Evidence map›Paper›PMID 42525322›Full record

ArticleInternational journal of clinical pharmacy2026

Effectiveness of continuous pharmacist intervention at maintaining dose intensity in postoperative adjuvant S-1 chemotherapy for gastric cancer: a multicentre retrospective study.

Toshinobu Hayashi, Makiko Go, Kenji Kawasumi, Kazuyoshi Kawakami, Reiko Matsui, Hironori Fujii, Takanori Miyoshi, Tomoaki Eto, Makoto Kajizono, Tatsuya Ohtsubo and 6 more

Abstract readMulticenter Study
In one paragraph

Article in International journal of clinical pharmacy, 2026. 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
–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

0 citing papers in PubMed.

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

16 authors.

Toshinobu Hayashi *Department of Pharmaceutical Sciences for Health Crisis Management, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.ORCID http://orcid.org/0000-0001-6183-4939
Makiko Go *Department of Pharmacy, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.ORCID http://orcid.org/0009-0001-6499-7060
Kenji KawasumiDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Chiba, Japan.
Kazuyoshi KawakamiDepartment of Pharmacy, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2023-1300
Reiko MatsuiDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Chiba, Japan.
Hironori FujiiDepartment of Pharmacy, Gifu University Hospital, Gifu, Japan.ORCID http://orcid.org/0000-0003-0944-7290
Takanori MiyoshiDepartment of Pharmacy, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.ORCID http://orcid.org/0000-0003-1644-9841
Tomoaki EtoDepartment of Pharmacy, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.ORCID http://orcid.org/0009-0004-2028-1476
Makoto KajizonoDepartment of Pharmacy, Okayama University Hospital, Okayama, Japan.ORCID http://orcid.org/0009-0000-4683-3225
Tatsuya OhtsuboDepartment of Pharmacy, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan.ORCID http://orcid.org/0009-0008-1378-2028
Yumi MoriokaDepartment of Pharmacy, Kagoshima Kouseiren Hospital, Kagoshima, Japan.
Kyohei YamaguchiDepartment of Pharmacy, Japanese Red Cross Matsuyama Hospital, Matsuyama, Ehime, Japan.
Akihiro OgawaDepartment of Pharmacy, Japanese Red Cross Ise Hospital, Ise, Mie, Japan.
Toshihisa NakashimaDepartment of Pharmacy, National Cancer Center Japan Hospital, Tokyo, Japan.ORCID http://orcid.org/0000-0002-6048-2502
Maki TodoDepartment of Pharmacy, Saitama Medical University International Medical Center, Hidaka, Saitama, Japan.ORCID http://orcid.org/0000-0001-5203-493X
Koichi MatsuoDepartment of Oncology and Infectious Disease Pharmacy, Faculty of Pharmaceutical Sciences, Fukuoka University, 8-19-1, Nanakuma, Jonan-Ku, Fukuoka, 814-0180, Japan. ko1matsuo@fukuoka-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMaintaining dose intensity is essential for ensuring the efficacy of adjuvant S-1 chemotherapy in gastric cancer. Although pharmacist interventions can reduce toxicity and improve adherence, multicentre evidence regarding their impact on dose maintenance is limited.

aimThis study aimed to evaluate the effectiveness of continuous pharmacist intervention on the eight-cycle treatment completion rate and relative performance (RP) in patients with gastric cancer undergoing outpatient S-1 adjuvant chemotherapy.

methodThis multicentre retrospective study analysed 225 patients across 12 institutions, categorised into the continuous intervention (n = 97) and non-continuous intervention (n = 128) groups. Continuous intervention was defined as systematic monitoring and management for at least 50% of the treatment duration. Inverse probability of treatment weighting was used to adjust for baseline covariates. The primary and secondary endpoints were the eight-cycle completion rate and RP value, respectively.

resultsThe eight-cycle completion rate did not differ significantly between the continuous and non-continuous intervention groups (53.0% vs. 55.2%, p = 0.775), nor did the frequency of treatment modification events, including discontinuation or dose reduction. However, the RP value was significantly higher in the continuous intervention group than in the non-continuous intervention group (73.7% vs. 64.9%, p = 0.038). This finding was robustly supported by sensitivity analysis between these two groups (75.1% vs. 61.1%, p = 0.0008). Overall, the continuous group maintained a high intervention rate (89.1%) throughout the final cycle, providing significantly more supportive care interventions than the non-continuous intervention group (53.2% vs. 4.9%, p < 0.001).

conclusionAlthough continuous pharmacist intervention did not improve the treatment completion rate, it was essential for maintaining RP values above the clinically essential 70% threshold through proactive toxicity management and dynamic dose optimisation. These findings suggest that systematic pharmaceutical care contributes significantly to ensuring the quality and intensity of adjuvant chemotherapy.

Indexed as

Antimetabolites, AntineoplasticOxonic AcidPharmacistsProfessional RoleStomach NeoplasmsTegafurAgedChemotherapy, AdjuvantDrug CombinationsFemaleHumansMaleMiddle AgedRetrospective StudiesAntimetabolites, AntineoplasticDrug CombinationsOxonic AcidS 1 (combination)TegafurAdjuvant chemotherapyContinuous interventionGastric cancerPharmacistS-1

Identifiers

PMID42525322
PMCPMC13569544

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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.