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Dive into the research topics where Medha Sasane is active.

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Featured researches published by Medha Sasane.


Pediatric Blood & Cancer | 2013

Age-related treatment patterns in sickle cell disease patients and the associated sickle cell complications and healthcare costs.

Morey A. Blinder; Francis Vekeman; Medha Sasane; Alex Trahey; Carole Paley; Mei Sheng Duh

This study explored the blood transfusion patterns, SCD complications, utilization of iron chelation therapies (ICT), healthcare resource use, and costs in pediatric, transitioning (18 years old) and adult patients with SCD.


Transfusion | 2012

Economic impact on US Medicare of a new diagnosis of myelodysplastic syndromes and the incremental costs associated with blood transfusion need

Stuart L. Goldberg; Er Chen; Medha Sasane; Carole Paley; Amy Guo; Marianne Laouri

BACKGROUND: Recent retrospective studies suggest myelodysplastic syndromes (MDSs) are more common than previously recognized and patients who develop transfusional dependence may be at risk for increased comorbid complications.


Journal of Medical Economics | 2015

Brain metastases in patients with ALK+ non-small cell lung cancer: clinical symptoms, treatment patterns and economic burden

Annie Guerin; Medha Sasane; Jie Zhang; Kenneth W. Culver; Katherine Dea; Roy Nitulescu; Eric Q. Wu

Abstract Objective: Brain metastases (BM) are highly prevalent among anaplastic lymphoma kinase positive (ALK+) non-small cell lung cancer (NSCLC) patients; yet little is known about their real-world treatment patterns and clinical and economic burdens. This study aimed to describe these patients’ treatment patterns, symptoms, and costs. Research design and methods: Retrospective study pooling data from three large administrative databases in the US (08/2011–06/2013). ALK+ NSCLC patients with BM and continuous enrollment for ≥ 60 days before and ≥30 days after the first observed BM diagnosis were identified by pharmacy records for crizotinib among patients with lung cancer and BM diagnostic codes. Main outcome measures: Treatment patterns, symptoms, healthcare resource utilization, and costs, before and after BM diagnosis. Results: Of the 213 crizotinib patients with BM diagnoses meeting the selection criteria, 23.0% had BM prior to NSCLC diagnosis; 47.4% had BM prior to crizotinib initiation; 19.2% during crizotinib treatment; and 10.3% post-crizotinib treatment. For those diagnosed with BM after NSCLC diagnosis, the median time between the NSCLC and BM diagnoses was 88 days. Following the first observed BM diagnosis, 88.7% used chemotherapy, 63.4% had radiotherapy, and 31.9% had stereotactic radiosurgery. The prevalence of BM-related symptoms substantially increased post-BM-diagnosis: fatigue (from 15% to 39%), headaches (from 5% to 24%), and depression (from 5% to 15%). Monthly costs per patient averaged


Journal of Comparative Effectiveness Research | 2015

Deferasirox therapy is associated with reduced mortality risk in a medicare population with myelodysplastic syndromes

Amer M. Zeidan; Franklin Hendrick; Erika Friedmann; Maria R. Baer; Steven D. Gore; Medha Sasane; Carole Paley; Amy J. Davidoff

5983 before the BM diagnosis and


Current Medical Research and Opinion | 2015

Treatment, overall survival, and costs in patients with ALK-positive non-small-cell lung cancer after crizotinib monotherapy

Annie Guerin; Medha Sasane; Heather A. Wakelee; Jack Zhang; Kenneth W. Culver; Katherine Dea; Roy Nitulescu; Philip Galebach; Alexander R. Macalalad

22,645 after diagnosis. Patients’ resource utilization increased significantly post-BM-diagnosis, with a 3-fold increase in OP visits and a 6-fold increase in IP stays. Post-BM-diagnosis costs were driven by pharmacy (42.0%), inpatient (29.6%), and outpatient costs (26.0%). Limitations: The study sample was limited to crizotinib-treated patients. Conclusions: Post-BM-diagnosis, patients experience high symptom burden. Post-BM-diagnosis, treatment is highly variable and costly: average monthly costs per patient almost quadrupled post-BM-diagnosis.


