High number of CD45RO+ tumor infiltrating lymphocytes is an independent prognostic factor in non-metastasized (stage I-IIA) esophageal adenocarcinoma
- Sandra Rauser†1,
- Rupert Langer†2,
- Sebastian Tschernitz1,
- Peter Gais1,
- Uta Jütting3,
- Marcus Feith4,
- Heinz Höfler1, 2 and
- Axel Walch1Email author
© Rauser et al; licensee BioMed Central Ltd. 2010
Received: 11 May 2010
Accepted: 5 November 2010
Published: 5 November 2010
The validation of novel prognostic indicators is of greatest interest for the management of esophageal adenocarcinoma (Barrett's cancer), particularly for non-metastasized (stage I-IIA) disease. The prognostic role of tumor infiltrating T-lymphocytes (TILs) in Barrett's cancer has not been reported so far. Here we evaluated the impact of TILs on survival, recurrence, and metastasis in Barrett's cancer, particularly in stage I-IIA patients.
The levels of the adaptive immune markers CD3, CD8, and CD45RO were analyzed by immunohistochemistry and image analysis in tissue microarrays consisting of tumor tissues of 118 patients with primary resected Barrett's cancer. The findings were correlated with clinicopathological parameters including patient outcome.
In multivariate analysis, a low density of intratumoral CD45RO+ immune cells was an independent unfavorable factor for disease-free survival in stages I-IIA patients (P = 0.004, RR = 4.7, 95% CI = 1.6-13.5) as well in the entire cohort (P = 0.048, RR = 2.0, 95% CI = 1.0-4.0). High CD3+ and CD45RO+ levels were associated with prolonged disease-free survival and overall survival as well with low recurrence rates of disease (P = 0.005 and P = 0.018, respectively). In addition, low CD3+ levels were correlated with a higher frequency of lymph node metastasis (P = 0.025).
This study demonstrates that the density of CD45RO+ TILs is an independent prognostic factor in non-metastasized (stage I-IIA) Barrett's cancer patients and indicates an important role for the adaptive immunologic microenvironment. The inclusion of CD45RO+ density may help to improve the management of stage I-IIA Barrett's cancer.
Barrett's cancer (esophageal adenocarcinoma), most frequently arising from intestinal metaplasia, has rapidly increased in incidence over the last decades, faster than any other gastrointestinal malignancy [1, 2]. Despite advances in the therapy of locally advanced tumors with multimodal treatment strategies including neoadjuvant chemo- or radiochemotherapy [3–5], it still remains one of the most deadly tumors in solid oncology. Therefore, there is the need of prognostic factors for improved individualized risk stratifications, and alternative treatment options, like targeted or immunologic therapeutic approaches.
Growth regulation and progression of cancer are not only influenced by the biological behavior of the tumor but also by the host defense mechanisms. Host immunity consists of a complex network of humoral and cellular components that interact with tumor cells and tumor stroma. On the cellular level, inflammatory elements encompass dendritic cells, macrophages, granulocytes and lymphocytes. Activated, memory- and cytotoxic tumor infiltrating T-lymphocytes (TILs) are considered to be manifestations of a specific host immune reaction against cancer cells, related to the cytotoxic activity and the production of growth modulating cytokines of TIL [6, 7]. Several studies have demonstrated the presence of TILs in various solid human cancers, most recently showing the association of an abundance of CD3+, CD8+ or CD45RO+ lymphocytic tumor infiltration with a survival benefit for patients with gastric  and colorectal [9–11] cancer, as well as for patients with endometrial , cervical , ovarian [14, 15], urothelial  and hepatocellular  carcinoma and melanoma . Furthermore, it was argued that the type, density, and location of immune cells in colorectal cancer have prognostic values that are superior to and independent of those of the UICC-TNM classification [10, 19]. However, the effect of TILs in the clinical course of Barrett's cancer is largely unknown. The validation of novel prognostic indicators are therefore of greatest interest for the management of esophageal adenocarcinoma, particularly for non-metastasized (stage I-IIA) disease.
