Autologous transplantation for Philadelphia chromosome-positive acute lymphoblastic leukemia achieves outcomes similar to allogeneic transplantation: results of CALGB Study 10001 (Alliance)
Meir Wetzler,
Dorothy Watson,
Wendy Stock,
Gregory Koval,
Flora A. Mulkey,
Eva E. Hoke,
John M. McCarty,
William G. Blum,
Bayard L. Powell,
Guido Marcucci,
Clara D. Bloomfield,
Charles A. Linker,
Richard A. Larson
Affiliations
Meir Wetzler
Roswell Park Cancer Institute, Buffalo, NY
Dorothy Watson
Alliance Biostatistics and Data Center, Duke University Medical Center, Durham, NC
Wendy Stock
University of Chicago, Chicago, IL
Gregory Koval
University of Chicago, Chicago, IL
Flora A. Mulkey
Alliance Biostatistics and Data Center, Duke University Medical Center, Durham, NC
Eva E. Hoke
Alliance Biostatistics and Data Center, Duke University Medical Center, Durham, NC
John M. McCarty
Virginia Commonwealth University, Richmond, VA
William G. Blum
The Ohio State University Comprehensive Cancer Center, Columbus, OH
Bayard L. Powell
Wake Forest University School of Medicine, Winston-Salem, NC
Guido Marcucci
The Ohio State University Comprehensive Cancer Center, Columbus, OH
Clara D. Bloomfield
The Ohio State University Comprehensive Cancer Center, Columbus, OH
Charles A. Linker
University of California at San Francisco, San Francisco, CA, USA
Allogeneic stem cell transplantation is the standard approach to Philadelphia chromosome positive acute lymphoblastic leukemia. We hypothesized that imatinib plus sequential chemotherapy will result in significant leukemia cell cytoreduction in patients with Philadelphia chromosome positive acute lymphoblastic leukemia, allowing collection of normal hematopoietic stem cells uncontaminated by residual BCR/ABL1+ lymphoblasts and thus reduce the likelihood of relapse after autologous stem cell transplantation for patients under 60 years of age without sibling donors. We enrolled 58 patients; 19 underwent autologous and 15 underwent allogeneic stem cell transplantation on study. Imatinib plus sequential chemotherapy resulted in reverse-transcriptase polymerase chain reaction-negative stem cells in 9 patients and remained minimally positive in 4 (6 were not evaluable). Overall survival (median 6.0 years vs. not reached) and disease-free survival (median 3.5 vs. 4.1 years) were similar between those who underwent autologous and those who underwent allogeneic stem cell transplantation. We conclude that autologous stem cell transplantation represents a safe and effective alternative for allogeneic stem cell transplantation in Philadelphia chromosome positive acute lymphoblastic leukemia patients without sibling donors (clinicaltrials.gov identifier:00039377).