Evidence map›Paper›PMID 41324998›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2026

Phase Ib/II Study of Zanidatamab in Combination with Tislelizumab and Chemotherapy in First-Line HER2-Positive Gastric/Gastroesophageal Junction Adenocarcinoma.

Keun-Wook Lee, Li-Yuan Bai, Minkyu Jung, Jieer Ying, Young-Hyuck Im, Do-Youn Oh, Jae Yong Cho, Sang Cheul Oh, Yee Chao, Jin Won Kim and 4 more

2 registry-linked trialsAbstract readClinical Trial, Phase IClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04276493 phase1 / phase2completednot on this map

Phase 1b/2 Study Investigating Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of Anti-HER2 Bispecific Antibody ZW25 in Combination With Chemotherapy With/Without Tislelizumab in Patients With Advanced HER2-positive Breast Cancer or Gastric/Gastroesophageal Junction Adenocarcinoma

TypeinterventionalSponsorBeiGeneRan2020 to 2024Enrolled71ConditionsBreast Cancer, Gastric Cancer, Gastroesophageal Junction CancerArmsZanidatamab, Docetaxel, Tislelizumab, Capecitabine, Oxaliplatin
NCT05152147 phase3active not recruitingnot on this map

A Randomized, Multicenter, Phase 3 Study of Zanidatamab in Combination With Chemotherapy With or Without Tislelizumab in Subjects With HER2-positive Unresectable Locally Advanced or Metastatic Gastroesophageal Adenocarcinoma (GEA)

TypeinterventionalSponsorJazz PharmaceuticalsRan2021 to 2027Enrolled920ConditionsGastric Neoplasms, Gastroesophageal Adenocarcinoma, Esophageal AdenocarcinomaArmsZanidatamab, Tislelizumab, Trastuzumab, Capecitabine, Oxaliplatin
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Keun-Wook LeeDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.ORCID 0000-0002-8491-703X
Li-Yuan BaiDivision of Hematology and Oncology, China Medical University Hospital and China Medical University, Taichung, Taiwan.ORCID 0000-0001-7739-4077
Minkyu JungDivision of Medical Oncology, Yonsei University College of Medicine, Yonsei Cancer Center, Seoul, Republic of Korea.ORCID 0000-0001-8281-3387
Jieer YingDepartment of Oncology, Zhejiang Cancer Hospital, Hangzhou, China.ORCID 0000-0001-9452-1242
Young-Hyuck ImDepartment of Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID 0000-0001-6459-8118
Do-Youn OhSeoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Integrated Major in Innovative Medical Science, Seoul National University Graduate School, Seoul, Republic of Korea.ORCID 0000-0003-1663-9901
Jae Yong ChoDepartment of Oncology, Gangnam Severance Hospital, Yonsei University Health System, Seoul, Republic of Korea.ORCID 0009-0006-2362-706X
Sang Cheul OhDepartment of Oncology, Korea University Guro Hospital, Seoul, Republic of Korea.ORCID 0000-0002-0527-6001
Yee ChaoDepartment of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.ORCID 0000-0001-5578-340X
Jin Won KimDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.ORCID 0000-0002-1357-7015
Ye ChenClinical Development, BeOne Medicines Ltd. (Beijing) Co., Ltd., Beijing, China.ORCID 0009-0007-0115-2566
Vincent LiClinical Development, BeOne Medicines Ltd. (Beijing) Co., Ltd., Beijing, China.ORCID 0000-0003-1923-5232
Shengnan ChenGlobal Statistics and Data Science, BeOne Medicines Ltd. (Shanghai) Co., Ltd., Shanghai, China.ORCID 0009-0000-8527-1464
Yoon-Koo KangDepartment of Oncology, Asan Medical Center, University of Ulsan, Seoul, Republic of Korea.ORCID 0000-0003-0783-6583

Funding

BeOne Medicines, Ltd.
6 · The paper itself

Abstract

purposeThis phase Ib/II trial (NCT04276493) assessed the antitumor activity, safety, and pharmacokinetics (PK) of zanidatamab in combination with tislelizumab and chemotherapy in patients with advanced HER2-positive (HER2+) gastric cancer/gastroesophageal junction cancer (GEJC). PATIENTS AND

methodsAdult patients with previously untreated, unresectable, locally advanced/metastatic HER2+ gastric cancer/GEJC received zanidatamab 30 mg/kg i.v. (cohort A) or zanidatamab 1800 mg i.v. (weight <70 kg)/2,400 mg i.v. (weight ≥70 kg; cohort B) once every 3 weeks (Q3W). Both cohorts received tislelizumab 200 mg i.v. once every 3 weeks and standard chemotherapy [capecitabine and oxaliplatin (CAPOX)] once every 3 weeks. Primary endpoints were investigator-assessed confirmed objective response rate (cORR) per RECIST v1.1, in addition to the frequency and severity of adverse events (AE) and serious AEs. Secondary endpoints included investigator-assessed progression-free survival (PFS), duration of response (DoR), overall survival (OS), PK, and immunogenicity of zanidatamab.

resultsAs of December 7, 2023, 33 patients (cohort A, n = 19; cohort B, n = 14) received treatment. The confirmed objective response rate was 75.8%; the median duration of response, progression-free survival, and overall survival were 23.3, 16.7, and 32.4 months, respectively. The most common treatment-related AEs (TRAEs) were diarrhea (100%), nausea (63.6%), and decreased appetite (48.5%). Treatment-related AEs of grade ≥3 were reported in 22 (66.7%) patients; diarrhea was the most common (27.3%).

conclusionsZanidatamab, in combination with tislelizumab and CAPOX, demonstrated clinically meaningful antitumor activity with a manageable safety profile as first-line therapy for patients with HER2+ gastric cancer/GEJC. These results support a further development of zanidatamab and tislelizumab with chemotherapy in this patient population in the ongoing phase III HERIZON-GEA-01 trial (NCT05152147).

Indexed as

AdenocarcinomaAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsErb-b2 Receptor Tyrosine KinasesEsophageal NeoplasmsEsophagogastric JunctionStomach NeoplasmsAdultAgedAntibodies, BispecificCapecitabineFemaleHumansMaleMiddle AgedOxaliplatinAntibodies, BispecificAntibodies, Monoclonal, HumanizedCapecitabineERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesOxaliplatintislelizumabzanidatamab

Identifiers

PMID41324998
PMCPMC12809114

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.