First-line Gemcitabine


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 16 01 2021
revised: 26 01 2021
accepted: 27 01 2021
entrez: 31 3 2021
pubmed: 1 4 2021
medline: 10 4 2021
Statut: ppublish

Résumé

This study aimed to investigate the efficacy of first-line gemcitabine monotherapy for metastatic breast cancer (MBC) and its effect on health-related quality of life (HRQoL) compared with treatment of physician's choice (TPC). We enrolled 96 patients into the first-line gemcitabine group (n=47) or other treatment of physician's choice (TPC) group (n=49) from May 2010 to April 2013. HRQoL was evaluated every 4 weeks. There was no significant difference in the median time to treatment failure (5.3 vs. 4.6 months, hazard ratio=0.87, p=0.546) and the incidence rates of grade 3/4 haematological toxicity (10.6% vs. 8.1%, p=0.677) and grade 3/4 non-haematological toxicity (4.2% vs. 8.1%, p=0.429) between the gemcitabine and TPC groups. Changes in HRQoL from baseline to 12 weeks were not significantly different. Gemcitabine achieves similar efficacy and HRQoL benefit to other chemotherapy and can be used as first-line treatment for MBC.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
This study aimed to investigate the efficacy of first-line gemcitabine monotherapy for metastatic breast cancer (MBC) and its effect on health-related quality of life (HRQoL) compared with treatment of physician's choice (TPC).
PATIENTS AND METHODS METHODS
We enrolled 96 patients into the first-line gemcitabine group (n=47) or other treatment of physician's choice (TPC) group (n=49) from May 2010 to April 2013. HRQoL was evaluated every 4 weeks.
RESULTS RESULTS
There was no significant difference in the median time to treatment failure (5.3 vs. 4.6 months, hazard ratio=0.87, p=0.546) and the incidence rates of grade 3/4 haematological toxicity (10.6% vs. 8.1%, p=0.677) and grade 3/4 non-haematological toxicity (4.2% vs. 8.1%, p=0.429) between the gemcitabine and TPC groups. Changes in HRQoL from baseline to 12 weeks were not significantly different.
CONCLUSION CONCLUSIONS
Gemcitabine achieves similar efficacy and HRQoL benefit to other chemotherapy and can be used as first-line treatment for MBC.

Identifiants

pubmed: 33788764
pii: 41/3/1671
doi: 10.21873/anticanres.14930
doi:

Substances chimiques

Deoxycytidine 0W860991D6
Gemcitabine 0

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1671-1676

Informations de copyright

Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Shinya Yamamoto (S)

Yokohama City University Medical Center, Department of Breast and Thyroid Surgery, Yokohama, Japan.

Kazutaka Narui (K)

Yokohama City University Medical Center, Department of Breast and Thyroid Surgery, Yokohama, Japan; nr1@gc5.so-net.ne.jp.

Takashi Ishikawa (T)

Yokohama City University Medical Center, Department of Breast and Thyroid Surgery, Yokohama, Japan.

Shoko Adachi (S)

Yokohama City University Medical Center, Department of Breast and Thyroid Surgery, Yokohama, Japan.

Kazuhiro Shimada (K)

Yokohama City University Medical Center, Department of Breast and Thyroid Surgery, Yokohama, Japan.

Daisuke Shimizu (D)

Yokohama City University Medical Center, Department of Breast and Thyroid Surgery, Yokohama, Japan.

Akimitsu Yamada (A)

Yokohama City University Graduate School of Medicine, Department of Gastroenterological Surgery, Yokohama, Japan.

Sadatoshi Sugae (S)

Yokohama City University Graduate School of Medicine, Department of Gastroenterological Surgery, Yokohama, Japan.

Mikiko Tanabe (M)

Yokohama City University Medical Center, Department of Pathology, Yokohama, Japan.

Mari Oba (M)

Yokohama City University Medical Center, Department of Biostatics and Epidemiology, Yokohama, Japan.

Satoshi Morita (S)

Kyoto University Graduate School of Medicine, Department of Biomedical Statistics and Bioinformatics, Kyoto, Japan.

Takako Doi (T)

Shonan Kinen Hospital, Breast Center, Kamakura, Japan.

Satoshi Hasegawa (S)

Saiseikai Yokohama-shi Nanbu Hospital, Department of Surgery, Yokohama, Japan.

Tomoyuki Morita (T)

Yokosuka Kyosai Hospital, Department of Surgery, Yokosuka, Japan.

Ayako Kito (A)

Yokohama Municipal Citizen's Hospital, Department of Breast Surgery, Yokohama, Japan.

Takashi Chishima (T)

Yokohama Rosai Hospital, Department of Breast Surgery, Yokohama, Japan.

Yasushi Ichikawa (Y)

Yokohama City University Graduate School of Medicine, Department of Clinical Oncology, Yokohama, Japan.

Itaru Endo (I)

Yokohama City University Graduate School of Medicine, Department of Gastroenterological Surgery, Yokohama, Japan.

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Classifications MeSH