Evidence map›Paper›PMID 32623573›Full record

Trial reportJournal of cancer research and clinical oncology2020

Camrelizumab in advanced or metastatic solid tumour patients with DNA mismatch repair deficient or microsatellite instability high: an open-label prospective pivotal trial.

Jingde Chen, Ming Quan, Zhiqin Chen, Tianmei Zeng, Yandong Li, Ying Zhou, Yanan Hai, Yong Gao

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Journal of cancer research and clinical oncology, 2020. 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
0.8field-weighted citation impact, top 26% 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.

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, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Current status and prospect of immunotherapy for colorectal cancer.International journal of colorectal disease · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

8 authors at 2 institutions in 1 country.

Jingde ChenShanghai East Hospital, Tongji University School of Medicine, No. 150 Ji-Mo Rd., Shanghai, 200120, China.
Ming QuanShanghai East Hospital, Tongji University School of Medicine, No. 150 Ji-Mo Rd., Shanghai, 200120, China.
Zhiqin ChenShanghai East Hospital, Tongji University School of Medicine, No. 150 Ji-Mo Rd., Shanghai, 200120, China.
Tianmei ZengEastern Hepatobiliary Surgery Hospital, Third Affiliated Hospital of Second Military Medical University, Shanghai, China.
Yandong LiShanghai East Hospital, Tongji University School of Medicine, No. 150 Ji-Mo Rd., Shanghai, 200120, China.
Ying ZhouShanghai East Hospital, Tongji University School of Medicine, No. 150 Ji-Mo Rd., Shanghai, 200120, China.
Yanan HaiShanghai East Hospital, Tongji University School of Medicine, No. 150 Ji-Mo Rd., Shanghai, 200120, China.
Yong GaoShanghai East Hospital, Tongji University School of Medicine, No. 150 Ji-Mo Rd., Shanghai, 200120, China. gaoyon@hotmail.com.ORCID http://orcid.org/0000-0001-7812-0932
Shanghai East Hospital · CNSecond Military Medical University · CN

Funding

National Natural Science Foundation of China 81772567
6 · The paper itself

Abstract

purposePatients with DNA mismatch repair-deficient (dMMR)/microsatellite instability-high (MSI-H) cancers are prone to response to programmed cell death-1 (PD-1) checkpoint inhibitors. Therefore, we explored the efficacy and safety of a PD-1 checkpoint inhibitor camrelizumab in advanced or metastatic solid tumour with dMMR/MSI-H.

methodsPatients with dMMR/MSI-H advanced or metastatic solid tumours who had received at least one line of prior systemic chemotherapy were recruited. Camrelizumab was given intravenously 200 mg every 2-week treatment cycle. The primary endpoint was objective response rate according to Response Evaluation Criteria in Solid Tumours v1.1.

resultsTwelve patients were enrolled. As data cutoff, eight patients (66.7%, 95% CI 34.9-90.1) achieved objective response. Disease control rate reached 100% (95% CI 73.5-100). Progression-free survival rate at 12 months was 83.3% (95% CI 48.2-95.6), and overall survival rate at 12 months was 90% (95% CI 47.3-98.5). The most common treatment-related adverse events were reactive cutaneous capillary endothelial proliferation (100%), increased alanine aminotransferase (41.7%), and increased aspartate aminotransferase (41.7%).

conclusionsCamrelizumab provided durable objective response and disease control in pre-treated patients with dMMR/MSI-H advanced or metastatic solid tumour, being a promising treatment option for these patients.

Indexed as

AdultAgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalDNA Mismatch RepairFemaleHumansMaleMicrosatellite InstabilityMiddle AgedNeoplasm MetastasisNeoplasmsProgrammed Cell Death 1 ReceptorProgression-Free SurvivalProspective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalcamrelizumabPDCD1 protein, humanProgrammed Cell Death 1 ReceptorCamrelizumabdMMR/MSI-HSHR-1210Solid tumour

Identifiers

PMID32623573
PMCPMC11804717
OpenAlexW3039410094

What OpenQuestion holds

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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.