TY - JOUR
T1 - Methotrexate, vinblastine, doxorubicin, and cisplatin in metastatic breast cancer. A phase II trial of the hoosier oncology group
AU - Roth, Bruce J.
AU - Sledge, George W.
AU - Williams, Stephen D.
AU - Meyer, Steven C.
AU - Ansari, Rafat
AU - Fisher, William B.
PY - 1991/7/15
Y1 - 1991/7/15
N2 - Forty‐six eligible patients with metastatic breast cancer (MBC) were treated with a combination of methotrexate, vinblastine, doxorubicin, and cisplatin (M‐VAC) as first‐line chemotherapy. Of 44 patients evaluable for response, 28 (64%) had an objective response, including seven (16%) who had a complete response. The median duration of response was 4 months (range, 0 to 38 months), and the median survival from the time of entry was 14 months (range, < 1 to > 45 months). Myelosuppression was the most common dose‐limiting toxicity, with 54% of patients experiencing Grade 3 or 4 leukopenia (including 28% with granulocytopenic fever and one septic death), and cumulative Grade 3 anemia occurred in 28% of patients. Grades 3 to 4 stomatitis was observed in 18% of patients. An active, although highly toxic regimen when used as first‐line therapy in MBC, M‐VAC has a response rate and survival duration similar to existing, less toxic combination regimens. As such, M‐VAC cannot be recommended in preference to other combination chemotherapy regimens in this clinical setting.
AB - Forty‐six eligible patients with metastatic breast cancer (MBC) were treated with a combination of methotrexate, vinblastine, doxorubicin, and cisplatin (M‐VAC) as first‐line chemotherapy. Of 44 patients evaluable for response, 28 (64%) had an objective response, including seven (16%) who had a complete response. The median duration of response was 4 months (range, 0 to 38 months), and the median survival from the time of entry was 14 months (range, < 1 to > 45 months). Myelosuppression was the most common dose‐limiting toxicity, with 54% of patients experiencing Grade 3 or 4 leukopenia (including 28% with granulocytopenic fever and one septic death), and cumulative Grade 3 anemia occurred in 28% of patients. Grades 3 to 4 stomatitis was observed in 18% of patients. An active, although highly toxic regimen when used as first‐line therapy in MBC, M‐VAC has a response rate and survival duration similar to existing, less toxic combination regimens. As such, M‐VAC cannot be recommended in preference to other combination chemotherapy regimens in this clinical setting.
UR - http://www.scopus.com/inward/record.url?scp=0026068147&partnerID=8YFLogxK
U2 - 10.1002/1097-0142(19910715)68:2<248::AID-CNCR2820680205>3.0.CO;2-4
DO - 10.1002/1097-0142(19910715)68:2<248::AID-CNCR2820680205>3.0.CO;2-4
M3 - Article
C2 - 2070321
AN - SCOPUS:0026068147
SN - 0008-543X
VL - 68
SP - 248
EP - 252
JO - Cancer
JF - Cancer
IS - 2
ER -