Immunotherapy Potentiates the Effect of Chemotherapy in Metastatic Melanoma-A Retrospective Study

被引:31
作者
Hadash-Bengad, Reut [1 ]
Hajaj, Emma [1 ]
Klein, Shiri [1 ]
Merims, Sharon [1 ]
Frank, Stephen [1 ]
Eisenberg, Galit [1 ]
Yakobson, Alexander [2 ,3 ]
Orevi, Marina [4 ]
Caplan, Nadia [5 ]
Peretz, Tamar [1 ]
Lotem, Michal [1 ]
Cohen, Jonatan E. [1 ,6 ]
机构
[1] Hebrew Univ Jerusalem, Fac Med, Hadassah Med Ctr, Sharett Inst Oncol, Jerusalem, Israel
[2] Ben Gurion Univ Negev, Soroka Univ Med Ctr, Dept Oncol, Beer Sheva, Israel
[3] Ben Gurion Univ Negev, Fac Hlth Sci, Beer Sheva, Israel
[4] Hebrew Univ Jerusalem, Fac Med, Hadassah Med Ctr, Dept Nucl Med, Jerusalem, Israel
[5] Hebrew Univ Jerusalem, Fac Med, Hadassah Med Ctr, Div Radiol & Med Imaging, Jerusalem, Israel
[6] Hadassah Med Ctr, Wohl Inst Translat Med, Jerusalem, Israel
来源
FRONTIERS IN ONCOLOGY | 2020年 / 10卷
基金
以色列科学基金会;
关键词
immune checkpoint inhibitors; malignant melanoma; chemotherapy; salvage therapy; immune-monitoring; IMMUNE CHECKPOINT INHIBITORS; SALVAGE CHEMOTHERAPY; RESPONSE RATES; SURVIVAL; AGENT;
D O I
10.3389/fonc.2020.00070
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Melanoma survival increased with targeted- and immunotherapy agents, yet most patients ultimately progress and require salvage therapy. In our experience, some progressive disease patients on immune-checkpoint inhibitors (ICIs) demonstrate deep and sustained responses to chemotherapy. We hypothesized that ICIs improve the response to subsequent chemotherapy in metastatic melanoma. We conducted a retrospective study to compare the efficacy of chemotherapy given with prior immunotherapy, to its efficacy given without it. We measured progression free survival (PFS), overall survival, and response rate. Immune-monitoring was performed on sequential peripheral blood mononuclear cell samples taken from a chemotherapy-responsive patient. The chemotherapy post-immunotherapy group (CpI) included 11 patients, the chemotherapy without prior immunotherapy (CNPI) group included 24 patients. Median PFS was 5.2 months in the CpI vs. 2.5 months in the CNPI groups; HR 0.37 [95% Confidence interval (CI) 0.144-0.983], P = 0.046. Immune-monitoring showed an increased proportion of CD8(+) cells, with elevated PD-1 and CD69 expression, while on chemotherapy, as compared with all-time points on ICIs, suggesting immune-activation. Immunotherapy potentiates the effect of chemotherapy in metastatic melanoma possibly through activation of CD8(+) T cells.
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页数:8
相关论文
共 24 条
[1]   Survival Outcomes in Patients With Previously Untreated BRAF Wild-Type Advanced Melanoma Treated With Nivolumab Therapy Three-Year Follow-up of a Randomized Phase 3 Trial [J].
Ascierto, Paolo A. ;
Long, Georgina V. ;
Robert, Caroline ;
Brady, Benjamin ;
Dutriaux, Caroline ;
Di Giacomo, Anna Maria ;
Mortier, Laurent ;
Hassel, Jessica C. ;
Rutkowski, Piotr ;
McNeil, Catriona ;
Kalinka-Warzocha, Ewa ;
Savage, Kerry J. ;
Hernberg, Micaela M. ;
Lebbe, Celeste ;
Charles, Julie ;
Mihalcioiu, Catalin ;
Chiarion-Sileni, Vanna ;
Mauch, Cornelia ;
Cognetti, Francesco ;
Ny, Lars ;
Arance, Ana ;
Svane, Inge Marie ;
Schadendorf, Dirk ;
Gogas, Helen ;
Saci, Abdel ;
Jiang, Joel ;
Rizzo, Jasmine ;
Atkinson, Victoria .
JAMA ONCOLOGY, 2019, 5 (02) :187-194
[2]   Qualitative differences between naive and memory T cells [J].
Berard, M ;
Tough, DF .
IMMUNOLOGY, 2002, 106 (02) :127-138
[3]   Immune-based mechanisms of cytotoxic chemotherapy: implications for the design of novel and rationale-based combined treatments against cancer [J].
Bracci, L. ;
Schiavoni, G. ;
Sistigu, A. ;
Belardelli, F. .
CELL DEATH AND DIFFERENTIATION, 2014, 21 (01) :15-25
[4]   5-(3,3-DIMETHYL-1-TRIAZENO)-IMIDAZOLE-4-CARBOXAMIDE (DTIC, DIC, NSC-45388) - NEW ANTITUMOR AGENT WITH ACTIVITY AGAINST MALIGNANT-MELANOMA [J].
CARTER, SK ;
FRIEDMAN, MA .
EUROPEAN JOURNAL OF CANCER, 1972, 8 (01) :85-&
[5]  
Caruso A, 1997, CYTOMETRY, V27, P71, DOI 10.1002/(SICI)1097-0320(19970101)27:1<71::AID-CYTO9>3.0.CO
[6]  
2-O
[7]   Vemurafenib in patients with BRAFV600 mutation-positive metastatic melanoma: final overall survival results of the randomized BRIM-3 study [J].
Chapman, P. B. ;
Robert, C. ;
Larkin, J. ;
Haanen, J. B. ;
Ribas, A. ;
Hogg, D. ;
Hamid, O. ;
Ascierto, P. A. ;
Testori, A. ;
Lorigan, P. C. ;
Dummer, R. ;
Sosman, J. A. ;
Flaherty, K. T. ;
Chang, I. ;
Coleman, S. ;
Caro, I. ;
Hauschild, A. ;
McArthur, G. A. .
ANNALS OF ONCOLOGY, 2017, 28 (10) :2581-2587
[8]   Excellent response to chemotherapy post immunotherapy [J].
Dwary, Ashish D. ;
Master, Samip ;
Patel, Abhishek ;
Cole, Constance ;
Mansour, Richard ;
Mills, Glenn ;
Koshy, Nebu ;
Peddi, Prakash ;
Burton, Gary ;
Hammoud, Dalia ;
Beedupalli, Kavitha .
ONCOTARGET, 2017, 8 (53) :91795-91802
[9]   Re-evaluating the role of dacarbazine in metastatic melanoma: what have we learned in 30 years? [J].
Eggermont, AMM ;
Kirkwood, JM .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (12) :1825-1836
[10]   Immune Monitoring of Patients Treated With a Whole-Cell Melanoma Vaccine Engineered to Express 4-1 BBL [J].
Engelstein, Roni ;
Merims, Sharon ;
Eisenberg, Galit ;
Cohen, Jonathan ;
Frank, Stephen ;
Hamburger, Tamar ;
Frankenburg, Shoshana ;
Ron, Ilan ;
Isacson, Ruth ;
Grenader, Tal ;
Steinberg, Hanna ;
Cohen, Cyrille J. ;
Peretz, Tamar ;
Lotem, Michal .
JOURNAL OF IMMUNOTHERAPY, 2016, 39 (08) :321-328