| Literature DB >> 33306213 |
Marie-Charlotte Laude1, Laure Lebras2, Pierre Sesques3, Herve Ghesquieres3, Simon Favre4, Krimo Bouabdallah4, Carolyne Croizier5, Romain Guieze5, Laurianne Drieu La Rochelle6, Emmanuel Gyan6, Roza Chin7, Thérèse Aurran-Schleinitz7, Amira Marouf8, Bénédicte Deau-Fischer8, Paul Coppo9, Sandrine Malot9, Xavier Roussel10, Adrien Chauchet11, Marianne Schwarz12, Charles Bescond13, Thierry Lamy de la Chapelle14, Lucile Bussot15, Sylvain Carras16, Bénédicte Burlet17, Cédric Rossi18, Adrien Daniel19, Franck Morschhauser20, Fabien Subtil21, Anne-Sophie Michallet2.
Abstract
Historically, double or triple hit lymphoma (DHL and THL) have poor outcomes with conventional chemotherapy, but there is currently no guideline. We report the French experience in managing DHL and THL in first line using collective data on both survival and tolerance. All consecutive patients with newly diagnosis of large B-cell lymphoma with MYC, BCL2, and/or BCL6 rearrangements, as determined by FISH between January 2013 and April 2019 were included. Based on the eligibility criteria, 160 patients were selected among the 184 patients identified. With a median follow-up of 32 months, 2- and 4-year progression free survival (PFS) rates were 40% and 28% with R-CHOP compared with 57% and 52% with intensive chemotherapy (P = .063). There was no difference in overall survival (OS). For advanced stages, PFS was significantly longer with intensive chemotherapy than with R-CHOP (P = .029). There was no impact of autologous stem cell transplantation among patient in remission. For patients with central nervous system (CNS) involvement, the 2-year PFS and OS rate was 21% and 39%, vs 57% and 75% without CNS disease (P = .007 and P < .001). By multivariate analysis, elevated IPI score and CNS disease were strongly and independently associated with a poorer survival, whereas treatment was not significantly associated with OS. This is the largest series reporting the treatment of DHL and THL in Europe. The PFS was significantly longer with an intensive regimen for advanced stage, but no difference in OS, supporting the need for a prospective randomized trial.Entities:
Year: 2020 PMID: 33306213 DOI: 10.1002/ajh.26068
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047