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PMID: 15365066 Published · ppublish English Clinical Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Effect of doxorubicin plus cyclophosphamide on left ventricular ejection fraction in patients with breast cancer in the North Central Cancer Treatment Group N9831 Intergroup Adjuvant Trial.

Perez EA, Suman VJ, Davidson NE, Kaufman PA, Martino S, Dakhil SR, Ingle JN, Rodeheffer RJ, Gersh BJ, Jaffe AS

Abstract

To evaluate changes in left ventricular ejection fraction (LVEF) after four cycles of adjuvant doxorubicin plus cyclophosphamide (AC) in women with human epidermal growth factor receptor 2-positive (node-positive or node-negative) breast cancer enrolled onto the North Central Cancer Treatment Group N9831 Intergroup Adjuvant Trial. Patients were randomly assigned to receive standard doxorubicin (60 mg/m2) plus cyclophosphamide (600 mg/m2) every 3 weeks for four cycles followed by (1) weekly paclitaxel for 12 weeks; (2) weekly paclitaxel for 12 weeks, then weekly trastuzumab for 52 weeks; or (3) weekly paclitaxel plus trastuzumab for 12 weeks, then weekly trastuzumab for 40 weeks. LVEF was monitored before and after AC. Of the 1,576 eligible patients who completed AC, 1,458 had pre- and post-AC LVEF measurements taken using the same methodology (multiple-gated acquisition in 1,153 patients and echocardiogram in 305 patients). Among these 1,458 patients, 745 (51.1%) had < or = 15% decrease in LVEF and LVEF that remained at or above the radiologic lower limit of normal (LLN); 42 patients (2.9%) had < or = 15% decrease in LVEF and LVEF that decreased to or below the LLN; and 37 patients (2.5%) had an LVEF decrease of more than 15%. There was grade 2 LVEF toxicity in 96 (6.6%) of the 1,458 patients. Standard AC chemotherapy is associated with frequent decreases in LVEF, which are noted when measured 3 weeks after completion of the fourth cycle. Patients are being observed to determine the long-term significance of this and the potential impact on subsequent treatment options.

MeSH Terms
Adolescent Adult Aged Antibodies, Monoclonal/administration & dosage Antibodies, Monoclonal, Humanized Antineoplastic Agents/administration & dosage Antineoplastic Agents, Phytogenic/administration & dosage Antineoplastic Combined Chemotherapy Protocols/administration & dosage,adverse effects,therapeutic use Breast Neoplasms/drug therapy,surgery Chemotherapy, Adjuvant Cyclophosphamide/administration & dosage,adverse effects Doxorubicin/administration & dosage,adverse effects Female Humans Middle Aged Paclitaxel/administration & dosage Stroke Volume/drug effects Trastuzumab Ventricular Dysfunction, Left/chemically induced
Chemicals
Antibodies, Monoclonal Antibodies, Monoclonal, Humanized Antineoplastic Agents Antineoplastic Agents, Phytogenic Doxorubicin Cyclophosphamide Trastuzumab Paclitaxel
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Perez Edith A
North Central Cancer Treatment Group, Division of Hematology/Oncology, Mayo Clinic, Jacksonville, FL 32224, USA. [email protected]
Suman Vera J
Davidson Nancy E
Kaufman Peter A
Martino Silvana
Dakhil Shaker R
Ingle James N
Rodeheffer Richard J
Gersh Bernard J
Jaffe Allan S
Supplementary Concepts
AC protocol (Protocol)
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
0732-183X
Published
2004-09-15
Pages
3700-4
Language
English
Region
United States
NLM ID
8309333
Subset
IM
Grants
NCI NIH HHS · CA25224 · United States
Corrections
ErratumIn
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