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Treatment of relapsed acute lymphoblastic leukemia: Approaches used by pediatric oncologists and bone marrow transplant physicians
Author(s) -
Burke Michael J.,
Lindgen Bruce,
Verneris Michael R.
Publication year - 2012
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.23269
Subject(s) - medicine , bone marrow transplant , blood cancer , bone marrow , minimal residual disease , chemotherapy , lymphoblastic leukemia , pediatric oncology , disease , oncology , blinatumomab , leukemia , bone marrow transplantation , cancer , intensive care medicine
Background Management of relapsed B‐precursor acute lymphoblastic leukemia (ALL) is challenging and varied. We hypothesized that treatment approaches differ between pediatric oncologists and bone marrow transplant (BMT) physicians. Procedure A survey addressing management of relapsed ALL was sent to pediatric oncologists (n = 883) and BMT (n = 86) physicians across North America. Results A number of similarities in treatment approaches were identified including: choice of chemotherapy for re‐induction/consolidation, preference for unrelated donors (URDs) in very early marrow relapse and the choice to not use URD donors in late marrow relapse. However, differences between the two disciplines were noted. For patients who relapsed 18–36 months from diagnosis, the majority of oncologists (53.7%) would retreat with chemotherapy while a majority BMT physicians (70.3%) recommended URD transplant ( P < 0.001). Oncologists were also less likely to use minimal residual disease (MRD) in relapse assessment compared to BMT physicians (52% vs. 67.2%; P = 0.028) and more oncologists believed MRD testing was experimental and/or not proven in relapsed ALL (27.1% vs. 12.3%; P = 0.011). Conclusions This study highlights management differences in children with ALL between pediatric oncologists and BMT physicians, identifying opportunities for collaborative clinical trials. Pediatr Blood Cancer 2012; 58: 840–845. © 2011 Wiley Periodicals, Inc.