The aim of this study was to evaluate the impact of TILs on survival, recurrence, and metastasis in primary resected Barrett's cancer, particularly in non-metastasized (stage I-IIA) patients.
In total, 118 patients with adenocarcinomas of the distal esophagus [(Barrett's cancer associated with histopathologically identified Barrett's esophagus (according to WHO 2000)]  were enrolled into this study. The patients had undergone primary surgical resection without chemo- or radiotherapy at the Department of Surgery, Klinikum rechts der Isar, Technische Universität München between 1991 and 2004. For all patients formalin-fixed paraffin-embedded tissue from surgical resection was available and individual patient data including outcome were acquired with approval from the ethics committee of the Technische Universität München. All tumor tissue specimens were procured from patients giving written informed consent.
Mean age of the patients was 63.6 years (range, 33-83). Female/male ratio was 9/109. 47 tumors were UICC stage I, 18 stage IIA, 16 stage IIB, 28 stage III, and 8 stage IV. Lymph node metastases were absent in 65 cases (pN0M0) and present in 51 cases (pN1M0/1). The medium follow-up of the patients was 33 months for overall (range: 0.8 to 164 months) and 31 months for disease-free survival (range: 1.6 to 164 months).
Using a tissue microarray instrument (Beecher Instruments, Sun Prairie, Wisconsin, USA), three representative areas of each tumor (1.0 mm diameter) were removed from paraffin-embedded tissue blocks which had been prepared at the time of resection. Serial sections were cut for the purpose of immunohistochemistry and transferred to adhesive slides using the "paraffin-tape-transfer-system" according to manufacturer's instructions (Instrumedics, Hackensack, NJ, USA).
Immunohistochemical stainings for CD3, CD8, and CD45RO were carried out using an automated stainer (Ventana Discovery, Tuscon, AZ, USA) and DAB Map kit (Ventana). Monoclonal antibodies against CD3 (total T-cell marker; NeoMarkers, Fremont, CA, USA) were used in dilution at 1:100, against CD8 (cytotoxic T-cell marker; Dako, Hamburg, Germany) in dilution at 1:50 and against CD45RO (memory T-cell marker; Dako, Hamburg, Germany) in dilution at 1:1200.
Slides were analyzed with the use of an image-analysis workstation (SAMBA microscopic image processor; Meylan, France), the hardware and software of which have been first described by Brugal et al . This system is fitted with a standard orthoplan microscope (Leica, Bensheim, Germany) and a colour TV-camera (JVC (KY-F30), 3-CCD, Tokyo, Japan). T-cells were analyzed in at least 10 randomly selected high-power fields (magnification x400 with the Leica microscope). Formal scoring (labeling index) for each antibody was then performed in one section for each TMA block. A labeling index resulted from the percentage of nuclear immunopositive area in relation to the total nuclear area of infiltrative tumor cells within the tissue. For feature extraction we applied the software running on SAMBA system .
Receiver operating characteristic (ROC) analyses were done to determine cut-off levels for labeling indices of TILs (CD3, CD8, CD45RO positive lymphocytes) that correlate with clinical outcome (overall survival). The optimization of the cut-off determination was done by significance. All cases were therefore classified into low- and high-density groups for each marker, that is CD3+ low, CD8+ low, and CD45RO+ low (low-density groups) and CD3+ high, CD8+ high, and CD45RO+ high (high-density groups). Correlations between parameters were performed using the Pearson's correlation for continuous variables, and for discrete variables the Chi square test or Fisher's exact test was used. Disease-free survival and overall survival were calculated from the date of surgical resection to the date of first recurrence, death, or last follow-up and the rates were determined according to the Kaplan-Meier method. Comparisons of survival curves were made using the log-rank test and multivariate analyses were done using the stepwise Cox regression analysis. Hazard ratios (risk ratios) were calculated univariate and multivariate and listed together with the confidence intervals. P values < 0.05 were considered statistically significant in all analyses, whereas P values of 0.05 to 0.1 were considered as trend. All statistical analyses were done using the SAS (SAS Institute, Cary, NC, USA) software package.
