| Literature DB >> 26010123 |
Kevin Hay1, Benny Lee2, Ozge Goktepe3, Joseph M Connors4, Laurie H Sehn4, Kerry J Savage4, Richard Klasa4, Tamara Shenkier4, Alina Gerrie4,5, Diego Villa4.
Abstract
Although it is generally regarded appropriate to start chemotherapy promptly after a diagnosis of diffuse large B-cell lymphoma (DLBCL), the optimal time from diagnosis to treatment (TDT) is unknown. A total of 689 patients diagnosed with DLBCL and treated with ≥ 1 cycle of CHOP-R with curative intent during 2003-2008 in British Columbia were identified: 347 (50%) TDT ≤ 4 weeks, 277 (40%) TDT 5-8 weeks, 65 (10%) TDT > 8 weeks. For the respective TDT groups, 5-year OS estimates were 61%, 74%, 63% (p = 0.006); 5-year PFS 57%, 70%, 61% (p = 0.006); and 5-year DSS 64%, 80%, 77% (p <0.001). In multivariate analysis, TDT >8 weeks was associated with worse OS (HR 1.20 (95% CI 1.03, 1.41), p = 0.020), PFS (HR 1.33 (95% CI 1.15, 1.54), p < 0.001), and DSS (HR 1.40 (95% CI 1.10, 1.78), p = 0.006). Clinicians should endeavor to initiate curative chemotherapy as soon as possible after a diagnosis of DLBCL is established.Entities:
Keywords: Antibody-based immunotherapy; chemotherapeutic approaches; lymphoma and Hodgkin disease
Year: 2015 PMID: 26010123 DOI: 10.3109/10428194.2015.1055480
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022