Evidence map›Paper›PMID 40830660›Full record

Trial reportNature medicine2025

First-line sacituzumab tirumotecan with tagitanlimab in advanced non-small-cell lung cancer: a phase 2 trial.

Shaodong Hong, Qiming Wang, Ying Cheng, Yongzhong Luo, Xiujuan Qu, Haibo Zhu, Zhenyu Ding, Xingya Li, Lin Wu, Yan Wang and 13 more

Abstract readClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Nature medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Trial
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  3. Article
  4. Review
  5. Review
  6. Review
  7. Current and future immunotherapies for NSCLC.Journal of hematology & oncology · 2026
    Review
  8. Review
  9. Review
  10. Review
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

23 authors.

Shaodong Hong *Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China.
Qiming Wang *The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.
Ying Cheng *Jilin Cancer Hospital, Changchun, China.ORCID http://orcid.org/0000-0001-9908-597X
Yongzhong Luo *Hunan Cancer Hospital, Changsha, China.
Xiujuan Qu *The First Hospital of China Medical University, Shenyang, China.
Haibo ZhuShanxi Cancer Hospital, Taiyuan, China.
Zhenyu DingWest China Hospital of Sichuan University, Chengdu, China.
Xingya LiThe First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Lin WuHunan Cancer Hospital, Changsha, China.ORCID http://orcid.org/0000-0001-7078-7767
Yan WangHarbin Medical University Cancer Hospital, Harbin, China.
Sheng HuHubei Cancer Hospital, Wuhan, China.
Enwen WangChongqing University Cancer Hospital, Chongqing, China.
Anwen LiuThe Second Affiliated Hospital of Nanchang University, Nanchang, China.
Yuping SunShandong Cancer Hospital, Jinan, China.
Yun FanZhejiang Cancer Hospital, Hangzhou, China.
Feng YeThe First Affiliated Hospital of Xiamen University, Xiamen, China.
Kaihua LuJiangsu Province Hospital, Nanjing, China.
Jian FangBeijing Cancer Hospital, Beijing, China.
Yuping ShenSichuan Kelun-Biotech Biopharmaceutical Co Ltd, Chengdu, China.
Xiaoping JinSichuan Kelun-Biotech Biopharmaceutical Co Ltd, Chengdu, China.
Junyou GeSichuan Kelun-Biotech Biopharmaceutical Co Ltd, Chengdu, China.
Li ZhangSun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China. zhangli@sysucc.org.cn.ORCID http://orcid.org/0000-0003-0595-0761
Wenfeng FangSun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China. fangwf@sysucc.org.cn.ORCID http://orcid.org/0000-0002-6440-8246

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sacituzumab tirumotecan (sac-TMT, also known as MK-2870 or SKB264) is an antibody-drug conjugate targeting trophoblast cell surface antigen 2. We report the initial findings from the ongoing phase 2 OptiTROP-Lung01 study, evaluating the combination of sac-TMT and tagitanlimab (KL-A167), an anti-PD-L1 antibody, as first-line therapy in patients with advanced or metastatic non-small-cell lung cancer who lack actionable genomic alterations (cohorts 1A and 1B). Cohort 1A received sac-TMT (5 mg kg

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCamptothecinCarcinoma, Non-Small-Cell LungImmunoconjugatesLung NeoplasmsAdultAgedB7-H1 AntigenFemaleHumansMaleMiddle AgedAntibodies, Monoclonal, HumanizedB7-H1 AntigenCamptothecinCD274 protein, humanImmunoconjugatessacituzumab govitecan

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.