Novel Treatment Options in Metastatic Esophageal Carcinoma: Checkpoint Inhibitors in Combination Therapies

被引:3
作者
Casari, Capucine [1 ,2 ]
Novysedlak, Rene [2 ,3 ]
Vachtenheim, Jiri, Jr. [2 ,3 ]
Lischke, Robert [2 ,3 ]
Strizova, Zuzana [2 ,4 ]
机构
[1] Charles Univ Prague, Fac Med 2, Prague, Czech Republic
[2] Univ Hosp Motol, Prague, Czech Republic
[3] Charles Univ Prague, Fac Med 1, Dept Surg 3, Prague, Czech Republic
[4] Charles Univ Prague, Fac Med 2, Dept Immunol, Prague, Czech Republic
关键词
Esophageal carcinoma; Anti-PD1; Anti-PD-L1; Anti-CTLA-4; Chemotherapy; Targeted therapy; Immunotherapy; SQUAMOUS-CELL CARCINOMA; RESECTED ESOPHAGEAL; RADIATION-THERAPY; SINGLE-ARM; CANCER; BLOCKADE; RADIOTHERAPY; FUTURE; IMMUNOTHERAPY; PEMBROLIZUMAB;
D O I
10.1159/000527697
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Metastatic esophageal carcinoma (EC) has a poor prognosis and only limited treatment options. While immune checkpoint inhibitors (ICIs) have improved the treatment of a broad spectrum of cancers, patients with EC mostly fail to respond to this treatment. For that reason, it is crucial to understand the immune phenotype of each cancer patient and moreover, to understand how different therapies modulate the cancer microenvironment and sensitize the tumors to the treatment with ICIs. Summary: We have conducted a systematic review of the literature to evaluate the potential of ICI therapy in combination with chemotherapy, radiotherapy, and/or biologic therapy in EC patients. In our review, we have discussed the effects of diverse treatment approaches on the tumor microenvironment of EC. In addition, we have reviewed the current phase II and III clinical trials in EC patients to provide a rationale for immunotherapy application in combination settings with chemotherapy, radiotherapy, and/or biologic therapy. Key Messages: A great effort is already underway in clinical trials evaluating the combinatorial administration of ICIs and other treatment modalities in metastatic EC patients. PD-L1 expression status was shown to be higher in the squamous cell carcinoma (SCC) as compared to adenocarcinoma. Thus, ICIs plus chemotherapy are being discussed as a particularly feasible option for patients with SCC. Radiation was shown to induce the expression of immune checkpoint molecules and to promote the priming and activation of cytotoxic T cells which provides a rationale for ICI administration in a combination with radiotherapy. The combination of ICIs with biologic therapy was shown to be safe; however, the impact on the clinical outcomes of EC patients varied among studies.
引用
收藏
页码:37 / 46
页数:10
相关论文
共 109 条
[1]   Esophageal and Esophagogastric Junction Cancers, Version 2.2019 [J].
Ajani, Jaffer A. ;
D'Amico, Thomas A. ;
Bentrem, David J. ;
Chao, Joseph ;
Corvera, Carlos ;
Das, Prajnan ;
Denlinger, Crystal S. ;
Enzinger, Peter C. ;
Fanta, Paul ;
Farjah, Farhood ;
Gerdes, Hans ;
Gibson, Michael ;
Glasgow, Robert E. ;
Hayman, James A. ;
Hochwald, Steven ;
Hofstetter, Wayne L. ;
Ilson, David H. ;
Jaroszewski, Dawn ;
Johung, Kimberly L. ;
Keswani, Rajesh N. ;
Kleinberg, Lawrence R. ;
Leong, Stephen ;
Ly, Quan P. ;
Matkowskyj, Kristina A. ;
McNamara, Michael ;
Mulcahy, Mary F. ;
Paluri, Ravi K. ;
Park, Haeseong ;
Perry, Kyle A. ;
Pimiento, Jose ;
Poultsides, George A. ;
Roses, Robert ;
Strong, Vivian E. ;
Wiesner, Georgia ;
Willett, Christopher G. ;
Wright, Cameron D. ;
McMillian, Nicole R. ;
Pluchino, Lenora A. .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2019, 17 (07) :855-883
[2]   PD-1 and PD-L1 Checkpoint Signaling Inhibition for Cancer Immunotherapy: Mechanism, Combinations, and Clinical Outcome [J].
Alsaab, Hashem O. ;
Sau, Samaresh ;
Alzhrani, Rami ;
Tatiparti, Katyayani ;
Bhise, Ketki ;
Kashaw, Sushil K. ;
Iyer, Arun K. .
FRONTIERS IN PHARMACOLOGY, 2017, 8
[3]   VEGF in Signaling and Disease: Beyond Discovery and Development [J].
Apte, Rajendra S. ;
Chen, Daniel S. ;
Ferrara, Napoleone .
CELL, 2019, 176 (06) :1248-1264
[4]   Global burden of oesophageal and gastric cancer by histology and subsite in 2018 [J].
Arnold, Melina ;
Ferlay, Jacques ;
Henegouwen, Mark I. van Berge ;
Soerjomataram, Isabelle .
GUT, 2020, 69 (09) :1564-1571
[5]   Predicting the Future Burden of Esophageal Cancer by Histological Subtype: International Trends in Incidence up to 2030 [J].
Arnold, Melina ;
Laversanne, Mathieu ;
Brown, Linda Morris ;
Devesa, Susan S. ;
Bray, Freddie .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2017, 112 (08) :1247-1255
[6]   Global incidence of oesophageal cancer by histological subtype in 2012 [J].
Arnold, Melina ;
Soerjomataram, Isabelle ;
Ferlay, Jacques ;
Forman, David .
GUT, 2015, 64 (03) :381-387
[7]   Predictive biomarkers for cancer immunotherapy with immune checkpoint inhibitors [J].
Bai, Rilan ;
Lv, Zheng ;
Xu, Dongsheng ;
Cui, Jiuwei .
BIOMARKER RESEARCH, 2020, 8 (01)
[8]   First-in-human phase 1 study of margetuximab (MGAH22), an Fc-modified chimeric monoclonal antibody, in patients with HER2-positive advanced solid tumors [J].
Bang, Y. J. ;
Giaccone, G. ;
Im, S. A. ;
Oh, D. Y. ;
Bauer, T. M. ;
Nordstrom, J. L. ;
Li, H. ;
Chichili, G. R. ;
Moore, P. A. ;
Hong, S. ;
Stewart, S. J. ;
Baughman, J. E. ;
Lechleider, R. J. ;
Burris, H. A. .
ANNALS OF ONCOLOGY, 2017, 28 (04) :855-861
[9]  
Bang YJ, 2010, LANCET, V376, P1302
[10]   Cancer and Radiation Therapy: Current Advances and Future Directions [J].
Baskar, Rajamanickam ;
Lee, Kuo Ann ;
Yeo, Richard ;
Yeoh, Kheng-Wei .
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2012, 9 (03) :193-199