Saurabh Ray
University of Toronto
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Publication
Featured researches published by Saurabh Ray.
Value in Health | 2012
A. Simon Pickard; Saurabh Ray; Arijit Ganguli; David Cella
OBJECTIVE Although utility-based algorithms have been developed for the Functional Assessment of Cancer Therapy (FACT), their properties are not well known compared with those of generic utility measures such as the EQ-5D. Our objective was to compare EQ-5D and FACT preference-based scores in cancer patients. METHODS A retrospective analysis was conducted on cross-sectional data collected from 472 cancer patients who completed both FACT-General and the EQ-5D. Preference-based scores were calculated by using published scoring functions for the EQ-5D (Dolan P. Modeling valuations for EuroQol health states. Med Care 1997;35:1095-108; Shaw JW, Johnson JA, Coons SJ. US valuation of the EQ-5D health states: development and testing of the D1 valuation model. Med Care 2005;43:203-20) and FACT (Dobrez D, Cella D, Pickard AS, et al. Estimation of patient preference-based utility weights from the Functional Assessment of Cancer Therapy-General. Value Health 2007;10:266-72; Kind P, Macran S. Eliciting social preference weights for Functional Assessment of Cancer Therapy-Lung health states. Pharmacoeconomics 2005;23:1143-53; Cheung YB, Thumboo J, Gao F, et al. Mapping the English and Chinese versions of the Functional Assessment of Cancer Therapy-General to the EQ-5D utility index. Value Health 2009;12:371-6). Scores were compared on the basis of clinical severity by using Eastern Cooperative Oncology Group performance status ratings by physicians and patients. Relative efficiency of each scoring function was examined by using ratios of F statistics. RESULTS Mean scores for the overall cohort were lowest when using Kind and Macrans FACT UK societal algorithm (0.55, SD 0.09) and highest when using Dobrez et al.s FACT US patient algorithm (0.83, SD 0.08). Mean difference scores associated with clinical severity, when extrapolated to quality-adjusted life-years (QALYs), had a range of 0.18 QALYs gained using FACT (Kind and Macran) to 0.45 QALYs gained using the EQ-5D (Dolan). However, relative efficiencies suggested that FACT (Kind and Macran) scores may provide greater statistical power to detect significant differences based on clinical severity. CONCLUSIONS We found important differences in utilities scores estimated by each algorithm, with FACT-based algorithms tending to underestimate the QALY benefit compared with algorithms based on the EQ-5D. These differences highlight some of the challenges in using disease-specific preference-based measures for decision making despite potentially more relevant disease-specific content.
Journal of Comparative Effectiveness Research | 2013
Saurabh Ray; Vijayveer Bonthapally; Donna McMorrow; Machaon Bonafede; Pamela Landsman-Blumberg
AIM Metastatic breast cancer guidelines contain multiple lines of treatment and regimens; however, little data on therapeutic patterns and costs is available from real-world clinical practice. This descriptive study reports chemotherapy and biologic use, healthcare utilization and costs by line of therapy in a large insured US population. MATERIALS & METHODS Adult women with newly diagnosed metastatic breast cancer (between 2005 and 2009) were identified from MarketScan® databases containing medical and pharmacy claims of >40 million enrollees insured with >100 US health plans. Descriptive statistics were reported for use, duration and mean per patient per month costs across four lines of therapy. RESULTS Out of 7767 patients identified (mean [standard deviation] age = 58.2 [12] years), ≥50% received a subsequent line of therapy across the four lines (line 2: n = 4077; line 3: n = 2033; line four: n = 1059). The top two chemotherapies were paclitaxel and capecitabine in lines one and two, and paclitaxel and gemcitabine in lines three and four. The top two biologics were trastuzumab and bevacizumab across the multiple lines of treatments. Duration (mean, standard deviation and median days) varied across multiple lines of treatments: 162.7, 176.9 and 108.0 in line one; 147.5, 146.7 and 99.0 in line two; 139.9, 131.1 and 99.0 in line three; and 130.9, 123.4 and 94.0 in line four, respectively. Mean per patient per month costs decreased with increasing follow-up from US
