Rohan C. Parikh
University of Texas Health Science Center at Houston
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Publication
Featured researches published by Rohan C. Parikh.
Journal of the American Geriatrics Society | 2015
Xianglin L. Du; Yefei Zhang; Rohan C. Parikh; David R. Lairson; Yi Cai
To compare the effectiveness of chemotherapy in prolonging survival according to age in breast and colon cancer.
Value in Health | 2014
David R. Lairson; Rohan C. Parikh; Janice N. Cormier; Xianglin L. Du
OBJECTIVES Most economic evaluations of chemotherapies for ovarian cancer patients have used hypothetical cohorts or randomized control trials, but evidence integrating real-world survival, cost, and utility data is limited. METHODS A propensity score-matched cohort of 6856 elderly (≥65 years) ovarian cancer patients diagnosed from 1991 to 2005 from the Surveillance, Epidemiology, and End Results-Medicare data cohort were included. Treatment regimens (i.e., no chemotherapy, platinum-based only, platinum plus taxane, and other nonplatinum) were identified in the 6 months postdiagnosis. Patients were followed until death or end of study (December 2006). Effectiveness was measured in quality-adjusted life-years (QALYs), and total health care costs were measured by using a payers perspective (2009 US dollars). Methodological and statistical uncertainties were accounted by including alternative scenarios (for utility values) and net monetary benefit approach. Incremental cost-effectiveness ratios (ICERs) were calculated, and stratified analyses were performed by tumor stages and age groups. RESULTS On comparing the platinum-based group versus no chemotherapy, we found that the ICER was
Journal of Managed Care Pharmacy | 2017
Rohan C. Parikh; Xianglin L. Du; Morgan O. Robert; David R. Lairson
30,073/QALY and
Lung Cancer | 2015
Xianglin L. Du; Rohan C. Parikh; David R. Lairson
58,151/QALY for early- and late-stage disease, respectively, while other nonplatinum and platinum plus taxane groups were dominated (less effective and more costly). Similar results were found across alternative scenarios and age groups. For patients 85 years or older, platinum plus taxane, however, was not dominated by the platinum-based group, with an ICER of
Drugs - real world outcomes | 2016
Rohan C. Parikh; Xianglin L. Du; Robert O. Morgan; David R. Lairson
133,892/QALY. CONCLUSIONS Following elderly ovarian cancer patients over a lifetime using real-world longitudinal data and adjusting for quality of life, we found that treatment with platinum-based regimen was the most cost-effective treatment alternative.
PharmacoEconomics | 2015
Insiya B. Poonawalla; Rohan C. Parikh; Xianglin L. Du; Helena M. VonVille; David R. Lairson
BACKGROUND Treatment patterns for metastatic colorectal cancer (mCRC) patients have changed considerably over the last decade with the introduction of new chemotherapies and targeted biologics. These treatments are often administered in various sequences with limited evidence regarding their cost-effectiveness. OBJECTIVE To conduct a pharmacoeconomic evaluation of commonly administered treatment sequences among elderly mCRC patients. METHODS A probabilistic discrete event simulation model assuming Weibull distribution was developed to evaluate the cost-effectiveness of the following common treatment sequences: (a) first-line oxaliplatin/irinotecan followed by second-line oxaliplatin/irinotecan + bevacizumab (OI-OIB); (b) first-line oxaliplatin/irinotecan + bevacizumab followed by second-line oxaliplatin/irinotecan + bevacizumab (OIB-OIB); (c) OI-OIB followed by a third-line targeted biologic (OI-OIB-TB); and (d) OIB-OIB followed by a third-line targeted biologic (OIB-OIB-TB). Input parameters for the model were primarily obtained from the Surveillance, Epidemiology, and End Results-Medicare linked dataset for incident mCRC patients aged 65 years and older diagnosed from January 2004 through December 2009. A probabilistic sensitivity analysis was performed to account for parameter uncertainty. Costs (2014 U.S. dollars) and effectiveness were discounted at an annual rate of 3%. RESULTS In the base case analyses, at the willingness-to-pay (WTP) threshold of
PharmacoEconomics | 2014
David R. Lairson; Rohan C. Parikh; Janice N. Cormier; Wenyaw Chan; Xianglin L. Du
100,000/quality-adjusted life-year (QALY) gained, the treatment sequence OIB-OIB (vs. OI-OIB) was not cost-effective with an incremental cost-effectiveness ratio (ICER) per patient of
Medical Oncology | 2013
Xianglin L. Du; Rohan C. Parikh; David R. Lairson; Sharon H. Giordano; Putao Cen
119,007/QALY; OI-OIB-TB (vs. OIB-OIB) was dominated; and OIB-OIB-TB (vs. OIB-OIB) was not cost-effective with an ICER of
Value in Health | 2015
David R. Lairson; Rohan C. Parikh; Janice N. Cormier; Wenyaw Chan; Xianglin L. Du
405,857/QALY. Results similar to the base case analysis were obtained assuming log-normal distribution. Cost-effectiveness acceptability curves derived from a probabilistic sensitivity analysis showed that at a WTP of
Value in Health | 2015
Rohan C. Parikh; Xianglin L. Du; Robert O. Morgan; David R. Lairson
100,000/QALY gained, sequence OI-OIB was 34% cost-effective, followed by OIB-OIB (31%), OI-OIB-TB (20%), and OIB-OIB-TB (15%). CONCLUSIONS Overall, survival increases marginally with the addition of targeted biologics, such as bevacizumab, at first line and third line at substantial costs. Treatment sequences with bevacizumab at first line and targeted biologics at third line may not be cost-effective at the commonly used threshold of