Early-stage Hodgkin lymphoma in the modern era: simulation modelling to delineate long-term patient outcomes.
Authors
Parsons, SKelly, M
Cohen, J
Castellino, S
Henderson, T
Kelly, K
Keller, F
Henzer, T
Kumar, A
Johnson, P
Meyer, R
Radford, John A
Raemaekers, J
Hodgson, D
Evens, A
Affiliation
Department of Pediatrics, Tufts University School of Medicine, Boston, MA, USAIssue Date
2018-04-29
Metadata
Show full item recordAbstract
We developed a novel simulation model integrating multiple data sets to project long-term outcomes with contemporary therapy for early-stage Hodgkin lymphoma (ESHL), namely combined modality therapy (CMT) versus chemotherapy alone (CA) via 18 F-fluorodeoxyglucose positron emission tomography response-adaption. The model incorporated 3-year progression-free survival (PFS), probability of cure with/without relapse, frequency of severe late effects (LEs), and 35-year probability of LEs. Furthermore, we generated estimates for quality-adjusted life years (QALYs) and unadjusted survival (life years, LY) and used model projections to compare outcomes for CMTversusCA for two index patients. Patient 1: a 25-year-old male with favourable ESHL (stage IA); Patient 2: a 25-year-old female with unfavourable ESHL (stage IIB). Sensitivity analyses assessed the impact of alternative assumptions for LE probabilities. For Patient 1, CMT was superior to CA (CMT incremental gain = 0·11 QALYs, 0·21 LYs). For Patient 2, CA was superior to CMT (CA incremental gain = 0·37 QALYs, 0·92 LYs). For Patient 1, the advantage of CMT changed minimally when the proportion of severe LEs was reduced from 20% to 5% (0·15 QALYs, 0·43 LYs), whereas increasing the severity proportion for Patient 2's LEs from 20% to 80% enhanced the advantage of CA (1·1 QALYs, 6·5 LYs). Collectively, this detailed simulation model quantified the long-term impact that varied host factors and alternative contemporary treatments have in ESHL.Citation
Early-stage Hodgkin lymphoma in the modern era: simulation modelling to delineate long-term patient outcomes. 2018 Br J HaematolJournal
British Journal of HaematologyDOI
10.1111/bjh.15255PubMed ID
29707774Type
ArticleLanguage
enDescription
Lymphoma Research TeamISSN
1365-2141ae974a485f413a2113503eed53cd6c53
10.1111/bjh.15255
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