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Treatment of Acute Lymphoblastic Leukemia in the Elderly: An Evaluation of Interferon Alpha Given as a Single Agent After Complete Remission
Although interferon (IFN) has been used in elderly patients with acute lymphoblastic leukemia (ALL), the benefits from IFN therapy have not been properly assessed, especially as it was given combined with other cytotoxic drugs, which obscured the role of IFN if any. In 1997, we started a study aimed...
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Published in: | Leukemia & lymphoma 2002, Vol.43 (1), p.75-81 |
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creator | Delannoy, A. Cazin, B. Thomas, X. Bouabdallah, R. Boiron, J.M. Huguet, F. Straetmans, N. Zérazhi, H. Vernant, J.P. Dombret, H. Bilhou-Nabera, C. Charrin, C. Boucheix, C. Sebban, C. Lhéritier, V. Fière, D. |
description | Although interferon (IFN) has been used in elderly patients with acute lymphoblastic leukemia (ALL), the benefits from IFN therapy have not been properly assessed, especially as it was given combined with other cytotoxic drugs, which obscured the role of IFN if any. In 1997, we started a study aimed at improving our previous results in elderly patients with ALL and at assessing the therapeutic role of IFN in this disease. Fifty-eight patients with ALL, aged 55-81 years (median: 64.9 years), were randomly allocated to treatment with vindesine or vincristine during induction. After a first consolidation course, IFN was administered as a single agent for three months together with cranial radiotherapy. Chemotherapy was then resumed with a second consolidation course and maintenance. A complete remission (CR) was obtained in 58% of patients (CI: 45-71%), significantly less than in our previous study which included IFN combined with chemotherapy during maintenance (CR: 85%, CI:70-94%, p =0.007 ). Overall survival (median: 289 vs 434 days in the previous study, p =0.01 ) and disease-free survival (median: 146 vs 427 days, p =0.009 ) were also inferior in the present study. In particular, the pattern of relapses over time suggested that the 3 month IFN treatment phase with no additional chemotherapy might have contributed to the comparatively poor outcome of this cohort. In addition, vindesine given during induction did not prove less neurotoxic than vincristine, did not improve the CR rate, and had no impact on survival. In conclusion, although similar to published studies in elderly patients with ALL, this study is inferior to our previous one. INF, given as a single drug, has a modest role if any in the treatment of older persons with ALL. |
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In 1997, we started a study aimed at improving our previous results in elderly patients with ALL and at assessing the therapeutic role of IFN in this disease. Fifty-eight patients with ALL, aged 55-81 years (median: 64.9 years), were randomly allocated to treatment with vindesine or vincristine during induction. After a first consolidation course, IFN was administered as a single agent for three months together with cranial radiotherapy. Chemotherapy was then resumed with a second consolidation course and maintenance. A complete remission (CR) was obtained in 58% of patients (CI: 45-71%), significantly less than in our previous study which included IFN combined with chemotherapy during maintenance (CR: 85%, CI:70-94%, p =0.007 ). Overall survival (median: 289 vs 434 days in the previous study, p =0.01 ) and disease-free survival (median: 146 vs 427 days, p =0.009 ) were also inferior in the present study. In particular, the pattern of relapses over time suggested that the 3 month IFN treatment phase with no additional chemotherapy might have contributed to the comparatively poor outcome of this cohort. In addition, vindesine given during induction did not prove less neurotoxic than vincristine, did not improve the CR rate, and had no impact on survival. In conclusion, although similar to published studies in elderly patients with ALL, this study is inferior to our previous one. INF, given as a single drug, has a modest role if any in the treatment of older persons with ALL.