Effect of SHR-1701 on chemotherapy (chemo)-induced myelosuppression: Data from a phase 3 study in HER2-negative gastric/gastroesophageal junction adenocarcinoma (G/GEJA).

Z Zhi Peng (Beijing Key Laboratory of Cell and Gene Therapy for Solid Tumor, State Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Beijing Key Laboratory of Carcinogenesis and Translational Research, Department of Gastrointestinal Oncology, Peking University Cancer Hospital and Institute, Beijing, China) J Jufeng Wang (Henan Cancer Hospital, Zhengzhou, China) Y Yanqiao Zhang H Hongli Li (Key Laboratory of Genetic Evolution and Animal Models of the Chinese Academy of Sciences, Key Laboratory of Animal Models and Human Disease Mechanisms of Yunnan Province, and Kunming Institute of Zoology and Chinese University of Hong Kong Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming Institute of Zoology, Chinese Academy of Sciences) Q Qun Zhao (State Key Laboratory of Medical Proteomics, National Chromatographic Research & Analysis Center, Chinese Academy of Sciences Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences) X Xiaodong Zhu S Shaozhong Wei (Department of Gastrointestinal Surgery, Hubei Cancer Hospital, Wuhan, China) Y Ying Cheng (Institute of Biomedical Research, Yunnan University) K Kangsheng Gu (The First Affiliated Hospital of Anhui Medical University, Hefei, China) J Jun Bai Y Yigui Chen (Fujian Provincial Cancer Hospital, Fuzhou, China) Z Zhongtao Zhang J Jun Zhang J Junsheng Wang Z Zuoxing Niu Y Yueyin Pan Z Zhigao Wang (Center for Regenerative Medicine, Heart Institute, Department of Internal Medicine, Morsani College of Medicine, University of South Florida) W Wenliang Wang H Hongxia Han (Jiangsu Hengrui Pharmaceuticals Co., Ltd., Shanghai, China) L Lin Shen

Abstract

335 Background: Blocking TGF-β signaling has the potential to facilitate the recovery from chemo-induced myelosuppression. SHR-1701 is a bifunctional agent targeting PD-L1 and TGF-β. Methods: In the multicenter, randomized, double-blind phase 3 study (NCT04950322), SHR-1701 plus CAPOX demonstrated a statistically significant and clinically meaningful benefit in OS compared with placebo plus CAPOX in patients (pts) with previously untreated, unresectable locally advanced or metastatic HER2-negative G/GEJA (ESMO 2024, LBA60). Here, we reported the effect of SHR-1701 on chemo-associated myelosuppression. Results: In total, 364 and 366 pts in the SHR-1701 and placebo arm received assigned treatment. As of May 20, 2024, with a KM estimated median follow-up of 13.6 mo, all study medications showed similar exposure duration between the two arms (Table). Occurrence of treatment-related adverse events was generally comparable (any grade, 97.8% in SHR-1701 arm vs 98.4% in placebo arm; grade ≥3, 62.6% vs 59.0%). SHR-1701 reduced the incidence of any grade decreased platelet count, decreased neutrophil count, and decreased white blood cell count by 8.7%, 10.1%, and 11.2%, and for grade ≥3, by 9.1%, 4.3%, and 1.6%, respectively (Table). Compared with the placebo arm, less pts in the SHR-1701 arm used platelet growth factors (30.2% vs 42.9%) and white blood cell growth factors (32.7% vs 39.6%). Conclusions: SHR-1701 showed the capacity to suppress chemo-associated myelosuppression. Clinical trial information: NCT04950322 . Safety. SHR-1701 plus CAPOX(N=364) Placebo plus CAPOX(N=366) Treatment difference (SHR-1701 vs placebo) Treatment exposure (day), median (IQR) SHR-1701/placebo 137.0 (65.5-251.5) 127.5 (62.0-190.0) NA Capecitabine 122.0 (83.0-138.0) 122.0 (73.5-135.0) NA Oxaliplatin 107.0 (66.0-123.0) 108.5 (64.0-121.0) NA Treatment-related hematological toxicities, n (%) or % Any grade Grade ≥ 3 Any grade Grade ≥ 3 Any grade Grade ≥ 3 Platelet count decreased 217 (59.6%) 69 (19.0%) 250 (68.3%) 103 (28.1%) -8.7% -9.1% Neutrophil count decreased 163 (44.8%) 44 (12.1%) 201 (54.9%) 60 (16.4%) -10.1% -4.3% White blood cell count decreased 147 (40.4%) 13 (3.6%) 189 (51.6%) 19 (5.2%) -11.2% -1.6%

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 335-335
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

Z

Zhi Peng

Beijing Key Laboratory of Cell and Gene Therapy for Solid Tumor, State Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Beijing Key Laboratory of Carcinogenesis and Translational Research, Department of Gastrointestinal Oncology, Peking University Cancer Hospital and Institute, Beijing, China

J

Jufeng Wang

Henan Cancer Hospital, Zhengzhou, China

Y

Yanqiao Zhang

H

Hongli Li

Key Laboratory of Genetic Evolution and Animal Models of the Chinese Academy of Sciences, Key Laboratory of Animal Models and Human Disease Mechanisms of Yunnan Province, and Kunming Institute of Zoology and Chinese University of Hong Kong Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming Institute of Zoology, Chinese Academy of Sciences

Q

Qun Zhao

State Key Laboratory of Medical Proteomics, National Chromatographic Research & Analysis Center, Chinese Academy of Sciences Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences

X

Xiaodong Zhu

S

Shaozhong Wei

Department of Gastrointestinal Surgery, Hubei Cancer Hospital, Wuhan, China

Y

Ying Cheng

Institute of Biomedical Research, Yunnan University

K

Kangsheng Gu

The First Affiliated Hospital of Anhui Medical University, Hefei, China

J

Jun Bai

Y

Yigui Chen

Fujian Provincial Cancer Hospital, Fuzhou, China

Z

Zhongtao Zhang

J

Jun Zhang

J

Junsheng Wang

Z

Zuoxing Niu

Y

Yueyin Pan

Z

Zhigao Wang

Center for Regenerative Medicine, Heart Institute, Department of Internal Medicine, Morsani College of Medicine, University of South Florida

W

Wenliang Wang

H

Hongxia Han

Jiangsu Hengrui Pharmaceuticals Co., Ltd., Shanghai, China

L

Lin Shen