Clinical Characteristics and Early Treatment Patterns of Newly Diagnosed Cystic Fibrosis–Related Diabetes in Two Tertiary Centers

Diabetes ◽  
2018 ◽  
Vol 67 (Supplement 1) ◽  
pp. 2374-PUB
Author(s):  
ERIN MCCORRY ◽  
HIBA BASHEER ◽  
JORGE E. LASCANO ◽  
JOHN YOON ◽  
JULIO A. LEEY
Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 5360-5360 ◽  
Author(s):  
Amanda M Farr ◽  
Marni Stott-Miller ◽  
Helen Varker ◽  
Danae Spencer ◽  
Manan Shah ◽  
...  

Abstract Background: Treatment of MM has undergone dramatic changes in the past decade. However, few studies have focused on treatment patterns among elderly patients. The present study sought to describe contemporary FL treatment patterns among elderly MM patients in a community practice setting. Methods: A retrospective cohort study of patients (≥65 years old) with newly diagnosed MM between 7/1/2011 and 5/31/2014 who had ≥1 oncologist visit within 90 days after diagnosis and ≥90 days of follow-up was conducted. Patients were selected from the Truven MarketScan Oncology Electronic Medical Records (EMR) database and followed until last visit in the EMR database or 8/31/2014, whichever occurred first. Baseline demographics and clinical characteristics were compared between treated patients and patients who did not receive anti-MM treatment in the EMR network (untreated). FL treatment included all anti-MM agents received from first anti-MM prescription/administration after initial diagnosis until the initiation of second-line treatment, which was defined as the first day of any gap in treatment >90 days or initiation of a new regimen. FL treatment patterns were characterized based on descriptive analyses of the EMR data. Time from diagnosis to FL therapy initiation and duration of FL treatment were analyzed using Kaplan-Meier (K-M) methods. Results: A total of 3,768 patients met eligibility criteria: 2,896 (77%) initiated systemic FL therapy (median age 75 years, 56% male) and 872 (23%) were untreated (median age 76 years, 49% male; Table 1). The K-M estimate of treatment rate at 12 months from MM diagnosis was 76% (Table 2). With a median follow-up of 13.2 months, 55% of patients had discontinued FL, while 34% remained on FL. Treated patients were younger (mean age 75.4 years versus 76.4 years, P<0.001) and had fewer baseline comorbidities (P=0.001) than untreated patients. The proportion of males was higher in the treated group (P=0.002). Of the 2,896 treated patients, 13% received a stem cell transplant at any time. Median time from diagnosis to FL therapy initiation was 28 days (95% CI 25-31; Table 2). The most common FL therapy was bortezomib +/- steroids (44%), followed by steroids only (14%), lenalidomide +/- steroids (13%), bortezomib + lenalidomide +/- steroids (10%), bortezomib + cyclophosphamide +/- steroids (8%), carfilzomib- or pomalidomide-containing regimens (4%), and conventional chemotherapy (4%). During FL therapy, 14% switched therapies. 17% of those who were treated with bortezomib + lenalidomide +/- steroids and 10% of those treated with bortezomib + cyclophosphamide +/- steroids received maintenance therapy. Median duration of FL treatment was 196 days (95% CI 180-208; Table 2). Conclusions: Results suggest that almost one-quarter of elderly patients newly diagnosed with MM remain untreated. In addition, about 20% of those treated in FL received suboptimal therapy (i.e., chemotherapy or steroids). Despite the advances in the treatment of MM with the availability of proteasome inhibitors/immunomodulatory agents, there still seems to be an unmet need in this patient population for novel therapies in the FL setting, especially for elderly patients who are at higher risk of comorbidities and clinical complications. Table 1. Demographics and baseline clinical characteristics of newly diagnosed MM patients Treated Patients n=2,896 Untreated Patients n=872 P Age at diagnosis, years (mean, SD) 75.4 6.9 76.4 7.3 <0.001 Age group, years (n, %) 65-69 714 25% 173 20% 0.007 70-74 706 24% 225 26% 75-79 651 22% 186 21% ≥80 825 28% 288 33% Male (n, %) 1,629 56% 431 49% 0.002 Another primary cancer (n, %) 804 28% 152 17% <0.001 Charlson Comorbidity Index (mean, SD) 0.2 0.7 0.3 0.8 0.001 Length of follow-up, months (mean, SD) 15.2 9.1 14.5 8.9 0.040 Table 2. K-M estimates of time from diagnosis to FL initiation and FL duration of treatment K-M Estimate 95% CI Median time to therapy initiation, days 28 25-31 % patients treated at 3 months 65% 63-66% % patients treated at 6 months 70% 69-72% % patients treated at 9 months 73% 71-74% % patients treated at 12 months 76% 74-77% Median duration of FL treatment, days 196 180-208 Still on treatment at 3 months 74% 72-75% Still on treatment at 6 months 52% 50-54% Still on treatment at 9 months 41% 39-43% Still on treatment at 12 months 35% 33-37% Disclosures Farr: Truven Health Analytics: Employment, Other: I am employed by Truven Health Analytics which received funding from Bristol-Myers Squibb to conduct this analysis.. Stott-Miller:Truven Health Analytics: Employment, Other: I am an employee of Truven Health Analytics which received funding from Bristol-Myers Squibb to conduct this analysis.. Varker:Truven Health Analytics: Employment, Other: I am an employee of Truven Health Analytics which received funding from Bristol-Myers Squibb to conduct this analysis.. Spencer:Truven Health Analytics: Employment, Other: I am an employee of Truven Health Analytics which received funding from Bristol-Myers Squibb to conduct this analysis.. Shah:Bristol-Myers Squibb: Employment, Other: Stocks. Chen:Bristol-Myers Squibb: Employment.


