Evidence map›Paper›PMID 35428212›Full record

ArticleBMC cancer2022

CA19-9 in combination with P-CRP as a predictive marker of immune-related adverse events in patients with recurrent or unresectable advanced gastric cancer treated with nivolumab.

Tomoyuki Matsunaga, Hiroaki Saito, Hirohiko Kuroda, Tomohiro Osaki, Sadamu Takahashi, Akemi Iwamoto, Yoji Fukumoto, Kenjiro Taniguchi, Kenji Fukuda, Wataru Miyauchi and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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

13 authors at 8 institutions in 1 country.

Tomoyuki MatsunagaDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, 683-8504, Japan.
Hiroaki SaitoDepartment of Surgery, Japanese Red Cross Tottori Hospital, Tottori, 680-8517, Japan.ORCID http://orcid.org/0000-0001-7675-0754
Hirohiko KurodaDepartment of Surgery, Japanese Red Cross Masuda Hospital, Masuda, 698-8501, Japan.
Tomohiro OsakiDepartment of Surgery, Tottori Prefectural Central Hospital, Tottori, 680-0901, Japan.
Sadamu TakahashiNational Hospital Organization, Hamada Medical Center, Hamada, 697-8511, Japan.
Akemi IwamotoDivisions of Digestive Surgery, Tottori Prefectural Kousei Hospital, Kurayoshi, 682-0804, Japan.
Yoji FukumotoDivision of Gastroenterology, Matsue City Hospital, Matsue, 690-8509, Japan.
Kenjiro TaniguchiDepartment of Surgery, Yonago Medical Center of National Hospital Organization, Yonago, 683-0006, Japan.
Kenji FukudaDepartment of Surgery, Sanin Rosai Hospital, Yonago, 683-8605, Japan.
Wataru MiyauchiDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, 683-8504, Japan.
Yuji ShishidoDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, 683-8504, Japan.
Kozo MiyataniDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, 683-8504, Japan.
Yoshiyuki FujiwaraDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, 683-8504, Japan.
Tottori University · JPTottori Prefectural Central Hospital · JPMatsudo City Hospital · JPNational Hospital Organization · JPNational Institute of Technology, Yonago College · JPSanin Rosai Hospital · JPTottori Prefectural Kousei Hospital · JPTsuda University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune-check point inhibitors (ICPIs) for treatment of cancer patients sometimes induce potentially life-threatening immune-related adverse events (irAEs), which predict ICPIs treatment efficacy. Prediction of irAEs would be useful for management of irAEs and prediction of ICPIs efficacy. This study aimed to determine predictors of irAEs in patients with recurrent or unresectable advanced gastric cancer (RUGC) treated with nivolumab.

methodsSeventy-eight RUGC patients treated with nivolumab at nine institutions between January 2017 and April 2020 were included in this study. The usefulness of specific blood test results as predictors of irAEs was evaluated.

resultsWe observed irAEs in 15 (19.2%) patients. The disease control rate was significantly higher in the patients with irAEs than in those without (86.7% vs. 42.9%; P < 0.001). The median progression-free survival was significantly longer for patients with irAEs than for patients without (4.9 vs. 2.6 months; P = 0.018). The median survival time was longer for patients with irAEs than for those without (9.4 vs. 5.8 months; P = 0.041). The receiver operating characteristic (ROC) curves for irAEs indicated that the area under the curve (AUC) of carbohydrate antigen 19-9 (CA19-9) was highest (0.692; P = 0.022), followed by that for the platelet count × serum C-reactive protein (P-CRP) value (0.680; P = 0.032). The AUC for the CA19-9 + P-CRP combination was 0.782, which was more useful than that for either component and significantly associated with overall survival of nivolumab-treated RUGC patients.

conclusionsThe CA19-9 + P-CRP combination was predictive of irAEs and prognosis in RUGC patients.

Indexed as

Lung NeoplasmsStomach NeoplasmsCA-19-9 AntigenC-Reactive ProteinHumansNeoplasm Recurrence, LocalNivolumabRetrospective StudiesCA-19-9 AntigenC-Reactive ProteinNivolumabGastric cancerImmune-related adverse eventsNivolumabPrognosis

Identifiers

PMID35428212
PMCPMC9013067
OpenAlexW4224044240

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.