Evidence map›Paper›PMID 42714605›Full record

ArticleBreast cancer research and treatment2026

Exploring trop-2-directed ADCs monotherapy and combination therapy in pretreated mTNBC: a real-world study.

Jingze Liu, Linxiaoxiao Ding, Jiayi Wang, Tao Chen, Tianzhu Long, Qian Li, Jie Chai, Herui Yao, Ying Wang, Jianli Zhao

Abstract read
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Article in Breast cancer research and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jingze Liu *Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China.
Linxiaoxiao Ding *Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China.
Jiayi Wang *Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China.
Tao Chen *Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China.
Tianzhu Long *Thyroid and Breast Surgery Department, Guangzhou Women and Children's Medical center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Qian LiBreast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China.
Jie ChaiBreast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China.
Herui YaoBreast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China. yaoherui@mail.sysu.edu.cn.
Ying WangBreast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China. wangy556@mail.sysu.edu.cn.
Jianli ZhaoBreast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou, 510120, P. R. China. zhaojli5@mail.sysu.edu.cn.

Funding

Guangdong Provincial Clinical Research Center for Breast Diseases 2023B110005Guangzhou Science and Technology Plan Project 2024A03J1195Guangzhou Science and Technology Plan Project 2025A03J4194Guangzhou Science and Technology Plan Project SL2023A03J01150National Natural Science Foundation of China 82203141National Natural Science Foundation of China 82271793; 82573593National Natural Science Foundation of China 82573479National Science and Technology Major Project for the Prevention and Treatment of Cancer, Cardiovascular, Respiratory, and Metabolic Diseases 2024ZD0519800; 2024ZD0519805Sun Yat-sen Memorial Hospital Clinical Research 5010 Program SYS-5010-202308Sun Yat-sen Memorial Hospital Clinical Research 5010 Program SYS-5010-202409Sun Yat-sen Memorial Hospital Clinical Research Cultivation Program SYS-Q-202101Sun Yat-sen University Clinical Research 5010 Program 81000-13130007
6 · The paper itself

Abstract

purposeAlthough Trop-2 antibody-drug conjugates (ADCs) have improved outcomes in pretreated metastatic triple-negative breast cancer (mTNBC), resistance remains common and the optimal combination strategy in routine practice is unclear.

methodsIn this retrospective real-world study, we identified patients with mTNBC from a health record-derived database who received sacituzumab govitecan or sacituzumab tirumotecan in the later-line setting between April 2020 and December 2025. Patients received at least two cycles of Trop-2 ADC therapy as monotherapy, plus a PD-1 inhibitor (dual-agent combination), or plus a PD-1 inhibitor and an antiangiogenic agent (triple-agent combination).

resultsDescriptively, the ORR was 57.1% in the triple-agent combination group, 38.5% in the dual-agent combination group, and 31.7% in the monotherapy group. Median follow-up was 15.2 months (95% CI, 8.7-20.6). Median progression-free survival (mPFS) was 15.4 months (95% CI, 5.3-NA) in the triple-agent combination group, 10.0 months (95% CI, 4.2-NA) in the dual-agent combination group, and 3.8 months (95% CI, 3.2-5.2) in the monotherapy group. Severe treatment-related toxicity was not increased in the combination groups. Exploratory analyses identified a genomic scoring system that may enable stratification of patients with a higher likelihood of benefiting from the triple-agent combination.

conclusionTo our knowledge, this study represents one of the earliest real-world evaluations of this triple-agent strategy in previously treated mTNBC, providing a basis for further prospective validation and biomarker-guided application.

Indexed as

Antigens, NeoplasmAntineoplastic Combined Chemotherapy ProtocolsCell Adhesion MoleculesImmunoconjugatesTriple Negative Breast NeoplasmsAgedAntibodies, Monoclonal, HumanizedCamptothecinFemaleHumansMiddle AgedRetrospective StudiesAntibodies, Monoclonal, HumanizedAntigens, NeoplasmCamptothecinCell Adhesion MoleculesImmunoconjugatessacituzumab govitecanTACSTD2 protein, humanAnti-angiogenic agentsImmune checkpoint inhibitorsMetastatic triple-negative breast cancerTriple-agent combination therapyTrop-2 antibody-drug conjugates

Identifiers

PMID42714605
PMCPMC13558290

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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.