A Phase II Multi-institutional Trial of Chemoradiation Using Weekly Docetaxel and Erythropoietin for High-Risk Postoperative Head and Neck Cancer Patients

Purpose: To determine efficacy and toxicities of postoperative concurrent chemoradiation using docetaxel in high-risk head and neck cancer. Methods and Materials: High-risk patients were enrolled 2–8 weeks after surgery. Treatment included 60 Gy for 6 weeks with weekly docetaxel 25 mg/m2 and erythro...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2007-04, Vol.67 (5), p.1323-1331
Hauptverfasser: Willey, Christopher D., M.D., Ph.D, Murphy, Barbara A., M.D, Netterville, James L., M.D, Burkey, Brian B., M.D, Shyr, Yu, Ph.D, Shakhtour, Bashar, B.S, Kish, Bonnie, R.N, Raben, David, M.D, Chen, Changhu, M.D, Song, John I., M.D, Kane, Madeleine A., M.D., Ph.D, Cmelak, Anthony J., M.D
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container_end_page 1331
container_issue 5
container_start_page 1323
container_title International journal of radiation oncology, biology, physics
container_volume 67
creator Willey, Christopher D., M.D., Ph.D
Murphy, Barbara A., M.D
Netterville, James L., M.D
Burkey, Brian B., M.D
Shyr, Yu, Ph.D
Shakhtour, Bashar, B.S
Kish, Bonnie, R.N
Raben, David, M.D
Chen, Changhu, M.D
Song, John I., M.D
Kane, Madeleine A., M.D., Ph.D
Cmelak, Anthony J., M.D
description Purpose: To determine efficacy and toxicities of postoperative concurrent chemoradiation using docetaxel in high-risk head and neck cancer. Methods and Materials: High-risk patients were enrolled 2–8 weeks after surgery. Treatment included 60 Gy for 6 weeks with weekly docetaxel 25 mg/m2 and erythropoietin alpha 40,000 U for hemoglobin ≤12 g/dL. Primary endpoints included locoregional control (LC), disease-free survival (DFS), and patterns of failure (POF). Secondary endpoints were toxicity and quality of life. Results: Eighteen patients were enrolled (14 male, 4 female), aged 24–70 years (median, 55 years). Primary site included oropharynx = 7, oral cavity = 8, hypopharynx = 1, and larynx = 2. Pathologic American Joint Committee on Cancer Stage was III = 3 patients, IV = 15 patients. High-risk eligibility included ≥2 positive lymph nodes = 13, extracapsular extension = 10, positive margins = 8 (11 patients with two or more risk factors). Docetaxel was reduced to 20 mg/m2 /week after 5 patients had prolonged Grade 3 or higher mucositis. Overall, number of doses delivered was 2 of 6 = 1, 3 of 6 = 2, 4 of 6 = 2, 5 of 6 = 4, 6 of 6 = 9 patients. With median follow-up of 30 months (range, 5–66), 10 (56%) patients are alive and have no evidence of disease (NED); POF: three local recurrences (two with distant) and 1 distant only. One-year survival was 76%, median PFS and DFS had not been reached. Three-year LC was 82%. No Grade 3 or higher late toxicities were observed, although a few cases of prolonged mucositis and taste loss (>3 months) were seen, particularly at 25 mg/m2 /week. Conclusion: Postoperative radiation therapy with weekly docetaxel 20 or 25 mg/m2 /week for high-risk postoperative head and neck cancer caused intolerable mucosal toxicity, prompting early study termination. Further studies should consider 15 mg/m2 . Actuarial 3-year LC is 82%, similar to cisplatin-based chemoradiation regimens. Distant metastasis remains an important issue requiring additional systemic interventions.
