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Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer
Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer
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Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer
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Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer
Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer

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Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer
Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer
Journal Article

Granulocyte-Colony Stimulating Factor Use and Medical Costs after Initial Adjuvant Chemotherapy in Older Patients with Early-Stage Breast Cancer

2012
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Overview
Background : Granulocyte-colony stimulating factor (G-CSF) reduces the risk of severe neutropenia associated with chemotherapy, but its cost implications following chemotherapy are unknown. Objective : Our objective was to examine associations between G-CSF use and medical costs after initial adjuvant chemotherapy in early-stage (stage I–III) breast cancer (ESBC). Methods : Women diagnosed with ESBC from 1999 to 2005, who had an initial course of chemotherapy beginning within 180 days of diagnosis and including ≥1 highly myelosuppressive agent, were identified from the Surveillance, Epidemiology, and End Results (SEER)-Medicare database. Medicare claims were used to describe the initial chemotherapy regimen according to the classes of agents used: anthracycline ([A]: doxorubicin or epirubicin); cyclophosphamide (C); taxane ([T]: paclitaxel or docetaxel); and fluorouracil (F). Patients were classified into four study groups according to their G-CSF use: (i) primary prophylaxis, if the first G-CSF claim was within 5 days of the start of the first chemotherapy cycle; (ii) secondary prophylaxis, if the first claim was within 5 days of the start of the second or subsequent cycles; (iii)G-CSF treatment, if the first claim occurred outside of prophylactic use; and (iv) no G-CSF. Patients were described by age, race, year of diagnosis, stage, grade, estrogen (ER) and progesterone (PR) receptor status, National Cancer Institute (NCI) Co-morbidity Index, chemotherapy regimen and G-CSF use. Total direct medical costs ($US, year 2009 values) to Medicare were estimated from 4 weeks after the last chemotherapy administration up to 48 months. Medical costs included those for ESBC treatment and all other medical services received after chemotherapy. Least squares regression, using inverse probability weighting (IPW) to account for censoring within the cohort, was used to evaluate adjusted associations between G-CSF use and costs. Results: A total of 7026 patients were identified, with an average age of 72 years, of which 63% had stage II disease, and 59% were ER and/or PR positive. Compared with no G-CSF, those receiving G-CSF primary prophylaxis were more likely to have stage III disease (30% vs 16%; p < 0.0001), to be diagnosed in 2003–5 (87% vs 26%; p < 0.0001), and to receive dose-dense AC-T (26% vs 1%; p < 0.0001), while they were less likely to receive an F-based regimen (12% vs 42%; p < 0.0001). Overall, the estimated average direct medical cost over 48months after initial chemotherapy was $US42 628. In multivariate analysis, stage II or III diagnosis (compared with stage I),NCI Co-morbidity Index score 1 or ≥2 (compared with 0), or FAC or standard AC-T (each compared with AC) were associated with significantly higher IPW 48-month costs. Adjusting for patient demographic and clinical factors, costs in the G-CSF primary prophylaxis group were not significantly different from those not receiving primary prophylaxis (the other three study groups combined). In an analysis that included four separate study groups, G-CSF treatment was associated with significantly greater costs (incremental cost = $US2938; 95% CI 285, 5590) than no G-CSF. Conclusions : Direct medical costs after initial chemotherapy were not statistically different between those receiving G-CSF primary prophylaxis and those receiving no G-CSF, after adjusting for potential confounders.
Publisher
Springer International Publishing,Adis International,Springer Healthcare | Adis,Springer,Springer Nature B.V
Subject

Adjuvant treatment

/ Age Factors

/ Aged

/ Aged patients

/ Aged, 80 and over

/ Analysis

/ Anthracyclines

/ Antineoplastic agents

/ Antineoplastic Combined Chemotherapy Protocols - adverse effects

/ Antineoplastic Combined Chemotherapy Protocols - therapeutic use

/ Beneficiaries

/ Biological and medical sciences

/ Breast cancer

/ Breast Neoplasms - diagnosis

/ Breast Neoplasms - drug therapy

/ Breast Neoplasms - economics

/ Cancer

/ Care and treatment

/ Chemotherapy

/ Chemotherapy, Adjuvant - adverse effects

/ Chemotherapy-induced-anaemia

/ Cost-analysis

/ Costs

/ Costs and Cost Analysis

/ Cyclophosphamide

/ Disease prevention

/ Early-breast-cancer

/ Economic theory

/ Epidemiology

/ Expenditures

/ Female

/ Filgrastim

/ Fluorouracil

/ Granulocyte colony-stimulating factor

/ Granulocyte Colony-Stimulating Factor - economics

/ Granulocyte Colony-Stimulating Factor - therapeutic use

/ Granulocyte-colony-stimulating-factors

/ Granulocytes

/ Growth factors

/ Gynecology. Andrology. Obstetrics

/ Health Administration

/ Health Care Costs - statistics & numerical data

/ Health care expenditures

/ Health Economics

/ Hospitalization - statistics & numerical data

/ Humans

/ Kaplan-Meier Estimate

/ Least-Squares Analysis

/ Long-Term Care - economics

/ Mammary gland diseases

/ Medical care, Cost of

/ Medical sciences

/ Medicare

/ Medicine

/ Medicine & Public Health

/ Miscellaneous

/ Morbidity

/ Neutropenia

/ Neutropenia - chemically induced

/ Neutropenia - drug therapy

/ Neutropenia - economics

/ Neutropenia - prevention & control

/ Original Research Article

/ Patients

/ Pharmaceuticals

/ Pharmacoeconomics and Health Outcomes

/ Pharmacology. Drug treatments

/ Polyethylene Glycols

/ Public Health

/ Public health. Hygiene

/ Public health. Hygiene-occupational medicine

/ Quality of Life Research

/ Racial Groups - statistics & numerical data

/ Recombinant Proteins - therapeutic use

/ Retrospective Studies

/ SEER Program

/ Studies

/ Taxanes.

/ Tumors

/ United States