Neoadjuvant exemestane or exemestane plus docetaxel and cyclophosphamide tailored by clinicopathological response to 12 weeks' exemestane exposure in patients with estrogen receptor-positive breast cancer: A multicenter, open-label, phase II study.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 19 03 2019
revised: 28 06 2019
accepted: 03 07 2019
pubmed: 31 7 2019
medline: 22 8 2020
entrez: 31 7 2019
Statut: ppublish

Résumé

Our aim was to investigate the efficacy and safety of initial neoadjuvant endocrine therapy with exemestane alone followed by tailored treatment, either continued exemestane monotherapy or exemestane plus docetaxel-cyclophosphamide (TC) combination therapy, in postmenopausal patients with primary invasive estrogen receptor-positive, human epidermal growth factor receptor 2-negative, stage I-IIIA breast cancer and Ki67 labeling index ≤30%. In this open-label phase II study, patients initially received exemestane 25 mg/d for 12 weeks. Responders were defined as patients who achieved complete response (CR), partial response (PR) with Ki67 labeling index ≤5% after treatment, or stable disease with Ki67 labeling index ≤5% both before and after treatment. For the subsequent 12 weeks, exemestane monotherapy was continued for responders (group A), whereas nonresponders received exemestane plus four cycles of TC (docetaxel 75 mg/m

Identifiants

pubmed: 31361400
doi: 10.1002/cam4.2423
pmc: PMC6745863
doi:

Substances chimiques

Androstadienes 0
Receptors, Estrogen 0
Docetaxel 15H5577CQD
Cyclophosphamide 8N3DW7272P
exemestane NY22HMQ4BX

Types de publication

Clinical Trial, Phase II Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

5468-5481

Subventions

Organisme : Japan Breast Cancer Research Group

Informations de copyright

© 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Nobuaki Sato (N)

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

Norikazu Masuda (N)

Department of Surgery, Breast Oncology, National Hospital Organization Osaka National Hospital, Osaka, Japan.

Takashi Morimoto (T)

Department of Breast Surgery, Yao Municipal Hospital, Osaka, Japan.

Takayuki Ueno (T)

Breast Surgical Oncology, Breast Oncology Center, Cancer Institute Hospital, Tokyo, Japan.

Chizuko Kanbayashi (C)

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

Koji Kaneko (K)

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

Hiroyuki Yasojima (H)

Department of Surgery, Breast Oncology, National Hospital Organization Osaka National Hospital, Osaka, Japan.

Shigehira Saji (S)

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

Hironobu Sasano (H)

Department of Pathology, Tohoku University, Miyagi, Japan.

Satoshi Morita (S)

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

Shinji Ohno (S)

Breast Oncology Center, Cancer Institute Hospital, Tokyo, Japan.

Masakazu Toi (M)

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

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Classifications MeSH