Evidence map›Paper›PMID 38110665›Full record

Trial reportBritish journal of cancer2024

A phase Ib/II study of cadonilimab (PD-1/CTLA-4 bispecific antibody) plus anlotinib as first-line treatment in patients with advanced non-small cell lung cancer.

Bolin Chen, Wenxiu Yao, Xingya Li, Gen Lin, Qian Chu, Hailong Liu, Yingying Du, Jie Lin, Huaxin Duan, Huijuan Wang and 14 more

2 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in British journal of cancer, 2024. 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 30 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 4 pooled it
8.3field-weighted citation impact, top 2% of its field
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.

NCT04646330 phase1 / phase2completednot on this map

A Phase Ib/II Trial of AK104 Plus Anlotinib in Patients With NSCLC

TypeinterventionalSponsorAkesoRan2020 to 2025Enrolled114ConditionsNSCLCArmsAK104+anlotinib
NCT07635290 phase2active not recruitingnot on this mapstarted 2026, after this paper: background citation

A Phase II Clinical Trial of Anlotinib Combined With Cadonilimab and PULSAR in Previously Treated Advanced Unresectable or Metastatic Biliary Tract Cancer

TypeinterventionalSponsorWest China HospitalRan2026 to 2028Enrolled26ConditionsPreviously Treated, Advanced, Biliary Tract CancersArmsAnlotinib + Cadonilimab, PULSAR
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 4 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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  8. Induced proximity-based therapeutic modalities.Nature reviews. Drug discovery · 2026
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  16. The next generation of immunotherapies for lung cancers.Nature reviews. Clinical oncology · 2025
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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

24 authors at 12 institutions in 1 country.

Bolin Chen *The Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Wenxiu Yao *Department of Oncology, Sichuan Cancer Hospital, Chengdu, China.
Xingya Li *The Second Ward, Oncology Department, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Gen Lin *Department of Thoracic Oncology, Fujian Cancer Hospital, Fuzhou, China.
Qian ChuDepartment of Thoracic Oncology, Tongji Hospital Affiliated to Tongji Medical College of HUST, Wuhan, China.ORCID 0000-0001-8192-7630
Hailong LiuDepartment of Oncology, Chenzhou First People's Hospital, Chenzhou, China.
Yingying DuDepartment of Oncology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Jie LinDepartment of Medical Oncology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Huaxin DuanDepartment of Oncology, Hunan Provincial People's Hospital /The First Affiliated Hospital of Hunan Normal University, Changsha, China.
Huijuan WangThe Second Department of Respiratory Medicine, Henan Cancer Hospital, Zhengzhou, China.
Zemin XiaoDepartment of Oncology, The First People's Hospital of Changde City, Changde, China.
Hong SunDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Liyu LiuThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Li XuThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Yan XuThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Fang XuThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Yi KongThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Xingxiang PuThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Kang LiThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Qianzhi WangThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Jia LiThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Baiyong LiAkeso Biopharma, Inc, Zhongshan, China.
Yu XiaAkeso Biopharma, Inc, Zhongshan, China.
Lin WuThe Second Department of Thoracic Medicine, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China. wulin-calf@vip.163.com.ORCID 0000-0001-7078-7767
Central South University · CNAnhui Medical University · CNChenzhou First People's Hospital · CNFirst Affiliated Hospital of Xi'an Jiaotong University · CNFirst Affiliated Hospital of Zhengzhou University · CNFujian Provincial Cancer Hospital · CNHenan Cancer Hospital · CNHunan Normal University · CNKunming Medical University · CNSichuan Cancer Hospital · CNThe First People's Hospital of Changde · CNTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCadonilimab is a bispecific antibody that simultaneously targets programmed cell death receptor-1 and cytotoxic T lymphocyte-associated antigen-4. This study aimed to assess the safety and efficacy of cadonilimab plus anlotinib for the first-line treatment of advanced non-small cell lung cancer (NSCLC) without sensitizing EGFR/ALK/ROS1 mutations.

methodsPatients received cadonilimab 15 mg/kg and 10 mg/kg every three weeks (Q3W) plus anlotinib at doses of 10 or 12 mg once daily for two weeks on a one-week-off schedule. The primary endpoints included safety and objective response rate (ORR).

resultsSixty-nine treatment-naïve patients received cadonilimab 15 mg/kg Q3W combination (n = 49) and 10 mg/kg Q3W combination (n = 20). Treatment-related adverse events (TRAEs) were reported in 48 (98.0%) and 19 (95.0%) patients, with grade ≥3 TRAEs occurring in 29 (59.2%) and five (25.0%) patients, respectively. TRAEs leading to cadonilimab discontinuation occurred in eight (16.3%) and one (5.0%) patients in the cadonilimab 15 mg/kg Q3W and 10 mg/kg Q3W dosing groups. The confirmed ORRs were 51.0% (25/49) and 60.0% (12/20) accordingly.

conclusionsCadonilimab 10 mg/kg Q3W plus anlotinib showed manageable safety and promising efficacy as a first-line chemo-free treatment for advanced NSCLC. CLINICALTRIALS: GOV IDENTIFIER: NCT04646330.

Indexed as

Carcinoma, Non-Small-Cell LungIndolesLung NeoplasmsQuinolinesAntineoplastic Combined Chemotherapy ProtocolsCTLA-4 AntigenHumansProgrammed Cell Death 1 ReceptorProtein-Tyrosine KinasesProto-Oncogene ProteinsanlotinibCTLA-4 AntigenIndolesProgrammed Cell Death 1 ReceptorProtein-Tyrosine KinasesProto-Oncogene ProteinsQuinolines

Identifiers

PMID38110665
PMCPMC10844309
OpenAlexW4389892188

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.