Evidence map›Paper›PMID 37634209›Full record

SynthesisInternational journal of clinical oncology2023

Meta-analysis of three randomized trials of capecitabine plus cisplatin (XP) versus S-1 plus cisplatin (SP) as first-line treatment for advanced gastric cancer.

Kazuhiro Nishikawa, Hisato Kawakami, Toshio Shimokawa, Kazumasa Fujitani, Shigeyuki Tamura, Shunji Endo, Michiya Kobayashi, Junji Kawada, Yukinori Kurokawa, Akira Tsuburaya and 4 more

Abstract readMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in International journal of clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 11 institutions in 1 country.

Kazuhiro Nishikawa *Cancer Treatment Center, Osaka Police Hospital, 10-31 Kitayama-cho, Tennoji-ku, Osaka, 543-0035, Japan. kazuno13@hotmail.co.jp.ORCID http://orcid.org/0000-0003-1213-2732
Hisato Kawakami *Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Toshio ShimokawaClinical Study Support Center, Wakayama Medical University, Wakayama, Japan.
Kazumasa FujitaniDepartment of Gastroenterological Surgery, Osaka General Medical Center, Osaka, Japan.
Shigeyuki TamuraDepartment of Surgery, Yao Municipal Hospital, Yao, Japan.
Shunji EndoDepartment of Digestive Surgery, Kawasaki Medical School Hospital, Kurashiki, Japan.
Michiya KobayashiCancer Treatment Center, Kochi Medical School Hospital, Nankoku, Japan.
Junji KawadaDepartment of Gastroenterological Surgery, Osaka General Medical Center, Osaka, Japan.
Yukinori KurokawaDepartment of Gastroenterological Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Akira TsuburayaDepartment of Surgery, AOI Nanasawa Rehabilitation Hospital, Atsugi, Japan.
Takaki YoshikawaDepartment of Gastric Surgery, National Cancer Center Hospital, Tokyo, Japan.
Junichi SakamotoTokai Central Hospital, Kakamigahara, Japan.
Taroh SatohPalliative Care Center, Osaka University Hospital, Suita, Japan.
for HERBIS-2, HERBIS-4A, XParTS I. I. study investigators
Osaka Prefectural Medical Center · JPKawasaki Medical School Hospital · JPKindai University · JPKochi Medical School Hospital · JPNaga Municipal Hospital · JPOsaka Police Hospital · JPOsaka University Hospital · JPThe University of Osaka · JPTokai Central Hospital · JPTokyo National Hospital · JPWakayama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundS-1 plus cisplatin (SP) and capecitabine plus cisplatin (XP) are standard first-line regimens for advanced gastric cancer (AGC) worldwide. We conducted a meta-analysis using individual participant data (IPD) to investigate which is more suitable.

methodsIPD from three randomized trials were collected. In these trials, patients with AGC were randomly allocated to SP (S-1 80-120 mg for 21 days plus cisplatin 60 mg/m

resultsIn 211 eligible patients, median overall survival (OS) for SP versus XP was 13.5 and 11.7 months (hazard ratio [HR], 0.787; p = 0.114), progression-free survival (PFS) was 6.2 and 5.1 months (HR, 0.767; P = 0.076), and TTF was 5.1 and 4.0 months (HR, 0.611; P = 0.001). The most common grade ≥ 3 adverse events with SP or XP were neutropenia (18% vs. 29%) and anorexia (16% vs.18%). Subgroup analysis demonstrated significant interaction between treatment effect and performance status > 1 (HR, 0.685; P = 0.036), measurable lesion (HR, 0.709; P = 0.049), primary upper third tumor (HR, 0.539; P = 0.040), and differentiated type (HR, 0.549; interaction, 0.236; P = 0.019). For the differentiated type, OS was significantly longer in the SP group (13.2 months) than in the XP group (11.1 months) (HR, 0.549; P = 0.019). For the undifferentiated type, OS was similar in the SP group (14.2 months) and in the XP group (12.4 months) (HR, 0.868; P = 0.476).

conclusionsSP and XP were both effective and well tolerated. SP might be suitable for the pathological differentiated subtype of AGC. CLINICAL

trial registrationThe HERBIS-2, HERBIS-4A, and XParTS II trials were registered with UMIN-CTR as UMIN000006105, UMIN000006755, and UMIN000006045, respectively.

Indexed as

Stomach NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsCapecitabineCisplatinDrug CombinationsHumansRandomized Controlled Trials as TopicCapecitabineCisplatinDrug CombinationsS-1 plus cisplatinAdvanced gastric cancerCapecitabine plus cisplatin (XP)First-line chemotherapyHistological subtypesMeta-analysisS-1 plus cisplatin (SP)

Identifiers

PMID37634209
OpenAlexW4386203695

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.