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Outcome of children with B cell lymphoma in Venezuela with the LMB-89 protocol.

AbstractBACKGROUND:
We analyzed the results of the LMB-89 protocol performed in seven centers in Venezuela in 96 children having B-cell non-Hodgkin lymphoma treated from 1995 to 2002.
PROCEDURE:
Mean age was 7.1 years with 71 (74%) been male. Eighty-two patients (85%) had diffuse small cell lymphoma Burkitt and Burkitt-like, and 14 (15%) had diffuse large B-cell lymphoma. Initial disease sites included the abdomen in 67%, peripheral nodes in 8%, and mediastinal in 4%. Treatment was directed to risk groups as described for LMB-89 protocol. Group A: seven patients (7%), group B: 80 patients (83%), and group C: nine patients (9%).
RESULTS:
Mean follow-up was 35 +/- 31 months. Complete remission (CR) occurred in 70 patients (73%); four patients (6%) had relapse during the first year and ten patients (10%) had progressive disease. Overall survival (OS) and event free survival (EFS) were 85 and 80% at 1 year, and 82 and 75% at 2 years, respectively. The EFS by therapeutic groups at 3 years was A: 100%; B: 76%, and C: 56%.
TOXICITY:
neutropenia in 75%, thrombocytopenia in 63%, febrile neutropenia in 39%. Viral infections: hepatitis B in 20%, hepatitis C in 2%, and Herpes zoster in 3%. Tumor lysis syndrome (TLS) occurred in 9% during induction phase with a high mortality of 44% (urate-oxidase was available only at the end of the study).
CONCLUSIONS:
The high mortality rate during induction phase prohibited a better EFS. Prophylactic use of xantine-oxidase may improve future results. The high incidence of hepatitis B requires a vaccination program.
AuthorsG Acquatella, C L Insausti, R García, R Gómez, M Hernández, M Carneiro, S Santos, A Nouel
JournalPediatric blood & cancer (Pediatr Blood Cancer) Vol. 43 Issue 5 Pg. 580-6 (Oct 2004) ISSN: 1545-5009 [Print] United States
PMID15382276 (Publication Type: Clinical Trial, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2004 Wiley-Liss, Inc.
Chemical References
  • Hepatitis B Vaccines
  • Cytarabine
  • Vincristine
  • Etoposide
  • Doxorubicin
  • Cyclophosphamide
  • Leucovorin
  • Prednisone
  • Hydrocortisone
  • Methotrexate
Topics
  • Antineoplastic Combined Chemotherapy Protocols (administration & dosage, therapeutic use)
  • Child
  • Cyclophosphamide (administration & dosage)
  • Cytarabine (administration & dosage)
  • Disease Progression
  • Disease-Free Survival
  • Doxorubicin (administration & dosage)
  • Etoposide (administration & dosage)
  • Female
  • Hepatitis B (complications, prevention & control)
  • Hepatitis B Vaccines (administration & dosage)
  • Humans
  • Hydrocortisone (administration & dosage)
  • Leucovorin (administration & dosage)
  • Lymphoma, B-Cell (drug therapy, pathology)
  • Lymphoma, Non-Hodgkin (drug therapy, pathology)
  • Male
  • Methotrexate (administration & dosage)
  • Prednisone (administration & dosage)
  • Recurrence
  • Treatment Outcome
  • Venezuela
  • Vincristine (administration & dosage)

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