymphoma relapsed or refractory to high-dose methotrexate-based chemotherapy. Hematol Oncol. 2013;31:143–50.

    Article  CAS  PubMed  Google Scholar 

  9. Thiel E, Korfel A, Martus P, Kanz L, Griesinger F, Rauch M, et al. High-dose methotrexate with or without whole brain radiotherapy for primary CNS lymphoma (G-PCNSL-SG-1): a phase 3, randomised, non-inferiority trial. Lancet Oncol. 2010;11:1036–47.

    Article  CAS  PubMed  Google Scholar 

  10. Shah GD, Yahalom J, Correa DD, Lai RK, Raizer JJ, Schiff D, et al. Combined immunochemotherapy with reduced whole-brain radiotherapy for newly diagnosed primary CNS lymphoma. J Clin Oncol. 2007;25:4730–5.

    Article  CAS  PubMed  Google Scholar 

  11. Gavrilovic IT, Hormigo A, Yahalom J, DeAngelis LM, Abrey LE. Long-term follow-up of high-dose methotrexate-based therapy with and without whole brain irradiation for newly diagnosed primary CNS lymphoma. J Clin Oncol. 2006;24:4570–4.

    Article  CAS  PubMed  Google Scholar 

  12. Chamberlain MC, Johnston SK. High-dose methotrexate and rituximab with deferred radiotherapy for newly diagnosed primary B-cell CNS lymphoma. Neuro Oncol. 2010;12:736–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Mead GM, Bleehen NM, Gregor A, Bullimore J, Shirley D, Rampling RP, et al. A medical research council randomized trial in patients with primary cerebral non-Hodgkin lymphoma: cerebral radiotherapy with and without cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy. Cancer. 2000;89:1359–70.

    Article  CAS  PubMed  Google Scholar 

  14. Aneja R, Liu M, Yates C, Gao J, Dong X, Zhou B, et al. Multidrug resistance-associated protein-overexpressing teniposide-resistant human lymphomas undergo apoptosis by a tubulin-binding agent. Cancer Res. 2008;68:1495–503.

    Article  CAS  PubMed  Google Scholar 

  15. Wu JJ, Wang XH, Li L, Li X, Zhang L, Sun ZC, et al. Fotemustine, teniposide and dexamethasone in treating patients with CNS lymphoma. Asian Pac J Cancer Prev. 2014;15:4733–8.

    Article  PubMed  Google Scholar 

  16. Zhang Y, Liu G, Lang M, Zhang J, Geng J. Patients treatment with neuroglioma by teniposide and semustine and its influence on Twist and E-cadherin expression. Saudi Pharm J. 2016;24:299–304.

    Article  PubMed  PubMed Central  Google Scholar 

  17. van Tellingen O, Boogerd W, Nooijen WJ, Beijnen JH. The vascular compartment hampers accurate determination of teniposide penetration into brain tumor tissue. Cancer Chemother Pharmacol. 1997;40:330–4.

    Article  PubMed  Google Scholar 

  18. Poortmans PM, Kluin-Nelemans HC, Haaxma-Reiche H, Van’t Veer M, Hansen M, Soubeyran P, et al. High-dose methotrexate-based chemotherapy followed by consolidating radiotherapy in non-AIDS-related primary central nervous system lymphoma: European Organization for Research and Treatment of Cancer Lymphoma Group Phase II Trial 20962. J Clin Oncol. 2003;21:4483–8.

    Article  CAS  PubMed  Google Scholar 

  19. Wang YX, Huang Y, Xu XP, Chen BB, Lin ZG, Ma Y, et al. Curative effect of methotrexate combined with teniposide in the treatment of primary central nervous system lymphoma. Oncol Lett. 2020;19:2097–106.

    CAS  PubMed  PubMed Central  Google Scholar 

  20. Zhong KL, Xia XB, Da Y, Chen XL, Liu J, Zhang WJ, et al. Teniposide-based regimen for 16 patients with primary central nervous system lymphoma. Cancer Res Clinic. 2015;27:445–338.

    Google Scholar 

  21. Abrey LE, Batchelor TT, Ferreri AJ, Gospodarowicz M, Pulczynski EJ, Zucca E, et al. Report of an international workshop to standardize baseline evaluation and response criteria for primary CNS lymphoma. J Clin Oncol. 2005;23:5034–43.

    Article  PubMed  Google Scholar 

  22. Ferreri AJ, Blay JY, Reni M, Pasini F, Spina M, Ambrosetti A, et al. Prognostic scoring system for primary CNS lymphomas: the International Extranodal Lymphoma Study Group experience. J Clin Oncol. 2003;21:266–72.

    Article  PubMed  Google Scholar 

  23. Holdhoff M, Ambady P, Abdelaziz A, Sarai G, Bonekamp D, Blakeley J, et al. High-dose methotrexate with or without rituximab in newly diagnosed primary CNS lymphoma. Neurology. 2014;83:235–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Fritsch K, Kasenda B, Schorb E, Hau P, Bloehdorn J, Mohle R, et al. High-dose methotrexate-based immuno-chemotherapy for elderly primary CNS lymphoma patients (PRIMAIN study). Leukemia. 2017;31:846–52.

