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

© 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved..

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.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:6

Enthalten in:

Blood advances - 6(2022), 19 vom: 11. Okt., Seite 5550-5555

Sprache:

Englisch

Beteiligte Personen:

Savage, Kerry J [VerfasserIn]
Horwitz, Steven M [VerfasserIn]
Advani, Ranjana [VerfasserIn]
Christensen, Jacob Haaber [VerfasserIn]
Domingo-Domenech, Eva [VerfasserIn]
Rossi, Giuseppe [VerfasserIn]
Morschhauser, Franck [VerfasserIn]
Alpdogan, Onder [VerfasserIn]
Suh, Cheolwon [VerfasserIn]
Tobinai, Kensei [VerfasserIn]
Shustov, Andrei [VerfasserIn]
Trneny, Marek [VerfasserIn]
Yuen, Sam [VerfasserIn]
Zinzani, Pier Luigi [VerfasserIn]
Trümper, Lorenz [VerfasserIn]
Ilidge, Tim [VerfasserIn]
O'Connor, Owen A [VerfasserIn]
Pro, Barbara [VerfasserIn]
Miao, Harry [VerfasserIn]
Bunn, Veronica [VerfasserIn]
Fenton, Keenan [VerfasserIn]
Fanale, Michelle [VerfasserIn]
Puhlmann, Markus [VerfasserIn]
Iyer, Swaminathan [VerfasserIn]

Links:

Volltext

Themen:

5J49Q6B70F
7XL5ISS668
80168379AG
8N3DW7272P
Brentuximab Vedotin
Cyclophosphamide
Doxorubicin
Journal Article
Ki-1 Antigen
Prednisone
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
VB0R961HZT
Vincristine

Anmerkungen:

Date Completed 07.10.2022

Date Revised 16.11.2022

published: Print

ClinicalTrials.gov: NCT01777152

Citation Status MEDLINE

doi:

10.1182/bloodadvances.2020003971

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM339994282