Evidence map›Paper›PMID 37852261›Full record

ArticleCell reports. Medicine2023

A phase 1a/1b first-in-human study (COMPASSION-01) evaluating cadonilimab in patients with advanced solid tumors.

Sophia Frentzas, Hui K Gan, Rasha Cosman, Jermaine Coward, Ben Tran, Michael Millward, Yiting Zhou, Wenjing Wang, Dennis Xia, Zhongmin Maxwell Wang and 3 more

4 registry-linked trialsOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 37 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 3 pooled it
8.5field-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.

NCT03261011 phase1completednot on this map

A Phase 1A/1B Multicenter, Open-label, Dose-escalation, and Dose-expansion Study to Evaluate the Safety, Pharmacokinetics, and Antitumor Activity of AK104 in Subjects With Advanced Solid Tumors

TypeinterventionalSponsorAkesobio Australia Pty LtdRan2017 to 2023Enrolled119ConditionsAdvanced CancerArmsAK-104
NCT06140589 recruitingnot on this mapstarted 2024, after this paper: background citation

Study on the Efficacy, Safety and Cost-effectiveness of Cadonilimab in the Treatment of Cervical Cancer

TypeobservationalSponsorFujian Cancer HospitalRan2024 to 2026Enrolled200ConditionsCervical CancerArmsCadonilimab
NCT06143748 phase2active not recruitingnot on this mapstarted 2024, after this paper: background citation

Cadonilimab Combined With Induction Chemotherapy and Definitive Radiotherapy for Patients With Locally Advanced Esophageal Squamous Cell Carcinoma: a Phase II, Single-arm Trial (EC-CRT-006)

TypeinterventionalSponsorSun Yat-sen UniversityRan2024 to 2027Enrolled46ConditionsEsophagus CancerArmsCadonilimab, Paclitaxel and cisplatin, intensity-modulated radiotherapy
NCT06455254 phase2unknown statusnot on this mapstarted 2024, after this paper: background citation

A Single-arm, Multicenter, Phase II Study to Evaluate the Efficacy and Safety of Candonilimab(AK104) Combined With Regorafenib For the Third-line Treatment of MSS Colorectal Liver Metastasis

TypeinterventionalSponsorJin-hong ChenRan2024 to 2026Enrolled44ConditionsCRCArmsCandonilimab (AK104), Regorafenib
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 3 syntheses or guidelines pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  4. Safety, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy from a First-in-Human Study of Volrustomig, a Novel PD-1/CTLA-4 Bispecific Antibody.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  15. 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

13 authors at 7 institutions in 1 country.

Sophia FrentzasDepartment of Medical Oncology, Monash Health, Melbourne, Australia; Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Australia.
Hui K GanMedical Oncology Department, Austin Health, Melbourne, Australia.
Rasha CosmanThe Kinghorn Cancer Centre, St Vincent's Hospital, Sydney, Australia; St. Vincent's Clinical School, University of New South Wales, Sydney, Australia.
Jermaine CowardICON Cancer Centre, Brisbane, Australia; University of Queensland, Faculty of Medicine, Brisbane, Australia.
Ben TranDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.
Michael MillwardLinear Clinical Research, Nedland, Perth, Australia; School of Medicine, University of Western Australia, Perth, Australia.
Yiting ZhouAkeso Biopharma, Inc., Zhongshan, China.
Wenjing WangAkeso Biopharma, Inc., Zhongshan, China.
Dennis XiaAkeso Biopharma, Inc., Zhongshan, China.
Zhongmin Maxwell WangAkeso Biopharma, Inc., Zhongshan, China.
Baiyong LiAkeso Biopharma, Inc., Zhongshan, China.
Michelle XiaAkeso Biopharma, Inc., Zhongshan, China.
Jayesh DesaiSir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Australia. Electronic address: jayesh.desai@petermac.org.
Austin Health · AUMonash Health · AUPeter MacCallum Cancer Centre · AUThe University of Melbourne · AUThe University of Queensland · AUThe University of Western Australia · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Simultaneous inhibition of programmed cell death protein-1 (PD-1) and cytotoxic T lymphocyte-associated protein-4 (CTLA-4) with bispecific antibodies may improve efficacy over single-agent treatment while limiting toxicity. Cadonilimab is a humanized, bispecific antibody targeting PD-1 and CTLA-4. This is a phase 1 study of cadonilimab including dose escalation (n = 39) and dose expansion (n = 80). One dose-limiting toxicity event is observed, with the maximum tolerated dose not reached. 6 mg/kg cadonilimab once every 2 weeks is established as the recommended dose for future studies. The most common treatment-related adverse event is infusion-related reaction (18.5%), mostly grade 1/2 in severity. The incidences of any grade and grade ≥3 immune-related adverse events are 44.5% and 6.7%, respectively. The confirmed overall response rate is 13.4%, and the median duration of response is 12.9 months. Cadonilimab is well tolerated and showed promising efficacy in patients with advanced solid tumors. This study is registered with ClinicalTrials.gov: NCT03261011.

Indexed as

NeoplasmsProgrammed Cell Death 1 ReceptorAntibodies, Monoclonal, HumanizedCTLA-4 AntigenEmpathyHumansAntibodies, Monoclonal, HumanizedCTLA-4 AntigenProgrammed Cell Death 1 Receptoradvanced solid tumorsbispecific antibodycadonilimabCTLA-4immune checkpoint inhibitorPD-1

Identifiers

PMID37852261
PMCPMC10694581
OpenAlexW4387709297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.