Tumor infiltrating lymphocytes (TILs)
Immunohistochemical stainings were available for CD3 in 99 cases, for CD8 in 107 cases, and for CD45RO in 110 cases. Labeling indices of CD3+ ranged from 0.3-18.8 (mean 5.65), of CD8+ from 0.01-6.2 (mean 0.9) and of CD45RO+ levels from 0-32.1 (mean 2.1). There was a significant correlation between the TIL levels of CD3+ and CD8+ TILs (P < 0.001; r = 0.54), CD3+ and CD45RO+ TILs (P < 0.001, r = 0.4) and CD8+ and CD45RO+ TILs (P < 0.001; r = 0.53). Cut-off levels with prognostic relevance were 0.9 for CD3+, 0.5 for CD8+ and 2.0 for CD45RO+.
Correlation between clinicopathologic features and TIL density
Clinical and pathological characteristics of the patients grouped by TIL density
n = 99
n = 107
n = 110
Total number of patients
Lymph node metastasis
Recurrence of disease
CD3+ and CD45RO+ TILs as predictors of patient survival
Univariate Cox proportional regression hazard models for disease-free survival showed a relative risk (RR) of 2.39 for patients whose tumors had a low density of CD45RO+ cells (95% confidence interval [CI] = 1.28-4.46, P = 0.007) (overall survival: RR = 2.28, 95% CI = 1.19-4.35, P = 0.013). Relative risks for disease-free and overall survival for patients with low densities of CD3+ were 1.96 (95% CI = 1.13-3.39, P = 0.016) and 2.06 (95% CI = 1.18-3.61, P = 0.012), respectively.
TIL as a predictor of regional lymph node metastasis
Multivariate Cox regression analysis within the pN0-group revealed that low densities of CD45RO+ cells were independently associated with an unfavorable disease-free survival (P = 0.004, RR = 4.7, 95% CI = 1.6-13.5) (Table 2). In pN1 patients, distant metastasis was an independent prognostic factor (P = 0.002, RR = 3.6, 95% CI = 1.6-8.0).
Furthermore, the CD3+ low group showed a higher frequency of lymph node metastasis than the corresponding high group (P = 0.025) and for the CD45RO+ low group there was a trend for a higher presence of lymph node metastases (P = 0.065) (Table 1).
In this study, we analyzed the impact of tumor infiltrating lymphocytes (TILs) on survival, recurrence, and metastasis in primary resected esophageal adenocarcinoma (Barrett's cancer), particularly in stage I-IIA patients. The presence of high numbers of CD45RO+ lymphocytes was an independent predictor of increased survival particularly in non-metastasized (stage I-IIA) patients as well in the entire cohort. A high CD3+ level was further associated with prolonged survival and the absence of regional lymph node metastasis. Moreover, high infiltration levels of CD45RO+ and CD3+ T-cells were correlated with a lower rate of recurrence.
Similar observations were made in different cancer types. A study on gastric cancer demonstrated the independent prognostic value of the density of CD3+, CD8+, and CD45RO+ lymphocytes for regional lymph node metastasis and patient survival . Studies on colorectal cancer showed that TILs predict survival better than conventional anatomical staging and that a high density of CD45RO+ lymphocytes is correlated with the absence of lymphatic vessel invasion [10, 11]. In melanoma patients it was found that brisk TIL infiltration in tumor predicts sentinel lymph node metastasis  and in early-stage cervical cancer it was demonstrated that a high number of intraepithelial CD8+ lymphocytes is associated with the absence of lymph node metastasis . Also, in vivo experiments and animal models have provided data supporting the role of TILs in cancer immunosurveillance [23, 24]. Although the influence of lymphocytic infiltration has been studied in squamous cell cancer (SCC) of the esophagus [25–27], so far less information is available about the role of TILs in adenocarcinomas of the esophagus (Barrett's cancer).
