A single-arm, open-label, phase Ⅱ study investigating anti-HER2 ADC plus anti-PD-1 antibody in patients with unresectable locally advanced or metastatic BTC with HER2 overexpression.

Authors

null

Xiaofeng Chen

The First Affiliated Hospital with Nanjing Medical University, Nanjing, China;

Xiaofeng Chen , Fen Guo , Xinyi Zhang , Jinrong Qiu , Tongsen Zheng , Hong Qiu , Yitong Tian , Lanlan Pan , Jiaguang Zhang , Yizhang Chen , Haoyang Shen , Chao Wang

Organizations

The First Affiliated Hospital with Nanjing Medical University, Nanjing, China; , Department of Oncology, Suzhou Municipal Hospital, Suzhou, China; , Department of Oncology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China; , Eastern Hepatobibiary Surgery Hospital, Shanghai, China; , Harbin Medical University Cancer Hospital, Haerbin, China; , Department of Oncology, Tongji Hospital, Huazhong University of Science and Technology, China, Wuhan, China; , Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China; , Department of Oncology, The First Affiliated Hospital of Nanjing Medical University (Jiangsu Province Hospital), Nanjing, China; , Guangzhou Gloria Biosciences Co. Ltd., Beijing, China, Beijing, China;

Research Funding

No funding received
None.

Background: 1. Biliary tract cancer (BTC) accounts for 4% of all digestive tract cancers. In 2016-2020, the incidence of BTC has gradually increased worldwide. In China, gallbladder carcinoma accounted for 1.7% of all tumors and 1.9% of deaths in some regions. 2. The standard second-line treatment regimen is mFOLFOX, with an ORR of 5%, PFS of 2 months and OS of 6.2 months. Methods: This is a single-arm, open-label, phase Ⅱ study, approximately 31 patients of unresectable locally advanced or metastatic BTC with HER2 overexpression will be enrolled. Each treatment cycle is 14 days. Therapeutic regimen: Disitamab Vedotin 2.5mg/kg IV, D1, Q2W + Zimberelimab 240mg IV, D1, Q2W All patients treated until a loss of clinical benefit or unacceptable toxicity is observed by the investigator. Objective: to evaluate the efficacy and safety of Disitamab Vedotin + Zimberelima in patients with unresectable locally advanced or metastatic BTC with HER2 overexpression Disitamab Vedotin: Vedecitumab is an antibody-drug conjugate (ADC), with a humanized antibody conjugated to four tubulin inhibitor molecules (DAR=4) Zimberelimab: Zimberelimab is a fully human IgG4 monoclonal antibody that specifically binds to PD-1 molecules on the surface of lymphocytes. This drug is approved for r/r cHL and is also effective in the cervical cancer. Clinical trial information: NCT05540483.

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Abstract Details

Meeting

2023 ASCO Gastrointestinal Cancers Symposium

Session Type

Trials in Progress Poster Session

Session Title

Trials in Progress Poster Session B: Cancers of the Pancreas, Small Bowel, and Hepatobiliary Tract

Track

Pancreatic Cancer,Hepatobiliary Cancer,Neuroendocrine/Carcinoid,Small Bowel Cancer

Sub Track

Therapeutics

Clinical Trial Registration Number

NCT05540483

Citation

J Clin Oncol 41, 2023 (suppl 4; abstr TPS619)

DOI

10.1200/JCO.2023.41.4_suppl.TPS619

Abstract #

TPS619

Poster Bd #

N8

Abstract Disclosures