A phase I study of gemcitabine followed by cisplatin concurrent with whole pelvic radiation therapy in locally advanced cervical cancer: A Gynecologic Oncology Group study

2007 ◽  
Vol 107 (2) ◽  
pp. 274-279 ◽  
Author(s):  
P ROSE ◽  
K DEGEEST ◽  
S MCMEEKIN ◽  
N FUSCO
2012 ◽  
Vol 125 (2) ◽  
pp. 315-319 ◽  
Author(s):  
Dana M. Chase ◽  
Helen Q. Huang ◽  
Lari Wenzel ◽  
David Cella ◽  
Richard McQuellon ◽  
...  

2020 ◽  
Vol 19 (11) ◽  
pp. 2363-2370 ◽  
Author(s):  
Krishnansu S. Tewari ◽  
Michael W. Sill ◽  
Bradley J. Monk ◽  
Richard T. Penson ◽  
David H. Moore ◽  
...  

2015 ◽  
Vol 33 (19) ◽  
pp. 2136-2142 ◽  
Author(s):  
Peter G. Rose ◽  
James Java ◽  
Charles W. Whitney ◽  
Frederick B. Stehman ◽  
Rachelle Lanciano ◽  
...  

Purpose To evaluate the prognostic factors in locally advanced cervical cancer limited to the pelvis and develop nomograms for 2-year progression-free survival (PFS), 5-year overall survival (OS), and pelvic recurrence. Patients and Methods We retrospectively reviewed 2,042 patients with locally advanced cervical carcinoma enrolled onto Gynecologic Oncology Group clinical trials of concurrent cisplatin-based chemotherapy and radiotherapy. Nomograms for 2-year PFS, five-year OS, and pelvic recurrence were created as visualizations of Cox proportional hazards regression models. The models were validated by bootstrap-corrected, relatively unbiased estimates of discrimination and calibration. Results Multivariable analysis identified prognostic factors including histology, race/ethnicity, performance status, tumor size, International Federation of Gynecology and Obstetrics stage, tumor grade, pelvic node status, and treatment with concurrent cisplatin-based chemotherapy. PFS, OS, and pelvic recurrence nomograms had bootstrap-corrected concordance indices of 0.62, 0.64, and 0.73, respectively, and were well calibrated. Conclusion Prognostic factors were used to develop nomograms for 2-year PFS, 5-year OS, and pelvic recurrence for locally advanced cervical cancer clinically limited to the pelvis treated with concurrent cisplatin-based chemotherapy and radiotherapy. These nomograms can be used to better estimate individual and collective outcomes.


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