doi_str_mv 10.1016/j.ijrobp.2006.11.033
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Methods and Materials: High-risk patients were enrolled 2–8 weeks after surgery. Treatment included 60 Gy for 6 weeks with weekly docetaxel 25 mg/m2 and erythropoietin alpha 40,000 U for hemoglobin ≤12 g/dL. Primary endpoints included locoregional control (LC), disease-free survival (DFS), and patterns of failure (POF). Secondary endpoints were toxicity and quality of life. Results: Eighteen patients were enrolled (14 male, 4 female), aged 24–70 years (median, 55 years). Primary site included oropharynx = 7, oral cavity = 8, hypopharynx = 1, and larynx = 2. Pathologic American Joint Committee on Cancer Stage was III = 3 patients, IV = 15 patients. High-risk eligibility included ≥2 positive lymph nodes = 13, extracapsular extension = 10, positive margins = 8 (11 patients with two or more risk factors). Docetaxel was reduced to 20 mg/m2 /week after 5 patients had prolonged Grade 3 or higher mucositis. Overall, number of doses delivered was 2 of 6 = 1, 3 of 6 = 2, 4 of 6 = 2, 5 of 6 = 4, 6 of 6 = 9 patients. With median follow-up of 30 months (range, 5–66), 10 (56%) patients are alive and have no evidence of disease (NED); POF: three local recurrences (two with distant) and 1 distant only. One-year survival was 76%, median PFS and DFS had not been reached. Three-year LC was 82%. No Grade 3 or higher late toxicities were observed, although a few cases of prolonged mucositis and taste loss (&gt;3 months) were seen, particularly at 25 mg/m2 /week. Conclusion: Postoperative radiation therapy with weekly docetaxel 20 or 25 mg/m2 /week for high-risk postoperative head and neck cancer caused intolerable mucosal toxicity, prompting early study termination. Further studies should consider 15 mg/m2 . Actuarial 3-year LC is 82%, similar to cisplatin-based chemoradiation regimens. 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Methods and Materials: High-risk patients were enrolled 2–8 weeks after surgery. Treatment included 60 Gy for 6 weeks with weekly docetaxel 25 mg/m2 and erythropoietin alpha 40,000 U for hemoglobin ≤12 g/dL. Primary endpoints included locoregional control (LC), disease-free survival (DFS), and patterns of failure (POF). Secondary endpoints were toxicity and quality of life. Results: Eighteen patients were enrolled (14 male, 4 female), aged 24–70 years (median, 55 years). Primary site included oropharynx = 7, oral cavity = 8, hypopharynx = 1, and larynx = 2. Pathologic American Joint Committee on Cancer Stage was III = 3 patients, IV = 15 patients. High-risk eligibility included ≥2 positive lymph nodes = 13, extracapsular extension = 10, positive margins = 8 (11 patients with two or more risk factors). Docetaxel was reduced to 20 mg/m2 /week after 5 patients had prolonged Grade 3 or higher mucositis. Overall, number of doses delivered was 2 of 6 = 1, 3 of 6 = 2, 4 of 6 = 2, 5 of 6 = 4, 6 of 6 = 9 patients. With median follow-up of 30 months (range, 5–66), 10 (56%) patients are alive and have no evidence of disease (NED); POF: three local recurrences (two with distant) and 1 distant only. One-year survival was 76%, median PFS and DFS had not been reached. Three-year LC was 82%. No Grade 3 or higher late toxicities were observed, although a few cases of prolonged mucositis and taste loss (&gt;3 months) were seen, particularly at 25 mg/m2 /week. Conclusion: Postoperative radiation therapy with weekly docetaxel 20 or 25 mg/m2 /week for high-risk postoperative head and neck cancer caused intolerable mucosal toxicity, prompting early study termination. Further studies should consider 15 mg/m2 . Actuarial 3-year LC is 82%, similar to cisplatin-based chemoradiation regimens. Distant metastasis remains an important issue requiring additional systemic interventions.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - administration &amp; dosage</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Chemoradiation</subject><subject>Clinical trial</subject><subject>CLINICAL TRIALS</subject><subject>Combined Modality Therapy - adverse effects</subject><subject>Disease-Free Survival</subject><subject>Docetaxel</subject><subject>Dose Fractionation</subject><subject>ELDERLY PEOPLE</subject><subject>ERYTHROPOIETIN</subject><subject>Erythropoietin - administration &amp; dosage</subject><subject>FAILURES</subject><subject>Female</subject><subject>HEAD</subject><subject>Head and neck cancer</subject><subject>Head and Neck Neoplasms - blood</subject><subject>Head and Neck Neoplasms - drug therapy</subject><subject>Head and Neck Neoplasms - radiotherapy</subject><subject>Head and Neck Neoplasms - surgery</subject><subject>HEALTH HAZARDS</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>HEMOGLOBIN</subject><subject>Hemoglobin A</subject><subject>Humans</subject><subject>LARYNX</subject><subject>LYMPH NODES</subject><subject>Male</subject><subject>METASTASES</subject><subject>Middle