@article{c760d4c263c844648933eeb96a1f416f,
title = "Utilization of real-world data in assessing treatment effectiveness for diffuse large B-cell lymphoma",
abstract = "Direct comparisons of the effectiveness of the numerous novel therapies in the diffuse large B-cell lymphoma (DLBCL) treatment landscape in a range of head-to-head randomized phase 3 trials would be time-consuming and costly. Comparative effectiveness studies using real-world data (RWD) represent a complementary approach. Recently, several studies of relapsed/refractory (R/R) DLBCL have used RWD to create observational cohorts to compare patient outcomes with cohorts derived from single-arm phase 2 trials. Using propensity score methods to balance clinically and prognostically relevant baseline covariates, closely matched patient-level cohorts can be generated. By incorporating appropriate measures to assess covariate balance and address potential bias in comparative effectiveness study designs, robust comparative analyses can be performed. Results from such studies have been used to supplement regulatory approval of therapies assessed in single-arm trials. While RWD studies have a greater susceptibility to bias compared to randomized controlled trials, well-designed and appropriately analyzed studies can provide complementary real-world evidence on treatment effectiveness.",
author = "Grzegorz Nowakowski and Maurer, {Matthew J.} and Cerhan, {James R.} and Debarshi Dey and Sehn, {Laurie H.}",
note = "Funding Information: This study was sponsored by MorphoSys AG. Medical writing assistance was provided by Eoin Duffy, PhD, of Syneos Health and funded by MorphoSys AG. Funding Information: This study was sponsored by MorphoSys AG. Medical writing assistance was provided by Eoin Duffy, PhD, of Syneos Health and funded by MorphoSys AG. About Tafasitamab Tafasitamab is a humanized Fc-modified cytolytic CD19 targeting monoclonal antibody. In 2010, MorphoSys licensed exclusive worldwide rights to develop and commercialize tafasitamab from Xencor, Inc. Tafasitamab incorporates an XmAb{\textregistered} engineered Fc domain, which mediates B-cell lysis through apoptosis and immune effector mechanisms including Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC) and Antibody-Dependent Cellular Phagocytosis (ADCP). In January 2020, MorphoSys and Incyte entered into a collaboration and licensing agreement to further develop and commercialize tafasitamab globally. Following accelerated approval by the U.S. Food and Drug Administration in July 2020, tafasitamab is being co-commercialized by MorphoSys and Incyte in the United States. Incyte has exclusive commercialization rights outside the United States. XmAb{\textregistered} is a registered trademark of Xencor Inc. Publisher Copyright: {\textcopyright} 2022 The Authors. American Journal of Hematology published by Wiley Periodicals LLC.",
year = "2023",
month = jan,
doi = "10.1002/ajh.26767",
language = "English (US)",
volume = "98",
pages = "180--192",
journal = "American Journal of Hematology",
issn = "0361-8609",
publisher = "Wiley-Liss Inc.",
number = "1",
}