Evidence map›Paper›PMID 41613151›Full record

ReviewFrontiers in immunology2025

Recent progress in cadonilimab research for oncology applications.

Ming-Zhen Dong, Ming Cui, En-Bo Zhu, Ming-Quan Lin, Guang-Hui Dong, Guang-Lin Jin, Lin-Zhuo Qu, Hui-Ying Che, Hong-Jian Guan

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  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.

Ming-Zhen DongDepartment of Neurology, Yanbian University Hospital, Yanji, Jilin, China.
Ming CuiReproductive Medicine Center, Yanbian University Hospital, Yanji, Jilin, China.
En-Bo ZhuDepartment of Neurology, Yanbian University Hospital, Yanji, Jilin, China.
Ming-Quan LinDepartment of Neurology, Yanbian University Hospital, Yanji, Jilin, China.
Guang-Hui DongDepartment of Neurology, Yanbian University Hospital, Yanji, Jilin, China.
Guang-Lin JinDepartment of Neurology, Yanbian University Hospital, Yanji, Jilin, China.
Lin-Zhuo QuDepartment of Neurology, Yanbian University Hospital, Yanji, Jilin, China.
Hui-Ying CheDepartment of General Medicine, Yanbian University Hospital, Yanji, Jilin, China.
Hong-Jian GuanDepartment of Neurology, Yanbian University Hospital, Yanji, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cadonilimab is the first bispecific antibody independently developed in China that simultaneously targets Programmed Cell Death Protein-1 (PD-1) and Cytotoxic T Lymphocyte-Associated Antigen-4 (CTLA-4), marking a significant milestone in both clinical applications and drug development. Through its dual mechanism of action, cadonilimab blocks PD-1 and CTLA-4 signaling pathways concurrently, thereby activating T cells and enhancing antitumor immune responses. Within the tumor microenvironment, cadonilimab promotes effector T-cell infiltration while reducing nonspecific attacks on normal tissues, thus lowering the incidence of immune-related adverse events. In comparison to conventional monospecific antibodies, cadonilimab exhibits superior selectivity and safety. Multiple studies have shown that, either as monotherapy or in combination regimens, cadonilimab exhibits promising antitumor activity and tolerability in refractory solid tumors such as advanced cervical cancer, hepatocellular carcinoma, non-small cell lung cancer, and gastric cancer, with notable efficacy even in patients with low or negative PD-L1 expression. The successful development of cadonilimab not only underscores China's innovative capabilities in the field of cancer immunotherapy but also provides valuable insights for global drug development and clinical practice. However, most signals derive from phase I/II single-arm or small-sample studies with limited follow-up, and no randomized head-to-head trials have yet confirmed superiority over standard PD-1+CTLA-4 approaches. This review summarizes the mechanism of action, structural characteristics, clinical research progress, and future applications of cadonilimab, with the aim of offering a useful reference for research and clinical treatment while promoting its broader application in oncology.

Indexed as

Antibodies, BispecificAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsNeoplasmsAnimalsCTLA-4 AntigenHumansImmunotherapyProgrammed Cell Death 1 ReceptorTumor MicroenvironmentAntibodies, BispecificAntineoplastic Agents, ImmunologicalCTLA-4 AntigenImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorbispecific antibodycadonilimabimmunotherapylung cancerother malignancies

Identifiers

PMID41613151
PMCPMC12847384

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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.