Aged</subject><subject>Mouth Mucosa - drug effects</subject><subject>Mouth Mucosa - radiation effects</subject><subject>NECK</subject><subject>NEOPLASMS</subject><subject>ORAL CAVITY</subject><subject>PATIENTS</subject><subject>Postoperative</subject><subject>Prospective Studies</subject><subject>RADIATION DOSES</subject><subject>Radiation Injuries</subject><subject>Radiation-Sensitizing Agents - administration &amp; 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Murphy, Barbara A., M.D ; Netterville, James L., M.D ; Burkey, Brian B., M.D ; Shyr, Yu, Ph.D ; Shakhtour, Bashar, B.S ; Kish, Bonnie, R.N ; Raben, David, M.D ; Chen, Changhu, M.D ; Song, John I., M.D ; Kane, Madeleine A., M.D., Ph.D ; Cmelak, Anthony J., M.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-98e7617c8685dbed378e4bc3003bdbf54ecb9d256b9ab8b52adb712364bd68443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - administration &amp; dosage</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Chemoradiation</topic><topic>Clinical trial</topic><topic>CLINICAL TRIALS</topic><topic>Combined Modality Therapy - adverse effects</topic><topic>Disease-Free Survival</topic><topic>Docetaxel</topic><topic>Dose Fractionation</topic><topic>ELDERLY PEOPLE</topic><topic>ERYTHROPOIETIN</topic><topic>Erythropoietin - administration &amp; 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Methods and Materials: High-risk patients were enrolled 2–8 weeks after surgery. Treatment included 60 Gy for 6 weeks with weekly docetaxel 25 mg/m2 and erythropoietin alpha 40,000 U for hemoglobin ≤12 g/dL. Primary endpoints included locoregional control (LC), disease-free survival (DFS), and patterns of failure (POF). Secondary endpoints were toxicity and quality of life. Results: Eighteen patients were enrolled (14 male, 4 female), aged 24–70 years (median, 55 years). Primary site included oropharynx = 7, oral cavity = 8, hypopharynx = 1, and larynx = 2. Pathologic American Joint Committee on Cancer Stage was III = 3 patients, IV = 15 patients. High-risk eligibility included ≥2 positive lymph nodes = 13, extracapsular extension = 10, positive margins = 8 (11 patients with two or more risk factors). Docetaxel was reduced to 20 mg/m2 /week after 5 patients had prolonged Grade 3 or higher mucositis. Overall, number of doses delivered was 2 of 6 = 1, 3 of 6 = 2, 4 of 6 = 2, 5 of 6 = 4, 6 of 6 = 9 patients. With median follow-up of 30 months (range, 5–66), 10 (56%) patients are alive and have no evidence of disease (NED); POF: three local recurrences (two with distant) and 1 distant only. One-year survival was 76%, median PFS and DFS had not been reached. Three-year LC was 82%. No Grade 3 or higher late toxicities were observed, although a few cases of prolonged mucositis and taste loss (&gt;3 months) were seen, particularly at 25 mg/m2 /week. Conclusion: Postoperative radiation therapy with weekly docetaxel 20 or 25 mg/m2 /week for high-risk postoperative head and neck cancer caused intolerable mucosal toxicity, prompting early study termination. Further studies should consider 15 mg/m2 . Actuarial 3-year LC is 82%, similar to cisplatin-based chemoradiation regimens. Distant metastasis remains an important issue requiring additional systemic interventions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>17289289</pmid><doi>10.1016/j.ijrobp.2006.11.033</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0360-3016
ispartof International journal of radiation oncology, biology, physics, 2007-04, Vol.67 (5), p.1323-1331
issn 0360-3016
1879-355X
language eng
recordid cdi_osti_scitechconnect_20951574
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Adult
Aged
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - adverse effects
Chemoradiation
Clinical trial
CLINICAL TRIALS
Combined Modality Therapy - adverse effects
Disease-Free Survival
Docetaxel
Dose Fractionation
ELDERLY PEOPLE
ERYTHROPOIETIN
Erythropoietin - administration & dosage
FAILURES
Female
HEAD
Head and neck cancer
Head and Neck Neoplasms - blood
Head and Neck Neoplasms - drug therapy
Head and Neck Neoplasms - radiotherapy
Head and Neck Neoplasms - surgery
HEALTH HAZARDS
Hematology, Oncology and Palliative Medicine
HEMOGLOBIN
Hemoglobin A
Humans
LARYNX
LYMPH NODES
Male
METASTASES
Middle Aged
Mouth Mucosa - drug effects
Mouth Mucosa - radiation effects
NECK
NEOPLASMS
ORAL CAVITY
PATIENTS
Postoperative
Prospective Studies
RADIATION DOSES
Radiation Injuries
Radiation-Sensitizing Agents - administration & dosage
Radiation-Sensitizing Agents - adverse effects
Radiology
RADIOLOGY AND NUCLEAR MEDICINE
RADIOTHERAPY
Radiotherapy Dosage
Stomatitis - etiology
SURGERY
Taxoids - administration & dosage
Taxoids - adverse effects
TOXICITY
title A Phase II Multi-institutional Trial of Chemoradiation Using Weekly Docetaxel and Erythropoietin for High-Risk Postoperative Head and Neck Cancer Patients
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