Evidence map›Paper›PMID 37422527›Full record

ArticleBritish journal of cancer2023

Trajectories of α-fetoprotein and unresectable hepatocellular carcinoma outcomes receiving atezolizumab plus bevacizumab: a secondary analysis of IMbrave150 study.

Linbin Lu, Peichan Zheng, Yan Pan, Shanshan Huang, Erqian Shao, Yan Huang, Xuewen Wang, Yayin Chen, Gongbao Cuo, Hongyi Yang and 4 more

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

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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

14 authors at 4 institutions in 1 country.

Linbin Lu *Department of Oncology, Mengchao Hepatobiliary Hospital of Fujian Medical University, 350025, Fuzhou, Fujian, PR China. doctorxiaolin@fjmu.edu.cn.ORCID 0000-0003-3779-3457
Peichan Zheng *Fujian Center for Safety Evaluation of New Drug, Fujian Medical University, 350122, Fuzhou, Fujian, PR China.ORCID 0000-0003-3149-9978
Yan Pan *Department of Oncology, Fujian Provincial Hospital of Fujian Medical University, 350001, Fuzhou, Fujian, PR China.ORCID 0009-0006-3445-8265
Shanshan Huang *Department of Oncology, the First Affiliated Hospital of Nanchang University, 330006, Nanchang, Jiangxi, PR China.ORCID 0000-0001-6706-5894
Erqian ShaoDepartment of Oncology, The Third Affiliated Hospital of Sun Yat-sen University Yuedong Hospital, 514000, Meizhou, Guangdong, PR China.ORCID 0009-0008-4892-0195
Yan HuangDepartment of Oncology, Quanzhou First Hospital Affiliated to Fujian Medical University, 362002, Quanzhou, Fujian, PR China.
Xuewen WangDepartment of Oncology, Mengchao Hepatobiliary Hospital of Fujian Medical University, 350025, Fuzhou, Fujian, PR China.
Yayin ChenDepartment of Oncology, Mengchao Hepatobiliary Hospital of Fujian Medical University, 350025, Fuzhou, Fujian, PR China.ORCID 0000-0001-9690-5063
Gongbao CuoDepartment of Oncology, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzong Clinical College of Fujian Medical University, 350025, Fuzhou, Fujian, PR China.
Hongyi YangDepartment of Oncology, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzong Clinical College of Fujian Medical University, 350025, Fuzhou, Fujian, PR China.
Wangting GuoDepartment of Oncology, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzong Clinical College of Fujian Medical University, 350025, Fuzhou, Fujian, PR China.ORCID 0009-0009-3363-6033
Yanhong ShiDepartment of Oncology, Mengchao Hepatobiliary Hospital of Fujian Medical University, 350025, Fuzhou, Fujian, PR China.
Zhixian WuDepartment of Hepatobiliary Disease, Dongfang Hospital of Xiamen University Medical College, 350025, Fuzhou, Fujian, PR China.ORCID 0000-0002-0708-6770
Xiong ChenDepartment of Oncology, Mengchao Hepatobiliary Hospital of Fujian Medical University, 350025, Fuzhou, Fujian, PR China. cxiongzpc@fjmu.edu.cn.ORCID 0000-0001-5316-6512
Fujian Medical University · CNNanchang University · CNSun Yat-sen University · CNXiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundα-fetoprotein (AFP) response has been demonstrated as a biomarker for unresectable hepatocellular carcinoma (uHCC) patients receiving immunotherapy, but its definition is still unclear. This exploratory study investigated the AFP trajectory and clinical outcomes of receiving atezolizumab plus bevacizumab (Atez/Bev) therapy.

methodsThis secondary analysis used the Atez/Bev arm data of phase III IMbrave150 study to distinguish potential AFP changing rate trajectories through latent class trajectory models. The multivariable Cox models were applied to calculate adjusted hazard ratios (HRs) and 95% CIs for clinical outcomes.

resultsThree distinct trajectories were identified among the uHCC patients with 7 times (range, 3 to 28) of AFP measurements: low-stable (50.0%, n = 132), sharp-falling (13.3%, n = 35), and high-rising (36.7%, n = 97). Compared with the high-rising class, HRs of disease progression were 0.52 (95% CI: 0.39, 0.70) and 0.26 (95% CI: 0.16, 0.43) for the low-stable class and sharp-falling class, respectively. In contrast, HRs of death were 0.59 (95% CI: 0.40, 0.81) and 0.30 (95% CI: 0.16, 0.57) for the two groups after propensity score adjustment. Besides, AFP trajectories had the highest relative importance of each covariate to survival. DISCUSSION: There are three distinct AFP trajectories in uHCC patients receiving Atez/Bev, and it is an independent biomarker for clinical outcomes.

Indexed as

Carcinoma, HepatocellularLiver Neoplasmsalpha-FetoproteinsAntibodies, Monoclonal, HumanizedBevacizumabHumansalpha-FetoproteinsAntibodies, Monoclonal, HumanizedatezolizumabBevacizumab

Identifiers

PMID37422527
PMCPMC10421902
OpenAlexW4383646282

What OpenQuestion holds

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Registered trials

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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.