| Literature DB >> 29265182 |
Nirav N Shah1, Aniko Szabo2, Scott F Huntington3, Narendranath Epperla1, Nishitha Reddy4, Siddhartha Ganguly5, Julie Vose6, Cynthia Obiozor5, Fahad Faruqi3, Alexandra E Kovach4, Luciano J Costa7, Ana C Xavier8, Ryan Okal9, Abraham S Kanate9, Nilanjan Ghosh10, Mohamed A Kharfan-Dabaja11, Lauren Strelec12, Mehdi Hamadani1,13, Timothy S Fenske1, Oscar Calzada14, Jonathon B Cohen14, Julio Chavez11, Jakub Svoboda12.
Abstract
Primary mediastinal (thymic) large B-cell lymphoma (PMBCL) is an uncommon subtype of non-Hodgkin lymphoma (NHL) that presents with a mediastinal mass and has unique clinicopathological features. Historically, patients with PMBCL were treated with R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) chemotherapy ± involved field radiation. Since a phase II trial, published in April 2013, demonstrated excellent results using dose-adjusted (DA) R-EPOCH (rituximab, etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin), this treatment has gained popularity. We performed a retrospective, multicentre analysis of patients aged ≥18 years with PMBCL since January 2011. Patients were stratified by frontline regimen, R-CHOP versus DA-R-EPOCH. 132 patients were identified from 11 contributing centres (56 R-CHOP and 76 DA-R-EPOCH). The primary outcome was overall survival. Secondary outcomes included progression-free survival, complete response (CR) rate, and rates of treatment-related complications. Demographic characteristics were similar in both groups. DA-R-EPOCH use increased after April 2013 (79% vs. 45%, P < 0·001), and there was less radiation use after DA-R-EPOCH (13% vs. 59%, P < 0·001). While CR rates were higher with DA-R-EPOCH (84% vs. 70%, P = 0·046), these patients were more likely to experience treatment-related toxicities. At 2 years, 89% of R-CHOP patients and 91% of DA-R-EPOCH patients were alive. To our knowledge, this represents the largest series comparing outcomes of R-CHOP to DA-R-EPOCH for PMBCL.Entities:
Keywords: zzm321990PMBCLzzm321990; chemotherapy; non-Hodgkin lymphoma
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Year: 2017 PMID: 29265182 DOI: 10.1111/bjh.15051
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998