Your browser doesn't support javascript.
loading
Role of stem cell transplant in CD30+ PTCL following frontline brentuximab vedotin plus CHP or CHOP in ECHELON-2.
Savage, Kerry J; Horwitz, Steven M; Advani, Ranjana; Christensen, Jacob Haaber; Domingo-Domenech, Eva; Rossi, Giuseppe; Morschhauser, Franck; Alpdogan, Onder; Suh, Cheolwon; Tobinai, Kensei; Shustov, Andrei; Trneny, Marek; Yuen, Sam; Zinzani, Pier Luigi; Trümper, Lorenz; Ilidge, Tim; O'Connor, Owen A; Pro, Barbara; Miao, Harry; Bunn, Veronica; Fenton, Keenan; Fanale, Michelle; Puhlmann, Markus; Iyer, Swaminathan.
Afiliação
  • Savage KJ; Centre for Lymphoid Cancer and Division of Medical Oncology, British Columbia Cancer, Vancouver, BC, Canada.
  • Horwitz SM; Memorial Sloan-Kettering Cancer Center, New York, NY.
  • Advani R; Blood and Marrow Transplant Program, Stanford Cancer Center, Stanford, CA.
  • Christensen JH; Department of Haematology, Odense University Hospital, Odense, Denmark.
  • Domingo-Domenech E; Institut Catala D'oncologia, L'Hospitalet de Llobregat, Barcelona, Spain.
  • Rossi G; Azienda Ospedaliera Spedali Civili di Brescia, Brescia, Italy.
  • Morschhauser F; Department of Hematology, Université de Lille, Centre Hospitalier Universitaire Lille, ULR 7365, Groupe de Recherche sur les formes Injectables et les Technologies Associées (GRITA), Lille, France.
  • Alpdogan O; Division of Hematologic Malignancies and Hematopoietic Stem Cell Transplantation, Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA.
  • Suh C; Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Tobinai K; Hematology Division, National Cancer Center Hospital, Tokyo, Japan.
  • Shustov A; University of Washington Medical Center, Seattle, WA.
  • Trneny M; First Department of Medicine-Hematology, Charles University General Hospital and First Faculty of Medicine, Nové Mesto, Czech Republic.
  • Yuen S; Calvary Mater Newcastle Hospital, Waratah, NSW, Australia.
  • Zinzani PL; 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.
  • Trümper L; Department of Hematology and Medical Oncology, Universitätsmedizin Göttingen, Göttingen, Germany.
  • Ilidge T; Division of Cancer Sciences, Faculty of Biology, Medicine, and Health, University of Manchester, Manchester, United Kingdom.
  • O'Connor OA; National Institutes of Health and Research Biomedical Research Center, Manchester Academic Health Sciences, Christie Hospital National Health Service Foundation Trust, Manchester, United Kingdom.
  • Pro B; E. Couric Cancer Center, University of Virginia, Charlottesville, Virginia, and TG Therapeutics, New York, NY.
  • Miao H; NewYork-Presbyterian/Columbia University Irving Medical Center, New York, NY.
  • Bunn V; Kite Pharma, Santa Monica, CA.
  • Fenton K; Millennium Pharmaceuticals Inc., Cambridge, MA.
  • Fanale M; Seagen Inc., Bothell, WA.
  • Puhlmann M; Seagen Inc., Bothell, WA.
  • Iyer S; Seagen Inc., Bothell, WA.
Blood Adv ; 6(19): 5550-5555, 2022 10 11.
Article em En | MEDLINE | ID: mdl-35470385
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Anaplásico de Células Grandes / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Blood Adv Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Anaplásico de Células Grandes / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Blood Adv Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá