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 inClinical cancer research Vol. 9; no. 5; pp. 1689 - 1697
Main Authors ROSEN, Fred R, HARAF, Daniel J, PELZER, Harold, WEICHSELBAUM, Ralph R, VOKES, Everett E, KIES, Merrill S, STENSON, Kerstin, PORTUGAL, Louis, LIST, Marcy A, BROCKSTEIN, Bruce E, MITTAL, Bharat B, RADEMAKER, Alfred W, WITT, Mary Ellyn
Format Journal Article
LanguageEnglish
Published Philadelphia, PA American Association for Cancer Research 01.05.2003
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Abstract 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.
AbstractList 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. 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. 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. 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.
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.
Author Bruce E. Brockstein
Bharat B. Mittal
Louis Portugal
Fred R. Rosen
Alfred W. Rademaker
Merrill S. Kies
Kerstin Stenson
Marcy A. List
Mary Ellyn Witt
Everett E. Vokes
Daniel J. Haraf
Harold Pelzer
Ralph R. Weichselbaum
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Issue 5
Keywords Antineoplastic agent
Human
Drug combination
Hydroxycarbamide
Erythropoietin
Enzyme
Transferases
Fluoropyrimidine derivatives
Enzyme inhibitor
Malignant tumor
Radiotherapy
Thymidylate synthase
Chemotherapy
Methyltransferases
Antimetabolic
Taxane derivatives
Phase II trial
Paclitaxel
Head and neck
ENT disease
Pyrimidine derivatives
Advanced stage
Combined treatment
Fluorouracil
Language English
License CC BY 4.0
LinkModel OpenURL
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Snippet Purpose: To expand on our experience with the combination of paclitaxel, fluorouracil, hydroxyurea, and twice daily irradiation (T-FHX) and to assess the...
To expand on our experience with the combination of paclitaxel, fluorouracil, hydroxyurea, and twice daily irradiation (T-FHX) and to assess the impact of...
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StartPage 1689
SubjectTerms Adult
Aged
Aged, 80 and over
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Carcinoma, Squamous Cell - drug therapy
Carcinoma, Squamous Cell - radiotherapy
Carcinoma, Squamous Cell - surgery
Chemotherapy
Combined Modality Therapy
Drug Administration Schedule
Erythropoietin - administration & dosage
Female
Fluorouracil - administration & dosage
Head and Neck Neoplasms - drug therapy
Head and Neck Neoplasms - radiotherapy
Head and Neck Neoplasms - surgery
Humans
Hydroxyurea - administration & dosage
Male
Medical sciences
Middle Aged
Paclitaxel - administration & dosage
Pharmacology. Drug treatments
Recombinant Proteins
Survival Rate
Treatment Outcome
Title 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
URI http://clincancerres.aacrjournals.org/content/9/5/1689.abstract
https://www.ncbi.nlm.nih.gov/pubmed/12738722
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