HEMATOPOIETIC PROGENITOR-CELL TRANSPLANT IN ACUTE LEUKEMIAS IN CHILDREN - INDICATIONS, RESULTS AND CONTROVERSIES

Authors
Citation
Jj. Ortega et T. Olive, HEMATOPOIETIC PROGENITOR-CELL TRANSPLANT IN ACUTE LEUKEMIAS IN CHILDREN - INDICATIONS, RESULTS AND CONTROVERSIES, Bone marrow transplantation, 21, 1998, pp. 11-16
Citations number
20
Categorie Soggetti
Hematology,Oncology,Immunology,Transplantation
Journal title
ISSN journal
02683369
Volume
21
Year of publication
1998
Supplement
2
Pages
11 - 16
Database
ISI
SICI code
0268-3369(1998)21:<11:HPTIAL>2.0.ZU;2-1
Abstract
The objective of this study was to update the role of different modali ties of haematopoietic progenitor cell transplants (PCT) in the therap y of acute leukaemias in children emphasizing the points of agreement and controversy. In ARIL in first remission, allogeneic PCT from an HL A-identical sibling is the treatment of choice in most cases, DFS of 6 0-80% has been attained in paediatric series, Indications appear clear except in M3 subtype, M7 in children with Down syndrome and possibly in patients with M2 and t(8;21) and M5-Eo and inv(16) who have a good early response to; induction treatment. In some paediatric series, res ults with autologous transplants (APCT) are similar to those obtained with allo-PCT and superior to those obtained with chemotherapy alone, but this point is controversial. Allo-PCT and APCT are indicated in ch ildren in second remission, yielding 40% DFS, In children with ALL in first remission, indications for PCT are limited to only 8-10% of pati ents with very-high risk of relapse, mainly those with certain chromos ome abnormalities or with poor or late response to induction treatment ; a favourable outcome has been registered in 60%, Allo-PCT is the bes t choice for patients in second remission after an early marrow relaps e and who have an adequate related or unrelated donor; DFS of 40-50% h as been described in several paediatric series. Indications of allo-PC T from related donors after late bone marrow relapses or early extrame dullary relapses appears more controversial but there are data in its favour. The role of APCT appears even more controversial but some auth ors favour its use in these situations. In more advanced stages of the disease the results obtained with allo-PCT are poorer (DFS between 10 and 20%), In summary, although many controversial points with regards to indications and modalities of transplants in acute leukaemia in ch ildren remain, it must be emphasized that with advances in both fields , chemotherapy and transplants, today 80% of children with ALL and 60- 70% of those with AML are cured and enjoy good quality of life.