Evidence map›Paper›PMID 38706247›Full record

Trial reportTechnology in cancer research & treatment

A Single-Arm Multi-Center Phase II Clinical Trial of Cadonilimab (anti-PD-1/CTLA-4) in Combination with or without Conventional Second-Line Treatment for Patients with Extensive Stage Small Cell Lung Cancer.

Can Chen, Minjun Chen, Yuju Bai, Yajun Li, Jie Peng, Biao Yao, Jiangping Feng, Jian-Guo Zhou, Hu Ma

Registry-linked trialAbstract readMulticenter StudyClinical Trial, Phase II
In one paragraph

Trial report in Technology in cancer research & treatment. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05901584 (A Single-arm Multicenter Phase II Clinical Trial of Cadunilumab), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT05901584 phase2unknown statusnot on this map

A Single-arm Multicenter Phase II Clinical Trial of Cadunilumab (Anti-PD-1/CTLA-4) in Combination With or Without Chemotherapy in Second-line Treatment for Patients With Extensive Stage Small Cell Lung Cancer

TypeinterventionalSponsorSecond Affiliated Hospital of Zunyi Medical UniversityRan2023 to 2024Enrolled30ConditionsImmunotherapy, Second-line TreatmentArmsCadonilimab
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
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  6. 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

9 authors.

Can ChenDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Minjun ChenDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Yuju BaiDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Yajun LiDepartment of Oncology, The First People's Hospital of Zunyi, Zunyi, Guizhou, China.
Jie PengDepartment of Oncology, The Second Affiliated Hospital of Guizhou Medical University, Kaili, Guizhou, China.
Biao YaoDepartment of Oncology, Tongren People's Hospital, Tongren, Guizhou, China.
Jiangping FengDepartment of Oncology, Xingyi People's Hospital, Xingyi, Guizhou, China.
Jian-Guo ZhouDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.ORCID 0000-0002-5021-3739
Hu MaDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCadonilimab (AK104) is a bispecific IgG-single-chain Fv fragment (ScFv) antibody that binds to PD-1 and CTLA-4. Cadonilimab has shown encouraging anti-tumour activity and a favourable safety profile in several tumour types. In second-line treatment, there is no defined standard of care for patients with extensive-stage small-cell lung cancer (ES-SCLC). Cadonilimab is expected to show substantial clinical efficacy.

objectiveTo assess the antitumor activity and safety of cadonilimab monotherapy or combination with conventional therapy in ES-SCLC patients who failed first-line treatment.

methodsIn this multicenter, open-label, phase II study, ES-SCLC patients who had failed first-line treatment, also aged 18 years to 70 years with histologically or cytologically confirmed ES-SCLC, and an Eastern Cooperative Oncology Group performance status (ECOG-PS) of 0-2 were eligible. Patients will receive cadonilimab 10 mg/kg every three weeks (Q3 W) among 24 months until progressive disease (PD) or adverse events (AE) discovery. The primary endpoint is progression-free survival (PFS).

trial registrationNCT05901584.

Indexed as

CTLA-4 AntigenLung NeoplasmsProgrammed Cell Death 1 ReceptorSmall Cell Lung CarcinomaAdolescentAdultAgedAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansImmune Checkpoint InhibitorsMaleMiddle AgedNeoplasm StagingTreatment OutcomeAntibodies, Monoclonal, HumanizedCTLA-4 AntigenCTLA4 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorcadonilimabcombination therapyimmunotherapysecond-line treatmentsmall cell lung cancer

Identifiers

PMID38706247
PMCPMC11072065

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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.