Journal of Comparative Effectiveness Research | 2012
Mitch DeKoven; Vijayveer Bonthapally; Xiaolong Jiao; Arijit Ganguli; Prathamesh Pathak; Won Chan Lee; Saurabh Ray
13,147 (<6 months) to US
Journal of Medical Economics | 2013
Saurabh Ray; Vijayveer Bonthapally; Kyle D. Holen; Geneviève Gauthier; Eric Q. Wu; Martin Cloutier; Annie Guerin
11,610 (7-12 months) to US
CNS oncology | 2015
Nemica Thavarajah; Saurabh Ray; Gillian Bedard; Liying Zhang; David Cella; Erin Wong; Cyril Danjoux; May Tsao; Elizabeth Barnes; Arjun Sahgal; Hany Soliman; Natalie Pulenzas; Breanne Lechner; Edward Chow
10,219 (12-24 months) to US
CNS oncology | 2014
Gillian Bedard; Saurabh Ray; Liying Zhang; Liang Zeng; David Cella; Erin Wong; Cyril Danjoux; May Tsao; Elizabeth Barnes; Arjun Sahgal; Lori Holden; Natalie Lauzon; Edward Chow
9,192 (24-36 months) to US
CNS oncology | 2016
Natalie Pulenzas; Saurabh Ray; Liying Zhang; Rachel McDonald; David Cella; Leigha Rowbottom; Arjun Sahgal; Hany Soliman; May Tsao; Cyril Danjoux; Breanne Lechner; Edward Chow
7,384 (>36 months). Cumulative costs increased with follow-up, from US
Annals of palliative medicine | 2016
Ronald Chow; Saurabh Ray; May Tsao; Natalie Pulenzas; Liying Zhang; Arjun Sahgal; David Cella; Hany Soliman; Cyril Danjoux; Carlo DeAngelis; Sherlyn Vuong; Rachel McDonald; Edward Chow
78,882 (<6 months) to US
Journal of Clinical Oncology | 2012
Saurabh Ray; Vijayveer Bonthapally; Donna McMorrow; Machaon Bonafede; Pamela Landsman-Blumberg
443,062 (>36 months). CONCLUSION Longer follow-up, regardless of number of lines of therapy, was associated with higher cumulative, but lower monthly, costs. Delaying progression and improving survival with more individualized treatment regimens may help slow the rate of increasing long-term costs of metastatic breast cancer treatment and care.
Journal of Neuro-oncology | 2013
Saurabh Ray; Stacey Dacosta-Byfield; Arijit Ganguli; Vijayveer Bonthapally; April Teitelbaum
BACKGROUND The differences in country-specific treatment patterns across Europe for metastatic breast cancer (mBC) patients have not been extensively studied. This study compared the treatment choices in aggregate, as well as by biomarker status, between various lines of therapy in clinical practice in the EU-5 countries among newly diagnosed mBC patients. MATERIALS & METHODS The IMS LifeLink™ Oncology Analyzer database, based on surveys of practicing oncologists, was used to identify mBC patients aged ≥21 years. In this database, sample-level data are projected to national-level estimates for each country using a sample projection technique. RESULTS The prevalence of hormone receptors (71-74%) is quite similar across different countries, while HER2 overexpression varies from 22 (France) to 34% (Italy); chemotherapy combined with HER2-targeted medicine was the mainstay of treatment for HER2(+) patients. The use of HER2-targeted medicine and bevacizumab greatly varied: while they were most frequently used in France, they were least frequently used in the UK. Fewer treatment options existed for triple-negative patients and patients with HER2(+) disease following trastuzumab treatment. Chemotherapy was the treatment choice for triple-negative patients, as these patients do not respond to hormonal therapy and HER2-targeted medicine. CONCLUSION This study found that, while a trastuzumab-based regimen is the preferred option for treating HER2(+) mBC patients in the EU-5, variations in this personalized medicine approach exist between different EU-5 countries. However, fewer treatment options exist for triple-negative and HER2(+) patients after trastuzumab treatment, highlighting the unmet need for these patient subgroups.