PROSTATE-CANCER VOLUME ADDS SIGNIFICANTLY TO PROSTATE-SPECIFIC ANTIGEN IN THE PREDICTION OF EARLY BIOCHEMICAL FAILURE AFTER EXTERNAL-BEAM RADIATION-THERAPY
Av. Damico et Kj. Propert, PROSTATE-CANCER VOLUME ADDS SIGNIFICANTLY TO PROSTATE-SPECIFIC ANTIGEN IN THE PREDICTION OF EARLY BIOCHEMICAL FAILURE AFTER EXTERNAL-BEAM RADIATION-THERAPY, International journal of radiation oncology, biology, physics, 35(2), 1996, pp. 273-279
Citations number
22
Categorie Soggetti
Oncology,"Radiology,Nuclear Medicine & Medical Imaging
Purpose: A new clinical pretreatment quantity that closely approximate
s the true prostate cancer volume is defined. Methods and Materials: T
he cancer-specific prostate-specific antigen (PSA), PSA density, prost
ate cancer volume (V (Ca)), and the volume fraction of the gland invol
ved with carcinoma (V (Ca)fx) were calculated for 227 prostate cancer
patients managed definitively with external beam radiation therapy. 1.
PSA density = PSA/ultrasound prostate gland volume 2. Cancer-specific
PSA = PSA - [PSA from benign epithelial tissue] 3. V-Ca = Cancer-spec
ific PSA/[PSA in serum per cm(3) of cancer] 4. V(Ca)fx = V-Ca/ultrasou
nd prostate gland volume A Cox multiple regression analysis was used t
o-test whether any of these clinical pretreatment parameters added sig
nificantly to PSA in predicting early postradiation PSA failure. Resul
ts: The prostate cancer volume (p = 0.039) and the volume fraction of
the gland involved by carcinoma (p = 0.035) significantly added to the
PSA in predicting postradiation PSA failure, Conversely, the PSA dens
ity and the cancer-specific PSA did not add significantly (p > 0.05) t
o PSA in predicting postradiation PSA failure, The 20-month actuarial
PSA failure-free rates for patients with calculated tumor volumes of l
ess than or equal to 0.5 cm(3), 0.5-4.0 cm(3), and >4.0 cm(3) were 92,
80, and 47%, respectively (p = 0.00004). Conclusion: The volume of pr
ostate cancer (V (Ca)) and the resulting volume fraction of cancer bot
h added significantly to PSA in their ability to predict for early pos
tradiation PSA failure. These new parameters may be used to select pat
ients in prospective randomized trials that examine the efficacy of co
mbining radiation and androgen ablative therapy in patients with clini
cally localized disease, who are at high risk for early postradiation
PSA failure.