Evidence map›Paper›PMID 38400680›Full record

Trial reportCancer medicine2024

Efficacy and safety of camrelizumab combined with oxaliplatin and S-1 as neoadjuvant treatment in locally advanced gastric or gastroesophageal junction cancer: A phase II, single-arm study.

Wen-Jin Zhong, Jian-An Lin, Chu-Ying Wu, Jiantian Wang, Jun-Xing Chen, Huida Zheng, Kai Ye

Open access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
6.3field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

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  4. Neoadjuvant camrelizumab plus trastuzumab and chemotherapy for HER2-positive gastric or gastroesophageal junction adenocarcinoma: a single-arm, phase 2 trial.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2025
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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

7 authors at 1 institution in 1 country.

Wen-Jin ZhongDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, QuanZhou City, Fujian, China.
Jian-An LinDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, QuanZhou City, Fujian, China.
Chu-Ying WuDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, QuanZhou City, Fujian, China.
Jiantian WangDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, QuanZhou City, Fujian, China.
Jun-Xing ChenDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, QuanZhou City, Fujian, China.
Huida ZhengDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, QuanZhou City, Fujian, China.
Kai YeDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, QuanZhou City, Fujian, China.ORCID 0000-0001-8567-6197
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn the present study, we aimed to evaluate the efficacy and safety of camrelizumab combined with oxaliplatin plus S-1 in patients with resectable gastric or gastroesophageal junction cancer.

methodsIn this single-arm, phase II clinical trial, patients with locally advanced gastric or gastroesophageal junction adenocarcinoma were enrolled to receive three cycles of neoadjuvant camrelizumab and oxaliplatin plus S-1 every 3 weeks, followed by surgical resection and adjuvant therapy with the same regimen. The primary endpoint was pathological complete response (pCR) (ypT0) rate and secondary endpoints were R0 resection rate, total pCR (tpCR, ypT0N0) rate, major pathological response (MPR) rate, downstaging, objective response rate (ORR), disease control rate (DCR), event-free survival (EFS), overall survival (OS), and safety.

resultsBetween September, 2020 and January, 2022, a total of 29 patients were enrolled in the present study, all of whom completed neoadjuvant therapy and underwent surgery. Three (10.3%) (95% CI: 2.2-27.4) patients achieved pCR as well as tpCR, 20 (69.0%) patients had MPR and 28 (96.6%) patients achieved R0 resection. Treatment-emergent adverse events (AEs) of any grade were observed in 24 (82.8%) patients. Immune-related adverse events of any grade were reported in 13 (44.8%) patients, whereas no grade 3 or higher adverse events occurred.

conclusionThe neoadjuvant therapy with camrelizumab in combination with oxaliplatin and S-1 showed a modest pCR rate, and favorable MPR rate and safety profile in patients with gastric or gastroesophageal junction cancer.

Indexed as

Antibodies, Monoclonal, HumanizedNeoadjuvant TherapyStomach NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsEsophagogastric JunctionHumansOxaliplatinAntibodies, Monoclonal, HumanizedcamrelizumabOxaliplatinCamrelizumabgastric cancergastroesophageal junction cancerimmune checkpoint inhibitorNeoadjuvant therapyS-1

Identifiers

PMID38400680
PMCPMC10891470
OpenAlexW4392133444

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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.