Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol

Background: We conducted a phase II study to evaluate in 72 adult patients the efficacy of the intensive LMB chemotherapy regimen, previously reported by the Société Française d'Oncologie Pédiatrique for children with Burkitt lymphoma and L3 acute lymphoblastic leukemia. Patients and method...

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Veröffentlicht in:Annals of oncology 2005-12, Vol.16 (12), p.1928-1935
Hauptverfasser: Diviné, M., Casassus, P., Koscielny, S., Bosq, J., Sebban, C., Le Maignan, C., Stamattoulas, A., Dupriez, B., Raphaël, M., Pico, J.-L., Ribrag, V.
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container_end_page 1935
container_issue 12
container_start_page 1928
container_title Annals of oncology
container_volume 16
creator Diviné, M.
Casassus, P.
Koscielny, S.
Bosq, J.
Sebban, C.
Le Maignan, C.
Stamattoulas, A.
Dupriez, B.
Raphaël, M.
Pico, J.-L.
Ribrag, V.
description Background: We conducted a phase II study to evaluate in 72 adult patients the efficacy of the intensive LMB chemotherapy regimen, previously reported by the Société Française d'Oncologie Pédiatrique for children with Burkitt lymphoma and L3 acute lymphoblastic leukemia. Patients and methods: Treatment began with a prephase (low-dose steroids, vincristine and cyclophosphamide), except in patients with low tumor burden. Group A (resected stage I and abdominal stage II disease) received three courses of vincristine, cyclophosphamide, doxorubicin and prednisone. Group B (not eligible for groups A or C) received five courses of chemotherapy comprising high-dose methotrexate, infusional cytarabine and intrathecal (IT) methotrexate. Group C (patients with central nervous system and/or bone marrow involvement with
doi_str_mv 10.1093/annonc/mdi403
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Patients and methods: Treatment began with a prephase (low-dose steroids, vincristine and cyclophosphamide), except in patients with low tumor burden. Group A (resected stage I and abdominal stage II disease) received three courses of vincristine, cyclophosphamide, doxorubicin and prednisone. Group B (not eligible for groups A or C) received five courses of chemotherapy comprising high-dose methotrexate, infusional cytarabine and intrathecal (IT) methotrexate. Group C (patients with central nervous system and/or bone marrow involvement with &lt;30% of blast cells) received eight courses containing intensified high-dose methotrexate, high-dose cytarabine, etoposide and triple IT injections. Results: The 2 year event-free survival and overall survival rates for the 72 patients were 65% and 70%, respectively. Age ≥33 years and high lactate dehydrogenase value were associated with a shorter survival. No response to COP was also associated with a poor outcome in group B. Conclusion: Patients with advanced-stage Burkitt lymphoma, including those with bone marrow and/or central nervous system involvement, can be cured with a short-term intensive chemotherapy regime tailored to the tumor burden.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1093/annonc/mdi403</identifier><identifier>PMID: 16284057</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; adult patients ; Aged ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Burkitt lymphoma ; Burkitt Lymphoma - drug therapy ; Burkitt Lymphoma - mortality ; Burkitt Lymphoma - pathology ; chemotherapy ; Cyclophosphamide - therapeutic use ; Cytarabine - therapeutic use ; Disease-Free Survival ; Doxorubicin - therapeutic use ; Etoposide - therapeutic use ; Female ; Hematologic and hematopoietic diseases ; Humans ; Hydrocortisone - therapeutic use ; Leucovorin - therapeutic use ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Methotrexate - therapeutic use ; Middle Aged ; Neoplasm Staging ; Pharmacology. Drug treatments ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology ; Prednisone - therapeutic use ; Prognosis ; prognostic factors ; Prospective Studies ; Survival Rate ; Vincristine - therapeutic use</subject><ispartof>Annals of oncology, 2005-12, Vol.16 (12), p.1928-1935</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Dec 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-c4171372f74a310cf6ec7b76ab19e3dbae37a7b8d13974e4d9f1279bb1453d053</citedby><cites>FETCH-LOGICAL-c456t-c4171372f74a310cf6ec7b76ab19e3dbae37a7b8d13974e4d9f1279bb1453d053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17379227$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16284057$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Diviné, M.</creatorcontrib><creatorcontrib>Casassus, P.</creatorcontrib><creatorcontrib>Koscielny, S.</creatorcontrib><creatorcontrib>Bosq, J.</creatorcontrib><creatorcontrib>Sebban, C.</creatorcontrib><creatorcontrib>Le Maignan, C.</creatorcontrib><creatorcontrib>Stamattoulas, A.</creatorcontrib><creatorcontrib>Dupriez, B.</creatorcontrib><creatorcontrib>Raphaël, M.</creatorcontrib><creatorcontrib>Pico, J.-L.</creatorcontrib><creatorcontrib>Ribrag, V.</creatorcontrib><creatorcontrib>GELA</creatorcontrib><creatorcontrib>GOELAMS</creatorcontrib><title>Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>Background: We conducted a phase II study to evaluate in 72 adult patients the efficacy of the intensive LMB chemotherapy regimen, previously reported by the Société Française d'Oncologie Pédiatrique for children with Burkitt lymphoma and L3 acute lymphoblastic leukemia. Patients and methods: Treatment began with a prephase (low-dose steroids, vincristine and cyclophosphamide), except in patients with low tumor burden. Group A (resected stage I and abdominal stage II disease) received three courses of vincristine, cyclophosphamide, doxorubicin and prednisone. Group B (not eligible for groups A or C) received five courses of chemotherapy comprising high-dose methotrexate, infusional cytarabine and intrathecal (IT) methotrexate. Group C (patients with central nervous system and/or bone marrow involvement with &lt;30% of blast cells) received eight courses containing intensified high-dose methotrexate, high-dose cytarabine, etoposide and triple IT injections. Results: The 2 year event-free survival and overall survival rates for the 72 patients were 65% and 70%, respectively. Age ≥33 years and high lactate dehydrogenase value were associated with a shorter survival. No response to COP was also associated with a poor outcome in group B. Conclusion: Patients with advanced-stage Burkitt lymphoma, including those with bone marrow and/or central nervous system involvement, can be cured with a short-term intensive chemotherapy regime tailored to the tumor burden.