PMID- 25085897 OWN - NLM STAT- MEDLINE DCOM- 20150514 LR - 20211021 IS - 1549-490X (Electronic) IS - 1083-7159 (Print) IS - 1083-7159 (Linking) VI - 19 IP - 9 DP - 2014 Sep TI - Investigation of adverse-event-related costs for patients with metastatic breast cancer in a real-world setting. PG - 901-8 LID - 10.1634/theoncologist.2014-0059 [doi] AB - BACKGROUND: Existing treatments for metastatic breast cancer (mBC) are often effective but can cause adverse events (AEs). This study aimed to identify AEs associated with chemotherapies commonly used in mBC treatment (phase 1) and to quantify the economic impact of these AEs (phase 2). MATERIALS AND METHODS: Patients in phase 1 had at least one claim for therapy for mBC, with at least one episode with single or multiple agents. The most common chemotherapy-related complications were identified using medical and pharmacy claims data. In phase 2, patients meeting study criteria were divided into four treatment cohorts by the line of treatment and chemotherapy received: first-line taxane-treated patients, second-line taxane-treated patients, first-line capecitabine-treated patients, and second-line capecitabine-treated patients. Average monthly AE-related health care costs per cohort were stratified by cost component. Total monthly costs per number of AEs were also calculated. RESULTS: On average, patients in phase 1 (n = 1,551) had 2 episodes of treatment, with a mean duration of 131 days. The most frequently noted complications were anemia (50.7% of mBC treatment episodes), bilirubin elevation (26.4%), and leukopenia (24.8%). In phase 2, costs related to AEs were primarily driven by incremental inpatient, outpatient, and pharmacy costs. Increases in average monthly costs ranged from $854 (9.0%) to $5,320 (69.5%), according to cohort. Overall costs increased with increasing numbers of AEs. CONCLUSION: Chemotherapy-related AEs in patients with mBC are associated with a substantial economic burden that increases with the number of AEs reported. CI - (c)AlphaMed Press. FAU - Hurvitz, Sara AU - Hurvitz S AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA. FAU - Guerin, Annie AU - Guerin A AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA aguerin@analysisgroup.com. FAU - Brammer, Melissa AU - Brammer M AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA. FAU - Guardino, Ellie AU - Guardino E AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA. FAU - Zhou, Zheng-Yi AU - Zhou ZY AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA. FAU - Latremouille Viau, Dominick AU - Latremouille Viau D AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA. FAU - Wu, Eric Q AU - Wu EQ AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA. FAU - Lalla, Deepa AU - Lalla D AD - University of California Los Angeles, Los Angeles, California, USA; Analysis Group, Inc., Montreal, Quebec, Canada; Genentech Inc., South San Francisco, California, USA; Analysis Group, Inc., Boston, Massachusetts, USA. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20140801 PL - England TA - Oncologist JT - The oncologist JID - 9607837 RN - 0 (Bridged-Ring Compounds) RN - 0 (Taxoids) RN - 0W860991D6 (Deoxycytidine) RN - 1605-68-1 (taxane) RN - 6804DJ8Z9U (Capecitabine) RN - U3P01618RT (Fluorouracil) SB - IM MH - Aged MH - Breast Neoplasms/drug therapy/*economics/epidemiology MH - Bridged-Ring Compounds/economics/therapeutic use MH - Capecitabine MH - Costs and Cost Analysis/*economics MH - Deoxycytidine/analogs & derivatives/economics/therapeutic use MH - Drug-Related Side Effects and Adverse Reactions/*economics/epidemiology MH - Female MH - Fluorouracil/analogs & derivatives/economics/therapeutic use MH - *Health Care Costs MH - Humans MH - Middle Aged MH - Neoplasm Metastasis MH - Taxoids/economics/therapeutic use PMC - PMC4153460 OTO - NOTNLM OT - Breast neoplasms OT - Costs and cost analysis OT - Drug-related side effects and adverse reactions OT - Neoplasm metastasis COIS- Disclosures of potential conflicts of interest may be found at the end of this article. EDAT- 2014/08/03 06:00 MHDA- 2015/05/15 06:00 PMCR- 2015/09/01 CRDT- 2014/08/03 06:00 PHST- 2014/08/03 06:00 [entrez] PHST- 2014/08/03 06:00 [pubmed] PHST- 2015/05/15 06:00 [medline] PHST- 2015/09/01 00:00 [pmc-release] AID - theoncologist.2014-0059 [pii] AID - T1459 [pii] AID - 10.1634/theoncologist.2014-0059 [doi] PST - ppublish SO - Oncologist. 2014 Sep;19(9):901-8. doi: 10.1634/theoncologist.2014-0059. Epub 2014 Aug 1.