External beam radiation for the treatment of castration‑resistant prostate cancer following primary hormonal therapy with androgen ablation: Analysis and outcome of 21 patients

  • Authors:
    • Teele Kuusk
    • Kristiina Pulliainen
    • Markku H. Vaarala
  • View Affiliations

  • Published online on: February 6, 2017     https://doi.org/10.3892/mco.2017.1156
  • Pages: 428-432
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Abstract

Patients who undergo early androgen‑deprivation therapy for prostate cancer may eventually develop castration-resistant prostate cancer. However, no optimal treatment for non‑metastasized castration-resistant prostate cancer has yet been established. In the present retrospective, single-institutional study, the radiotherapy (RT) outcomes were evaluated in patients who underwent androgen‑deprivation therapy for non‑metastatic prostate cancer and subsequently developed castration-resistant disease. Following a thorough chart review, the data of 21 patients with castration-resistant prostate cancer who were treated between 2000 and 2010 with external beam radiation therapy (EBRT) at a prostate radiation dose of >45 Gy were evaluated. Of the 21 patients, 16 (76%) developed biochemical recurrence after RT, with a mean time to biochemical recurrence of 17 months. A total of 18 patients succumbed to the disease during follow-up, with a mean survival of 3 years after RT. A radiation dose of >66 Gy was associated with a longer time to biochemical recurrence after RT (P=0.011) and a longer survival, compared with a dose of ≤66 Gy (P=0.028). The mean overall survival time after RT was 42 months and did not depend on the primary hormonal treatment. Prostate‑specific survival time was negatively associated with the Gleason score at diagnosis. The prostate‑specific antigen (PSA) concentration prior to RT was a prognostic factor for biochemical recurrence of prostate cancer after RT, as well as for prostate cancer-specific survival. Finally, the multivariate analysis revealed that age, PSA concentration prior to RT and a high Gleason score were independent prognostic factors for prostate cancer-specific survival. Overall, our study findings demonstrated that disease progression was common after EBRT for castration‑resistant prostate cancer and that survival was limited. However, young patients and those with low-risk disease at the time of diagnosis may benefit from RT.

Introduction

Prostate cancer is the most common cancer among European men, comprising 12% of all new cancer cases and 5% of all cancer deaths in 2012 (1). There is no evidence that one radical treatment for localized disease is more effective compared with another (2). In a recently published randomized trial, it was demonstrated that radical prostatectomy and radiotherapy (RT) achieved comparable disease control after a 10-year follow-up (3). External beam radiation therapy (EBRT) is a treatment option available at different stages of non-metastatic prostate cancer (4). Androgen-deprivation therapy has also been used as primary treatment for localized prostate cancer (5), leading to apoptotic regression of androgen-dependent tumors. Possible androgen-deprivation therapy regimens include orchiectomy, gonadotropin hormone-releasing hormone (GnRH) agonists, GnRH antagonists and androgen receptor antagonists (6). Use of early androgen-deprivation therapy for prostate cancer may lead to the development of castration-resistant prostate cancer. The median time to bone metastasis in this group of patients is 9–30 months (7,8); the wide time range indicates the heterogeneity of this patient group. Additionally, the treatments and outcomes vary. No consensus on the treatment of non-metastasized castration-resistant prostate cancer has yet been reached. Few published studies have evaluated RT for castration-resistant prostate cancer (916). The aim of the present study was to evaluate the outcome of RT among patients who underwent androgen-deprivation therapy as a primary therapy for non-metastatic prostate cancer with progression to castration-resistant disease at our institution between 2000 and 2010.

Patients and methods

Patient chart review

Patient data were obtained through retrospective chart reviews from 2000 to 2010 and based on RT treatment codes. In total, 1,463 patients were treated with EBRT during this period. Of those, 68 had castration-resistant prostate cancer. Furthermore, 21 of those patients received a prostate radiation dose of >45 Gy. For these patients, RT was administered as salvage treatment for non-metastatic, castration-resistant prostate cancer. Nodal status was systematically assessed only by RT dose planning native computed tomography. Patients with evidently enlarged pelvic lymph nodes were excluded from higher (>45 Gy) prostate radiation doses. Castration-resistant prostate cancer was defined as a progressive increase in the prostate-specific antigen (PSA) concentration in repeated measurements during surgical or chemical (i.e., GnRH agonist therapy) castration. Baseline characteristics, radiation dose, lowest PSA concentration after RT, time to PSA increase (PSA nadir + 2 µg/l) and survival were recorded. The gross tumor volume (GTV) for RT was the prostate gland. The clinical target volume (CTV) was defined as GTV + 1 cm. The seminal vesicles were included in the CTV. The planning target volume (PTV) was defined as the CTV + 1 cm, except for 0.5 cm towards the rectum. If fiducial markers were used in the prostate, the CTV was GTV + 0.5 cm and the PTV was CTV + 0.5 cm, except 0 cm towards the rectum. Only conventional fractionation (2 Gy/fraction) was applied.

