Beneficial and harmful effects of anthracyclines in the treatment of childhood acute lymphoblastic leukaemia: a systematic review and meta‐analysis

Summary Anthracyclines are used to treat childhood acute lymphoblastic leukaemia (ALL) but non‐randomized studies suggest that cardiotoxicity may be a problem. Individual patient data from trials in childhood ALL that randomized anthracyclines or methods of reducing cardiotoxicity were analysed by s...

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Veröffentlicht in:British journal of haematology 2009-05, Vol.145 (3), p.376-388
1. Verfasser: Childhood Acute Lymphoblastic Leukaemia Collaborative Group (CALLCG),  
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description Summary Anthracyclines are used to treat childhood acute lymphoblastic leukaemia (ALL) but non‐randomized studies suggest that cardiotoxicity may be a problem. Individual patient data from trials in childhood ALL that randomized anthracyclines or methods of reducing cardiotoxicity were analysed by standard meta‐analysis methods. Results were grouped and combined according to: addition of an anthracycline to standard therapy, type of anthracycline, mode of administration, and the use of a cardioprotectant. Data from 958 patients in 4 trials, recruiting between 1972 and 1984, showed that addition of an anthracycline reduced bone marrow relapse and, non‐significantly, non‐bone marrow relapse, resulting in an increased relapse‐free interval. However there was a non‐significant increase in induction failures, and in deaths in first remission. Event‐free survival at 5 years was 56·7% with anthracycline versus 52·8% without (Odds Ratio = 0·91; 95% Confidence Interval = 0·76–1·10; P = 0·3). There were no significant differences found in other treatment comparisons. The limited data from trials did not demonstrate differences in clinically evident cardiotoxicity. Anthracyclines are effective against bone marrow relapse but have not been shown to significantly increase event free survival in childhood ALL. The evidence on type of anthracycline, method of administration or use of cardioprotectant was insufficient to be able to rule out important differences.
doi_str_mv 10.1111/j.1365-2141.2009.07624.x
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Individual patient data from trials in childhood ALL that randomized anthracyclines or methods of reducing cardiotoxicity were analysed by standard meta‐analysis methods. Results were grouped and combined according to: addition of an anthracycline to standard therapy, type of anthracycline, mode of administration, and the use of a cardioprotectant. Data from 958 patients in 4 trials, recruiting between 1972 and 1984, showed that addition of an anthracycline reduced bone marrow relapse and, non‐significantly, non‐bone marrow relapse, resulting in an increased relapse‐free interval. However there was a non‐significant increase in induction failures, and in deaths in first remission. Event‐free survival at 5 years was 56·7% with anthracycline versus 52·8% without (Odds Ratio = 0·91; 95% Confidence Interval = 0·76–1·10; P = 0·3). There were no significant differences found in other treatment comparisons. The limited data from trials did not demonstrate differences in clinically evident cardiotoxicity. Anthracyclines are effective against bone marrow relapse but have not been shown to significantly increase event free survival in childhood ALL. The evidence on type of anthracycline, method of administration or use of cardioprotectant was insufficient to be able to rule out important differences.</description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1111/j.1365-2141.2009.07624.x</identifier><identifier>PMID: 19236609</identifier><identifier>CODEN: BJHEAL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; anthracycline ; Anthracyclines - adverse effects ; Anthracyclines - therapeutic use ; Antibiotics, Antineoplastic - adverse effects ; Antibiotics, Antineoplastic - therapeutic use ; Antineoplastic agents ; Biological and medical sciences ; Cardiotonic Agents - therapeutic use ; Chemotherapy ; Child ; Child, Preschool ; childhood ALL ; Disease-Free Survival ; Female ; Heart Diseases - chemically induced ; Hematologic and hematopoietic diseases ; Humans ; Infant ; leukaemia ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; meta‐analysis ; Odds Ratio ; Pharmacology. 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Individual patient data from trials in childhood ALL that randomized anthracyclines or methods of reducing cardiotoxicity were analysed by standard meta‐analysis methods. Results were grouped and combined according to: addition of an anthracycline to standard therapy, type of anthracycline, mode of administration, and the use of a cardioprotectant. Data from 958 patients in 4 trials, recruiting between 1972 and 1984, showed that addition of an anthracycline reduced bone marrow relapse and, non‐significantly, non‐bone marrow relapse, resulting in an increased relapse‐free interval. However there was a non‐significant increase in induction failures, and in deaths in first remission. Event‐free survival at 5 years was 56·7% with anthracycline versus 52·8% without (Odds Ratio = 0·91; 95% Confidence Interval = 0·76–1·10; P = 0·3). There were no significant differences found in other treatment comparisons. The limited data from trials did not demonstrate differences in clinically evident cardiotoxicity. Anthracyclines are effective against bone marrow relapse but have not been shown to significantly increase event free survival in childhood ALL. The evidence on type of anthracycline, method of administration or use of cardioprotectant was insufficient to be able to rule out important differences.