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 |
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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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fullrecord | <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_20951574</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0360301606035048</els_id><sourcerecordid>21245660</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-98e7617c8685dbed378e4bc3003bdbf54ecb9d256b9ab8b52adb712364bd68443</originalsourceid><addsrcrecordid>eNqFktuKFDEQhhtR3HH1DUQCgnfdJp306UZYxnVnYNVBd9G7kEPNTmZ6ktkkvey8ik9r2h4QvBFC6qK--quov7LsNcEFwaR-vy3M1jt5KEqM64KQAlP6JJuRtulyWlU_n2YzTGuc0wSfZS9C2GKMCWnY8-yMNGXbpTfLfl2g1UYEQMsl-jz00eTGhmjiEI2zokc33qTfrdF8A3vnhTZizKDbYOwd-gGw64_oo1MQxSP0SFiNLv0xbrw7OAPRWLR2Hi3M3Sb_ZsIOrVyI7gA-qTwAWoDQf2q-gNqhubAKPFqlHNgYXmbP1qIP8OoUz7PbT5c380V-_fVqOb-4zhVrWMy7FpqaNKqt20pL0LRpgUlFMaZSy3XFQMlOl1UtOyFbWZVCy4aUtGZS1y1j9Dx7O-mm0QwPykRQG-WsBRV5ibuKVM1IvZuog3f3A4TI9yYo6HthwQ2Bl6RkVV3jBLIJVN6F4GHND97shT9ygvnoHN_yyTk-OscJ4cm5VPbmpD_IPei_RSerEvBhAiDt4sGAH0eFtDFt_DipduZ_Hf4VUL2xRol-B0cIWzf45HjghIeSY_59vJ7xeHAKFWYt_Q2_BMKS</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>21245660</pqid></control><display><type>article</type><title>A Phase II Multi-institutional Trial of Chemoradiation Using Weekly Docetaxel and Erythropoietin for High-Risk Postoperative Head and Neck Cancer Patients</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><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</creator><creatorcontrib>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</creatorcontrib><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.</description><identifier>ISSN: 0360-3016</identifier><identifier>EISSN: 1879-355X</identifier><identifier>DOI: 10.1016/j.ijrobp.2006.11.033</identifier><identifier>PMID: 17289289</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>International journal of radiation oncology, biology, physics, 2007-04, Vol.67 (5), p.1323-1331</ispartof><rights>Elsevier Inc.</rights><rights>2007 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-98e7617c8685dbed378e4bc3003bdbf54ecb9d256b9ab8b52adb712364bd68443</citedby><cites>FETCH-LOGICAL-c474t-98e7617c8685dbed378e4bc3003bdbf54ecb9d256b9ab8b52adb712364bd68443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijrobp.2006.11.033$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,315,781,785,886,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17289289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/20951574$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Willey, Christopher D., M.D., Ph.D</creatorcontrib><creatorcontrib>Murphy, Barbara A., M.D</creatorcontrib><creatorcontrib>Netterville, James L., M.D</creatorcontrib><creatorcontrib>Burkey, Brian B., M.D</creatorcontrib><creatorcontrib>Shyr, Yu, Ph.D</creatorcontrib><creatorcontrib>Shakhtour, Bashar, B.S</creatorcontrib><creatorcontrib>Kish, Bonnie, R.N</creatorcontrib><creatorcontrib>Raben, David, M.D</creatorcontrib><creatorcontrib>Chen, Changhu, M.D</creatorcontrib><creatorcontrib>Song, John I., M.D</creatorcontrib><creatorcontrib>Kane, Madeleine A., M.D., Ph.D</creatorcontrib><creatorcontrib>Cmelak, Anthony J., M.D</creatorcontrib><title>A Phase II Multi-institutional Trial of Chemoradiation Using Weekly Docetaxel and Erythropoietin for High-Risk Postoperative Head and Neck Cancer Patients</title><title>International journal of radiation oncology, biology, physics</title><addtitle>Int J Radiat Oncol Biol Phys</addtitle><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.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - administration & 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 & 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 & dosage</subject><subject>Radiation-Sensitizing Agents - adverse effects</subject><subject>Radiology</subject><subject>RADIOLOGY AND NUCLEAR MEDICINE</subject><subject>RADIOTHERAPY</subject><subject>Radiotherapy Dosage</subject><subject>Stomatitis - etiology</subject><subject>SURGERY</subject><subject>Taxoids - administration & dosage</subject><subject>Taxoids - adverse effects</subject><subject>TOXICITY</subject><issn>0360-3016</issn><issn>1879-355X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFktuKFDEQhhtR3HH1DUQCgnfdJp306UZYxnVnYNVBd9G7kEPNTmZ6ktkkvey8ik9r2h4QvBFC6qK--quov7LsNcEFwaR-vy3M1jt5KEqM64KQAlP6JJuRtulyWlU_n2YzTGuc0wSfZS9C2GKMCWnY8-yMNGXbpTfLfl2g1UYEQMsl-jz00eTGhmjiEI2zokc33qTfrdF8A3vnhTZizKDbYOwd-gGw64_oo1MQxSP0SFiNLv0xbrw7OAPRWLR2Hi3M3Sb_ZsIOrVyI7gA-qTwAWoDQf2q-gNqhubAKPFqlHNgYXmbP1qIP8OoUz7PbT5c380V-_fVqOb-4zhVrWMy7FpqaNKqt20pL0LRpgUlFMaZSy3XFQMlOl1UtOyFbWZVCy4aUtGZS1y1j9Dx7O-mm0QwPykRQG-WsBRV5ibuKVM1IvZuog3f3A4TI9yYo6HthwQ2Bl6RkVV3jBLIJVN6F4GHND97shT9ygvnoHN_yyTk-OscJ4cm5VPbmpD_IPei_RSerEvBhAiDt4sGAH0eFtDFt_DipduZ_Hf4VUL2xRol-B0cIWzf45HjghIeSY_59vJ7xeHAKFWYt_Q2_BMKS</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Willey, Christopher D., M.D., Ph.D</creator><creator>Murphy, Barbara