Following written assurance that patient information would remain coded and anonymous, this retrospective chart review was exempted from formal Institutional Review Board approval according to Finnish legislation and directions from Finnish ethics committees. The study was conducted according to the principles of the Helsinki Declaration.

Statistical analysis

Data were analyzed using SPSS software, version 22.0 (IBM Corp., Armonk, NY, USA). Between-group comparisons were performed using a t-test. Two-tailed P-values were reported, and P-values <0.05 were considered to indicate statistically significant differences. Prostate cancer-specific survival rates were calculated using the Kaplan-Meier method, and statistical significance between groups was analyzed using the log-rank test. Multivariate prognostic factor analyses were performed using Cox regression analyses.

Results

Patient characteristics

In total, 21 patients with castration-resistant prostate cancer were treated with EBRT with a prostate dose of >45 Gy. The median age of the patients at diagnosis was 68 years (range, 58–75 years). The median age of the patients at the start of EBRT was 74 years (range, 62–80 years). Another concurrent malignancy was present in 3 (14.3%) patients (lung cancer, n=1; malignant melanoma, n=1; and renal cancer, n=1). The Gleason score at diagnosis, clinical T-class [TNM classification (17)], and primary hormonal therapy are presented in Table I. None of the patients had histologically confirmed lymph node metastases at diagnosis. A bone scan was performed to exclude bone metastases at the time of diagnosis in 20 of the 21 patients. The median PSA concentration at the time of diagnosis was 50.2 µg/l (range, 4.8–335.0 µg/l).

Table I.

Gleason score and clinical T stage at diagnosis and primary hormonal therapy among the study population (n=21).

Table I.

Gleason score and clinical T stage at diagnosis and primary hormonal therapy among the study population (n=21).

TNM classificationN (%)
Gleason score at diagnosis
≤65 (23.8)
711 (52.4)
8–105 (23.8)
Clinical T stage
  1a-c3 (14.3)
  2a-c5 (23.8)
  3a,b9 (42.9)
  44 (19.0)
Primary hormonal therapy
  Antiandrogens4 (19.0)
  Chemical castration13 (61.9)
  Chemical castration + antiandrogen3 (14.3)
  Surgical castration1 (4.8)

[i] TNM, tumor-node-metastasis.

The median time until the PSA nadir was reached was 10 weeks (range, 2–96 weeks). Biochemical progression developed in a median of 41 months (range, 8–110 months). The median lowest PSA concentration was 0.8 µg/l (range, 0.2–25.0 µg/l). All the patients underwent a bone scan prior to RT to exclude metastatic disease; 6 patients (28.6%) also underwent a computed tomography scan and 6 patients (28.6%) underwent abdominal ultrasonography, whereas 1 patient (4.8%) underwent all three diagnostic modalities. The individual patient baseline characteristics are presented in Table II.

Table II.

Baseline characteristics of the patients (n=21).

Table II.

Baseline characteristics of the patients (n=21).

Patient no.Age at diagnosis, yearsPSA at diagnosis, µg/lGleason scoreClinical T stageLowest PSA prior to RT, µg/lPSA prior to RT, µg/lTime to nadir PSA prior to RT, monthsTime to biochemical progression prior to RT, months
16812.0  630.82.112  98
27328.6  812.51.0a10  24
36422.4  620.42.412  82
46916.2  731.33.0  4  41
57436.71041.426.7  4  8
65830.7  730.41.510  39
768214.0  845.668.211  27
87345.1  730.715.412  43
963335.0  7425.0219.010  25
106810.8  410.440.1  3  55
116635.4  730.88.6  5  35
126537.7  740.416.1  2  55
137521.1  733.232.7  3  39
147053.3  6212.3106.896110
157210.3  733.95.919  34
167042.3  720.427.431  52
176297.6  830.459.6  5  25
187035.8  730.29.728  49
197339.9  923.610.0  8  11
20624.8  611.214.413  48
216511.6  720.2130.037  84

a The patient had castration-resistant prostate cancer, as determined by an increasing PSA concentration, but maximal androgen blockade was initiated prior to RT. This PSA concentration was the actuarial last measurement prior to RT. RT, radiotherapy; PSA, prostate-specific antigen.

The median PSA concentration prior to RT was 15.4 µg/l (range, 1.0–219.0 µg/l). The median RT dose was 66 Gy (range, 46–72 Gy) and 10 patients (43.5%) received a dose of 72 Gy. Additionally, 19 patients received pelvic lymph node irradiation, with a median dose of 46 Gy (range, 46–56 Gy).

