A phase II study of irinotecan combined with S-1 in patients with advanced or recurrent cervical cancer previously treated with platinum based chemotherapy.


Journal

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
ISSN: 1525-1438
Titre abrégé: Int J Gynecol Cancer
Pays: England
ID NLM: 9111626

Informations de publication

Date de publication:
03 2019
Historique:
received: 25 08 2018
revised: 25 10 2018
accepted: 02 11 2018
entrez: 6 3 2019
pubmed: 6 3 2019
medline: 23 1 2020
Statut: ppublish

Résumé

We conducted a phase II study to investigate the efficacy and toxicities of irinotecan plus oral S-1 in patients with advanced or recurrent uterine cervical cancer. Patients with advanced or recurrent cervical cancer previously treated with platinum based chemotherapy were enrolled. Irinotecan (150 mg/m A total of 19 patients were enrolled and treated. The response rate was 29.4%. Grade 3-4 hematologic toxicities were observed in three patients (15.7%). The only grade 3-4 non-hematologic toxicity observed was grade 3 diarrhea. The median progression free survival and overall survival were 3 months and 9 months, respectively. S-1 plus irinotecan in a 3 weekly setting is safe and active in women with advanced or recurrent cervical cancer previously treated with platinum based chemotherapy. Future corroborative clinical studies are warranted.

Identifiants

pubmed: 30833436
pii: ijgc-2018-000070
doi: 10.1136/ijgc-2018-000070
doi:

Substances chimiques

Drug Combinations 0
S 1 (combination) 150863-82-4
Tegafur 1548R74NSZ
Oxonic Acid 5VT6420TIG
Irinotecan 7673326042

Types de publication

Clinical Trial, Phase II Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

474-479

Informations de copyright

© IGCS and ESGO 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Seiji Mabuchi (S)

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan smabuchi@gyne.med.osaka-u.ac.jp.

Eriko Yokoi (E)

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan.

Kotaro Shimura (K)

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan.

Naoko Komura (N)

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan.

Yuri Matsumoto (Y)

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan.

Kenjiro Sawada (K)

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan.

Aki Isobe (A)

Department of Obstetrics and Gynecology, Hyogo Prefectural Nishinomiya Hospital, Hyogo, Japan.

Tateki Tsutsui (T)

Department of Obstetrics and Gynecology, Japan Community Health Care Organization Osaka Hospital, Osaka, Japan.

Fuminori Kitada (F)

Department of Obstetrics and Gynecology, Suita Tokusyukai Hospital, Osaka, Japan.

Tadashi Kimura (T)

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan.

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Classifications MeSH