TY - JOUR
T1 - Phase II trial of doxorubicin and paclitaxel plus granulocyte colony- stimulating factor in metastatic breast cancer
T2 - An eastern cooperative oncology group study
AU - Sparano, Joseph A.
AU - Hu, Ping
AU - Rao, Radha M.
AU - Falkson, Carla I.
AU - Wolff, Antonio C.
AU - Wood, William C.
PY - 1999/12
Y1 - 1999/12
N2 - Purpose: Several groups have reported that the combination of doxorubicin plus paclitaxel given as a 3-hour intravenous (IV) infusion for up to eight cycles produces a high response rate (> 80%) and complete response rate (> 20%) in metastatic breast cancer, but is also complicated by a 20% incidence of congestive heart failure (CHF). The purpose of this phase II trial was to evaluate the antineoplastic activity of the regimen in a multi-institutional setting and to reduce the incidence of cardiotoxicity by limiting treatment to a maximum of six cycles. Patients and Methods: Fifty- two patients with advanced breast cancer received doxorubicin (60 mg/m2 by IV injection) followed 15 minutes later by paclitaxel (200 mg/m2 by IV infusion over 3 hours) every 3 weeks for four to six cycles. Results: Objective responses occurred in 25 of 48 assessable patients (52%; 95% confidence interval [Cl], 38% to 66%), including four complete responses (8%; 95% Cl, 0% to 16%). The median cumulative doxorubicin dose given was 240 mg/m2 (range, 132 to 360 mg/m2). Eleven patients (21%) were documented as having a decrease in the LVEF below normal, including three patients (6%; 95% Cl, 0% to 12%) who developed CHF. Conclusion: The doxorubicin/paclitaxel regimen that we used is unlikely to produce an objective response rate of more than 70% and a complete response rate of more than 20% in patients with metastatic breast cancer, and proved to be excessively cardiotoxic for use in the adjuvant setting.
AB - Purpose: Several groups have reported that the combination of doxorubicin plus paclitaxel given as a 3-hour intravenous (IV) infusion for up to eight cycles produces a high response rate (> 80%) and complete response rate (> 20%) in metastatic breast cancer, but is also complicated by a 20% incidence of congestive heart failure (CHF). The purpose of this phase II trial was to evaluate the antineoplastic activity of the regimen in a multi-institutional setting and to reduce the incidence of cardiotoxicity by limiting treatment to a maximum of six cycles. Patients and Methods: Fifty- two patients with advanced breast cancer received doxorubicin (60 mg/m2 by IV injection) followed 15 minutes later by paclitaxel (200 mg/m2 by IV infusion over 3 hours) every 3 weeks for four to six cycles. Results: Objective responses occurred in 25 of 48 assessable patients (52%; 95% confidence interval [Cl], 38% to 66%), including four complete responses (8%; 95% Cl, 0% to 16%). The median cumulative doxorubicin dose given was 240 mg/m2 (range, 132 to 360 mg/m2). Eleven patients (21%) were documented as having a decrease in the LVEF below normal, including three patients (6%; 95% Cl, 0% to 12%) who developed CHF. Conclusion: The doxorubicin/paclitaxel regimen that we used is unlikely to produce an objective response rate of more than 70% and a complete response rate of more than 20% in patients with metastatic breast cancer, and proved to be excessively cardiotoxic for use in the adjuvant setting.
UR - http://www.scopus.com/inward/record.url?scp=0032760998&partnerID=8YFLogxK
U2 - 10.1200/JCO.1999.17.12.3828
DO - 10.1200/JCO.1999.17.12.3828
M3 - Article
AN - SCOPUS:0032760998
SN - 0732-183X
VL - 17
SP - 3828
EP - 3834
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 12
ER -