Journal of Clinical Oncology, Vol 18, Issue 18
(September), 2000: 3256-3261
© 2000 American Society for Clinical Oncology
High Survival Rate in Infant Acute Leukemia Treated With Early High-Dose Chemotherapy and Stem-Cell Support
By Fernando Marco,
Encarna Bureo,
Juan J. Ortega,
Isabel Badell,
Amparo Verdaguer,
Ana Martínez,
Arturo Muñoz,
Luis Madero,
Teresa Olivé,
Josep Cubells,
Victoria Castel,
Ana Sastre,
M. Soledad Maldonado,
Miguel A. Díaz,
from the Grupo Español de Trasplante de Médula Ósea en Niños
From the Hospital Universitario Marqués de Valdecilla, Santander; Hospital Materno-Infantil Vall DHebrón; Hospital de la Santa Creu i Sant Pau, Barcelona; Hospital Universitario La Fe, Valencia; Hospital La Paz; Hospital Ramón y Cajal; and Hospital del Niño Jesús, Madrid, Spain.
Address reprint requests to Fernando Marco, MD, Servicio de Hematología, Hospital Universitario Marqués de Valdecilla, Avenida de Valdecilla 1, 39008 Santander, Spain; email fernandomarco{at}hotmail.com
PURPOSE: Infants with acute leukemia have a poor prognosis when treated with conventional chemotherapy. It is still unknown if stem-cell transplantation (SCT) can improve the outcome of these patients. In the present study, we review our experience with SCT in infant acute leukemia to clarify this issue.
PATIENTS AND METHODS: We report the results of 26 infants who were submitted to a SCT for acute leukemia. There were 15 cases of acute myeloid leukemia and 10 cases of acute lymphoid leukemia. One patient had a bilineal leukemia. Twenty-two patients were in their first complete response (CR1), three were in their second CR, and one was in relapse. Eight patients were submitted to allogeneic SCT, and 18 underwent autologous SCT.
RESULTS: With a median follow-up of 67 months, the 5-year overall survival and disease-free survival (DFS) are 64% (SE = 9%) and 63% (SE = 10%), respectively. Autologous and allogeneic SCT offered similar outcome. There was not any transplant-related mortality, and all deaths were caused by relapse in the first 6 months after SCT. In multivariate analysis, the single factor associated with better DFS was an interval between CR1 and SCT of less than 4 months (P < .025).
CONCLUSION: SCT is a valid option in the treatment of infant acute leukemia, and it may overcome the high risk of relapse with conventional chemotherapy showing very reduced toxicity. This study suggests that SCT should be performed in CR1 in the early phase of the disease.

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