Improved outcome with hematopoietic stem cell transplantation in a poor prognostic subgroup of infants with mixed-lineage-leukemia (MLL)–rearranged acute lymphoblastic leukemia: results from the Interfant-99 Study

Author:

Mann Georg1,Attarbaschi Andishe1,Schrappe Martin2,De Lorenzo Paola3,Peters Christina1,Hann Ian4,De Rossi Giulio5,Felice Maria6,Lausen Birgitte7,LeBlanc Thierry8,Szczepanski Tomasz9,Ferster Alina10,Janka-Schaub Gritta11,Rubnitz Jeffrey12,Silverman Lewis B.13,Stary Jan14,Campbell Myriam15,Li Chi Kong16,Suppiah Ram17,Biondi Andrea5,Vora Ajay4,Valsecchi Maria Grazia3,Pieters Rob18,

Affiliation:

1. Berlin-Frankfurt-Münster Study Group, Austria;

2. Berlin-Frankfurt-Münster Study Group, Germany;

3. Interfant-99 Trial Data Center, Department of Clinical Medicine and Prevention, University of Milano-Bicocca, Milan, Italy;

4. United Kingdom Children's Cancer Study Group, United Kingdom;

5. Associazione Italiana Ematologia Oncologia Pediatrica, Italy;

6. Argentinean Group of Pediatric Hematology and Oncology, Buenos Aires, Argentina;

7. Nordic Society of Pediatric Hematology and Oncology, Norway, Sweden, Denmark, Finland, and Iceland;

8. French Acute Lymphoblastic Leukemia Study Group, France;

9. Polish Pediatric Leukemia and Lymphoma Study Group, Poland;

10. Children's Leukemia Group, France, Belgium, and Portugal;

11. Cooperative Acute Lymphoblastic Leukemia Study Group, Germany;

12. St Jude Children's Research Hospital, Memphis, TN;

13. Dana-Farber Cancer Institute ALL Consortium, Boston, MA;

14. Czech Pediatric Haematology, Czech Republic;

15. Programa Infantil Nacional de Drogas Antineoplásicas, Chile;

16. Hong Kong Pediatric Hematology and Oncology Study Group, Hong Kong, China;

17. Australian and New Zealand Children's Haematology and Oncology Study Group, Australia; and

18. Dutch Childhood Oncology Study Group, Erasmus MC-Sophia Children's Hospital, The Netherlands

Abstract

AbstractTo define a role for hematopoietic stem cell transplantation (HSCT) in infants with acute lymphoblastic leukemia and rearrangements of the mixed-lineage-leukemia gene (MLL+), we compared the outcome of MLL+ patients from trial Interfant-99 who either received chemotherapy only or HSCT. Of 376 patients with a known MLL status in the trial, 297 (79%) were MLL+. Among the 277 of 297 MLL+ patients (93%) in first remission (CR), there appeared to be a significant difference in disease-free survival (adjusted by waiting time to HSCT) between the 37 (13%) who received HSCT and the 240 (87%) who received chemotherapy only (P = .03). However, the advantage was restricted to a subgroup with 2 additional unfavorable prognostic features: age less than 6 months and either poor response to steroids at day 8 or leukocytes more than or equal to 300 g/L. Ninety-seven of 297 MLL+ patients (33%) had such high-risk criteria, with 87 achieving CR. In this group, HSCT was associated with a 64% reduction in the risk of failure resulting from relapse or death in CR (hazard ratio = 0.36, 95% confidence interval, 0.15-0.86). In the remaining patients, there was no advantage for HSCT over chemotherapy only. In summary, HSCT seems to be a valuable option for a subgroup of infant MLL+ acute lymphoblastic leukemia carrying further poor prognostic factors. The trial was registered at www.clinicaltrials.gov as #NCT00015873 and at www.controlled-trials.com as #ISRCTN24251487.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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