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.
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Breast Neoplasms
/ drug therapy
Carcinoma, Ductal, Breast
/ drug therapy
Carcinoma, Lobular
/ drug therapy
Cyclophosphamide
/ administration & dosage
Docetaxel
/ administration & dosage
Epirubicin
/ administration & dosage
Female
Fluorouracil
/ administration & dosage
Follow-Up Studies
Humans
Middle Aged
Prognosis
Receptor, ErbB-2
/ metabolism
Receptors, Estrogen
/ metabolism
Receptors, Progesterone
/ metabolism
Survival Rate
Young Adult
Breast cancer
Cyclophosphamide
Docetaxel
Doxorubicin
Neoadjuvant chemotherapy
Randomized clinical trial
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
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
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