EBMT prospective observational study on allogeneic hematopoietic stem cell transplantation in T-prolymphocytic leukemia (T-PLL).


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
09 2019
Historique:
received: 23 07 2018
accepted: 04 01 2019
revised: 27 12 2018
pubmed: 22 1 2019
medline: 12 9 2020
entrez: 22 1 2019
Statut: ppublish

Résumé

Preliminary data suggest that allogeneic stem cell transplantation (allo-SCT) may be effective in T-prolymphocytic leukemia (T-PLL). The purpose of the present observational study was to assess the outcome of allo-SCT in patients aged 65 years or younger with a centrally confirmed diagnosis of T-PLL. Patients were consecutively registered with the EBMT at the time of transplantation and followed by routine EBMT monitoring but with an extended dataset. Between 2007 and 2012, 37 evaluable patients (median age 56 years) were accrued. Pre-treatment contained alemtuzumab in 95% of patients. Sixty-two percent were in complete remission (CR) at the time of allo-SCT. Conditioning contained total body irradiation with 6 Gy or more (TBI6) in 30% of patients. With a median follow-up of 50 months, the 4-year non-relapse mortality, relapse incidence, progression-free (PFS) and overall survival were 32, 38, 30 and 42%, respectively. By univariate analysis, TBI6 in the conditioning was the only significant predictor for a low relapse risk, and an interval between diagnosis and allo-SCT of more than 12 months was associated with a lower NRM. This study confirms for the first time prospectively that allo-SCT can provide long-term disease control in a sizable albeit limited proportion of patients with T-PLL.

Identifiants

pubmed: 30664723
doi: 10.1038/s41409-019-0448-x
pii: 10.1038/s41409-019-0448-x
doi:

Types de publication

Clinical Trial Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1391-1398

Auteurs

W Wiktor-Jedrzejczak (W)

Medical University of Warsaw, Warsaw, Poland. wieslaw.jedrzejczak@wum.edu.pl.

J Drozd-Sokolowska (J)

Medical University of Warsaw, Warsaw, Poland.

D J Eikema (DJ)

EBMT Statisticians, Leiden, The Netherlands.

J Hoek (J)

Data Office Leiden, Leiden, The Netherlands.

M Potter (M)

Royal Marsden Hospital, London, UK.

G Wulf (G)

Universitätsklinikum Göttingen, Göttingen, Germany.

L Sellner (L)

University of Heidelberg, Heidelberg, Germany.

P Ljungman (P)

Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.

P Chevallier (P)

CHU Nantes, Nantes, France.

L Volin (L)

HUCH Comprehensive Cancer Center, Helsinki, Finland.

Y Koc (Y)

Medical Park Hospitals, Antalya, Turkey.

S Martin (S)

Robert-Bosch-Krankenhaus, Stuttgart, Germany.

D Bunjes (D)

Universitätsklinikum Ulm, Ulm, Germany.

M Rovira (M)

Hospital Clinic, Barcelona, Spain.

M Itälä-Remes (M)

Turku University Hospital, Turku, Finland.

R Foá (R)

Univ. 'La Sapienza', Rome, Italy.

E Deconinck (E)

Hopital Jean Minjoz, Besancon, France.

T Gedde-Dahl (T)

Oslo University Hospital, Rikshospitalet, Oslo, Norway.

J Cornelissen (J)

Erasmus MC Cancer Institute, Rotterdam, Netherlands.

M Collin (M)

Freeman Hospital, Newcastle, UK.

A Brecht (A)

Deutsche Klinik für Diagnostik, KMT Zentrum, Wiesbaden, Germany.

A Patel (A)

Clatterbridge Cancer centre, Liverpool, UK.

M de Groot (M)

University Medical Center Groningen, Groningen, Netherlands.

P Reményi (P)

St. Istvan & St. Laszlo Hospital, Budapest, Hungary.

A Nagler (A)

Chaim Sheba Medical Center, Tel-Hashomer, Israel.

J Finke (J)

University of Freiburg, Freiburg, Germany.

P Turlure (P)

CHRU Limoges, Limoges, France.

S Iacobelli (S)

Tor Vergata University, Rome, Italy.

A van Biezen (A)

Data Office Leiden, Leiden, The Netherlands.

J Schetelig (J)

Universitätsklinikum Dresden, Dresden, Germany.

N Kröger (N)

University Hospital Eppendorf, Hamburg, Germany.

P Dreger (P)

University of Heidelberg, Heidelberg, Germany.

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Classifications MeSH