</description><subject>Adolescent</subject><subject>Adult</subject><subject>adult patients</subject><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Burkitt lymphoma</subject><subject>Burkitt Lymphoma - drug therapy</subject><subject>Burkitt Lymphoma - mortality</subject><subject>Burkitt Lymphoma - pathology</subject><subject>chemotherapy</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Cytarabine - therapeutic use</subject><subject>Disease-Free Survival</subject><subject>Doxorubicin - therapeutic use</subject><subject>Etoposide - therapeutic use</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Hydrocortisone - therapeutic use</subject><subject>Leucovorin - therapeutic use</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methotrexate - therapeutic use</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Pharmacology. Drug treatments</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology</subject><subject>Prednisone - therapeutic use</subject><subject>Prognosis</subject><subject>prognostic factors</subject><subject>Prospective Studies</subject><subject>Survival Rate</subject><subject>Vincristine - therapeutic use</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd1rVDEQxYNY7Lr66KsEQd9um6-bbHxrq3UrKyIoFF_C3CSXpr1fJrna_e_NsosLvmQI85szwzkIvaLkjBLNz2EYxsGe9y4Iwp-gBa2lrlZE0KdoQTTjlaq5OEXPU7onhEjN9DN0SiVbCVKrBeov5_gQcsbdtp_uxh5wGDC4ucvpPQY8xTFN3ubw2-OUZ7fFY4sVwxPk4IeccI4esnf4T8h3GHajMO3-k3cBcgwWb75c7mTyaMfuBTppoUv-5aEu0Y_rj9-v1tXm66ebq4tNZUUtc3mpolyxVgnglNhWeqsaJaGh2nPXgOcKVLNylGslvHC6pUzppqGi5o7UfIne7XXL4l-zT9n0IVnfdTD4cU6GljFFhS7gm__A-3GOQ7mtMFIySYuFS1TtIVvcSNG3Zoqhh7g1lJhdCGYfgtmHUPjXB9G56b070gfXC_D2AECy0LURBhvSkVNcacbUcXFI2T_-60N8MLIwtVnf_jSf6bf69lquzQf-F_ShoNo</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>Diviné, M.</creator><creator>Casassus, P.</creator><creator>Koscielny, S.</creator><creator>Bosq, J.</creator><creator>Sebban, C.</creator><creator>Le Maignan, C.</creator><creator>Stamattoulas, A.</creator><creator>Dupriez, B.</creator><creator>Raphaël, M.</creator><creator>Pico, J.-L.</creator><creator>Ribrag, V.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><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>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope></search><sort><creationdate>20051201</creationdate><title>Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol</title><author>Diviné, M. ; Casassus, P. ; Koscielny, S. ; Bosq, J. ; Sebban, C. ; Le Maignan, C. ; Stamattoulas, A. ; Dupriez, B. ; Raphaël, M. ; Pico, J.-L. ; Ribrag, V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-c4171372f74a310cf6ec7b76ab19e3dbae37a7b8d13974e4d9f1279bb1453d053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>adult patients</topic><topic>Aged</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Burkitt lymphoma</topic><topic>Burkitt Lymphoma - drug therapy</topic><topic>Burkitt Lymphoma - mortality</topic><topic>Burkitt Lymphoma - pathology</topic><topic>chemotherapy</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>Cytarabine - therapeutic use</topic><topic>Disease-Free Survival</topic><topic>Doxorubicin - therapeutic use</topic><topic>Etoposide - therapeutic use</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Hydrocortisone - therapeutic use</topic><topic>Leucovorin - therapeutic use</topic><topic>Leukemias. 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Patients and methods: Treatment began with a prephase (low-dose steroids, vincristine and cyclophosphamide), except in patients with low tumor burden. Group A (resected stage I and abdominal stage II disease) received three courses of vincristine, cyclophosphamide, doxorubicin and prednisone. Group B (not eligible for groups A or C) received five courses of chemotherapy comprising high-dose methotrexate, infusional cytarabine and intrathecal (IT) methotrexate. Group C (patients with central nervous system and/or bone marrow involvement with &lt;30% of blast cells) received eight courses containing intensified high-dose methotrexate, high-dose cytarabine, etoposide and triple IT injections. Results: The 2 year event-free survival and overall survival rates for the 72 patients were 65% and 70%, respectively. Age ≥33 years and high lactate dehydrogenase value were associated with a shorter survival. No response to COP was also associated with a poor outcome in group B. 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subjects Adolescent
Adult
adult patients
Aged
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Burkitt lymphoma
Burkitt Lymphoma - drug therapy
Burkitt Lymphoma - mortality
Burkitt Lymphoma - pathology
chemotherapy
Cyclophosphamide - therapeutic use
Cytarabine - therapeutic use
Disease-Free Survival
Doxorubicin - therapeutic use
Etoposide - therapeutic use
Female
Hematologic and hematopoietic diseases
Humans
Hydrocortisone - therapeutic use
Leucovorin - therapeutic use
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Male
Medical sciences
Methotrexate - therapeutic use
Middle Aged
Neoplasm Staging
Pharmacology. Drug treatments
Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy
Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality
Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology
Prednisone - therapeutic use
Prognosis
prognostic factors
Prospective Studies
Survival Rate
Vincristine - therapeutic use
title Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol
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