Diabetes ◽  
2018 ◽  
Vol 67 (Supplement 1) ◽  
pp. 1648-P
Author(s):  
JIANMIN WU ◽  
JIN XIE ◽  
HOONG WONG-JACOBOSN SIEW ◽  
VIRGINIA S. HAYNES ◽  
ZHENXIANG ZHAO

2021 ◽  
pp. 247412642097887
Author(s):  
Terry Lee ◽  
Cason B. Robbins ◽  
Akshay S. Thomas ◽  
Sharon Fekrat

Purpose: This work aims to investigate real-world treatment patterns and outcomes in eyes with branch retinal vein occlusion in the antivascular endothelial growth factor (anti-VEGF) era. Methods: A retrospective, nonrandomized, comparative study was conducted on eyes diagnosed with branch retinal vein occlusion at a single tertiary center between 2009 and 2017. Medical history, treatment patterns, and visual acuity outcomes were examined. Subanalysis was performed for eyes that met the eligibility criteria for the BRAVO (Ranibizumab for the Treatment of Macular Edema Following Branch Retinal Vein Occlusion) trial. Results: A total of 315 eyes were included, of which 244 were treatment naive. In all eyes, the most common first treatment was the following: intravitreal bevacizumab (38.4%), aflibercept (15.1%), ranibizumab (8.1%), sectoral scatter laser (6.2%), and triamcinolone (3.1%). At 1 year, treatment-naive eyes had received an average of 2.43 anti-VEGF injections. During follow-up, treatment-naive eyes gained an average of 0.21 Early Treatment Diabetic Retinopathy Study lines. Forty eyes that met BRAVO trial criteria received an average of 5.05 anti-VEGF injections in the first year and gained an average of 1.83 Early Treatment Diabetic Retinopathy Study lines. Conclusions: This real-world cohort received fewer anti-VEGF injections at year 1 and experienced less improvement in visual acuity during the course of treatment than clinical trial participants. Trial-eligible patients received more injections and had greater visual gains than those who would not have been eligible for the trial.


2021 ◽  
Vol 16 (3) ◽  
pp. S284
Author(s):  
L. Kathmann ◽  
J. Roeper ◽  
K. Wedeken ◽  
K. Willborn ◽  
F. Griesinger

2021 ◽  
Vol 11 (7) ◽  
Author(s):  
Hans C. Lee ◽  
Sikander Ailawadhi ◽  
Cristina J. Gasparetto ◽  
Sundar Jagannath ◽  
Robert M. Rifkin ◽  
...  

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