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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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. |
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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 |
Author_xml | – sequence: 1 givenname: Fred R surname: ROSEN fullname: ROSEN, Fred R organization: Department of Medicine, Section of Hematology/Oncology, University of Illinois at Chicago, Chicago, Illinois, United States – sequence: 2 givenname: Daniel J surname: HARAF fullname: HARAF, Daniel J organization: Department of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois, United States – sequence: 3 givenname: Harold surname: PELZER fullname: PELZER, Harold organization: Department of Otolaryngology/Head and Neck Surgery, Northwestern University, Chicago, Illinois, United States – sequence: 4 givenname: Ralph R surname: WEICHSELBAUM fullname: WEICHSELBAUM, Ralph R organization: Department of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois, United States – sequence: 5 givenname: Everett E surname: VOKES fullname: VOKES, Everett E organization: Department of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois, United States – sequence: 6 givenname: Merrill S surname: KIES fullname: KIES, Merrill S organization: Department of Medicine, Northwestern University, Chicago, Illinois, United States – sequence: 7 givenname: Kerstin surname: STENSON fullname: STENSON, Kerstin organization: Section of Otolaryngology/Head and Neck Surgery, University of Chicago, Chicago, Illinois, United States – sequence: 8 givenname: Louis surname: PORTUGAL fullname: PORTUGAL, Louis organization: Department of Radiation Oncology, and Department of Otolaryngology/Head and Neck Surgery, University of Illinois at Chicago, Chicago, Illinois, United States – sequence: 9 givenname: Marcy A surname: LIST fullname: LIST, Marcy A organization: Center, University of Chicago, Chicago, Illinois, United States – sequence: 10 givenname: Bruce E surname: BROCKSTEIN fullname: BROCKSTEIN, Bruce E organization: Department of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois, United States – sequence: 11 givenname: Bharat B surname: MITTAL fullname: MITTAL, Bharat B organization: Department of Radiation Oncology, Northwestern University, Chicago, Illinois, United States – sequence: 12 givenname: Alfred W surname: RADEMAKER fullname: RADEMAKER, Alfred W organization: Department of Cancer Research Center, Northwestern University, Chicago, Illinois, United States – sequence: 13 givenname: Mary Ellyn surname: WITT fullname: WITT, Mary Ellyn organization: Department of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois, United States |
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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 |
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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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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 |
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