</description><identifier>ISSN: 1042-8194</identifier><identifier>EISSN: 1029-2403</identifier><identifier>DOI: 10.1080/10428190210180</identifier><identifier>PMID: 11908739</identifier><language>eng</language><publisher>United States: Informa UK Ltd</publisher><subject>Acute Lymphoblastic Leukemia ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - toxicity ; Brain Neoplasms - prevention & control ; Brain Neoplasms - radiotherapy ; Elderly ; Female ; Humans ; Interferon ; Interferon-alpha - administration & dosage ; Interferon-alpha - therapeutic use ; Male ; Middle Aged ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - radiotherapy ; Random Allocation ; Recurrence ; Remission Induction - methods ; Survival Analysis ; Treatment Outcome ; Vincristine - administration & dosage ; Vincristine - toxicity ; Vindesine ; Vindesine - administration & dosage ; Vindesine - toxicity</subject><ispartof>Leukemia & lymphoma, 2002, Vol.43 (1), p.75-81</ispartof><rights>2002 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-6945e90b0979e7337bbe8167288532aa9df57df29cf82f6f4bbc6320a72e64593</citedby><cites>FETCH-LOGICAL-c423t-6945e90b0979e7337bbe8167288532aa9df57df29cf82f6f4bbc6320a72e64593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11908739$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Delannoy, A.</creatorcontrib><creatorcontrib>Cazin, B.</creatorcontrib><creatorcontrib>Thomas, X.</creatorcontrib><creatorcontrib>Bouabdallah, R.</creatorcontrib><creatorcontrib>Boiron, J.M.</creatorcontrib><creatorcontrib>Huguet, F.</creatorcontrib><creatorcontrib>Straetmans, N.</creatorcontrib><creatorcontrib>Zérazhi, H.</creatorcontrib><creatorcontrib>Vernant, J.P.</creatorcontrib><creatorcontrib>Dombret, H.</creatorcontrib><creatorcontrib>Bilhou-Nabera, C.</creatorcontrib><creatorcontrib>Charrin, C.</creatorcontrib><creatorcontrib>Boucheix, C.</creatorcontrib><creatorcontrib>Sebban, C.</creatorcontrib><creatorcontrib>Lhéritier, V.</creatorcontrib><creatorcontrib>Fière, D.</creatorcontrib><creatorcontrib>LALA Group, France and Belgium</creatorcontrib><title>Treatment of Acute Lymphoblastic Leukemia in the Elderly: An Evaluation of Interferon Alpha Given as a Single Agent After Complete Remission</title><title>Leukemia & lymphoma</title><addtitle>Leuk Lymphoma</addtitle><description>Although interferon (IFN) has been used in elderly patients with acute lymphoblastic leukemia (ALL), the benefits from IFN therapy have not been properly assessed, especially as it was given combined with other cytotoxic drugs, which obscured the role of IFN if any. In 1997, we started a study aimed at improving our previous results in elderly patients with ALL and at assessing the therapeutic role of IFN in this disease. Fifty-eight patients with ALL, aged 55-81 years (median: 64.9 years), were randomly allocated to treatment with vindesine or vincristine during induction. After a first consolidation course, IFN was administered as a single agent for three months together with cranial radiotherapy. Chemotherapy was then resumed with a second consolidation course and maintenance. A complete remission (CR) was obtained in 58% of patients (CI: 45-71%), significantly less than in our previous study which included IFN combined with chemotherapy during maintenance (CR: 85%, CI:70-94%, p =0.007 ). Overall survival (median: 289 vs 434 days in the previous study, p =0.01 ) and disease-free survival (median: 146 vs 427 days, p =0.009 ) were also inferior in the present study. In particular, the pattern of relapses over time suggested that the 3 month IFN treatment phase with no additional chemotherapy might have contributed to the comparatively poor outcome of this cohort. In addition, vindesine given during induction did not prove less neurotoxic than vincristine, did not improve the CR rate, and had no impact on survival. In conclusion, although similar to published studies in elderly patients with ALL, this study is inferior to our previous one. INF, given as a single drug, has a modest role if any in the treatment of older persons with ALL.