    Article  CAS  PubMed  Google Scholar 

  25. Wu J, Duan L, Zhang L, Sun Z, Fu X, Li X, et al. Fotemustine, teniposide and dexamethasone versus high-dose methotrexate plus cytarabine in newly diagnosed primary CNS lymphoma: a randomised phase 2 trial. J Neurooncol. 2018;140:427–34.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Chan H, Moraes FY, Berlin A, Crump M, Mason W, Laperriere N, et al. Significance of treatment response when managing patients with primary central nervous system lymphoma. Leuk Lymphoma. 2019;60:349–57.

    Article  PubMed  Google Scholar 

  27. Kasenda B, Loeffler J, Illerhaus G, Ferreri AJ, Rubenstein J, Batchelor TT. The role of whole brain radiation in primary CNS lymphoma. Blood. 2016;128:32–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Ferreri AJ, Cwynarski K, Pulczynski E, Ponzoni M, Deckert M, Politi LS, et al. Chemoimmunotherapy with methotrexate, cytarabine, thiotepa, and rituximab (MATRix regimen) in patients with primary CNS lymphoma: results of the first randomisation of the International Extranodal Lymphoma Study Group-32 (IELSG32) phase 2 trial. Lancet Haematol. 2016;3:e217–27.

    Article  PubMed  Google Scholar 

  29. Schmitt AM, Herbrand AK, Fox CP, Bakunina K, Bromberg JEC, Cwynarski K, et al. Rituximab in primary central nervous system lymphoma-A systematic review and meta-analysis. Hematol Oncol. 2019;37:548–57.

    Article  CAS  PubMed  Google Scholar 

  30. Bromberg JEC, van der Meulen M, Doorduijn JK. The Role of Rituximab in Primary Central Nervous System Lymphoma. Curr Oncol Rep. 2020;22:78.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Mendez JS, Ostrom QT, Gittleman H, Kruchko C, DeAngelis LM, Barnholtz-Sloan JS, et al. The elderly left behind-changes in survival trends of primary central nervous system lymphoma over the past 4 decades. Neuro Oncol. 2018;20:687–94.

    Article  PubMed  Google Scholar 

  32. Martinez-Calle N, Poynton E, Alchawaf A, Kassam S, Horan M, Rafferty M, et al. Outcomes of older patients with primary central nervous system lymphoma treated in routine clinical practice in the UK: methotrexate dose intensity correlates with response and survival. Br J Haematol. 2020;190:394–404.

    Article  CAS  PubMed  Google Scholar 

  33. Tempaku A, Takahashi Y, Kamada H. Therapeutic outcomes and toxicity of high-dose methotrexate-based chemotherapy for elderly patients with primary central nervous system lymphoma: a report on six cases. Acta Haematol. 2019;142:190–2.

    Article  PubMed  Google Scholar 

  34. Abrey LE, Ben-Porat L, Panageas KS, Yahalom J, Berkey B, Curran W, et al. Primary central nervous system lymphoma: the Memorial Sloan-Kettering Cancer Center prognostic model. J Clin Oncol. 2006;24:5711–5.

    Article  PubMed  Google Scholar 

  35. Jahr G, Broi MD, Holte H Jr, Beiske K, Meling TR. Evaluation of Memorial Sloan-Kettering Cancer Center and International Extranodal Lymphoma Study Group prognostic scoring systems to predict Overall Survival in intracranial Primary CNS lymphoma. Brain Behav. 2018;8:e00928.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

The authors thank all patients who participated in this study. They also acknowledge the cooperation of all members from the Lymphoma Group of Chinese Geriatric Oncology Society.

Funding

This work was supported by the Research and Cultivation Fund of Capital Medical University (PYZ21157); Institutional Grant of Beijing Shijitan Hospital, Capital Medical University (2017-c04); Capital’s Funds for Health Improvement and Research (2018–1-2151).

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Authors

Contributions

KZ, YS, YG, HZ, MZ, QZ, XC, MX, YQ, YZ, LZ, RL, NW, YX, YY, AL, HB, JW, BC, WZ, and WJ Z carried out the studies, participated in collecting data, and drafted the manuscript. KZ, YS, WZ and WJ Z performed the statistical analysis and participated in its design. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Kaili Zhong or Weijing Zhang.

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Ethics approval and consent to participate

The study was conducted in accordance with the Declaration of Helsinki. The scientific research project was approved by the Scientific Research Ethics Committee of Beijing Shijitan Hospital, Capital Medical University (# Research Ethics Review of 2019 No. (56)). Informed consent was waived by the Scientific Research Ethics Committee of Beijing Shijitan Hospital, Capital Medical University due to the retrospective nature of the study.

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Not applicable.

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The authors declare no competing interests.

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Zhong, K., Shi, Y., Gao, Y. et al. First-line induction chemotherapy with high-dose methotrexate versus teniposide in patients with newly diagnosed primary central nervous system lymphoma: a retrospective, multicenter cohort study. BMC Cancer 23, 746 (2023). https://doi.org/10.1186/s12885-023-11268-5

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