Chemoimmunotherapy with hyper‐CVAD plus rituximab for the treatment of adult Burkitt and Burkitt‐type lymphoma or acute lymphoblastic leukemia

BACKGROUND Adult Burkitt‐type lymphoma (BL) and acute lymphoblastic leukemia (B‐ALL) are rare entities composing 1% to 5% of non‐Hodgkin lymphomas NHL) or ALL. Prognosis of BL and B‐ALL has been poor with conventional NHL or ALL regimens, but has improved with dose‐intensive regimens. METHODS To eva...

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Published inCancer Vol. 106; no. 7; pp. 1569 - 1580
Main Authors Thomas, Deborah A., Faderl, Stefan, O'Brien, Susan, Bueso‐Ramos, Carlos, Cortes, Jorge, Garcia‐Manero, Guillermo, Giles, Francis J., Verstovsek, Srdan, Wierda, William G., Pierce, Sherry A., Shan, Jianqin, Brandt, Mark, Hagemeister, Fredrick B., Keating, Michael J., Cabanillas, Fernando, Kantarjian, Hagop
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.04.2006
Wiley-Liss
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BL
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Abstract BACKGROUND Adult Burkitt‐type lymphoma (BL) and acute lymphoblastic leukemia (B‐ALL) are rare entities composing 1% to 5% of non‐Hodgkin lymphomas NHL) or ALL. Prognosis of BL and B‐ALL has been poor with conventional NHL or ALL regimens, but has improved with dose‐intensive regimens. METHODS To evaluate the addition of rituximab, a CD20 monoclonal antibody, to intensive chemotherapy in adults with BL or B‐ALL, 31 patients with newly diagnosed BL or B‐ALL received the hyper‐fractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (hyper‐CVAD) regimen with rituximab. Their median age was 46 years; 29% were 60 years or older. Rituximab 375 mg/m2 was given on Days 1 and 11 of hyper‐CVAD courses and on Days 1 and 8 of methotrexate and cytarabine courses. RESULTS Complete remission (complete response [CR]) was achieved in 24 of 28 (86%) evaluable patients; 3 had a partial response, and 1 had resistant disease. There were no induction deaths. The 3‐year overall survival (OS), event‐free survival, and disease‐free survival rates were 89%, 80%, and 88%, respectively. Nine elderly patients achieved CR with all of them in continuous CR (except 1 death in CR from infection), with a 3‐year OS rate of 89%. Multivariate analysis of current and historical (those treated with hyper‐CVAD alone) groups identified age and treatment with rituximab as favorable factors. CONCLUSIONS The addition of rituximab to hyper‐CVAD may improve outcome in adult BL or B‐ALL, particularly in elderly patients. Cancer 2006. © 2006 American Cancer Society. The addition of rituximab to hyper‐CVAD may improve outcome in adult Burkitt lymphoma and acute lymphoblastic leukemia, particularly in elderly patients.
AbstractList Adult Burkitt-type lymphoma (BL) and acute lymphoblastic leukemia (B-ALL) are rare entities composing 1% to 5% of non-Hodgkin lymphomas NHL) or ALL. Prognosis of BL and B-ALL has been poor with conventional NHL or ALL regimens, but has improved with dose-intensive regimens. To evaluate the addition of rituximab, a CD20 monoclonal antibody, to intensive chemotherapy in adults with BL or B-ALL, 31 patients with newly diagnosed BL or B-ALL received the hyper-fractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (hyper-CVAD) regimen with rituximab. Their median age was 46 years; 29% were 60 years or older. Rituximab 375 mg/m(2) was given on Days 1 and 11 of hyper-CVAD courses and on Days 1 and 8 of methotrexate and cytarabine courses. Complete remission (complete response [CR]) was achieved in 24 of 28 (86%) evaluable patients; 3 had a partial response, and 1 had resistant disease. There were no induction deaths. The 3-year overall survival (OS), event-free survival, and disease-free survival rates were 89%, 80%, and 88%, respectively. Nine elderly patients achieved CR with all of them in continuous CR (except 1 death in CR from infection), with a 3-year OS rate of 89%. Multivariate analysis of current and historical (those treated with hyper-CVAD alone) groups identified age and treatment with rituximab as favorable factors. The addition of rituximab to hyper-CVAD may improve outcome in adult BL or B-ALL, particularly in elderly patients.