</description><subject>Acute Lymphoblastic Leukemia</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - toxicity</subject><subject>Brain Neoplasms - prevention & control</subject><subject>Brain Neoplasms - radiotherapy</subject><subject>Elderly</subject><subject>Female</subject><subject>Humans</subject><subject>Interferon</subject><subject>Interferon-alpha - administration & dosage</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - radiotherapy</subject><subject>Random Allocation</subject><subject>Recurrence</subject><subject>Remission Induction - methods</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><subject>Vincristine - administration & dosage</subject><subject>Vincristine - toxicity</subject><subject>Vindesine</subject><subject>Vindesine - administration & dosage</subject><subject>Vindesine - toxicity</subject><issn>1042-8194</issn><issn>1029-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp1kE9v1DAQxSMEoqXlyhH5xC3Fdv6aW7RaSqWVkKA9WxNn3KQ4drCdov0O_dD1aldCPfQ0Hvn33hu9LPvE6BWjLf3KaMlbJihnlLX0TXbOKBc5L2nx9vAueZ5-y7PsQwgPlNJK1Px9dsaSom0KcZ493XqEOKONxGnSqTUi2e3nZXS9gRAnRXa4_sF5AjJZEkckWzOgN_tvpLNk-whmhTg5e1Df2Iheo09bZ5YRyPX0iJZAIEB-T_beIOnuD0mdTiDZuHkxmPJ-JfsQksll9k6DCfjxNC-yu-_b282PfPfz-mbT7XJV8iLmtSgrFLSnohHYFEXT99iyuuFtWxUcQAy6agbNhdIt17Uu-17VBafQcKzLShQX2Zej7-Ld3xVDlOkAhcaARbcGyUSdgpoqgVdHUHkXgkctFz_N4PeSUXnoX77sPwk-n5zXfsbhP34qPAHiCExWOz_DP-fNICPsjfPag1VTkMWr5u0L7Yhg4qjAo3xwq7epstfuega7naQv</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Delannoy, A.</creator><creator>Cazin, B.</creator><creator>Thomas, X.</creator><creator>Bouabdallah, R.</creator><creator>Boiron, J.M.</creator><creator>Huguet, F.</creator><creator>Straetmans, N.</creator><creator>Zérazhi, H.</creator><creator>Vernant, J.P.</creator><creator>Dombret, H.</creator><creator>Bilhou-Nabera, C.</creator><creator>Charrin, C.</creator><creator>Boucheix, C.</creator><creator>Sebban, C.</creator><creator>Lhéritier, V.</creator><creator>Fière, D.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>7T5</scope><scope>H94</scope></search><sort><creationdate>2002</creationdate><title>Treatment of Acute Lymphoblastic Leukemia in the Elderly: An Evaluation of Interferon Alpha Given as a Single Agent After Complete Remission</title><author>Delannoy, A. ; Cazin, B. ; Thomas, X. ; Bouabdallah, R. ; Boiron, J.M. ; Huguet, F. ; Straetmans, N. ; Zérazhi, H. ; Vernant, J.P. ; Dombret, H. ; Bilhou-Nabera, C. ; Charrin, C. ; Boucheix, C. ; Sebban, C. ; Lhéritier, V. ; Fière, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-6945e90b0979e7337bbe8167288532aa9df57df29cf82f6f4bbc6320a72e64593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Acute Lymphoblastic Leukemia</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - toxicity</topic><topic>Brain Neoplasms - prevention & control</topic><topic>Brain Neoplasms - radiotherapy</topic><topic>Elderly</topic><topic>Female</topic><topic>Humans</topic><topic>Interferon</topic><topic>Interferon-alpha - administration & dosage</topic><topic>Interferon-alpha - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - radiotherapy</topic><topic>Random Allocation</topic><topic>Recurrence</topic><topic>Remission Induction - methods</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><topic>Vincristine - administration & dosage</topic><topic>Vincristine - toxicity</topic><topic>Vindesine</topic><topic>Vindesine - administration & dosage</topic><topic>Vindesine - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Delannoy, A.</creatorcontrib><creatorcontrib>Cazin, B.</creatorcontrib><creatorcontrib>Thomas, X.</creatorcontrib><creatorcontrib>Bouabdallah, R.</creatorcontrib><creatorcontrib>Boiron, J.M.</creatorcontrib><creatorcontrib>Huguet, F.</creatorcontrib><creatorcontrib>Straetmans, N.</creatorcontrib><creatorcontrib>Zérazhi, H.</creatorcontrib><creatorcontrib>Vernant, J.P.</creatorcontrib><creatorcontrib>Dombret, H.</creatorcontrib><creatorcontrib>Bilhou-Nabera, C.