Serum tumor markers in metastatic breast cancer comparative study between CEA, CA-15.3 and MCA

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

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.


1993 ◽  
Vol 11 (5-6) ◽  
pp. 217-223 ◽  
Author(s):  
J. S. Y. Ng ◽  
C. M. Sturgeon ◽  
J. Seth ◽  
G. M. Paterson ◽  
J. E. Roulston ◽  
...  

Three serum markers, TPS, CA 15.3 and CEA, were used to monitor the response to treatment of 20 patients with metastatic breast cancer. At the time of the first evidence of metastases or at the time of progression of known metastatic disease, 84% of TPS values were above the reference limit, as compared to 74% for CA 15.3 and 84% forCEA. If the treatment instituted was effective, 60% of TPS values showed an early (within 2 or 3 weeks after commencement or change of therapy) reduction in level against only 27% of CA 15.3 and 27% of CEA levels. This suggests that TPS provides a more sensitive and earlier predictor of therapeutic response. In patients with clinical evidence of further progression of disease while on therapy , 86% ofTPS values showed persistent elevation or increase, as compared to 71 % of CA 15.3 levels and only 36% ofCEA levels. It was also noted in these patients that TPS values rose earlier than either CA 15.3 or CEA. This indicates that TPS is a more reliable predictor of response to treatment than the other two markers. In addition, we found that, at the time of presentation, in women who had visceral metastases (liver, lung, or brain alone or in combination), 87% ofTPS values were raised, as compared to 80% of CA 15.3 and 73% of CEA values. In women who had bone and soft tissue metastases at presentation, 75% ofTPS values were elevated, against 50% ofCA 15.3 and 75% of CEA values. We also noted that in patients without raised TPS levels, the sites of subsequent disease progression were limited to bones, regional lymph nodes, skin and soft tissues.


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