Should Transplantation Still Be Considered for Ph1-Negative Myeloproliferative Neoplasms in Transformation?

Allogeneic transplantation First-line treatment Ph1-negative myeloproliferative neoplasms in transformation Prognostic factors Survival

Journal

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628

Informations de publication

Date de publication:
06 2020
Historique:
received: 31 12 2019
revised: 19 02 2020
accepted: 20 02 2020
pubmed: 3 3 2020
medline: 24 6 2021
entrez: 3 3 2020
Statut: ppublish

Résumé

BCR-ABL-negative myeloproliferative neoplasms (MPNs) in transformation have a dismal prognosis, and allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered the sole curative therapeutic option. We retrospectively analyzed 53 molecularly annotated patients treated at Saint Louis Hospital, Paris, diagnosed with MPN in transformation between 2008 and 2018. The median patient age was 65 years, and the median interval between MPN diagnosis and MPN transformation was 46 months. The median overall survival (OS) of the entire cohort after transformation was 7.1 months. OS was better for patients treated with hypomethylating agents (HMAs) or with chemotherapy compared than for those treated by best supportive care or single-agent targeted therapy (median, 9.1 months versus 1.5 months; P < .001). Patients treated with chemotherapy more often achieved complete remission compared with those treated with HMAs (68% versus 29%; P = .02), and were more often candidates for transplantation (59% versus 14%; P = .02), but the median OS was similar in the 2 groups. We then compared the outcomes in transplant recipients and nonrecipients using the Mantel-Byar methodology and found that allo-HSCT did not improve survival. In multivariate analysis, independent factors in prognosis were performance status at transformation (P < .01), initial treatment with HMAs or chemotherapy (P = .02), and the ability to achieve complete remission during follow-up (P < .01). Our data demonstrate that the indication for allo-HSCT for high-risk MPN should be discussed before transformation, because transplantation rescues few patients after transformation.

Identifiants

pubmed: 32119970
pii: S1083-8791(20)30105-1
doi: 10.1016/j.bbmt.2020.02.019
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1160-1170

Informations de copyright

Copyright © 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Mathilde Ruggiu (M)

Hematology and Transplantation, Saint Louis Hospital, Paris, France.

Bruno Cassinat (B)

Cellular Biology, Saint Louis Hospital, Paris, France; University of Paris, INSERM U1131, Paris, France.

Jean-Jacques Kiladjian (JJ)

Clinical Investigation Center, Saint Louis Hospital, Paris, France.

Emmanuel Raffoux (E)

Adult Hematology Unit, Saint Louis Hospital, Paris, France.

Stéphane Giraudier (S)

Cellular Biology, Saint Louis Hospital, Paris, France; University of Paris, INSERM U1131, Paris, France.

Marie Robin (M)

Hematology and Transplantation, Saint Louis Hospital, Paris, France.

Raphael Itzykson (R)

Adult Hematology Unit, Saint Louis Hospital, Paris, France.

Emmanuelle Clappier (E)

Hematology Central Laboratory, Saint Louis Hospital, Paris, France; University of Paris, INSERM U944, Paris, France.

David Michonneau (D)

Hematology and Transplantation, Saint Louis Hospital, Paris, France; University of Paris, INSERM U976, Paris, France.

Flore Sicre de Fontbrune (FS)

Hematology and Transplantation, Saint Louis Hospital, Paris, France.

Régis Peffault de Latour (RP)

Hematology and Transplantation, Saint Louis Hospital, Paris, France.

Lionel Ades (L)

Hematology Senior Unit, Saint Louis Hospital, Paris, France; University of Paris, INSERM U944, Paris, France.

Gérard Socié (G)

Hematology and Transplantation, Saint Louis Hospital, Paris, France; University of Paris, INSERM U976, Paris, France. Electronic address: gerard.socie@aphp.fr.

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