PMID- 32054500 OWN - NLM STAT- MEDLINE DCOM- 20210618 LR - 20210618 IS - 1750-1172 (Electronic) IS - 1750-1172 (Linking) VI - 15 IP - 1 DP - 2020 Feb 13 TI - Adverse event rates and economic burden associated with purine nucleoside analogs in patients with hairy cell leukemia: a US population-retrospective claims analysis. PG - 47 LID - 10.1186/s13023-020-1325-9 [doi] LID - 47 AB - BACKGROUND: Purine nucleoside analogs (PNAs) are the recommended first-line treatment for patients with hairy cell leukemia (HCL), but they are associated with adverse events (AEs). Due to a lack of real-world evidence regarding AEs that are associated with PNAs, we used commercial data to assess AE rates, AE-related health care resource utilization (HCRU), and costs among PNA-treated patients with HCL. Adults aged >/=18 years with >/=2 claims for HCL >/=30 days apart from 1 January 2006 through 31 December 2015 were included. Included patients had >/=1 claim for HCL therapy (cladribine +/- rituximab or pentostatin +/- rituximab [index date: first claim date]) and continuous enrollment for a >/= 6-month baseline and >/= 12-month follow-up period. Patient sub-cohorts were based on the occurrence of myelosuppression and opportunistic infections (OIs). Generalized linear models were used to compare HCRU and costs. RESULTS: In total, 647 PNA-treated patients were identified (mean age: 57.1 years). Myelosuppression and OI incidence were 461 and 42 per 1000 patient-years, respectively. Adjusted results indicated that those with myelosuppression had higher rates of hospitalization (47.4% vs 12.4%; P < .0001) and incurred higher mean inpatient costs ($23,517 vs $12,729; P = .011) and total costs ($57,325 vs $34,733; P = .001) as compared with those without myelosuppression. Similarly, patients with OIs had higher rates of hospitalization (53.8% vs 30.8%; P = .025) and incurred higher mean inpatient costs ($21,494 vs $11,229; P < .0001) as compared with those without OIs. CONCLUSIONS: PNA therapy is highly effective but associated with significant toxicities that increase costs; these findings indicate a need for therapies with improved toxicity profiles and better risk stratification of patients at risk of developing myelosuppression and OIs. FAU - Epperla, Narendranath AU - Epperla N AD - Division of Hematology, The James Cancer Hospital and Solove Research Institute, The Ohio State University Comprehensive Cancer Center, A346 Starling Loving Hall, 320W 10th Ave, Columbus, OH, 43210, USA. Narendranath.Epperla@osumc.edu. FAU - Pavilack, Melissa AU - Pavilack M AD - AstraZeneca, Gaithersburg, MD, USA. FAU - Olufade, Temitope AU - Olufade T AD - AstraZeneca, Gaithersburg, MD, USA. FAU - Bashyal, Richa AU - Bashyal R AD - STATinMED Research, Plano, TX, USA. FAU - Li, Jieni AU - Li J AD - STATinMED Research, Plano, TX, USA. FAU - Kabadi, Shaum M AU - Kabadi SM AD - AstraZeneca, Gaithersburg, MD, USA. FAU - Yuce, Huseyin AU - Yuce H AD - New York City College of Technology, New York, NY, USA. FAU - Andritsos, Leslie AU - Andritsos L AD - Division of Hematology and Oncology, The University of New Mexico, Albuquerque, NM, USA. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20200213 PL - England TA - Orphanet J Rare Dis JT - Orphanet journal of rare diseases JID - 101266602 RN - 0 (Nucleosides) RN - 0 (Purine Nucleosides) SB - IM MH - Adolescent MH - Adult MH - Cost of Illness MH - Health Care Costs MH - Humans MH - Insurance Claim Review MH - *Leukemia, Hairy Cell/drug therapy MH - Middle Aged MH - Nucleosides MH - Purine Nucleosides MH - Retrospective Studies PMC - PMC7020358 OTO - NOTNLM OT - Adverse events OT - Hairy cell leukemia OT - Myelosuppression OT - Purine nucleoside analogs COIS- N Epperla, H Yuce, and L Andritsos have no conflicts to disclose. M Pavilack, T Olufade, and S Kabadi are employees of AstraZeneca, the study sponsor. R Bashyal and J Li are employees of STATinMED Research, a paid consultant to the study sponsor. EDAT- 2020/02/15 06:00 MHDA- 2021/06/22 06:00 PMCR- 2020/02/13 CRDT- 2020/02/15 06:00 PHST- 2019/10/31 00:00 [received] PHST- 2020/01/28 00:00 [accepted] PHST- 2020/02/15 06:00 [entrez] PHST- 2020/02/15 06:00 [pubmed] PHST- 2021/06/22 06:00 [medline] PHST- 2020/02/13 00:00 [pmc-release] AID - 10.1186/s13023-020-1325-9 [pii] AID - 1325 [pii] AID - 10.1186/s13023-020-1325-9 [doi] PST - epublish SO - Orphanet J Rare Dis. 2020 Feb 13;15(1):47. doi: 10.1186/s13023-020-1325-9.