A., M.D</creator><creator>Netterville, James L., M.D</creator><creator>Burkey, Brian B., M.D</creator><creator>Shyr, Yu, Ph.D</creator><creator>Shakhtour, Bashar, B.S</creator><creator>Kish, Bonnie, R.N</creator><creator>Raben, David, M.D</creator><creator>Chen, Changhu, M.D</creator><creator>Song, John I., M.D</creator><creator>Kane, Madeleine A., M.D., Ph.D</creator><creator>Cmelak, Anthony J., M.D</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope><scope>OTOTI</scope></search><sort><creationdate>20070401</creationdate><title>A Phase II Multi-institutional Trial of Chemoradiation Using Weekly Docetaxel and Erythropoietin for High-Risk Postoperative Head and Neck Cancer Patients</title><author>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</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 & 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 & dosage</topic><topic>FAILURES</topic><topic>Female</topic><topic>HEAD</topic><topic>Head and neck cancer</topic><topic>Head and Neck Neoplasms - blood</topic><topic>Head and Neck Neoplasms - drug therapy</topic><topic>Head and Neck Neoplasms - radiotherapy</topic><topic>Head and Neck Neoplasms - surgery</topic><topic>HEALTH HAZARDS</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>HEMOGLOBIN</topic><topic>Hemoglobin A</topic><topic>Humans</topic><topic>LARYNX</topic><topic>LYMPH NODES</topic><topic>Male</topic><topic>METASTASES</topic><topic>Middle Aged</topic><topic>Mouth Mucosa - drug effects</topic><topic>Mouth Mucosa - radiation effects</topic><topic>NECK</topic><topic>NEOPLASMS</topic><topic>ORAL CAVITY</topic><topic>PATIENTS</topic><topic>Postoperative</topic><topic>Prospective Studies</topic><topic>RADIATION DOSES</topic><topic>Radiation Injuries</topic><topic>Radiation-Sensitizing Agents - administration & dosage</topic><topic>Radiation-Sensitizing Agents - adverse effects</topic><topic>Radiology</topic><topic>RADIOLOGY AND NUCLEAR MEDICINE</topic><topic>RADIOTHERAPY</topic><topic>Radiotherapy Dosage</topic><topic>Stomatitis - etiology</topic><topic>SURGERY</topic><topic>Taxoids - administration & dosage</topic><topic>Taxoids - adverse effects</topic><topic>TOXICITY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Willey, Christopher D., M.D., Ph.D</creatorcontrib><creatorcontrib>Murphy, Barbara A., M.D</creatorcontrib><creatorcontrib>Netterville, James L., M.D</creatorcontrib><creatorcontrib>Burkey, Brian B., M.D</creatorcontrib><creatorcontrib>Shyr, Yu, Ph.D</creatorcontrib><creatorcontrib>Shakhtour, Bashar, B.S</creatorcontrib><creatorcontrib>Kish, Bonnie, R.N</creatorcontrib><creatorcontrib>Raben, David, M.D</creatorcontrib><creatorcontrib>Chen, Changhu, M.D</creatorcontrib><creatorcontrib>Song, John I., M.D</creatorcontrib><creatorcontrib>Kane, Madeleine A., M.D., Ph.D</creatorcontrib><creatorcontrib>Cmelak, Anthony J., M.D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>OSTI.GOV</collection><jtitle>International journal of radiation oncology, biology, physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Willey, Christopher D., M.D., Ph.D</au><au>Murphy, Barbara A., M.D</au><au>Netterville, James L., M.D</au><au>Burkey, Brian B., M.D</au><au>Shyr, Yu, Ph.D</au><au>Shakhtour, Bashar, B.S</au><au>Kish, Bonnie, R.N</au><au>Raben, David, M.D</au><au>Chen, Changhu, M.D</au><au>Song, John I., M.D</au><au>Kane, Madeleine A., M.D., Ph.D</au><au>Cmelak, Anthony J., M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Phase II Multi-institutional Trial of Chemoradiation Using Weekly Docetaxel and Erythropoietin for High-Risk Postoperative Head and Neck Cancer Patients</atitle><jtitle>International journal of radiation oncology, biology, physics</jtitle><addtitle>Int J Radiat Oncol Biol Phys</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>67</volume><issue>5</issue><spage>1323</spage><epage>1331</epage><pages>1323-1331</pages><issn>0360-3016</issn><eissn>1879-355X</eissn><abstract>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.</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> |
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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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T03%3A13%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Phase%20II%20Multi-institutional%20Trial%20of%20Chemoradiation%20Using%20Weekly%20Docetaxel%20and%20Erythropoietin%20for%20High-Risk%20Postoperative%20Head%20and%20Neck%20Cancer%20Patients&rft.jtitle=International%20journal%20of%20radiation%20oncology,%20biology,%20physics&rft.au=Willey,%20Christopher%20D.,%20M.D.,%20Ph.D&rft.date=2007-04-01&rft.volume=67&rft.issue=5&rft.spage=1323&rft.epage=1331&rft.pages=1323-1331&rft.issn=0360-3016&rft.eissn=1879-355X&rft_id=info:doi/10.1016/j.ijrobp.2006.11.033&rft_dat=%3Cproquest_osti_%3E21245660%3C/proquest_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=21245660&rft_id=info:pmid/17289289&rft_els_id=1_s2_0_S0360301606035048&rfr_iscdi=true |