Exclusive image-guided IMRT versus radical prostatectomy followed by postoperative IMRT for localized prostate cancer: A matched-pair analysis based on risk groups.

2012 ◽  
Vol 30 (5_suppl) ◽  
pp. 135-135
Author(s):  
Caroline Azelie ◽  
Mélanie Gauthier ◽  
Céline Mirjolet-Didelot ◽  
Luc Cormier ◽  
Etienne Martin ◽  
...  

135 Background: To investigate whether patients treated for a localized prostate cancer require prior radical prostatectomy followed by postoperative radiotherapy or exclusive radiotherapy, in the modern era of image-guided IMRT. Methods: One hundred and seventy-eight patients with localized prostate cancer were referred for daily on-line exclusive image-guided IMRT (IG-IMRT), while 69 patients were referred for postoperative IMRT without image guidance after radical prostatectomy (RP+IMRT). The patients were matched in a 1:1 ratio according to their baseline risk group before any treatment. Late toxicity was scored using the CTV v3.0 scale. Biochemical failure was defined as a postoperative PSA ≥ 0.1 ng/mL followed by 1 consecutive rise in PSA for the postoperative group of patients and by the Phoenix definition (nadir+2 ng/mL) for the group of patients treated with exclusive radiotherapy. Results: A total of 98 patients were matched (49:49). Thirty patients had a low-risk (30.6%), 62 patients an intermediate risk (63.3%) and 6 patients a high risk (6.1%). In the RP+IMRT group, the median PSA value before radiotherapy in the RP+IMRT group was 0.28 ng/mL [undetectable-6.99]. The median radiation dose in the IG-IMRT group was 77.4Gy [73.0-79.8 Gy] whereas it was 66.0 Gy [31.4-70.3 Gy] in the RP+IMRT group. The duration of the hormones was similar in both groups (p= 0.438). From the start of any treatment, the median follow-up was 56.6 months (95% CI = [49.6-61.2], range [18.2-115.1]. No patients had late gastrointestinal grade ≥ 2 toxicity in the IG-IMRT group vs. 4% in the RP+IMRT group. Forty-two percent of the patients in both groups had late grade ≥ 2 genitourinary toxicity. The 5-year freedom from biochemical failure rates in the IG-IMRT group and in the RP+IMRT groups were 93.1% [80.0-97.8] and 76.5% [58.3-87.5], respectively (p= 0.031). Conclusions: Patients with localized prostate cancer treated with IG-IMRT had a better oncological outcome than patients treated with RP+IMRT. Further improvements in postoperative IMRT using image guidance and dose escalation need to be evaluated to determine whether it could eventually be superior to IG-IMRT.

2000 ◽  
pp. 101-105 ◽  
Author(s):  
CHRISTOPHER L. AMLING ◽  
MICHAEL L. BLUTE ◽  
ERIK J. BERGSTRALH ◽  
THOMAS M. SEAY ◽  
JEFFREY SLEZAK ◽  
...  

2002 ◽  
Vol 20 (15) ◽  
pp. 3213-3218 ◽  
Author(s):  
John Thomas ◽  
Manjula Gupta ◽  
Ying Grasso ◽  
Chandana A. Reddy ◽  
Warren D. Heston ◽  
...  

PURPOSE: We report a prospective study examining the ability of preoperative nested reverse transcriptase polymerase chain reaction (RT-PCR) for prostate-specific antigen (PSA) and prostate-specific membrane antigen (PSM) to predict pathologic stage and biochemical recurrence in patients with clinically localized prostate cancer treated with radical prostatectomy.PATIENTS AND METHODS: One hundred forty-one patients were entered onto the study. Preoperative evaluation included clinical T stage, serum PSA, biopsy Gleason score, and serum RT-PCR for PSA/PSM. Univariate and multivariate logistic regression models, Kaplan-Meier estimates, and Cox proportional hazards modeling were used to identify predictors of pathologic stage and biochemical failure.RESULTS: Seventy-three patients (51.8%) were RT-PCR positive for PSA, PSM, or both. In the multivariate logistic regression model, only initial PSA was an independent predictor of pathologic stage as defined by organ-confined disease (odds ratio [OR], 1.06; 95% confidence interval [CI], 1.00 to 1.13; P = .026) or organ-/specimen-confined disease (OR, 1.09; 95% CI, 1.02 to 1.16; P = .009). Overall Kaplan-Meier biochemical relapse-free survival (bRFS) was 85% at 59 months. Multivariate analysis of predictors for bRFS with the Cox proportional hazards model indicated that only initial PSA (OR, 1.05; 95% CI, 1.02 to 1.09; P = .004) and biopsy Gleason score (OR, 3.57; 95% CI, 1.37 to 9.58; P = .009) were independent predictors of biochemical failure. RT-PCR status did not predict pathologic stage or biochemical failure. Repeat analysis excluding 27 patients who received preoperative androgen-deprivation therapy did not change the results.CONCLUSION: Combined nested RT-PCR for PSA and PSM is not an independent predictor of pathologic stage or biochemical failure in patients with localized prostate cancer undergoing radical prostatectomy. This assay has no clinical utility in this patient population.


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