Multicenter Randomized Phase II Study of Paclitaxel (1-Hour Infusion), Fluorouracil, Hydroxyurea, and Concomitant Twice Daily Radiation with or without Erythropoietin for Advanced Head and Neck Cancer
Purpose: To expand on our experience with the combination of paclitaxel, fluorouracil, hydroxyurea, and twice daily irradiation (T-FHX) and to assess the impact of weekly administration of erythropoietin (r-HuEpo) on transfusion requirements, we conducted a Phase II multi-institutional trial with a...
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Published in | Clinical cancer research Vol. 9; no. 5; pp. 1689 - 1697 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
American Association for Cancer Research
01.05.2003
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Subjects | |
Online Access | Get full text |
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Summary: | Purpose: To expand on our experience with the combination of paclitaxel, fluorouracil, hydroxyurea, and twice daily irradiation (T-FHX)
and to assess the impact of weekly administration of erythropoietin (r-HuEpo) on transfusion requirements, we conducted a
Phase II multi-institutional trial with a simplified 1-h paclitaxel infusion schedule and randomized patients to receive weekly
doses of r-HuEpo.
Patients and Methods: A total of 90 patients with locally advanced head and neck cancers (stage IV, 96%; N 2 /N 3 , 66%) were treated on a regimen of 1-h infusion of paclitaxel (100 mg/m 2 /day, day 1), 120-h infusion of 5-fluorouracil (600 mg/m 2 /day, days 0–5); hydroxyurea 500 mg p.o. every 12 h for 11 doses; and radiation 150cGy bid, days 1–5 of each 14-day cycle
repeated for five cycles over 10 weeks (7200–7500 cGy). Before initiating therapy, patients were randomized to receive r-HuEpo
40,000 IU s.c. once weekly.
Results: At median follow-up of 40 months, 3-year progression-free survival is 62%, locoregional control is 84%, and systemic control
is 79%. Overall survival is 59%. Anemia, leucopenia, dermatitis, and mucositis were the most frequent grade 3 or 4 toxicities.
Patients randomized to erythropoietin experienced less grade 2/3 anemia (52 versus 77%; P = 0.02), but transfusion requirements were not significantly different.
Conclusions: T-FHX is an active and tolerable regimen inducing local tumor control and promising survival with organ preservation in high-risk
patients. One h infusion of paclitaxel simplified the regimen without compromising efficacy. Addition of erythropoietin does
not reduce the need for transfusion with this nonplatinum-containing regimen. T-FHX should be advanced to a randomized trial
and compared with a cisplatin-based concomitant regimen. |
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ISSN: | 1078-0432 1557-3265 |