Retrospective study on the effectiveness of medroxyprogesterone acetate in the treatment of ER-positive/HER2-negative post-menopausal advanced breast cancer: an additional analysis of the JBCRG-C06 Safari study.


Journal

Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225

Informations de publication

Date de publication:
07 Mar 2023
Historique:
received: 24 07 2022
accepted: 08 11 2022
pubmed: 10 12 2022
medline: 10 3 2023
entrez: 9 12 2022
Statut: ppublish

Résumé

Only old evidence exists to back up the use of medroxyprogesterone acetate. Therefore, this study aimed to explore the factors that influence the time to treatment failure of medroxyprogesterone acetate in real-world settings as late-line treatment. This was a cohort study that used the database of the Safari study on oestrogen receptor-positive post-menopausal advanced breast cancer (UMIN000015168). We created Kaplan-Meier curves for time to treatment failure with medroxyprogesterone acetate. Further, univariate and multivariate analyses were performed using a Cox hazard model of the clinicopathological factors involved in the time to treatment failure of medroxyprogesterone acetate. From the 1031 patients in the Safari study, 279 patients were selected as the population for the analysis of effectiveness of medroxyprogesterone acetate monotherapy. In the analysis of medroxyprogesterone acetate by treatment line, the median time to treatment failure was 3.0 months for third-line treatment and 4.1 months for fourth and subsequent treatment lines. In cases where medroxyprogesterone acetate was used as a third-line or later endocrine treatment, multivariate analysis showed that the length of the disease-free interval was correlated with the length of time to treatment failure of medroxyprogesterone acetate (P = 0.004). With medroxyprogesterone acetate monotherapy as the fourth-line or later treatment, 20% of the patients achieved a time to treatment failure of 12 months or longer. In actual clinical practice, patients treated with medroxyprogesterone acetate alone as the fourth or subsequent treatment lines showed a time to treatment failure of 4 months, suggesting that there is merit in using medroxyprogesterone acetate even in late treatment lines, especially in patients with long disease-free interval and those who are difficult to treat using other antineoplastic agents.

Sections du résumé

BACKGROUND BACKGROUND
Only old evidence exists to back up the use of medroxyprogesterone acetate. Therefore, this study aimed to explore the factors that influence the time to treatment failure of medroxyprogesterone acetate in real-world settings as late-line treatment.
METHODS METHODS
This was a cohort study that used the database of the Safari study on oestrogen receptor-positive post-menopausal advanced breast cancer (UMIN000015168). We created Kaplan-Meier curves for time to treatment failure with medroxyprogesterone acetate. Further, univariate and multivariate analyses were performed using a Cox hazard model of the clinicopathological factors involved in the time to treatment failure of medroxyprogesterone acetate.
RESULTS RESULTS
From the 1031 patients in the Safari study, 279 patients were selected as the population for the analysis of effectiveness of medroxyprogesterone acetate monotherapy. In the analysis of medroxyprogesterone acetate by treatment line, the median time to treatment failure was 3.0 months for third-line treatment and 4.1 months for fourth and subsequent treatment lines. In cases where medroxyprogesterone acetate was used as a third-line or later endocrine treatment, multivariate analysis showed that the length of the disease-free interval was correlated with the length of time to treatment failure of medroxyprogesterone acetate (P = 0.004). With medroxyprogesterone acetate monotherapy as the fourth-line or later treatment, 20% of the patients achieved a time to treatment failure of 12 months or longer.
CONCLUSION CONCLUSIONS
In actual clinical practice, patients treated with medroxyprogesterone acetate alone as the fourth or subsequent treatment lines showed a time to treatment failure of 4 months, suggesting that there is merit in using medroxyprogesterone acetate even in late treatment lines, especially in patients with long disease-free interval and those who are difficult to treat using other antineoplastic agents.

Identifiants

pubmed: 36484305
pii: 6884062
doi: 10.1093/jjco/hyac184
doi:

Substances chimiques

Medroxyprogesterone Acetate C2QI4IOI2G
Medroxyprogesterone HSU1C9YRES

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

203-211

Subventions

Organisme : AstraZeneca
Organisme : Kumamoto University

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Hidetoshi Kawaguchi (H)

Department of Breast Surgery, Matsuyama Red Cross Hospital, Matsuyama, Japan.

Yutaka Yamamoto (Y)

Department of Breast and Endocrine Surgery, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.

Shigehira Saji (S)

Department of Medical Oncology, Fukushima Medical University, Fukushima, Japan.

Norikazu Masuda (N)

Department of Department of Breast and Endocrine Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Takahiro Nakayama (T)

Department of Breast and Endocrine Surgery, Osaka International Cancer Institute, Osaka, Japan.

Kenjiro Aogi (K)

Department of Breast Oncology, NHO Shikoku Cancer Center, Matsuyama, Japan.

Keisei Anan (K)

Department of Surgery, Kitakyushu Municipal Medical Center, Kitakyushu , Japan.

Shoichiro Ohtani (S)

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

Nobuaki Sato (N)

Department of Breast Oncology, Niigata Cancer Center Hospital, Niigata, Japan.

Toshimi Takano (T)

Department of Medical Oncology, Toranomon Hospital, Tokyo, Japan.

Eriko Tokunaga (E)

Department of Breast Oncology, Kyushu Cancer Center, Fukuoka, Japan.

Seigo Nakamura (S)

Department of Surgery, Division of Breast Surgical Oncology, Showa University School of Medicine, Tokyo, Japan.

Yoshie Hasegawa (Y)

Department of Breast Surgery, Hachinohe City Hospital, Hachinohe, Japan.

Masaya Hattori (M)

Department of Breast Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.

Tomomi Fujisawa (T)

Department of Breast Oncology, Gunma Prefectural Cancer Center, Ohta, Japan.

Satoshi Morita (S)

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

Miki Yamaguchi (M)

Department of Breast Surgery, JCHO Kurume General Hospital, Kurume, Japan.

Toshinari Yamashita (T)

Department of Breast and Endocrine Surgery, Kanagawa Cancer Center, Yokohama, Japan.

Daisuke Yotsumoto (D)

Department of Breast and Thyroid Surgery, Hakuaikai Social Medical Corporation, Sagara Hospital, Kagoshima, Japan.

Masakazu Toi (M)

Department of Breast Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Shinji Ohno (S)

Breast Oncology Center, The Cancer Institute Hospital of JFCR, Tokyo, Japan.

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Classifications MeSH