</creatorcontrib><creatorcontrib>Charrin, C.</creatorcontrib><creatorcontrib>Boucheix, C.</creatorcontrib><creatorcontrib>Sebban, C.</creatorcontrib><creatorcontrib>Lhéritier, V.</creatorcontrib><creatorcontrib>Fière, D.</creatorcontrib><creatorcontrib>LALA Group, France and Belgium</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Leukemia & lymphoma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Delannoy, A.</au><au>Cazin, B.</au><au>Thomas, X.</au><au>Bouabdallah, R.</au><au>Boiron, J.M.</au><au>Huguet, F.</au><au>Straetmans, N.</au><au>Zérazhi, H.</au><au>Vernant, J.P.</au><au>Dombret, H.</au><au>Bilhou-Nabera, C.</au><au>Charrin, C.</au><au>Boucheix, C.</au><au>Sebban, C.</au><au>Lhéritier, V.</au><au>Fière, D.</au><aucorp>LALA Group, France and Belgium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of Acute Lymphoblastic Leukemia in the Elderly: An Evaluation of Interferon Alpha Given as a Single Agent After Complete Remission</atitle><jtitle>Leukemia & lymphoma</jtitle><addtitle>Leuk Lymphoma</addtitle><date>2002</date><risdate>2002</risdate><volume>43</volume><issue>1</issue><spage>75</spage><epage>81</epage><pages>75-81</pages><issn>1042-8194</issn><eissn>1029-2403</eissn><abstract>Although interferon (IFN) has been used in elderly patients with acute lymphoblastic leukemia (ALL), the benefits from IFN therapy have not been properly assessed, especially as it was given combined with other cytotoxic drugs, which obscured the role of IFN if any. In 1997, we started a study aimed at improving our previous results in elderly patients with ALL and at assessing the therapeutic role of IFN in this disease. Fifty-eight patients with ALL, aged 55-81 years (median: 64.9 years), were randomly allocated to treatment with vindesine or vincristine during induction. After a first consolidation course, IFN was administered as a single agent for three months together with cranial radiotherapy. Chemotherapy was then resumed with a second consolidation course and maintenance. A complete remission (CR) was obtained in 58% of patients (CI: 45-71%), significantly less than in our previous study which included IFN combined with chemotherapy during maintenance (CR: 85%, CI:70-94%, p =0.007 ). Overall survival (median: 289 vs 434 days in the previous study, p =0.01 ) and disease-free survival (median: 146 vs 427 days, p =0.009 ) were also inferior in the present study. In particular, the pattern of relapses over time suggested that the 3 month IFN treatment phase with no additional chemotherapy might have contributed to the comparatively poor outcome of this cohort. In addition, vindesine given during induction did not prove less neurotoxic than vincristine, did not improve the CR rate, and had no impact on survival. In conclusion, although similar to published studies in elderly patients with ALL, this study is inferior to our previous one. INF, given as a single drug, has a modest role if any in the treatment of older persons with ALL.</abstract><cop>United States</cop><pub>Informa UK Ltd</pub><pmid>11908739</pmid><doi>10.1080/10428190210180</doi><tpages>7</tpages></addata></record> |
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subjects | Acute Lymphoblastic Leukemia Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - therapeutic use Antineoplastic Combined Chemotherapy Protocols - toxicity Brain Neoplasms - prevention & control Brain Neoplasms - radiotherapy Elderly Female Humans Interferon Interferon-alpha - administration & dosage Interferon-alpha - therapeutic use Male Middle Aged Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality Precursor Cell Lymphoblastic Leukemia-Lymphoma - radiotherapy Random Allocation Recurrence Remission Induction - methods Survival Analysis Treatment Outcome Vincristine - administration & dosage Vincristine - toxicity Vindesine Vindesine - administration & dosage Vindesine - toxicity |
title | Treatment of Acute Lymphoblastic Leukemia in the Elderly: An Evaluation of Interferon Alpha Given as a Single Agent After Complete Remission |
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