BACKGROUND Adult Burkitt‐type lymphoma (BL) and acute lymphoblastic leukemia (B‐ALL) are rare entities composing 1% to 5% of non‐Hodgkin lymphomas NHL) or ALL. Prognosis of BL and B‐ALL has been poor with conventional NHL or ALL regimens, but has improved with dose‐intensive regimens. METHODS To evaluate the addition of rituximab, a CD20 monoclonal antibody, to intensive chemotherapy in adults with BL or B‐ALL, 31 patients with newly diagnosed BL or B‐ALL received the hyper‐fractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (hyper‐CVAD) regimen with rituximab. Their median age was 46 years; 29% were 60 years or older. Rituximab 375 mg/m2 was given on Days 1 and 11 of hyper‐CVAD courses and on Days 1 and 8 of methotrexate and cytarabine courses. RESULTS Complete remission (complete response [CR]) was achieved in 24 of 28 (86%) evaluable patients; 3 had a partial response, and 1 had resistant disease. There were no induction deaths. The 3‐year overall survival (OS), event‐free survival, and disease‐free survival rates were 89%, 80%, and 88%, respectively. Nine elderly patients achieved CR with all of them in continuous CR (except 1 death in CR from infection), with a 3‐year OS rate of 89%. Multivariate analysis of current and historical (those treated with hyper‐CVAD alone) groups identified age and treatment with rituximab as favorable factors. CONCLUSIONS The addition of rituximab to hyper‐CVAD may improve outcome in adult BL or B‐ALL, particularly in elderly patients. Cancer 2006. © 2006 American Cancer Society. The addition of rituximab to hyper‐CVAD may improve outcome in adult Burkitt lymphoma and acute lymphoblastic leukemia, particularly in elderly patients.
Abstract BACKGROUND Adult Burkitt‐type lymphoma (BL) and acute lymphoblastic leukemia (B‐ALL) are rare entities composing 1% to 5% of non‐Hodgkin lymphomas NHL) or ALL. Prognosis of BL and B‐ALL has been poor with conventional NHL or ALL regimens, but has improved with dose‐intensive regimens. METHODS To evaluate the addition of rituximab, a CD20 monoclonal antibody, to intensive chemotherapy in adults with BL or B‐ALL, 31 patients with newly diagnosed BL or B‐ALL received the hyper‐fractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (hyper‐CVAD) regimen with rituximab. Their median age was 46 years; 29% were 60 years or older. Rituximab 375 mg/m 2 was given on Days 1 and 11 of hyper‐CVAD courses and on Days 1 and 8 of methotrexate and cytarabine courses. RESULTS Complete remission (complete response [CR]) was achieved in 24 of 28 (86%) evaluable patients; 3 had a partial response, and 1 had resistant disease. There were no induction deaths. The 3‐year overall survival (OS), event‐free survival, and disease‐free survival rates were 89%, 80%, and 88%, respectively. Nine elderly patients achieved CR with all of them in continuous CR (except 1 death in CR from infection), with a 3‐year OS rate of 89%. Multivariate analysis of current and historical (those treated with hyper‐CVAD alone) groups identified age and treatment with rituximab as favorable factors. CONCLUSIONS The addition of rituximab to hyper‐CVAD may improve outcome in adult BL or B‐ALL, particularly in elderly patients. Cancer 2006. © 2006 American Cancer Society. The addition of rituximab to hyper‐CVAD may improve outcome in adult Burkitt lymphoma and acute lymphoblastic leukemia, particularly in elderly patients.
Author O'Brien, Susan
Garcia‐Manero, Guillermo
Kantarjian, Hagop
Bueso‐Ramos, Carlos
Verstovsek, Srdan
Giles, Francis J.
Pierce, Sherry A.
