Sociodemographic associations with uptake of novel therapies for acute myeloid leukemia.
Sociodemographic associations with uptake of novel therapies for acute myeloid leukemia.
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DOI:
10.1038/s41408-023-00964-x
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发表时间:
2023-12-21
影响因子:
12.8
通讯作者:
Abel, Gregory A.
中科院分区:
文献类型:
--
作者:
Hantel, Andrew;Cernik, Colin;Uno, Hajime;Walsh, Thomas P.;Calip, Gregory S.;DeAngelo, Daniel J.;Lathan, Christopher S.;Abel, Gregory A.
Inequitable uptake of novel therapies (NT) in non-cancer settings are known for patients with lower socioeconomic status (SES), People of Color (POC), and older adults. NT uptake equity in acute myeloid leukemia (AML) is not well known. We performed a retrospective cohort study (1/2014-8/2022) of the United States nationwide Flatiron HealthTM electronic health record-derived, de-identified database. We estimated sociodemographic associations with AML NT receipt using incidence rate ratios (IRR). Odds ratios (OR) assessed differences in venetoclax (the most common NT) receipt at community sites and between site characteristics and NT adoption. Of 8081 patients (139 sites), 3102 (38%) received a NT. NT use increased annually (IRR 1.14, 95% confidence interval [1.07, 1.22]). NT receipt was similar between Non-Hispanic-Whites and POC (IRR 1.03, [0.91, 1.17]) and as age increased (IRR 1.02 [0.97, 1.07]). At community sites, Non-Hispanic-Whites were less likely to receive venetoclax (OR 0.77 [0.66, 0.91]); older age (OR 1.05 [1.04, 1.05]) and higher area-level SES were associated with venetoclax receipt (OR 1.23 [1.05, 1.43]). Early NT adopting sites had more prescribing physicians (OR 1.25 [1.13, 1.43]) and higher SES strata patients (OR 2.81 [1.08, 7.66]). Inequities in AML NT uptake were seen by SES; for venetoclax, differential uptake reflects its label indication for older adults and those with comorbidities.
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影响因子:
28.2
作者:
Bhatnagar B;Kohlschmidt J;Mrózek K;Zhao Q;Fisher JL;Nicolet D;Walker CJ;Mims AS;Oakes C;Giacopelli B;Orwick S;Boateng I;Blachly JS;Maharry SE;Carroll AJ;Powell BL;Kolitz JE;Stone RM;Byrd JC;Paskett ED;de la Chapelle A;Garzon R;Eisfeld AK
通讯作者:
Eisfeld AK
影响因子:
7.5
作者:
Hantel A;Luskin MR;Garcia JS;Stock W;DeAngelo DJ;Abel GA
通讯作者:
Abel GA
影响因子:
20.3
作者:
Abraham, Ivy Elizabeth;Rauscher, Garth H.;Khan, Irum
通讯作者:
Khan, Irum
DOI:
10.1097/coc.0b013e3181dea934
发表时间:
2011-06-01
影响因子:
2.6
作者:
Byrne, Margaret M.;Halman, L. Jill;Cheung, Michael C.
通讯作者:
Cheung, Michael C.
影响因子:
28.4
作者:
O'Connor, Jeremy M.;Fessele, Kristen L.;Gross, Cary P.
通讯作者:
Gross, Cary P.