Lymphopenia combined with low TCR diversity (divpenia) predicts poor overall survival in metastatic breast cancer patients

Lymphopenia (< 1Giga/L) detected before initiation of chemotherapy is a predictive factor for death in metastatic solid tumors. Combinatorial T cell repertoire (TCR) diversity was investigated and tested either alone or in combination with lymphopenia as a prognostic factor at diagnosis for overall survival (OS) in metastatic breast cancer (MBC) patients. The combinatorial TCR diversity was measured by semi quantitative multi-N-plex PCR on blood samples before the initiation of the first line chemotherapy in a development (n = 66) and validation (n = 67) MBC patient cohorts. A prognostic score, combining lymphocyte count and TCR diversity was evaluated. Univariate and multivariate analyses of prognostic factors for OS were performed in both cohorts. Lymphopenia and severe restriction of TCR diversity called “divpenia” (diversity ≤ 33%) were independently associated with shorter OS. Lympho-divpenia combining lymphopenia and severe divpenia accurately identified patients with poor OS in both cohorts (7.6 and 10.6 vs 24.5 and 22.9 mo). In multivariate analysis including other prognostic clinical factors, lympho-divpenia was found to be an independent prognostic factor in the pooled cohort (p = 0.005) along with lack of HER2 and hormonal receptors expression (p = 0.011) and anemia (p = 0.009). Lympho-divpenia is a novel prognostic factor that will be used to improve quality of MBC patients’ medical care.

[1]  M. Morre,et al.  Interleukin-7 and immune reconstitution in cancer patients: a new paradigm for dramatically increasing overall survival , 2012, Targeted Oncology.

[2]  D. Klatzmann,et al.  Half of the T‐cell repertoire combinatorial diversity is genetically determined in humans and humanized mice , 2012, European journal of immunology.

[3]  J. Blay,et al.  Early detection of tumor cells by innate immune cells leads to T(reg) recruitment through CCL22 production by tumor cells. , 2011, Cancer research.

[4]  J. Blay,et al.  Quantitative and functional alterations of plasmacytoid dendritic cells contribute to immune tolerance in ovarian cancer. , 2011, Cancer research.

[5]  Ian O Ellis,et al.  Tumor-infiltrating CD8+ lymphocytes predict clinical outcome in breast cancer. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[6]  J. Castillo,et al.  Lymphopenia and breast cancer subtypes as prognostic factors in patients with locally advanced breast cancer. , 2011, Journal of Clinical Oncology.

[7]  Yuan Zhang,et al.  Normalization of T cell receptor repertoire diversity in patients with advanced colorectal cancer who responded to chemotherapy , 2011, Cancer science.

[8]  G. Thibault,et al.  Pre-treatment lymphopenia as a prognostic biomarker in colorectal cancer patients receiving chemotherapy , 2011, Cancer Chemotherapy and Pharmacology.

[9]  J. Wolchok,et al.  Anti-CTLA-4 antibody therapy: immune monitoring during clinical development of a novel immunotherapy. , 2010, Seminars in oncology.

[10]  P. Natali,et al.  Dacarbazine treatment before peptide vaccination enlarges T-cell repertoire diversity of melan-a-specific, tumor-reactive CTL in melanoma patients. , 2010, Cancer research.

[11]  D. Schadendorf,et al.  Improved survival with ipilimumab in patients with metastatic melanoma. , 2010, The New England journal of medicine.

[12]  S. Maiella,et al.  In vivo expansion of naive and activated CD4+CD25+FOXP3+ regulatory T cell populations in interleukin-2–treated HIV patients , 2010, Proceedings of the National Academy of Sciences.

[13]  D. Klatzmann,et al.  High diversity of the immune repertoire in humanized NOD.SCID.γc−/− mice , 2009, European journal of immunology.

[14]  J. Blay,et al.  Lymphopenia as a prognostic factor for overall survival in advanced carcinomas, sarcomas, and lymphomas. , 2009, Cancer research.

[15]  C. Rouzioux,et al.  Enhanced T cell recovery in HIV-1-infected adults through IL-7 treatment. , 2009, The Journal of clinical investigation.

[16]  J. Blay,et al.  Regulatory T cells recruited through CCL22/CCR4 are selectively activated in lymphoid infiltrates surrounding primary breast tumors and lead to an adverse clinical outcome. , 2009, Cancer research.

