Evidence map›Paper›PMID 33688593›Full record

ReviewGlobal health & medicine2021

Current status of doublet combinations of platinum and fluoropyrimidines using oxaliplatin for advanced gastric cancer.

Shusuke Yagi, Kazuhiko Yamada, Masayoshi Terayama, Hitomi Wake, Naoki Enomoto, Kyoko Nohara, Nobuyuki Takemura, Tomomichi Kiyomatsu, Norihiro Kokudo

Open access · bronzeAbstract readReview
In one paragraph

Review in Global health & medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. NJournal of cancer research and clinical oncology · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. 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 at 1 institution in 1 country.

Shusuke YagiDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Kazuhiko YamadaDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Masayoshi TerayamaDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Hitomi WakeDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Naoki EnomotoDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Kyoko NoharaDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Nobuyuki TakemuraDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Tomomichi KiyomatsuDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
Norihiro KokudoDepartment of Surgery, National Center for Global Health and Medicine, Tokyo, Japan.
National Center for Global Health and Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most common treatment for advanced gastric cancer (AGC) is systemic chemotherapy. The standard treatment for advanced gastric cancer differs worldwide. In Japan, two phase III clinical trials demonstrated the non-inferiority of S-1 compared with 5-fluorouracil (5-FU) and superiority of cisplatin plus S-1 (CS), compared with S-1, with respect to overall survival (SPIRITS trial). Oxaliplatin (L-OHP) has a favorable toxicity profile compared with cisplatin; hence, a phase III clinical trial (G-SOX trial) demonstrated the progression-free survival (PFS) and overall survival in CS was 5.4 and 13.1 months and those in SOX was 5.5 and 14.1 months, respectively. Serious adverse events were more frequently seen in CS than in SOX. So, SOX is as effective as CS for advanced gastric cancer with favorable safety profile. After the publication of this G-SOX trial, the combination of oral or intravenous 5-FU and various doses of L-OHP have been reported. And FOLFOX6 regimen (FOLFOX: a combination of 1-LV and FU with L-OHP) was approved for the treatment of AGC in Japan in 2017. FOLFOX was promising for patients with severe peritoneal metastasis from AGC, because the FOLFOX regimen does not require hydration and does not include oral agents. This review summarizes the efficacy and safety of doublet combinations of platinum and fluoropyrimidines using L-OHP for advanced gastric cancer.

Indexed as

advanced gastric cancerFOLFOXoxaliplatinS-1

Identifiers

PMID33688593
PMCPMC7936367
OpenAlexW3116418363

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.