| Literature DB >> 33216888 |
Ho-Young Yhim1,2, Yael Eshet3, Ur Metser3, Chae-Hong Lim4,5, Katherine Lajkosz6, Keren Isaev1, Matthew Cooper1,7, Anca Prica1, Vishal Kukreti1, Sita Bhella1, Noémie Lang1, Kyung-Han Lee4, Wei Xu6, David Hodgson8, Richard Tsang8, Sang Eun Yoon9, Seok Jin Kim9, Won Seog Kim9, Michael Crump1, John Kuruvilla1, Robert Kridel1.
Abstract
There are limited data regarding the combined value of the pretransplant Deauville score (DS) from a positron emission tomography scan and clinical risk factors in patients with relapsed/refractory aggressive non-Hodgkin lymphoma (NHL). We performed a retrospective analysis to assess the prognostic role of pretransplant DS in patients with relapsed/refractory aggressive NHL who underwent salvage chemotherapy and autologous stem cell transplantation (ASCT). We identified 174 eligible patients between January 2013 and March 2019. In multivariable analysis, pretransplant DS, B symptoms, and secondary International Prognostic Index (sIPI) were independent risk factors for event-free survival (EFS). These variables were used to derive an integrated risk score that categorized 166 patients with available information for all risk factors into 3 groups: low (n = 92; 55.4%), intermediate (n = 48; 28.9%), and high (n = 26; 15.7%). The new prognostic index showed a strong association with EFS (low-risk vs intermediate-risk hazard ratio [HR], 3.94; 95% confidence interval [CI], 2.16-7.17; P < .001; low-risk vs high-risk HR, 10.83; 95% CI, 5.81-20.19; P < .001) and outperformed models based on clinical risk factors or DS alone. These results were validated in 60 patients from an independent external cohort (low-risk vs intermediate-risk HR, 4.04; 95% CI, 1.51-10.82; P = .005; low-risk vs high-risk HR, 10.49; 95% CI, 4.11-26.73; P < .001). We propose and validate a new prognostic index that risk-stratifies patients undergoing salvage chemotherapy followed by ASCT, thereby identifying patients at high risk for posttransplant treatment failure.Entities:
Mesh:
Year: 2020 PMID: 33216888 PMCID: PMC7686897 DOI: 10.1182/bloodadvances.2020002814
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529