## Abstract Previous studies have demonstrated continuousโinfusion 5โfluorouracil (Cl 5โFU) to be an active singleโagent treatment for breast cancer without significant myelotoxicity. These qualities made Cl 5โFU an attractive agent for combination with other effective but myelosuppressive agents.
Doxorubicin/vinblastine and doxorubicin/cyclophosphamide combination chemotherapy by continuous infusion
โ Scribed by Jacob J. Lokich; Thomas E. Zipoli; Cherie Moore; Henry Sonneborn; Stephen Paul; Robert Greene
- Book ID
- 101329444
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 404 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
โฆ Synopsis
Fifty-two patients received one of two doxorubicin (D0X)-based admixtures; DOX plus cyclophosphamide (CTX) or DOX plus vinblastine (VBL) administered as a continuous 24-hour infusion for protracted periods. Compatibility and stability of the two-drug admixture was established for a minimum of 7 days. Twenty patients on the DOX/CTX admixture were infused for a median of 20 days (range, 7-56 days). DOX/VLB was infused in 32 patients for a median of 18 days (range, 5-48 days). Dose limiting toxicity was leukopenia observed in 14/52 patients; 4/20 on DOX/CTX and 10/32 on DOX/VLB. Additional toxicities observed included stomatitis (15%) and subclavian vein thrombosis (23%). Tumor responses were observed in 11 patients, including 6/13 breast cancer; 2/2 hepatoma; 2/4 sarcoma and 1/1 ovarian cancer. Responses were relatively short-lived and no responses were noted in known anthracycline resistant tumors. Admixtures of chemotherapeutic agents represents a novel, but feasible, mechanism for delivery of multiple drugs with an infusion schedule and can be considered for Phase 111 comparative clinical trials.
๐ SIMILAR VOLUMES
Two hundred and seventy-four consecutive patients with measurable metastatic breast cancer, without prior exposure to cytotoxic agents were treated with tamoxifen, 5-fluorouracil, doxorubicin, and cyclophosphamide (FAC). The initial 133 patients received doxorubicin by bolus IV administration and fo