The mean follow-up duration was 108 months (range, 35–219 months). A total of 18 patients died during the follow-up period: 14 patients (66.7%) succumbed to prostate cancer, whereas 4 (19%) died from other causes, namely chronic obstructive pulmonary disease, intracerebral hemorrhage, gastric cancer and myocardial infarction. Three (14.3%) patients remained alive at the time of the chart review. The individual patient RT dose data and follow-up data are presented in Table III.

Table III.

Radiation therapy dose data and follow-up data of the patients (n=21).

Table III.

Radiation therapy dose data and follow-up data of the patients (n=21).

Patient no.Prostate radiation dose, GyPelvic lymph node radiation dose, GyLowest PSA after RT, µg/lTime to PSA nadir after RT, monthsTime to biochemical recurrence after RT, monthsCause of deathSurvival after RT, monthsOverall survival/follow-up months
  172460.86.012.4Prostate cancer47.8158
  266560.14.8 Other diseasea9.536
  372500.17.9 Alive 154
  472460.44.759.9Alive 174
  566461.93.09.9Prostate cancer30.540
  672460.25.6 Alive 131
  7505072.95.47.3Prostate cancer45.295
  87246 Other diseaseb3.862
  96646105.04.69.0Prostate cancer19.462
10725638.71.94.9Prostate cancer38.6131
1172460.49.735.0Prostate cancer86.8115
12505086.24.04.7Prostate cancer6.164
1350 65.47.79.6Prostate cancer21.981
145050126.93.56.6Prostate cancer16.1128
1550 1.63.77.9Prostate cancer59.2106
1650500.917.0 Other diseasec27.8120
1772463.44.09.5Prostate cancer57.885
1872460.28.833.4Prostate cancer89.6145
1950503.07.310.5Prostate cancer20.335
2072460.45.735.8Other diseased218.8219
214646158.74.19.3Prostate cancer32.9129

a Chronic obstructive pulmonary disease.

b Intracerebral hemorrhage.

c Gastric cancer.

d Myocardial infarction.PSA, prostate-specific antigen; RT, radiotherapy.

The median nadir PSA concentration after RT was 1.8 µg/l (range, 0.1–158 µg/l).

The mean time to the PSA nadir after RT was 5.9 months (range, 1.9–17.0 months). Among patients who developed biochemical recurrence after RT (n=16), the mean time to biochemical recurrence was 17 months [range, 4.7–60.0; 95% confidence interval (CI), 8.4–24.0 months]. Among patients who died during follow-up (n=18), the mean survival after RT was 36 months (range, 3.8–90.0 months).

The radiation dose was associated with the lowest PSA concentration after RT, time to biochemical recurrence after RT, and survival. For patients treated with a prostate radiation dose of ≤66 vs. >66 Gy, the mean lowest PSA concentration after RT was 56.6 and 5.0 µg/l, respectively (P=0.18). The time to biochemical recurrence and survival after RT for patients treated with a prostate radiation dose of ≤66 vs. >66 Gy were 8.3 vs. 27 months (P=0.011) and 26 vs. 54 months (P=0.028), respectively.

After RT, the mean overall survival was 42 months (95% CI: 29–55 months). The overall survival did not depend on the primary hormonal treatment. There were no significant differences between different hormonal treatments (data not shown).

The mean prostate-specific survival was negatively associated with the Gleason score at diagnosis (Fig. 1). The mean (95% CI) survival among patients with a Gleason score of ≤6, 7 and ≥8 was 165 (130–201), 119 (95–144), and 66 (36–95) months, respectively (P=0.002).

The PSA level prior to RT was a prognostic factor for biochemical recurrence of prostate cancer after RT [hazard ratio (HR)=1.02; 95% CI: 1.01–1.04; P=0.002). Furthermore, it was a prognostic factor for prostate cancer-specific survival (HR=1.01; 95% CI: 1.00–1.02; P=0.03).

A multivariate analysis was performed, including age, PSA concentration prior to RT and the Gleason score groups. Age, PSA concentration prior to RT and a high Gleason score were independent prognostic factors for prostate cancer-specific survival (Table IV).

Table IV.

Cox proportional multivariate analysis of patient age at diagnosis, PSA concentration prior to RT and Gleason score at diagnosis as risk factors for prostate cancer death.

Table IV.

Cox proportional multivariate analysis of patient age at diagnosis, PSA concentration prior to RT and Gleason score at diagnosis as risk factors for prostate cancer death.

VariablesHR95% CIP-value
Age at diagnosis1.251.01–1.540.04
PSA value prior to RT1.021.00–1.030.02
Gleason score
  ≤61 (ref.)
  71.940.49–7.740.35
  ≥815.92.38–1060.004

[i] PSA, prostate-specific antigen; RT, radiotherapy; HR, hazard ratio; CI, confidence interval.