Brandt, Mark
Cortes, Jorge
Wierda, William G.
Faderl, Stefan
Cabanillas, Fernando
Keating, Michael J.
Thomas, Deborah A.
Shan, Jianqin
Hagemeister, Fredrick B.
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https://www.ncbi.nlm.nih.gov/pubmed/16502413$$D View this record in MEDLINE/PubMed
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ISSN 0008-543X
IngestDate Fri Aug 23 02:13:02 EDT 2024
Sat Sep 28 07:47:43 EDT 2024
Sun Oct 22 16:06:47 EDT 2023
Sat Aug 24 01:04:09 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 7
Keywords Antineoplastic agent
B-ALL
chemoimmunotherapy
BL
Monoclonal antibody
Glucocorticoid
Doxorubicin
Alkaloid
Isomerases
Cancerology
Lymphoproliferative syndrome
Immunotherapy
Anticytokine
Adult
Acute lymphocytic leukemia
Antimitotic
Human
Corticosteroid
DNA topoisomerase (ATP-hydrolysing)
Drug combination
Dexamethasone
Enzyme
Acute
Burkitt lymphoma
Enzyme inhibitor
Acute leukemia
Rituximab
Malignant hemopathy
Non Hodgkin lymphoma
Vincristine
Fractionated dose
Infection
Alkylating agent
Antibiotic
Oxazaphosphinane derivatives
Chemotherapy
Cyclophosphamide
acute lymphoblastic leukemia
Nitrogen mustard
Viral disease
adult Burkitt lymphoma
Anthracyclins
Combined treatment
Therapeutic protocol
hyper-CVAD
Language English
License CC BY 4.0
Copyright 2006 American Cancer Society.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3576-fc05a2e44687ecbcb0814e4c8284f10de6147bed355cf6796de54d4625af178f3
Notes Fax: (713) 794‐4297
PMID 16502413
PageCount 12
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PublicationTitle Cancer
PublicationTitleAlternate Cancer
PublicationYear 2006
Publisher Wiley Subscription Services, Inc., A Wiley Company
Wiley-Liss
Publisher_xml – name: Wiley Subscription Services, Inc., A Wiley Company
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Snippet BACKGROUND Adult Burkitt‐type lymphoma (BL) and acute lymphoblastic leukemia (B‐ALL) are rare entities composing 1% to 5% of non‐Hodgkin lymphomas NHL) or ALL....
Adult Burkitt-type lymphoma (BL) and acute lymphoblastic leukemia (B-ALL) are rare entities composing 1% to 5% of non-Hodgkin lymphomas NHL) or ALL. Prognosis...
Abstract BACKGROUND Adult Burkitt‐type lymphoma (BL) and acute lymphoblastic leukemia (B‐ALL) are rare entities composing 1% to 5% of non‐Hodgkin lymphomas...
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pubmed
pascalfrancis
wiley
SourceType Aggregation Database
Index Database
Publisher
StartPage 1569
SubjectTerms acute lymphoblastic leukemia
adult Burkitt lymphoma
Antibodies, Monoclonal - therapeutic use
Antibodies, Monoclonal, Murine-Derived
Antineoplastic agents
Antineoplastic Agents - therapeutic use
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Burkitt Lymphoma - drug therapy
B‐ALL
chemoimmunotherapy
Combined Modality Therapy
Combined treatments (chemotherapy of immunotherapy associated with an other treatment)
Cyclophosphamide - administration & dosage
Dexamethasone - administration & dosage
Doxorubicin - administration & dosage
Drug Administration Schedule
Female
Humans
hyper‐CVAD
Immunotherapy
Infusions, Intravenous
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy
Rituximab
Survival Analysis
Treatment Outcome
Tumors
Vincristine - administration & dosage
Title Chemoimmunotherapy with hyper‐CVAD plus rituximab for the treatment of adult Burkitt and Burkitt‐type lymphoma or acute lymphoblastic leukemia
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcncr.21776
https://www.ncbi.nlm.nih.gov/pubmed/16502413
Volume 106
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