[17]  M. Leal,et al.  Thymopoiesis in elderly human is associated with systemic inflammatory status , 2009, AGE.

[18]  D. Venzon,et al.  Administration of rhIL-7 in humans increases in vivo TCR repertoire diversity by preferential expansion of naive T cell subsets , 2008, The Journal of experimental medicine.

[19]  W. Tan,et al.  Functional polymorphisms in FAS and FASL contribute to increased apoptosis of tumor infiltration lymphocytes and risk of breast cancer , 2006 .

[20]  Alison A Motsinger,et al.  Immunogenetics of CD4 lymphocyte count recovery during antiretroviral therapy: An AIDS Clinical Trials Group study. , 2006, The Journal of infectious diseases.

[21]  T. Gingeras,et al.  CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4+ T reg cells , 2006, The Journal of experimental medicine.

[22]  Howard I. Grossman AIDS at 25: a quarter century of medical miracles. , 2006, MedGenMed : Medscape general medicine.

[23]  A. Qattan,et al.  The B7-H1 (PD-L1) T lymphocyte-inhibitory molecule is expressed in breast cancer patients with infiltrating ductal carcinoma: correlation with important high-risk prognostic factors. , 2006, Neoplasia.

[24]  J. Blay,et al.  CD4 lymphopenia as a risk factor for febrile neutropenia and early death after cytotoxic chemotherapy in adult patients with cancer , 2004, Cancer.

[25]  J. Blay,et al.  Dendritic Cell Infiltration and Prognosis of Early Stage Breast Cancer , 2004, Clinical Cancer Research.

[26]  J. Blay,et al.  Baseline and early lymphopenia predict for the risk of febrile neutropenia after chemotherapy , 2003, British Journal of Cancer.

[27]  Jacques Demongeot,et al.  Quantitative and Qualitative Changes in V-J α Rearrangements During Mouse Thymocytes Differentiation , 2002, The Journal of Experimental Medicine.

[28]  G Rassner,et al.  Metastatic pathways and time courses in the orderly progression of cutaneous melanoma , 2002, The British journal of dermatology.

[29]  J. Demongeot,et al.  Quantitative and qualitative changes in V-J alpha rearrangements during mouse thymocytes differentiation: implication for a limited T cell receptor alpha chain repertoire. , 2002, The Journal of experimental medicine.

[30]  J. Blay,et al.  Identification of patients at risk for early death after conventional chemotherapy in solid tumours and lymphomas , 2001, British Journal of Cancer.

[31]  M. Lotze,et al.  Decreased zeta chain expression and apoptosis in CD3+ peripheral blood T lymphocytes of patients with melanoma. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.

[32]  D. Schatz,et al.  Factors and forces controlling V(D)J recombination. , 2001, Advances in immunology.

[33]  J. Blay,et al.  Inhibition of the differentiation of dendritic cells from CD34(+) progenitors by tumor cells: role of interleukin-6 and macrophage colony-stimulating factor. , 1998, Blood.

[34]  C. Copie-Bergman,et al.  CD3 hyporesponsiveness and in vitro apoptosis are features of T cells from both malignant and nonmalignant secondary lymphoid organs. , 1998, The Journal of clinical investigation.

[35]  J. Blay,et al.  A risk model for thrombocytopenia requiring platelet transfusion after cytotoxic chemotherapy. , 1998, Blood.

[36]  C. Katlama,et al.  Perturbation of CD4+ and CD8+ T-cell repertoires during progression to AIDS and regulation of the CD4+ repertoire during antiviral therapy , 1998, Nature Medicine.

[37]  C. Mackall,et al.  Constraints on CD4 recovery postchemotherapy in adults: thymic insufficiency and apoptotic decline of expanded peripheral CD4 cells. , 1997, Blood.

[38]  J. Blay,et al.  Early lymphopenia after cytotoxic chemotherapy as a risk factor for febrile neutropenia. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[39]  P. Rosenberg,et al.  Determining the value of additional surrogate exposure data for improving the estimate of an odds ratio. , 1995, Statistics in medicine.

[40]  A. Shad,et al.  Lymphocyte depletion during treatment with intensive chemotherapy for cancer. , 1994, Blood.

[41]  C. C. Chen,et al.  The bootstrap and identification of prognostic factors via Cox's proportional hazards regression model. , 1985, Statistics in medicine.

[42]  S. Tonegawa,et al.  Somatic generation of antibody diversity. , 1976, Nature.