Author/Authors :
Burke Michael J. نويسنده , Bhatt Neel S. نويسنده Division of Pediatric Hematology-Oncology-Blood and Marrow
Transplantation, Medical College of Wisconsin, Milwaukee,
WI , Phelan Rachel نويسنده Division of Pediatric Hematology-Oncology-Blood and Marrow
Transplantation, Medical College of Wisconsin, Milwaukee,
WI
Abstract :
Context Survival after allogeneic hematopoietic stem-cell
transplantation (HSCT) for children with hematologic malignancies
including acute lymphoblastic leukemia (ALL) continues to improve in
part due to advancement in HLA typing and enhanced supportive care.
Despite improved outcomes with HSCT, the decision to offer it in first
remission (CR1) in children with ALL remains a topic of debate and
uncertainty. This review aims to discuss the role of HSCT in CR1 for
children with high-risk subsets of ALL in the current era. Evidence
Acquisition A thorough review of the literature was performed using
electronic databases: PubMed, Google Scholar, and bibliographies.
Studies focusing on high-risk subsets of ALL (Primary Induction Failure,
Severe Hypodiploidy, Philadelphia-chromosome positive ALL, T-Cell ALL,
Infant ALL, ALL with persistent minimal residual disease (MRD), and
Philadelphia-like ALL) were included. Publications in non- English
language were excluded. Results Based on our review of the current
literature, HSCT should be considered in first remission for patients
with primary induction failure, severe hypodiploidy, T-cell ALL with
poor response, high-risk infant ALL, and persistently positive MRD. In
contrast, HSCT in CR1 may not be warranted for patients with early
T-cell progenitor ALL or Philadelphia-chromosome positive ALL. Further
data are needed to make specific recommendations regarding
Philadelphia-like ALL. Conclusions As our understanding of high-risk
leukemia biology continues to develop, the role of HSCT in ALL CR1 will
need to be revisited.