Efficacy of Postoperative Chemotherapy After Resection that Leaves No Macroscopically Visible Disease of Gastric Cancer with Positive Peritoneal Lavage Cytology (CY1) or Localized Peritoneum Metastasis (P1a): A Multicenter Retrospective Study.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 18 04 2019
pubmed: 20 9 2019
medline: 10 6 2020
entrez: 20 9 2019
Statut: ppublish

Résumé

Gastric cancer (GC) patients with positive peritoneal lavage cytology (CY1) and/or localized peritoneum metastasis (P1a) are defined as stage IV in the 15th edition of the Japanese Classification of Gastric Cancer. In Japan, the most common treatment for patients with CY1 and/or P1a is gastrectomy followed by postoperative chemotherapy. Subjects in this multi-institutional retrospective study were GC patients with CY1 and/or P1a who received surgical resection that leaves no macroscopically visible disease. Patients were selected from 34 institutions in Japan between 2007 and 2012. Selection criteria included adenocarcinoma, no distant metastasis except CY1 and P1a, and no prior treatment for GC before surgery. Among 824 patients registered, 506 were identified as eligible, with a background of P0CY1, P1aCY0, or P1aCY1 (72.5%, 16.0%, and 11.5% of subjects, respectively). Sixty-two patients had not received postoperative chemotherapy (no-Cx), whereas 444 patients had received postoperative chemotherapy: S-1 monotherapy (S-1; n = 267, 52.7%), cisplatin plus S-1 (CS; n = 114, 22.5%), and others (n = 63, 12.6%). Overall survival (OS) was 29.5, 24.7, 25.4 and 9.9 months in the S-1, CS, 'others', and no-Cx groups, respectively [CS vs. S-1: hazard ratio (HR) 1.15, 95% confidence interval (CI) 0.89-1.50; p = 0.275]. In multivariate analysis, OS was similar between the S-1 and CS groups (CS vs. S-1: HR 1.19, 95% CI 0.92-1.55; p = 0.18). Postoperative chemotherapy after gastrectomy that leaves no macroscopically visible disease may have some survival benefits for GC patients with CY1 and/or P1a. In contrast, S-1 plus cisplatin seems to have no additional benefit over S-1 treatment alone.

Sections du résumé

BACKGROUND BACKGROUND
Gastric cancer (GC) patients with positive peritoneal lavage cytology (CY1) and/or localized peritoneum metastasis (P1a) are defined as stage IV in the 15th edition of the Japanese Classification of Gastric Cancer. In Japan, the most common treatment for patients with CY1 and/or P1a is gastrectomy followed by postoperative chemotherapy.
PATIENTS AND METHODS METHODS
Subjects in this multi-institutional retrospective study were GC patients with CY1 and/or P1a who received surgical resection that leaves no macroscopically visible disease. Patients were selected from 34 institutions in Japan between 2007 and 2012. Selection criteria included adenocarcinoma, no distant metastasis except CY1 and P1a, and no prior treatment for GC before surgery.
RESULTS RESULTS
Among 824 patients registered, 506 were identified as eligible, with a background of P0CY1, P1aCY0, or P1aCY1 (72.5%, 16.0%, and 11.5% of subjects, respectively). Sixty-two patients had not received postoperative chemotherapy (no-Cx), whereas 444 patients had received postoperative chemotherapy: S-1 monotherapy (S-1; n = 267, 52.7%), cisplatin plus S-1 (CS; n = 114, 22.5%), and others (n = 63, 12.6%). Overall survival (OS) was 29.5, 24.7, 25.4 and 9.9 months in the S-1, CS, 'others', and no-Cx groups, respectively [CS vs. S-1: hazard ratio (HR) 1.15, 95% confidence interval (CI) 0.89-1.50; p = 0.275]. In multivariate analysis, OS was similar between the S-1 and CS groups (CS vs. S-1: HR 1.19, 95% CI 0.92-1.55; p = 0.18).
CONCLUSIONS CONCLUSIONS
Postoperative chemotherapy after gastrectomy that leaves no macroscopically visible disease may have some survival benefits for GC patients with CY1 and/or P1a. In contrast, S-1 plus cisplatin seems to have no additional benefit over S-1 treatment alone.

Identifiants

pubmed: 31535301
doi: 10.1245/s10434-019-07697-x
pii: 10.1245/s10434-019-07697-x
doi:

Substances chimiques

Drug Combinations 0
S 1 (combination) 150863-82-4
Tegafur 1548R74NSZ
Oxonic Acid 5VT6420TIG
Cisplatin Q20Q21Q62J

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

284-292

Auteurs

Toshifumi Yamaguchi (T)

Cancer Chemotherapy Center and Second Department of Internal Medicine, Osaka Medical College, Osaka, Japan.
Gastrointestinal Oncology Division, National Cancer Center Hospital, Tokyo, Japan.

Atsuo Takashima (A)

Gastrointestinal Oncology Division, National Cancer Center Hospital, Tokyo, Japan. atakashi@ncc.go.jp.

Kengo Nagashima (K)

Research Center for Medical and Health Data Science, The Institute of Statistical Mathematics, Tokyo, Japan.

Rie Makuuchi (R)

Division of Gastric Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Masaki Aizawa (M)

Department of Gastroenterological Surgery, Niigata Cancer Center Hospital, Niigata, Japan.

Manabu Ohashi (M)

Department of Gastroenterological Surgery, Cancer Institute Hospital, Tokyo, Japan.

Keitaro Tashiro (K)

Departments of General and Gastroenterological Surgery, Osaka Medical College Hospital, Osaka, Japan.

Tatsuya Yamada (T)

Department of Gastroenterological Surgery, Saitama Cancer Center, Saitama, Japan.

Takahiro Kinoshita (T)

Gastric Surgery Division, National Cancer Center Hospital East, Kashiwa, Japan.

Hiroaki Hata (H)

Department of Surgery, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.

Yasuyuki Kawachi (Y)

Department of Surgery, Nagaoka Chuo General Hospital, Niigata, Japan.

Ryohei Kawabata (R)

Department of Surgery, Osaka Rosai Hospital, Osaka, Japan.

Toshikatsu Tsuji (T)

Department of Gastroenterological Surgery, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.

Jun Hihara (J)

Department of Surgery, Hiroshima City Asa Citizens Hospital, Hiroshima, Japan.

Takeshi Sakamoto (T)

Department of Gastroenterology, Hyogo Cancer Center, Hyogo, Japan.

Takeo Fukagawa (T)

Department of Surgery, Teikyo University Hospital, Tokyo, Japan.

Hitoshi Katai (H)

Department of Gastric Surgery, National Cancer Center Hospital, Tokyo, Japan.

Kazuhide Higuchi (K)

Cancer Chemotherapy Center and Second Department of Internal Medicine, Osaka Medical College, Osaka, Japan.

Narikazu Boku (N)

Gastrointestinal Oncology Division, National Cancer Center Hospital, Tokyo, Japan.

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