Evidence map›Paper›PMID 42129335›Full record

ArticleNPJ precision oncology2026

A Phase II study of SHR-A1921, a TROP2-targeted antibody-drug conjugate, in patients with recurrent or metastatic salivary gland carcinoma.

Guang-Liang Chen, Yanjing Guo, Ya'nan Yang, Youzhou Sang, Si Sun, Xin Liu, Xin Zhou, Chun-Ying Sheng, Xiayun He, Jianfei Wang and 4 more

Registry-linked trialAbstract read
In one paragraph

Article in NPJ precision oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05924256 (A Phase II Study of Advanced Salivary Gland Carcinoma Based on Molecular Typing), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT05924256 phase2active not recruitingnot on this map

A Phase II Study of Advanced Salivary Gland Carcinoma Based on Molecular Typing

TypeinterventionalSponsorFudan UniversityRan2023 to 2026Enrolled88ConditionsAdvanced Salivary Gland CarcinomaArmsSHR-A1811, SHR 3680 + leuprolide, SHR-A1921
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Guang-Liang Chen *Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yanjing Guo *Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ya'nan YangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Youzhou SangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Si SunDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xin LiuDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xin ZhouDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Chun-Ying ShengDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Xiayun HeDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Jianfei WangClinical Research & Development, Jiangsu Hengrui Pharmaceuticals Co., Ltd, Shanghai, China.
Rongliang ShiDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Yu WangDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Qinghai JiDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Dongmei JiDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China. jid09@fudan.edu.cn.

Funding

the National Natural Science Foundation of China No. 82573874
6 · The paper itself

Abstract

Advanced salivary gland carcinoma (SGC) lacking both human epidermal growth factor receptor 2 (HER2) and androgen receptor (AR) expression has limited treatment options. In this single-center, phase II trial, patients with recurrent/metastatic HER2-negative/AR-negative SGC received SHR-A1921, a TROP-2-directed antibody-drug conjugate, every 3 weeks until disease progression or unacceptable toxicity. The primary endpoint was objective response rate (ORR) per RECIST v1.1; secondary endpoints included progression-free survival (PFS), safety, and exploratory analyses of baseline TROP-2 expression by immunohistochemistry. As of August 1, 2025, 17 patients were treated and 15 were evaluable for efficacy, including 10 with non-adenoid cystic carcinoma (non-ACC) and 5 with adenoid cystic carcinoma (ACC). In non-ACC SGC, confirmed ORR was 20.0%, disease control rate was 80.0%, and clinical benefit rate was 60.0%. All patients with ACC achieved stable disease, with median PFS of 15.4 months. Treatment-related adverse events were manageable; oral mucositis was most common. No grade 4-5 treatment-related adverse events or treatment-related serious adverse events occurred; one patient discontinued treatment due to toxicity. Baseline TROP-2 expression was heterogeneous, with numerically higher H-scores in responders but no significant association with PFS. SHR-A1921 showed preliminary activity in non-ACC SGC and disease stabilization in ACC, supporting further evaluation in stratified cohorts. Trial registration: ClinicalTrials.gov, NCT05924256. Registered on June 29, 2023.

Identifiers

PMID42129335
PMCPMC13518839

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