Abstract P1-07-21: Use of serum tumor markers and high cost imaging in women with metastatic breast cancer

Author(s):  
MK Accordino ◽  
JD Wright ◽  
S Vasan ◽  
AI Neugut ◽  
JC Hu ◽  
...  
2005 ◽  
Vol 23 (16_suppl) ◽  
pp. 9516-9516
Author(s):  
A. Stopeck ◽  
M. Cristofanilli ◽  
G. T. Budd ◽  
M. J. Ellis ◽  
J. Matera ◽  
...  

2017 ◽  
Vol 15 (3) ◽  
pp. 316-324 ◽  
Author(s):  
Antonio Di Meglio ◽  
Nancy U. Lin ◽  
Rachel A. Freedman ◽  
William T. Barry ◽  
Eric P. Winer ◽  
...  

1998 ◽  
Vol 34 ◽  
pp. S43 ◽  
Author(s):  
C. Carneiro ◽  
L. Costa ◽  
M. Melo ◽  
A. Quintela ◽  
I. Miranda ◽  
...  

2017 ◽  
Vol 470 ◽  
pp. 51-55 ◽  
Author(s):  
Weigang Wang ◽  
Xiaoqin Xu ◽  
Baoguo Tian ◽  
Yan Wang ◽  
Lili Du ◽  
...  

2021 ◽  
pp. 600-614
Author(s):  
Jennifer L. Caswell-Jin ◽  
Alison Callahan ◽  
Natasha Purington ◽  
Summer S. Han ◽  
Haruka Itakura ◽  
...  

PURPOSE Treatment and monitoring options for patients with metastatic breast cancer (MBC) are increasing, but little is known about variability in care. We sought to improve understanding of MBC care and its correlates by analyzing real-world claims data using a search engine with a novel query language to enable temporal electronic phenotyping. METHODS Using the Advanced Cohort Engine, we identified 6,180 women who met criteria for having estrogen receptor–positive, human epidermal growth factor receptor 2–negative MBC from IBM MarketScan US insurance claims (2007-2014). We characterized treatment, monitoring, and hospice usage, along with clinical and nonclinical factors affecting care. RESULTS We observed wide variability in treatment modality and monitoring across patients and geography. Most women received first-recorded therapy with endocrine (67%) versus chemotherapy, underwent more computed tomography (CT) (76%) than positron emission tomography-CT, and were monitored using tumor markers (58%). Nearly half (46%) met criteria for aggressive disease, which were associated with receiving chemotherapy first, monitoring primarily with CT, and more frequent imaging. Older age was associated with endocrine therapy first, less frequent imaging, and less use of tumor markers. After controlling for clinical factors, care strategies varied significantly by nonclinical factors (median regional income with first-recorded therapy and imaging type, geographic region with these and with imaging frequency and use of tumor markers; P < .0001). CONCLUSION Variability in US MBC care is explained by patient and disease factors and by nonclinical factors such as geographic region, suggesting that treatment decisions are influenced by local practice patterns and/or resources. A search engine designed to express complex electronic phenotypes from longitudinal patient records enables the identification of variability in patient care, helping to define disparities and areas for improvement.


2008 ◽  
Vol 26 (15_suppl) ◽  
pp. 1072-1072
Author(s):  
I. Ertl ◽  
V. Heinemann ◽  
I. Bauerfeind ◽  
M. Untch ◽  
D. Laessig ◽  
...  

2018 ◽  
Vol 2 (2) ◽  
Author(s):  
Ana Elisa Lohmann ◽  
Ryan J O Dowling ◽  
Marguerite Ennis ◽  
Eitan Amir ◽  
Christine Elser ◽  
...  

Abstract Background Circulating tumor cells (CTCs) are associated with worse prognosis in metastatic breast cancer (BC). We evaluated the association of metabolic, inflammatory, and tumor markers with CTCs in women with metastatic BC before commencing a new systemic therapy. Methods Ninety-six patients with newly diagnosed or progressing metastatic BC without current diabetes or use of anti-inflammatory agents were recruited from four Ontario hospitals. Women provided fasting blood for measurement of metabolic, inflammatory, and tumor markers and CTCs. CTCs were assayed within 72 hours of collection using CellSearch. Other blood was frozen at –80°C, and assays were performed in a single batch. Associations between CTC counts with study factors were evaluated using Spearman correlation, and the chi-square or Fisher exact test. All statistical tests were two-sided and P value ≤ .05 was considered statistically significant. Results The median age was 60.5 years; 90.6% were postmenopausal. The cohort included hormone receptor–positive (87.5%), HER2–positive (15.6%), and triple-negative (10.4%) BCs. Patients were starting firstline (35.5%), second-line (26.0%), or third-or-later-line therapy (38.5%). CTC counts (per 7.5 mL of blood) ranged from 0 to 1238 (median 2); an elevated CTC count, defined as five or more CTCs, was detected in 42 (43.8%) patients. Those with liver metastases (vs not) more frequently had an elevated CTC count (59.0% vs 33.3%, P = .02). CTCs were significantly associated with C-reactive protein (R = .22, P = .02), interleukin (IL)-6 (R = .25, P = .01), IL-8 (R = .38, P = .0001), plasminogen activator inhibitor 1 (R = .31, P = .001), carcinoembryonic antigen (R = .31, P = .002), and cancer antigen 15-3 (R = .40, P = .0001) and inversely associated with body mass index (R = –.23, P = .02) and leptin (R = –.26, P = .01). Conclusions CTC counts were positively associated with tumor and inflammatory markers and inversely associated with some metabolic markers, potentially reflecting tumor burden and cachexia.


1987 ◽  
Vol 28 ◽  
pp. 109
Author(s):  
V. Möbus ◽  
G.P. Breitbach ◽  
R. Kreienberg ◽  
G. Bastert ◽  
H.J. Staab

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