To our knowledge, the current study is the first one to examine the prognostic influence of intratumoral CD3+ total T-lymphocytes, CD8+ cytotoxic T-lymphocytes, and CD45RO+ memory T-lymphocytes in a large cohort of primary resected Barrett's cancer patients (n = 118). In a previous study of a smaller series of human esophageal carcinomas (n = 70), which encompassed both squamous cell carcinomas and adenocarcinomas, the presence of a dense intratumoral CD8+ lymphocytic infiltration was associated with good prognosis independent from tumor stage and nodal stage . However, we did not find CD8+ TILs to be a prognostic factor in Barrett's cancer. A recent work with a cohort of 106 adenocarcinomas of the esophagus failed to show a prognostic influence of CD3+ and CD8+ TILs , whereas in our cohort patients benefit from a high CD3+ lymphocytic infiltration. A possible explanation may be different methods applied to quantify TILs. In the study of Schumacher et al the number of CD8+ lymphocytes was counted by fluorescence microscopy and individual cases were classified in groups according to their location and quantification . Zingg et al used high power field light microscopy and assessed the number of lymphocytes in two different locations, at the periphery and in the center of the tumors . In our study, we used tissue microarrays with core biopsies taken randomized from the tumor area and the quantification of lymphocytic infiltration was done by image analysis. This approach has been demonstrated to be representative and has been used in different types of cancer [8-10, 12, 30].
Metastatic relapse attributable to the presence of tumor cells within lymph nodes is the most frequent cause leading to cancer-related death in patients with esophageal tumors . In the current study, high levels of CD45RO+ TILs were significantly associated with improved survival in Barrett's cancer, on the one hand in the whole study cohort as well in the subgroup of non-metastasized patients. We also showed that high densities of CD45RO+ cells were an independent predictor of improved overall and disease-free survival. We found, that recurrence of disease less often occurred in the presence of high levels of CD45RO+ TILs. This observation is in line with the functional mechanism of memory T-lymphocytes, namely providing a more rapid and effective secondary immune response to previously encountered antigens . Our data suggest that CD45RO+ T-lymphocytes within esophageal adenocarcinomas function not only locally but also systemically in tumor-draining lymph nodes to suppress micrometastasis.
Our results show that the presence of intratumoral CD45RO+ T-cells is associated with the lack of tumor metastases in the lymph nodes of Barrett's cancer patients. Because the absence of lymph node metastases is strongly associated with a better prognosis, patients with high CD45RO+ lymphocyte levels are likely to display an improved clinical outcome in Barrett's cancer. CD45RO+ and CD3+ TILs within Barrett's cancer may serve as criteria for selection and monitoring of patients for adjuvant immunotherapeutic strategies and can be a reliable prognostic marker to predict favorable outcome in patient subgroups. In our study, we focused on the T-lymphocytic cellular component, but additional studies are in need to elucidate the mechanisms and potency of host immunity. This is in particular concern for the purpose of the development of potential immunomodulatory or targeted cancer therapies that are highly required for the treatment of esophageal adenocarcinoma due to its aggressive behavior and the limited success of conventional therapy regimes. Our findings may provide a basis for risk adopted tumor treatment through predicting clinical outcome and definition of patient subgroups with different prognosis. The inclusion of CD45RO+ TIL density may help to improve the prognostication of stage I-IIA Barrett's cancer. Moreover, our results may be highly valuable in the context of future promising adjuvant immunotherapy and for potential immunomodulatory targeted therapy approaches.
A. Walch acknowledges the financing support of the Deutsche Krebshilfe (108096) and the MolBioMed Programme (EndoMed 01EZ0802) of the BMBF, Germany.
We thank Ulrike Buchholz, Andrea Harwardt, Claudia-Mareike Pflüger, and Eleonore Samson for excellent technical assistance performing the laboratory work.
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