Prospective outcome data on 267 unselected adult patients with Philadelphia chromosome–positive acute lymphoblastic leukemia confirms superiority of allogeneic transplantation over chemotherapy in the pre-imatinib era: results from the International ALL Trial MRC UKALLXII/ECOG2993

Author:

Fielding Adele K.1,Rowe Jacob M.2,Richards Susan M.3,Buck Georgina3,Moorman Anthony V.4,Durrant I. Jill3,Marks David I.5,McMillan Andrew K.6,Litzow Mark R.7,Lazarus Hillard M.8,Foroni Letizia9,Dewald Gordon7,Franklin Ian M.10,Luger Selina M.11,Paietta Elisabeth12,Wiernik Peter H.12,Tallman Martin S.13,Goldstone Anthony H.14

Affiliation:

1. University College London, London, United Kingdom;

2. Rambam Medical Center and Technicon, Israel Institute of Technology, Haifa, Israel;

3. Clinical Trial Service Unit, Oxford, United Kingdom;

4. Northern Institute for Cancer Research, Newcastle University, Newcastle, United Kingdom;

5. Bristol Haematology and Oncology Centre, Bristol, United Kingdom;

6. Nottingham University, Nottingham, United Kingdom;

7. Mayo Clinic College of Medicine, Rochester, MN;

8. Ireland Cancer Center, University Hospitals of Cleveland, OH;

9. Imperial College London, London, United Kingdom;

10. University of Glasgow, National Blood Transfusion Service, Glasgow, United Kingdom;

11. Abramson Cancer Center, University of Pennsylvania, Philadelphia;

12. Montefiore Medical Center North Division and New York Medical College, Bronx;

13. Northwestern University Feinberg School of Medicine, Chicago, IL; and

14. University College London Hospitals, London, United Kingdom

Abstract

Abstract Prospective data on the value of allogeneic hematopoietic stem cell transplantation (alloHSCT) in Philadelphia chromosome–positive (Ph+) acute lymphoblastic leukemia (ALL) are limited. The UKALLXII/ECOG 2993 study evaluated the outcome of assigning alloHSCT with a sibling (sib) or matched unrelated donor (MUD) to patients younger than 55 years of age achieving complete remission (CR). The CR rate of 267 patients, median age 40, was 82%. Twenty-eight percent of patients proceeded to alloHSCT in first CR. Age older than 55 years or a pre-HSCT event were the most common reasons for failure to progress to alloHSCT. At 5 years, overall survival (OS) was 44% after sib alloHSCT, 36% after MUD alloHSCT, and 19% after chemotherapy. After adjustment for sex, age, and white blood count and excluding chemotherapy-treated patients who relapsed or died before the median time to alloHSCT, only relapse-free survival remained significantly superior in the alloHSCT group (odds ratio 0.31, 95% confidence interval 0.16-0.61). An intention-to-treat analysis, using the availability or not of a matched sibling donor, showed 5-year OS to be nonsignificantly better at 34% with a donor versus 25% with no donor. This prospective trial in adult Ph+ ALL indicates a modest but significant benefit to alloHSCT. This trial has been registered with clinicaltrials.gov under identifier NCT00002514 and as ISRCTN77346223.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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