TY - JOUR
T1 - Combination chemotherapy and high‐dose cyclophosphamide intensification for poor prognosis breast cancer. A southwest oncology group study
AU - Ellis, Georgiana K.
AU - Green, Stephanie
AU - Schulman, Susan
AU - Tranum, Bill L.
AU - Goldberg, Ronald S.
AU - Livingston, Robert B.
PY - 1989/12/15
Y1 - 1989/12/15
N2 - Thirty‐seven patients with poor prognosis, metastatic breast cancer were treated with 5‐fluorouracil, vinblastine, and Adriamycin (doxorubicin; Adria Laboratories, Columbus, OH) (FUVA) induction chemotherapy. All 26 patients (74%) with responsive or stable disease after induction chemotherapy received intensification with high‐dose cyclophosphamide (120 mg/kg). Continued responders received additional FUVA as consolidation. The response rate to induction therapy was 54% (with complete response [CR] in 11%). With intensification, three patients (11%) showed improved response (partial response [PR] in one, PR to complete response [CR] in two); however, six patients (23%) progressed within 2 months of cyclophosphamide intensification, three within 1 month. The overall response rate to all three phases of the study was 69%, with CR in 23%. The median survival of all patients entered in this study was 15 months. For cyclophosphamide intensification, major toxicity consisted of leukopenia with fever requiring broad‐spectrum antibiotics in 27%. The authors conclude that a single cycle of high‐dose cyclophosphamide intensification in metastatic breast cancer does not result in significantly improved responses or prolonged survival. Cancer 64:2409–2415, 1989.
AB - Thirty‐seven patients with poor prognosis, metastatic breast cancer were treated with 5‐fluorouracil, vinblastine, and Adriamycin (doxorubicin; Adria Laboratories, Columbus, OH) (FUVA) induction chemotherapy. All 26 patients (74%) with responsive or stable disease after induction chemotherapy received intensification with high‐dose cyclophosphamide (120 mg/kg). Continued responders received additional FUVA as consolidation. The response rate to induction therapy was 54% (with complete response [CR] in 11%). With intensification, three patients (11%) showed improved response (partial response [PR] in one, PR to complete response [CR] in two); however, six patients (23%) progressed within 2 months of cyclophosphamide intensification, three within 1 month. The overall response rate to all three phases of the study was 69%, with CR in 23%. The median survival of all patients entered in this study was 15 months. For cyclophosphamide intensification, major toxicity consisted of leukopenia with fever requiring broad‐spectrum antibiotics in 27%. The authors conclude that a single cycle of high‐dose cyclophosphamide intensification in metastatic breast cancer does not result in significantly improved responses or prolonged survival. Cancer 64:2409–2415, 1989.
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U2 - 10.1002/1097-0142(19891215)64:12<2409::AID-CNCR2820641202>3.0.CO;2-T
DO - 10.1002/1097-0142(19891215)64:12<2409::AID-CNCR2820641202>3.0.CO;2-T
M3 - Article
C2 - 2684382
AN - SCOPUS:0024851971
SN - 0008-543X
VL - 64
SP - 2409
EP - 2415
JO - Cancer
JF - Cancer
IS - 12
ER -