Long-term outcome of patients with newly diagnosed chronic myeloid leukemia: a randomized comparison of stem cell transplantation with drug treatment.

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Etat: Public
Version: de l'auteur⸱e
ID Serval
serval:BIB_E928980A6C80
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Long-term outcome of patients with newly diagnosed chronic myeloid leukemia: a randomized comparison of stem cell transplantation with drug treatment.
Périodique
Leukemia
Auteur⸱e⸱s
Gratwohl A., Pfirrmann M., Zander A., Kröger N., Beelen D., Novotny J., Nerl C., Scheid C., Spiekermann K., Mayer J., Sayer H.G., Falge C., Bunjes D., Döhner H., Ganser A., Schmidt-Wolf I., Schwerdtfeger R., Baurmann H., Kuse R., Schmitz N., Wehmeier A., Th Fischer J., Ho A.D., Wilhelm M., Goebeler M.E., Lindemann H.W., Bormann M., Hertenstein B., Schlimok G., Baerlocher G.M., Aul C., Pfreundschuh M., Fabian M., Staib P., Edinger M., Schatz M., Fauser A., Arnold R., Kindler T., Wulf G., Rosselet A., Hellmann A., Schäfer E., Prümmer O., Schenk M., Hasford J., Heimpel H., Hossfeld D.K., Kolb H.J., Büsche G., Haferlach C., Schnittger S., Müller M.C., Reiter A., Berger U., Saußele S., Hochhaus A., Hehlmann R.
ISSN
1476-5551 (Electronic)
ISSN-L
0887-6924
Statut éditorial
Publié
Date de publication
2016
Peer-reviewed
Oui
Volume
30
Numéro
3
Pages
562-569
Langue
anglais
Résumé
Tyrosine kinase inhibitors represent today's treatment of choice in chronic myeloid leukemia (CML). Allogeneic hematopoietic stem cell transplantation (HSCT) is regarded as salvage therapy. This prospective randomized CML-study IIIA recruited 669 patients with newly diagnosed CML between July 1997 and January 2004 from 143 centers. Of these, 427 patients were considered eligible for HSCT and were randomized by availability of a matched family donor between primary HSCT (group A; N=166 patients) and best available drug treatment (group B; N=261). Primary end point was long-term survival. Survival probabilities were not different between groups A and B (10-year survival: 0.76 (95% confidence interval (CI): 0.69-0.82) vs 0.69 (95% CI: 0.61-0.76)), but influenced by disease and transplant risk. Patients with a low transplant risk showed superior survival compared with patients with high- (P<0.001) and non-high-risk disease (P=0.047) in group B; after entering blast crisis, survival was not different with or without HSCT. Significantly more patients in group A were in molecular remission (56% vs 39%; P=0.005) and free of drug treatment (56% vs 6%; P<0.001). Differences in symptoms and Karnofsky score were not significant. In the era of tyrosine kinase inhibitors, HSCT remains a valid option when both disease and transplant risk are considered.
Pubmed
Web of science
Open Access
Oui
Création de la notice
05/04/2016 17:57
Dernière modification de la notice
20/08/2019 17:11
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