MAHOGANY: margetuximab combination in HER2+ unresectable/metastatic gastric/gastroesophageal junction adenocarcinoma

被引:81
作者
Catenacci, Daniel V. T. [1 ]
Rosales, Minori [2 ]
Chung, Hyun Cheol [3 ]
Yoon, Harry H. [4 ]
Shen, Lin [5 ]
Moehler, Markus [6 ]
Kang, Yoon-Koo [7 ]
机构
[1] Univ Chicago, Dept Med, Sect Hematol & Oncol, Chicago, IL 60637 USA
[2] MacroGenics Inc, Clin Res, Rockville, MD 20850 USA
[3] Univ Coll Med, Yonsei Canc Ctr, Seoul 03722, South Korea
[4] Mayo Clin, Canc Ctr, Rochester, MN 55905 USA
[5] Peking Univ Canc Hosp & Inst, Beijing 100142, Peoples R China
[6] Univ Med Ctr Mainz, D-55131 Mainz, Germany
[7] Univ Ulsan, Asan Med Ctr, Coll Med, Seoul 05505, South Korea
关键词
checkpoint inhibitor; first-line therapy; gastric cancer; gastroesophageal adenocarcinoma; gastroesophageal junction cancer; HER2; immuno-oncology; I-O combination; LAG-3; PD-1; SINGLE-ARM; CANCER; PEMBROLIZUMAB;
D O I
10.2217/fon-2020-1007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Standard-of-care, first-line therapy for patients with advanced human epidermal growth factor receptor 2 (HER2)-positive gastric/gastroesophageal junction adenocarcinoma is chemotherapy plus trastuzumab, a monoclonal antibody (mAb) targeting HER2. Margetuximab is an Fc-optimized mAb that binds HER2. Retifanlimab, a humanized IgG4 mAb, binds to PD-1 and blocks its interaction with PD-L1/2. Tebotelimab, an IgG4 kappa bispecific DART(R) molecule, binds PD-1 and lymphocyte activation gene 3 concomitantly, disrupting these nonredundant inhibitory pathways to further restore exhausted T-cell function. Here, we describe the design and rationale of the randomized, open-label, Phase II/III MAHOGANY trial evaluating margetuximab plus retifanlimab with/without chemotherapy and margetuximab plus tebotelimab with chemotherapy in first-line unresectable metastatic/locally advanced gastroesophageal junction adenocarcinoma. Primary end points include objective response rate, overall survival and safety/tolerability.
引用
收藏
页码:1155 / 1164
页数:10
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