Discussion

Castration-resistant prostate cancer without metastases represents a challenge for physicians. Medical or surgical castration has been historically used to treat prostate cancer in patients unfit for radical prostatectomy. Castration is currently not recommended for asymptomatic patients with non-metastatic prostate cancer (18). Furthermore, castration may increase the risk of cardiovascular side effects (19). Thus, there must be clear indications, such as severe obstructive voiding symptoms in a patient unsuitable for transurethral resection of the prostate, for castration to be applied; however, some patients are still primarily treated with castration, and this may lead to the need for radical EBRT when primary hormonal therapy fails.

Previous studies have reported the outcome of RT in patients with non-metastatic castration-resistant prostate cancer: To the best of our knowledge, the earliest patient series with a number of patients sufficient for statistical analyses was performed by Lankford et al (9), reporting the outcomes of 29 patients: At 4 years, 80% exhibited disease progression or an increasing PSA concentration (9). Botticella et al (20) reported that, during a 5-year follow-up, 60% of the 42 patients benefited from EBRT. This was the case for patients with a lower Gleason score, lower T stage and low PSA concentration prior to RT. Moreover, at a median follow-up of 53 months after EBRT, 21 of 42 (50%) patients developed biochemical failure, defined as the nadir PSA + 2 µg/l (20). Among Japanese patients, 66 of 140 (47%) exhibited clinical progression after EBRT during a median follow-up of 20.7 months (12). Another Japanese study presented results from 84 patients with a 3-year progression-free survival (PFS) rate of 61% (21). In an earlier Japanese report containing data from 61 patients (14), the 5-year PFS rate was 43.5%. Another study from Japan (11) presented results from 53 patients: The 3-year clinical relapse-free survival rate was 78%, and 15 patients developed clinical metastases during a median follow-up of 35 months (11). An Italian study published at the same time reported the data from 29 patients, 24 (83%) of whom had developed biochemical failure after a median of 9.2 months from EBRT (13). A study from Australia reported an actuarial median locoregional PFS duration of 43 months in 34 patients (15); in that study, however, 14 of the 34 patients had metastatic disease at baseline, and the outcome of patients with non-metastatic disease was not specified (15).

In our cohort, 16 of 21 (76%) patients developed biochemical recurrence after RT with a mean time to biochemical recurrence of 17 months. Among patients who died during follow-up (n=18), the mean survival following RT was 3 years.

Our study included a limited population and was retrospective in nature. Possible toxicities were not recorded. The outcomes in our institutional cohort are comparable with those published earlier. However, the benefit of EBRT for castration-refractory prostate cancer appears to be limited, and similar survival may be reached in this population with the novel hormonal treatments abiraterone and enzalutamide. Currently, the use of castration is limited among patients without metastasis, and the need for EBRT with curative intent may be on the decrease.

In conclusion, disease progression following EBRT for castration-resistant prostate cancer was common and survival was limited in the present study. However, certain patients, more likely those who are younger and have low-risk disease at diagnosis, may benefit significantly from RT.

Glossary

Abbreviations

Abbreviations:

CI

confidence interval

CTV

clinical target volume

GnRH

gonadotropin hormone-releasing hormone

GTV

gross tumor volume

HR

hazard ratio

PSA

prostate-specific antigen

PTV

planning target volume

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Spandidos Publications style
Kuusk T, Pulliainen K and Vaarala MH: External beam radiation for the treatment of castration‑resistant prostate cancer following primary hormonal therapy with androgen ablation: Analysis and outcome of 21 patients. Mol Clin Oncol 6: 428-432, 2017.
APA
Kuusk, T., Pulliainen, K., & Vaarala, M.H. (2017). External beam radiation for the treatment of castration‑resistant prostate cancer following primary hormonal therapy with androgen ablation: Analysis and outcome of 21 patients. Molecular and Clinical Oncology, 6, 428-432. https://doi.org/10.3892/mco.2017.1156
MLA
Kuusk, T., Pulliainen, K., Vaarala, M. H."External beam radiation for the treatment of castration‑resistant prostate cancer following primary hormonal therapy with androgen ablation: Analysis and outcome of 21 patients". Molecular and Clinical Oncology 6.3 (2017): 428-432.
Chicago
Kuusk, T., Pulliainen, K., Vaarala, M. H."External beam radiation for the treatment of castration‑resistant prostate cancer following primary hormonal therapy with androgen ablation: Analysis and outcome of 21 patients". Molecular and Clinical Oncology 6, no. 3 (2017): 428-432. https://doi.org/10.3892/mco.2017.1156