Evidence map›Paper›PMID 37740797›Full record

ArticleCancer chemotherapy and pharmacology2024

Correlation analysis between camrelizumab trough concentration levels and efficacy or safety in East Asian patients with advanced lung cancer.

Mengfei Cheng, Fang Yang, Yanchao Yang, Xinyue Gao, Yang Yu, Nan Wang, Xinyu Luo, Shuo Zhang, Shuai Jiang, Mei Dong

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In one paragraph

Article in Cancer chemotherapy and pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
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

10 authors at 1 institution in 1 country.

Mengfei Cheng *Department of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Fang YangThe First Department of Respiratory Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Yanchao Yang *Department of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Xinyue GaoDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Yang YuDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Nan WangDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Xinyu LuoDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Shuo ZhangDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Shuai JiangDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China. jdyhmu3@163.com.ORCID 0000-0003-1235-6269
Mei DongDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China. 13804567370@163.com.
Harbin Medical University · CN

Funding

Beijing Hongdingxiang Public Welfare Development Center BJ-HDX-20220437The General Program of Harbin Medical University Cancer Hospital Haiyan Fund JJMS2022-19the Project of Beijing Medical Award Foundation YXJL-2022-0187-0013
6 · The paper itself

Abstract

backgroundCamrelizumab combined with chemotherapy is approved across tumor types. However, only a fraction of patients benefits from immunotherapy, and biomarkers such as the expression of PD-L1, tumor mutational burden, and CXCL11 are expensive and suboptimal specificity for cancer patients. An exposure-response (E-R) relationship has been reported in many immune checkpoint inhibitors (ICIs), and the trough concentrations and other drug exposure metrics are broadly used to guide dosing decisions, assess exposure-outcomes relationships, and ultimately predict outcomes based on those relationships. However, the potential use of trough concentration levels for camrelizumab is still not clear.

methodsBlood samples were obtained at trough levels after doses 3 and 4 from 77 patients with advanced lung cancer who received camrelizumab (200 mg Q3 W) monotherapy or combined with chemotherapy. We optimized a competitive ELISA method to measure the trough concentration.

resultsWe found that the trough concentration was steady after 3 dose cycles, and the trough concentration level of camrelizumab was higher in patients who developed immune-related adverse effects (irAEs) than in those who did not (P < 0.05) but was not observed in disease progression and PFS (P > 0.05). Age (< 65 years old), no smoking history, and efficacy evaluation after 4-dose treatment were associated with PFS (P < 0.05), but no significance was observed in other clinical characteristics. Total bilirubin and albumin had an influence on trough concentration, and monocytes and albumin were independent risk factors for PFS (P < 0.05).

conclusionsOur results suggest that the trough concentration level of camrelizumab might be a risk factor for the occurrence of irAEs in advanced lung cancer, and using the immunotherapy as early as possible may bring better clinical outcomes.

Indexed as

Antibodies, Monoclonal, HumanizedDrug-Related Side Effects and Adverse ReactionsLung NeoplasmsAgedAlbuminsEast Asian PeopleHumansAlbuminsAntibodies, Monoclonal, HumanizedcamrelizumabCamrelizumabExposure–responseImmune-related adverse effectsImmunotherapyLung cancer

Identifiers

PMID37740797
OpenAlexW4386981066

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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.