</description><subject>Adolescent</subject><subject>Adult</subject><subject>anthracycline</subject><subject>Anthracyclines - adverse effects</subject><subject>Anthracyclines - therapeutic use</subject><subject>Antibiotics, Antineoplastic - adverse effects</subject><subject>Antibiotics, Antineoplastic - therapeutic use</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Cardiotonic Agents - therapeutic use</subject><subject>Chemotherapy</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>childhood ALL</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Heart Diseases - chemically induced</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>leukaemia</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>meta‐analysis</subject><subject>Odds Ratio</subject><subject>Pharmacology. Drug treatments</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</subject><subject>randomized</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Remission Induction</subject><subject>Young Adult</subject><issn>0007-1048</issn><issn>1365-2141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAQgCMEokvhFZAvcMvin8SJkUBqK6CgSlzgbM3aY-LFSZbYaZsbj8CFF-RJSLqrBW74Ymvmmx_ryzLC6JrN58V2zYQsc84KtuaUqjWtJC_Wt_ey1TFxP1tRSquc0aI-yR7FuKWUCVqyh9kJU1xISdUq-3mOHTpvPAQCnSUNDK0bA0Hn0KRIejeHUzOAmUzwHUbiO5IaJGlASC12aUFM44Nt-t4SMGNCEqZ21_SbADF5QwKOXwFbDy8JkDjFhC0s8QGvPd7cjW0xwa_vP6CDMEUfH2cPHISITw73afb57ZtPF5f51cd37y_OrnJTClHkrBaVsFUtlVXMWWdsIQVU1NpNReuyFBtqOTdGKS5NVTvpQG6kMpIDLwteitPs9b7vbty0aM38nQGC3g2-hWHSPXj9b6bzjf7SX2teM14JPjd4fmgw9N9GjEm3PhoMATrsx6g5LWumhJrBeg-aoY9xQHccwqhenOqtXtTpRZ1enOo7p_p2Ln3695J_Cg8SZ-DZAYBoILgBOuPjkeNM1KVU1cy92nM3PuD03wvo8w-Xy0v8BhOwwjU</recordid><startdate>200905</startdate><enddate>200905</enddate><creator>Childhood Acute Lymphoblastic Leukaemia Collaborative Group (CALLCG),  </creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><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><scope>5PM</scope></search><sort><creationdate>200905</creationdate><title>Beneficial and harmful effects of anthracyclines in the treatment of childhood acute lymphoblastic leukaemia: a systematic review and meta‐analysis</title><author>Childhood Acute Lymphoblastic Leukaemia Collaborative Group (CALLCG),  </author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5334-18373d7869d91fdfcd463a70ddb708553b0d22cc9926c78f6fa6b69c62a254253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>anthracycline</topic><topic>Anthracyclines - adverse effects</topic><topic>Anthracyclines - therapeutic use</topic><topic>Antibiotics, Antineoplastic - adverse effects</topic><topic>Antibiotics, Antineoplastic - therapeutic use</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Cardiotonic Agents - therapeutic use</topic><topic>Chemotherapy</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>childhood ALL</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Heart Diseases - chemically induced</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>leukaemia</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>meta‐analysis</topic><topic>Odds Ratio</topic><topic>Pharmacology. Drug treatments</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</topic><topic>randomized</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Remission Induction</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Childhood Acute Lymphoblastic Leukaemia Collaborative Group (CALLCG),  </creatorcontrib><creatorcontrib>Childhood Acute Lymphoblastic Leukaemia Collaborative Group (CALLCG)</creatorcontrib><collection>Pascal-Francis</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Childhood Acute Lymphoblastic Leukaemia Collaborative Group (CALLCG),  </au><aucorp>Childhood Acute Lymphoblastic Leukaemia Collaborative Group (CALLCG)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beneficial and harmful effects of anthracyclines in the treatment of childhood acute lymphoblastic leukaemia: a systematic review and meta‐analysis</atitle><jtitle>British journal of haematology</jtitle><addtitle>Br J Haematol</addtitle><date>2009-05</date><risdate>2009</risdate><volume>145</volume><issue>3</issue><spage>376</spage><epage>388</epage><pages>376-388</pages><issn>0007-1048</issn><eissn>1365-2141</eissn><coden>BJHEAL</coden><abstract>Summary Anthracyclines are used to treat childhood acute lymphoblastic leukaemia (ALL) but non‐randomized studies suggest that cardiotoxicity may be a problem. Individual patient data from trials in childhood ALL that randomized anthracyclines or methods of reducing cardiotoxicity were analysed by standard meta‐analysis methods. Results were grouped and combined according to: addition of an anthracycline to standard therapy, type of anthracycline, mode of administration, and the use of a cardioprotectant. Data from 958 patients in 4 trials, recruiting between 1972 and 1984, showed that addition of an anthracycline reduced bone marrow relapse and, non‐significantly, non‐bone marrow relapse, resulting in an increased relapse‐free interval. However there was a non‐significant increase in induction failures, and in deaths in first remission. Event‐free survival at 5 years was 56·7% with anthracycline versus 52·8% without (Odds Ratio = 0·91; 95% Confidence Interval = 0·76–1·10; P = 0·3). There were no significant differences found in other treatment comparisons. The limited data from trials did not demonstrate differences in clinically evident cardiotoxicity. Anthracyclines are effective against bone marrow relapse but have not been shown to significantly increase event free survival in childhood ALL. The evidence on type of anthracycline, method of administration or use of cardioprotectant was insufficient to be able to rule out important differences.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19236609</pmid><doi>10.1111/j.1365-2141.2009.07624.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
anthracycline
Anthracyclines - adverse effects
Anthracyclines - therapeutic use
Antibiotics, Antineoplastic - adverse effects
Antibiotics, Antineoplastic - therapeutic use
Antineoplastic agents
Biological and medical sciences
Cardiotonic Agents - therapeutic use
Chemotherapy
Child
Child, Preschool
childhood ALL
Disease-Free Survival
Female
Heart Diseases - chemically induced
Hematologic and hematopoietic diseases
Humans
Infant
leukaemia
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Male
Medical sciences
meta‐analysis
Odds Ratio
Pharmacology. Drug treatments
Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy
Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality
randomized
Randomized Controlled Trials as Topic
Remission Induction
Young Adult
title Beneficial and harmful effects of anthracyclines in the treatment of childhood acute lymphoblastic leukaemia: a systematic review and meta‐analysis
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