TY - JOUR
T1 - Combination chemotherapy using cyclophosphamide, vincristine, methotrexate and 5‐fluorouracil in solid tumors
AU - Costanzi, John J.
AU - Coltman, Charles A.
AU - Col, Lt
PY - 1969/3
Y1 - 1969/3
N2 - Results of a combination chemotherapeutic regimen consisting of cyclophosphamide, vincristine, methotrexate and 5‐fluorouracil for disseminated solid tumors in 31 patients are presented. Objective response was noted in 16 of these cases. Particularly responsive were malignant melanoma, pancreatic adenocarcinoma and certain mesenchymal sarcomas. Of those patients achieving a good objective response, the average survival is as follows: malignant melanoma = 9.4 months; pancreatic adenocarcinoma = 20.0+ months; and mesenchymal sarcomas = 13.5 months. Two patients achieved a complete remission after three courses of therapy. One with synovial sarcoma is alive at 27+ months, and the other with melanoma is alive at 11.0+ months. Toxicity was noted in 25 cases with 13 noting moderate toxicity, producing a delay in treatment. Patients' performance status paralleled objective response in most cases. These data reflect some support for the theoretical basis for efficacy of combined drugs in the treatment of disseminated solid tumors.
AB - Results of a combination chemotherapeutic regimen consisting of cyclophosphamide, vincristine, methotrexate and 5‐fluorouracil for disseminated solid tumors in 31 patients are presented. Objective response was noted in 16 of these cases. Particularly responsive were malignant melanoma, pancreatic adenocarcinoma and certain mesenchymal sarcomas. Of those patients achieving a good objective response, the average survival is as follows: malignant melanoma = 9.4 months; pancreatic adenocarcinoma = 20.0+ months; and mesenchymal sarcomas = 13.5 months. Two patients achieved a complete remission after three courses of therapy. One with synovial sarcoma is alive at 27+ months, and the other with melanoma is alive at 11.0+ months. Toxicity was noted in 25 cases with 13 noting moderate toxicity, producing a delay in treatment. Patients' performance status paralleled objective response in most cases. These data reflect some support for the theoretical basis for efficacy of combined drugs in the treatment of disseminated solid tumors.
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U2 - 10.1002/1097-0142(196903)23:3<589::AID-CNCR2820230310>3.0.CO;2-A
DO - 10.1002/1097-0142(196903)23:3<589::AID-CNCR2820230310>3.0.CO;2-A
M3 - Article
C2 - 4304025
AN - SCOPUS:0014480425
VL - 23
SP - 589
EP - 596
JO - Cancer
JF - Cancer
SN - 0008-543X
IS - 3
ER -