Factors associated with improved biochemical response to neoadjuvant androgen deprivation therapy before definitive radiation therapy in prostate cancer patients
Background: In prostate cancer patients treated with androgen deprivation therapy (ADT) and radiation therapy (RT), a pre-RT PSA level ⩾0.5 ng ml −1 , determined after neoadjuvant ADT and before RT, predicts for worse survival measures. The present study sought to identify patient, tumor and treatme...
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Published in | Prostate cancer and prostatic diseases Vol. 16; no. 4; pp. 346 - 351 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.12.2013
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Background:
In prostate cancer patients treated with androgen deprivation therapy (ADT) and radiation therapy (RT), a pre-RT PSA level ⩾0.5 ng ml
−1
, determined after neoadjuvant ADT and before RT, predicts for worse survival measures. The present study sought to identify patient, tumor and treatment characteristics associated with the pre-RT PSA in prostate cancer patients.
Methods:
We reviewed the charts of all patients diagnosed with intermediate- and high-risk prostate cancer and treated with a combination of neoadjuvant (median, 2.2 and 2.5 months, respectively), concurrent, and adjuvant ADT and RT between 1990 and 2011.
Results:
A total of 170 intermediate- and 283 high-risk patients met inclusion criteria. On multivariate analysis, both intermediate- and high-risk patients with higher pre-treatment PSA (iPSA) were significantly less likely to achieve a pre-RT PSA <0.5 ng ml
−1
(iPSA 10.1–20 ng ml
−1
:
P
=0.005 for intermediate risk; iPSA 10.1–20 ng ml
−1
:
P
=0.005, iPSA >20 ng ml
−1
:
P
<0.001 for high risk). High-risk patients undergoing total androgen blockade were more likely to achieve a pre-RT PSA <0.5 ng ml
−1
(
P
=0.031). We observed an interaction between race and type of neoadjuvant ADT (
P
=0.074); whereas African-American men on total androgen blockade reached pre-RT PSA <0.5 ng ml
−1
as frequently as other men on total androgen blockade (
P
=0.999), African-American men on luteinizing hormone-releasing hormone (LH-RH) agonist monotherapy/orchiectomy were significantly less likely to reach pre-RT PSA <0.5 ng ml
−1
compared with other men on LH-RH monotherapy/orchiectomy (
P
=0.001).
Conclusions:
Our findings suggest that total androgen blockade in the neoadjuvant period may be beneficial compared with LH-RH monotherapy for achieving a pre-RT PSA <0.5 ng ml
−1
in African-American men with high-risk prostate cancer. In addition, men with higher iPSA are more likely to have a pre-RT PSA greater than 0.5 ng ml
−1
in response to neoadjuvant ADT and are therefore candidates for clinical trials testing newer, more aggressive hormone-ablative therapies. |
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ISSN: | 1365-7852 1476-5608 |
DOI: | 10.1038/pcan.2013.26 |