Evidence map›Paper›PMID 39494102›Full record

Trial reportWorld journal of gastroenterology2024

Inetetamab combined with S-1 and oxaliplatin as first-line treatment for human epidermal growth factor receptor 2-positive gastric cancer.

Ying Kong, Qi Dong, Peng Jin, Ming-Yan Li, Li Ma, Qi-Jun Yi, Yu-E Miao, Hai-Yan Liu, Jian-Gang Liu

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in World journal of gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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.

Ying KongDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.
Qi DongDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.
Peng JinDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.
Ming-Yan LiDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.
Li MaDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.
Qi-Jun YiDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.
Yu-E MiaoDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.
Hai-Yan LiuDepartment of Oncology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China. liuhaiyan@sdfmu.edu.cn.
Jian-Gang LiuDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Shandong First Medical University, Tai'an 271000, Shandong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with human epidermal growth factor receptor 2 (HER2)-positive advanced gastric cancer have poor outcomes. Trastuzumab combined with chemotherapy is the first-line standard treatment for HER2-positive advanced gastric cancer. Inetetamab is a novel anti-HER2 drug, and its efficacy and safety in gastric cancer have not yet been reported.

aimTo evaluate the efficacy and safety of the S-1 plus oxaliplatin (SOX) regimen combined with inetetamab as a first-line treatment for HER2-positive advanced gastric cancer.

methodsThirty-eight patients with HER2-positive advanced gastric cancer or gastroesophageal junction adenocarcinoma were randomly divided into two groups: One group received inetetamab combined with the SOX regimen, and the other group received trastuzumab combined with the SOX regimen. After 4-6 cycles, patients with stable disease received maintenance therapy. The primary endpoints were progression-free survival (PFS) and overall survival (OS), and the secondary endpoints were the objective response rate, disease control rate, and adverse events (AEs).

resultsThirty-seven patients completed the trial, with 18 patients in the inetetamab group and 19 patients in the trastuzumab group. In the inetetamab group, the median PFS was 8.5 months, whereas it was 7.3 months in the trastuzumab group (

conclusionIn the first-line treatment of HER2-positive advanced gastric cancer, inetetamab and trastuzumab showed comparable efficacy. The inetetamab group showed superior PFS, and both groups had good safety.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsErb-b2 Receptor Tyrosine KinasesOxaliplatinOxonic AcidStomach NeoplasmsTegafurAdenocarcinomaAdultAgedDrug CombinationsEsophagogastric JunctionFemaleHumansMaleMiddle AgedAntibodies, Monoclonal, HumanizedDrug CombinationsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesOxaliplatinOxonic AcidS 1 (combination)TegafurTrastuzumabAdvanced gastric cancerEfficacyHuman epidermal growth factor receptor 2-positiveInetetamabSafetyTrastuzumab

Identifiers

PMID39494102
PMCPMC11525863

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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.