scholarly journals Racial Disparities in Oncologic Outcomes After Radical Prostatectomy: Long-term Follow-up

Urology ◽  
2014 ◽  
Vol 84 (6) ◽  
pp. 1434-1441 ◽  
Author(s):  
Farzana A. Faisal ◽  
Debasish Sundi ◽  
John L. Cooper ◽  
Elizabeth B. Humphreys ◽  
Alan W. Partin ◽  
...  
2014 ◽  
Vol 191 (4S) ◽  
Author(s):  
Farzana Faisal ◽  
Debasish Sundi ◽  
Ashley Ross ◽  
Elizabeth Humphreys ◽  
Alan Partin ◽  
...  

1991 ◽  
Vol 19 (4) ◽  
pp. 279-283 ◽  
Author(s):  
H. Frohmüller ◽  
M. Theiss ◽  
M.P. Wirth

2012 ◽  
Vol 11 (1) ◽  
pp. e352
Author(s):  
A. Forgues ◽  
F. Rozet ◽  
A. Ouzzane ◽  
R.E. Sanchez-Salas ◽  
E. Barret ◽  
...  

2014 ◽  
Vol 19 (2) ◽  
pp. 251-257 ◽  
Author(s):  
David Luyimbazi ◽  
Rebecca A. Nelson ◽  
Audrey H. Choi ◽  
Lily Li ◽  
Joseph Chao ◽  
...  

2019 ◽  
Vol 37 (7_suppl) ◽  
pp. 60-60
Author(s):  
Noelia Sanmamed ◽  
Rachel Glicksman ◽  
John Thoms ◽  
Alexandre Zlotta ◽  
Antonio Finelli ◽  
...  

60 Background: Pre-operative radiotherapy (PreORT) improves local control in various cancer types, and has become an established oncologic treatment strategy. During 2001-2004, we conducted a phase I pilot study assessing the role of short-course PreORT for men with unfavourable intermediate- and high-risk localized prostate cancer (PCa). We present long-term follow-up toxicity and oncologic outcomes. Methods: Eligible patients had histologically proven PCa, cT1-T2N0M0, PSA > 15-35 ng/ml with any Gleason score, or PSA 10-15 ng/ml with Gleason score ≥7. Patients received 25 Gy in five consecutive daily fractions to the prostate, followed by radical prostatectomy (RadP) within 14 days after RT completion. Primary outcomes were intra-operative morbidity, and late genitourinary (GU) and gastrointestinal (GI) toxicities. Acute toxicity was assessed during radiotherapy treatment on daily basis using RTOG grade scoring scale. Patients were assessed post-RadP clinically and with PSA at 1 and 6 months, and every 6 months. Intra- and Post-RadP toxicity was documented prospectively and scored as per Common Terminology Criteria for Adverse Events v4.0. Biochemical failure (BF) was determined based on two consecutive post-RadP PSA > 0.2 ng/ml. Results: Fifteen patients were enrolled; 14 patients completed PreORT followed by RadP, which also included bilateral lymph node dissections in 13 cases. Median follow-up was 12.2 years (range 6.7-16.3 years). Late GU toxicity was common, with 2 patients (14.3%) experiencing G2 toxicity, and 6 patients (42.8%) G3 toxicity. There were no G4-5 late GU toxicity. Late GI toxicity was infrequent, with only 1 patient (7.1%) experiencing transient G2 proctitis. At last follow-up, 8 (57.1%) and 6 (42.8%) patients experienced BF and metastatic disease recurrence, respectively. Conclusions: The use of PreORT in men with high-risk PCa is associated with unexpected high-rates of late GU toxicity. Future studies examining the role of RT pre-RadP must cautiously select RT technique and dose schedule. Importantly, long-term follow-up data is essential to fully determine the therapeutic index of PreORT in the management of localized PCa. Clinical trial information: NCT00252447.


Author(s):  
Philipp Dahm

This chapter provides a summary of the landmark PIVOT trial that randomized men with clinically localized prostate cancer from the early prostate-specific antigen (PSA) era to radical prostatectomy versus watchful waiting. Based on long-term follow-up, the study found that surgery provided only small reductions in disease-specific survival but caused substantial side effects. It suggested that many men with clinically localized prostate cancer fare well with watchful waiting.


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