Allogeneic Hematopoietic Stem-Cell Transplantation for Myeloid Sarcoma: A Retrospective Study From the SFGM-TC

被引:86
作者
Chevallier, Patrice
Mohty, Mohamad
Lioure, Bruno
Michel, Gerard
Contentin, Nathalie
Deconinck, Eric
Bordigoni, Pierre
Vernant, Jean-Paul
Hunault, Mathilde
Vigouroux, Stephane
Blaise, Didier
Tabrizi, Reza
Buzyn, Agnes
Socie, Gerard
Michallet, Mauricette
Volteau, Christelle
Harousseau, Jean-Luc
机构
[1] CHU Hotel Dieu, Cellule Promot Rech Clin, Nantes, France
[2] CHU Haute Pierre, Strasbourg, France
[3] Inst J Paoli I Calmettes, F-13009 Marseille, France
[4] Ctr Henri Becquerel, F-76038 Rouen, France
[5] CHU Minjoz, Besancon, France
[6] CHU Brabois, Nancy, France
[7] Hop Necker Enfants Malad, AP HP, Paris, France
[8] CHU St Louis, AP HP, Paris, France
[9] CHU Angers, Angers, France
[10] CHU Pontchaillou, Rennes, France
[11] CHU Haut Leveque, Bordeaux, France
[12] CHU Edouard Herriot, Lyon, France
关键词
D O I
10.1200/JCO.2007.15.6315
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose This retrospective multicenter study assessed the outcome of 51 patients with myeloid sarcoma (MS) who underwent allogeneic hematopoietic stem-cell transplantation (alloHSCT). Patients and Methods Most patients had MS presenting in conjunction with acute myeloid leukemia (AML) or after AML. Six patients had isolated MS. The median time between diagnosis and alloHSCT was 8 months (range, 2.8 to 67). Forty patients were in complete remission (CR) at time of alloHSCT. Results With a median follow-up of 33 (range, 1 to 182) months, the Kaplan-Meier estimates of overall survival (OS) and disease-free survival were 47% (95% CI, 33% to 61%) and 36% (95% CI, 24% to 50%) at 5 years. Twenty patients (39%) relapsed at a median of 204 (range, 35 to 1151) days after alloHSCT, with relapse being the major cause of death. In a Cox multivariate analysis, age >= 15 years and remission status at time of alloHSCT (CR v other) were associated with improved OS (hazard ratio [HR], 0.27; 95% CI, 0.12 to 0.65; P = .003; and HR, 0.22; 95% CI, 0.08 to 0.57; P = .002, respectively). Conclusion We conclude that first-line alloHSCT performed early in the course of MS is a valid therapeutic option.
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页码:4940 / 4943
页数:4
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