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Role of stem cell transplant in CD30+ PTCL following frontline brentuximab vedotin plus CHP or CHOP in ECHELON-2

Authors :
Kerry J. Savage
Steven M. Horwitz
Ranjana Advani
Jacob Haaber Christensen
Eva Domingo-Domenech
Giuseppe Rossi
Franck Morschhauser
Onder Alpdogan
Cheolwon Suh
Kensei Tobinai
Andrei Shustov
Marek Trneny
Sam Yuen
Pier Luigi Zinzani
Lorenz Trümper
Tim Ilidge
Owen A. O’Connor
Barbara Pro
Harry Miao
Veronica Bunn
Keenan Fenton
Michelle Fanale
Markus Puhlmann
Swaminathan Iyer
Source :
Blood Advances. 6:5550-5555
Publication Year :
2022
Publisher :
American Society of Hematology, 2022.

Abstract

Peripheral T-cell lymphomas (PTCLs) are a heterogeneous group of aggressive non-Hodgkin lymphomas, the majority of which have high relapse rates following standard therapy. Despite use of consolidative stem cell transplant (SCT) following frontline therapy, there remains no consensus on its utility. The double-blind randomized phase 3 ECHELON-2 study (#NCT01777152; clinicaltrials.gov) demonstrated improved progression-free survival (PFS) and overall survival with frontline brentuximab vedotin plus cyclophosphamide, doxorubicin, and prednisone (A+CHP). Herein, we conducted an exploratory subgroups analysis of the impact of consolidative SCT on PFS in patients with previously untreated CD30+ PTCL (ALK− anaplastic large cell lymphoma [ALCL] and non-ALCL) who were in complete response (CR) after frontline treatment with A+CHP or cyclophosphamide, doxorubicin, vincristine, and prednisone. Median PFS follow-up was 47.57 months. The PFS hazard ratio was 0.36, equating to a 64% reduction in the risk of a PFS event in patients who underwent SCT. The median PFS in patients who underwent SCT was not reached, vs 55.66 months in patients who did not undergo SCT. PFS results favored the use of SCT in both ALK− ALCL and non-ALCL subgroups. These data support the consideration of consolidative SCT in patients with CD30+PTCL who achieve CR following treatment with A+CHP.

Details

ISSN :
24739537 and 24739529
Volume :
6
Database :
OpenAIRE
Journal :
Blood Advances
Accession number :
edsair.doi.dedup.....6b02787ddbf580ba2112ede2cb297584
Full Text :
https://doi.org/10.1182/bloodadvances.2020003971