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

. 2022 Oct 11 ; 6 (19) : 5550-5555.

Jazyk angličtina Země Spojené státy americké Médium print

Typ dokumentu časopisecké články, randomizované kontrolované studie, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid35470385

Grantová podpora
P30 CA008748 NCI NIH HHS - United States

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.

1st Department of Medicine Hematology Charles University General Hospital and 1st Faculty of Medicine Nové Město Czech Republic

Azienda Ospedaliera Spedali Civili di Brescia Brescia Italy

Blood and Marrow Transplant Program Stanford Cancer Center Stanford CA

Calvary Mater Newcastle Hospital Waratah NSW Australia

Centre for Lymphoid Cancer and Division of Medical Oncology British Columbia Cancer Vancouver BC Canada

Department of Haematology Odense University Hospital Odense Denmark

Department of Hematology and Medical Oncology Universitätsmedizin Göttingen Göttingen Germany

Department of Hematology Université de Lille Centre Hospitalier Universitaire Lille ULR 7365 Groupe de Recherche sur les formes Injectables et les Technologies Associées Lille France

Department of Oncology Asan Medical Center University of Ulsan College of Medicine Seoul Republic of Korea

Division of Cancer Sciences Faculty of Biology Medicine and Health University of Manchester Manchester United Kingdom

Division of Hematologic Malignancies and Hematopoietic Stem Cell Transplantation Department of Medical Oncology Thomas Jefferson University Philadelphia PA

E Couric Cancer Center University of Virginia Charlottesville Virginia and TG Therapeutics New York NY

Hematology Division National Cancer Center Hospital Tokyo Japan

Institut Catala D'oncologia L'Hospitalet de Llobregat Barcelona Spain

Kite Pharma Santa Monica CA

MD Anderson Cancer Center University of Texas Houston TX

Memorial Sloan Kettering Cancer Center New York NY

Millennium Pharmaceuticals Inc Cambridge MA

National Institutes of Health and Research Biomedical Research Center Manchester Academic Health Sciences Christie Hospital National Health Service Foundation Trust Manchester United Kingdom

NewYork Presbyterian Columbia University Irving Medical Center New York NY

Scientific Institute for Research Hospitalization and Healthcare Azienda Ospedaliero Universitaria di Bologna Istituto di Ematologia Seràgnoli Dipartimento di Medicina Specialistica Diagnostica e Sperimentale Università degli Studi Bologna Italy

Seagen Inc Bothell WA

University of Washington Medical Center Seattle WA

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ClinicalTrials.gov
NCT01777152

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