Journal of Emergency Medicine | 2015

Age-Related Emergency Department Reliance in Patients with Sickle Cell Disease.

Morey A. Blinder; Mei Sheng Duh; Medha Sasane; Alex Trahey; Carole Paley; Francis Vekeman

AIMS Iron overload adversely affects patients with myelodysplastic syndromes (MDS), but benefits of iron chelation therapy have not been clearly demonstrated. We examined the association between deferasirox (DFX) therapy and mortality in transfusion-receiving Medicare patients. PATIENTS & METHODS MDS patients from 2005 to 2008 were identified using ICD-9 codes from 100% Medicare claims. Patients receiving ≥20 blood units were observed until death or end of study. Marginal structural models were used for estimation. RESULTS 3926 patients (10.1% used DFX) were observed for a mean of 48.8 weeks. Each incremental week of DFX was associated with a significant reduction in mortality risk (hazard ratio [HR]: 0.989; 95% CI: 0.983-0.996; p = 0.001). CONCLUSION DFX therapy is associated with a reduced mortality risk among older MDS patients who received a minimum transfusion threshold.


Lung Cancer | 2016

Characteristics, treatment patterns, and survival among ALK+ non-small cell lung cancer (NSCLC) patients treated with crizotinib: A chart review study

Jacques Cadranel; Keunchil Park; Oscar Arrieta; Miklos Pless; Edmond Bendaly; Dony Patel; Medha Sasane; Adam Nosal; Elyse Swallow; Philip Galebach; Andrew Kageleiry; Karen Stein; Ravi Degun; Jie Zhang

Abstract Background: Limited post-crizotinib treatment options for ALK-positive non-small cell lung cancer (NSCLC) might lead to poor survival and high economic burden. Objective: To evaluate real-world treatment patterns, overall survival (OS), and costs following crizotinib discontinuation. Methods: This study used chart review and claims data. First, 27 participating US oncologists reviewed medical records of ALK-positive NSCLC patients who discontinued crizotinib monotherapy and reported patient demographic and clinical information, including post-crizotinib treatment and mortality. OS was estimated using Kaplan–Meier analyses. Second, three large administrative US claims databases were pooled. NSCLC patients were selected if they discontinued crizotinib monotherapy. Post-crizotinib costs were analyzed separately for patients who did or did not discontinue antineoplastic treatment after crizotinib monotherapy. All data were collected prior to ceritinib approval for this patient population. Results: A total of 119 ALK-positive NSCLC patients discontinued crizotinib monotherapy. Upon discontinuation, 42% had no additional antineoplastic treatment and 13% received radiation therapy only. The median OS post-crizotinib was 61 days; patients with brain metastases had shorter OS than those who did not (44 vs. 69 days, P = 0.018), and patients without further antineoplastic treatment had shorter OS than those who did (17 vs. 180 days, P < 0.001). From claims data, 305 ALK-positive NSCLC patients discontinued crizotinib monotherapy. After discontinuation, 72% had no additional antineoplastic treatment. Among patients who continued antineoplastic treatment, monthly healthcare costs averaged


Journal of Medical Economics | 2013

Cost-effectiveness of 3-years of adjuvant imatinib in gastrointestinal stromal tumors (GIST) in the United States

Myrlene Sanon; Douglas C. A. Taylor; Anju Parthan; John Coombs; Marc Paolantonio; Medha Sasane

22,160, driven by pharmacy (


Journal of Medical Economics | 2016

Adherence to iron chelation therapy and associated healthcare resource utilization and costs in Medicaid patients with sickle cell disease and thalassemia

Francis Vekeman; Medha Sasane; Wendy Y. Cheng; Agnihotram V. Ramanakumar; Jonathan Fortier; Ying Qiu; Mei Sheng Duh; Carole Paley; Patricia Adams-Graves

9202), inpatient (


Current Medical Research and Opinion | 2012

Effectiveness of adjuvant imatinib in patients with gastrointestinal stromal tumor: results of a population-based, matched-cohort study.

Hind T. Hatoum; Swu-Jane Lin; Medha Sasane; Jonathan C. Trent

6419), and outpatient radiotherapy (

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