Primary intermittent chemo-hormonal therapy (CHT) for high risk locally advanced (LAPC) or metastatic prostate cancer (MPC): Preliminary results and quality of life (QOL)

2005 ◽  
Vol 23 (16_suppl) ◽  
pp. 4734-4734
Author(s):  
S. Tucker ◽  
R. Leibowitz
2017 ◽  
Vol 41 (6) ◽  
pp. 368-375
Author(s):  
I. López-Calderero ◽  
L. López-Fando ◽  
E. Ríos-González ◽  
P. Maisonobe ◽  
E. Hernández-Yuste ◽  
...  

2008 ◽  
Vol 7 (3) ◽  
pp. 206 ◽  
Author(s):  
P.C.M.S. Verhagen ◽  
L.D. Wissenburg ◽  
M.F. Wildhagen ◽  
W.A.B.M. Bolle ◽  
A.M. Verkerk ◽  
...  

2018 ◽  
Vol 15 (7) ◽  
pp. S285-S286
Author(s):  
K. Chaker ◽  
A. Sellami ◽  
Y. Ouanes ◽  
M.A. Essid ◽  
K. Mrad Dali ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
S. Rausch ◽  
C. Schmitt ◽  
T. Kälble

Introduction. High-risk prostate cancer represents a therapeutic challenge. The role of radical prostatectomy (RP) in patients with extreme PSA values is under discussion.Material and Methods. We retrospectively analysed our data of 56 consecutive patients with preoperative PSA ≥ 40 mg/mL undergoing open radical retropubic prostatectomy from 1999 to 2009. Patient survival and time to PSA recurrence were recorded, and the Kaplan-Meier survival analysis was performed. Postoperative quality of life and functional status were investigated using a SF-12 questionnaire and determining the number of pads used per day.Results. Overall 56 patients were available for followup after a median time of 83.84 months. Locally advanced carcinoma was present in 84% while 16% of patients had organ-confined stages. A positive nodal status was observed in 46%. Overall survival was 95% at five and 81% at 10 years. Cancer-specific survival was 100% for five years and 83% for 10 years. Corresponding biochemical recurrence-free survival was low (52% and 11%, resp.). Quality of life and functional outcomes were favourable.Conclusions. In patients with PSA ≥ 40 mg/mL, RP allows long-term control, exact planning of adjuvant treatment, and identification of curable disease.


2011 ◽  
Vol 29 (7_suppl) ◽  
pp. 75-75
Author(s):  
H. C. Quon ◽  
P. Cheung ◽  
D. A. Loblaw ◽  
G. Morton ◽  
E. Szumacher ◽  
...  

75 Background: Combined radiotherapy (RT) and long-term hormonal therapy (HT) is a standard treatment option for high-risk prostate cancer. Dose escalated RT alone has been shown to improve disease free survival. Increased sensitivity of prostate cancer to high doses per fraction has led to hypofractionation as a method to radiobiologically escalate dose.We report on the quality of life of patients treated with combined hypofractionated RT and HT. Methods: A prospective phase I/II study enrolling patients with any of: clinical T3, PSA ≥20, or Gleason 8-10. Forty-five Gy (1.8 Gy/fraction) was delivered to the pelvic nodes with a concomitant 22.5 Gy intensity-modulated RT boost to the prostate, for a total of 67.5 Gy (2.7 Gy/fraction) in 25 fractions over 5 weeks. Hormonal therapy was administered for 2-3 years. Patient reported outcomes were measured at baseline and every 6 months using the validated Expanded Prostate Cancer Index Composite (EPIC) questionnaire, which measures urinary, bowel, sexual, and hormonal domains. Results: Sixty patients with a minimum 24 months of patient-reported outcomes were analyzed. Mean scores comparing baseline to 24 month values are reported. There were no statistically significant changes in the urinary summary scores (86.3 vs. 86.0, p=0.45) or any of the urinary subscales (function, bother, incontinence, irritative/obstructive). Domain summary score decreases were observed in: bowel by 4.4% (94.7 vs. 90.3, p<0.01), sexual by 27% (44.5 vs. 17.5, p<0.01), and hormonal by 11.9% (93.1 vs. 81.2, p<0.01). Examining time trends in outcomes, most changes occurred within the first 6 months with smaller changes thereafter. Conclusions: Hypofractionated RT combined with long-term HT is associated with good patient-reported urinary and bowel outcomes at 24 months. Sexual and hormonal summary scores are affected, largely due to continued androgen deprivation therapy. Further follow-up is needed to document patient reported outcomes after testosterone recovery. No significant financial relationships to disclose.


2018 ◽  
Author(s):  
Kays Chaker ◽  
Ahmed Sellami ◽  
Yassine Ouanes ◽  
Mohamed Ali Essid ◽  
Karem Abid ◽  
...  

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