A randomized study comparing docetaxel/cyclophosphamide (TC), 5-fluorouracil/epirubicin/cyclophosphamide (FEC) followed by TC, and TC followed by FEC for patients with hormone receptor-positive HER2-negative primary breast cancer.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 25 11 2019
accepted: 06 03 2020
pubmed: 15 3 2020
medline: 15 12 2020
entrez: 15 3 2020
Statut: ppublish

Résumé

Our primary objective was to determine the benefit/risk of anthracycline-free regimens by comparing docetaxel + cyclophosphamide (TC) alone, fluorouracil + epirubicin + cyclophosphamide (FEC) followed by TC, or TC followed by FEC as a primary treatment for patients with HR-positive, HER2-negative BC. We randomized patients with stage I-III HR-positive HER2-negative, operable BC to receive either six cycles of TC (TC6), three cycles of FEC followed by three cycles of TC (FEC-TC), or three cycles of TC followed by three cycles of FEC (TC-FEC). The primary endpoint was the pathological response. Secondary endpoints included clinical response, type of surgical procedure, recurrence, death, and adverse events (by NCI-Common Terminology Criteria for Adverse Events v.3.0). We conducted all statistical analyses using SAS Version 9.2. We enrolled 195 patients and analyzed data from 193 as the intention-to-treat population. Pathological complete response rates were numerically higher in the TC6 group than in the other groups (p = 0.321). The breast conservation rate was significantly higher in the TC6 group (73%) than in the other groups (FEC-TC 51%, TC-FEC 45%, p = 0.007). Adverse events with grade > 3 were not common in the treatment groups (p = 0.569). The overall and distant disease-free survivals were similar among the groups with median follow-up of 5.80 years. Despite similar long-term efficacy and safety profile, the higher breast conservation rate in the TC6 group suggests that preoperative chemotherapy without an anthracycline may benefit patients with HR-positive HER2-negative BC. UMIN000003283 https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003873.

Identifiants

pubmed: 32170634
doi: 10.1007/s10549-020-05590-w
pii: 10.1007/s10549-020-05590-w
pmc: PMC7103001
doi:

Substances chimiques

Receptors, Estrogen 0
Receptors, Progesterone 0
Docetaxel 15H5577CQD
Epirubicin 3Z8479ZZ5X
Cyclophosphamide 8N3DW7272P
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Fluorouracil U3P01618RT

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

715-724

Références

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Auteurs

Hiroshi Ishiguro (H)

International University of Health and Welfare, 4-3 Kozunomori, Narita, 286-8686, Japan. hishiguro@iuhw.ac.jp.

Norikazu Masuda (N)

National Hospital Organization Osaka National Hospital, Osaka, Japan.

Nobuaki Sato (N)

Niigata Cancer Center Hospital, Niigata, Japan.

Kenji Higaki (K)

Higaki Breastcare Clinic, Osaka, Japan.

Takashi Morimoto (T)

Yao Municipal Hospital, Osaka, Japan.

Yasuhiro Yanagita (Y)

Gunma Prefectural Cancer Center, Maebashi, Japan.

Makiko Mizutani (M)

National Hospital Organization Osaka National Hospital, Osaka, Japan.

Shoichiro Ohtani (S)

Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.

Koji Kaneko (K)

Niigata Cancer Center Hospital, Niigata, Japan.

Tomomi Fujisawa (T)

Gunma Prefectural Cancer Center, Maebashi, Japan.

Masato Takahashi (M)

National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan.

Takayuki Kadoya (T)

Hiroshima University Hospital, Hiroshima, Japan.

Nobuki Matsunami (N)

Shuto General Hospital, Yamaguchi, Japan.

Yutaka Yamamoto (Y)

Kumamoto University Hospital, Kumamoto, Japan.

Shinji Ohno (S)

Cancer Institute Hospital of JFCR, Tokyo, Japan.

Toshimi Takano (T)

Toranomon Hospital, Tokyo, Japan.

Satoshi Morita (S)

Kyoto University Hospital, Kyoto, Japan.

Sachiko Tanaka-Mizuno (S)

Kyoto University Hospital, Kyoto, Japan.
Shiga University of Medical Science, Otsu, Japan.

Masakazu Toi (M)

Kyoto University Hospital, Kyoto, Japan.

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Classifications MeSH