Immunotherapy-based combinations: an update

被引:23
作者
Fuca, Giovanni [1 ]
de Braud, Filippo [1 ,2 ]
Di Nicola, Massimo [1 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Med Oncol Dept, Milan, Italy
[2] Univ Milan, Dept Oncol & Hematooncol, Milan, Italy
关键词
cancer immunotherapy; immune checkpoint inhibitors; immunotherapy combinations; CELL LUNG-CANCER; CLINICAL ACTIVITY; PHASE-I; IMMUNE CHECKPOINTS; PLUS IPILIMUMAB; OPEN-LABEL; BEVACIZUMAB; PEMBROLIZUMAB; RADIOTHERAPY; ATEZOLIZUMAB;
D O I
10.1097/CCO.0000000000000466
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose of reviewThe advent of immunotherapy significantly improved clinical outcomes in cancer patients, although immune checkpoint blockade (ICB) still lack of efficacy in a consistent proportion of treated patients. The purpose of this article is to review the most innovative and clinically promising ICB-based combinations designed to improve the efficacy of cancer immunotherapy.Recent findingsFirst-line combinatorial treatment with ipilimumab and nivolumab has recently shown to be superior to the standard of care in a subset of metastatic nonsmall cell lung cancer (NSCLC) and renal cell carcinoma (RCC). The combination of programmed cell death protein 1 (PD-1)/PD-L1 blockade with antiangiogenics has demonstrated a consistent clinical efficacy, especially for the combination of bevacizumab and atezolizumab as first-line therapy in metastatic RCC. The sequential combination of definitive chemoradiotherapy followed by durvalumab maintenance in advanced, unresectable NSCLC became the new standard of care, while the addition of pembrolizumab to first-line chemotherapy in metastatic NSCLC significantly improves overall survival. Despite promising results for the combination of ICBs with v-raf murine sarcoma viral oncogene homolog B/MAPK/ERK kinase inhibitors or epidermal growth factor receptor inhibitors, especially in melanoma and NSCLC, safety concerns slowed down the development of such strategies.SummaryImmunotherapy-based combinations are becoming the standard of care for cancer treatment, in particularly for advanced melanoma, NSCLC and RCC.
引用
收藏
页码:345 / 351
页数:7
相关论文
共 77 条
[1]
Phase Ib trial of atezolizumab in combination with nab-paclitaxel in patients with metastatic triple negative breast cancer (mTNBC). [J].
Adams, Sylvia ;
Diamond, Jennifer Robinson ;
Hamilton, Erika Paige ;
Pohlmann, Paula Raffin ;
Tolaney, Sara M. ;
Molinero, Luciana ;
He, Xian ;
Waterkamp, Daniel ;
Funke, Roel Peter ;
Powderly, John D. .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
[2]
Osimertinib combined with durvalumab in EGFR-mutant non-small cell lung cancer: Results from the TATTON phase Ib trial [J].
Ahn, M. -J. ;
Yang, J. ;
Yu, H. ;
Saka, H. ;
Ramalingam, S. ;
Goto, K. ;
Kim, S. -W. ;
Yang, L. ;
Walding, A. ;
Oxnard, G. R. .
JOURNAL OF THORACIC ONCOLOGY, 2016, 11 (04) :S115-S115
[3]
Chemotherapeutic Targeting of Cancer-Induced Immunosuppressive Cells [J].
Alizadeh, Darya ;
Larmonier, Nicolas .
CANCER RESEARCH, 2014, 74 (10) :2663-2668
[4]
Phase II study of vemurafenib followed by ipilimumab in patients with previously untreated BRAF-mutated metastatic melanoma [J].
Amin, Asim ;
Lawson, David H. ;
Salama, April K. S. ;
Koon, Henry B. ;
Guthrie, Troy, Jr. ;
Thomas, Sajeve S. ;
O'Day, Steven J. ;
Shaheen, Montaser F. ;
Zhang, Bin ;
Francis, Stephen ;
Hodi, F. Stephen .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2016, 4
[5]
Lag-3, Tim-3, and TIGIT: Co-inhibitory Receptors with Specialized Functions in Immune Regulation [J].
Anderson, Ana C. ;
Joller, Nicole ;
Kuchroo, Vijay K. .
IMMUNITY, 2016, 44 (05) :989-1004
[6]
[Anonymous], 2015, J CLIN ONCOL S
[7]
[Anonymous], 2017, P AM SOC CLIN ON S15
[8]
[Anonymous], J CLIN ONCOL S15
[9]
[Anonymous], 2016, J CLIN ONCOL, DOI DOI 10.1200/JCO.2016.34.2_SUPPL.559
[10]
Durvalumab after Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer [J].
Antonia, S. J. ;
Villegas, A. ;
Daniel, D. ;
Vicente, D. ;
Murakami, S. ;
Hui, R. ;
Yokoi, T. ;
Chiappori, A. ;
Lee, K. H. ;
de Wit, M. ;
Cho, B. C. ;
Bourhaba, M. ;
Quantin, X. ;
Tokito, T. ;
Mekhail, T. ;
Planchard, D. ;
Kim, Y. -C. ;
Karapetis, C. S. ;
Hiret, S. ;
Ostoros, G. ;
Kubota, K. ;
Gray, J. E. ;
Paz-Ares, L. ;
de Castro Carpeno, J. ;
Wadsworth, C. ;
Melillo, G. ;
Jiang, H. ;
Huang, Y. ;
Dennis, P. A. ;
Ozguroglu, M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (20) :1919-1929