Prostate radiotherapy for metastatic hormone sensitive prostate cancer—myth or reality?

Previously, local radiotherapy (RT) was only limited to palliate local symptoms, including bleeding or obstructive symptoms in metastatic prostate cancer patients. However, a population-based database and retrospective studies suggested that the local treatment of the prostate could improve survival in metastatic hormone-naïve prostate cancer with a small metastatic burden, ‘oligometastatic’ state (1-3). Recently two randomized trials demonstrated the efficacy of local RT to prostate in metastatic prostate cancer patients (4,5).

In STAMPEDE trial comparing hormonotherapy ± docetaxel with RT to prostate, 2,061 newly diagnosed metastatic prostate cancer patients were analyzed (4). Although overall survival (OS) was not improved with local RT (HR =0.92, 95% CI: 0.80–1.06; P=0.266), a significant improvement in failure-free survival (FFS) was observed with prostate RT compared to standard of care alone (HR =0.76, 95% CI: 0.68–0.84; P<00001). However, in subgroup analysis according to metastatic burden defined in CHAARTED study (6), an OS (HR =0.68, 95% CI: 0.52–0.90; P=0.007) and FFS (HR =0.59, 95% CI: 0.49–0.72; P<0.0001) benefit was observed in patients with a low metastatic burden. However, patients with a high metastatic burden did not benefit from radiotherapy in terms of OS and FFS. The authors concluded that RT to primary tumor should be an option for newly diagnosed metastatic prostate cancer patients with low metastatic burden.

In second randomized trial, HORRAD trial, 432 men with metastatic prostate cancer were randomly allocated androgen deprivation therapy either alone or with prostate RT (5). Addition of external RT to primary tumor did not significantly improve OS compared to androgen deprivation alone (HR =0.90, 95% CI: 0.70–1.14; P=0.4). However in subgroup analysis, in patients with less than 5 bone metastasis including 160 patients, prostate RT improved OS with borderline significance (HR =0.68, 95% CI: 0.42–1.10).

These two randomized studies addressed the importance of local RT to prostate in newly diagnosed metastatic prostate cancer with low metastatic burden. Although the definition of metastatic burden (high vs. low) is well-described in STAMPEDE study, HORRAD trial collected the number of bone metastasis in three subcategories (<5, 5–15 and >15). Thus, a meta-analysis is crucial to define the patient population that benefits from primary tumor RT. The STOPCAP meta-analysis (7) is a prospective framework adaptive meta-analysis including one ongoing PEACE-1 study and two completed STAMPEDE and HORRAD studies (4,5). The pooled results of 2,126 patients de novo metastatic prostate cancer did not demonstrate a significant improvement in OS (HR =0.92, 95% CI: 0.81–1.04; P=0.195) and progression-free survival (PFS) (HR =0.94, 95% CI: 0.84–1.05; P=0.238) with prostate RT. There was no significant effect of adding prostate RT to androgen deprivation treatment on OS by patient age, performance status, clinical T-stage and Gleason score. However, the effect of prostate RT on OS (HR =1.47, 95% CI: 1.11–1.94; P=0.007), PFS (HR =1.32, 95% CI: 1.04–1.67; P=0.021), and FFS (HR =1.35, 95% CI: 1.10–1.66; P=0.004) was evident in patients with less than five bone metastasis, when stratification was made on number of bone metastasis (<5 vs. ≥5 metastases).

Although STOPCAP meta-analysis is important in demonstrating the effect of prostate RT on survival according to metastatic burden, there are some limitations. Most important limitation is the methods of metastasis detection with conventional imaging modalities, which has a limited value. Recent studies have demonstrated that the sensitivity and specificity of bone scintigraphy in detecting osseous metastases were 46–89% and 32–57%, respectively (8). However, several studies have demonstrated the benefits of ⁶⁸Ga-PSMA-PET/CT in identifying metastasis (9). Thus, staging with ⁶⁸Ga-PSMA-PET/CT is essential for appropriate staging. Furthermore, the RT doses to prostate delivered in STAMPEDE (either 36 Gy in 6 fractions or 55 Gy in 20 fractions) and HORRAD (70 Gy in 35 fractions or 57.76 Gy in 19 fractions) were significantly lower than suggested doses for high-risk prostate cancer patients (10). Therefore, studies with higher prostate irradiation doses may be more beneficial to demonstrate true effect of local RT.

Based on the findings of STOPCAP (7), primary prostate RT could be considered for newly diagnosed metastatic prostate cancer patients with less than five bone metastases. But further studies with better staging and higher local RT doses are needed to better define the benefit of prostate RT and also to delineate the clinical implementation of such treatment.

Acknowledgments

Funding: None.

Footnote

Provenance and Peer Review: This article was commissioned and reviewed by the Section Editor Peng Zhang, MD, PhD (Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China).

Conflicts of Interest: The author has completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr.2019.05.11). The author has no conflicts of interest to declare.

Ethical Statement: The author is accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.

References

1. Fossati N, Trinh QD, Sammon J, et al. Identifying optimal candidates for local treatment of the primary tumor among patients diagnosed with metastatic prostate cancer: a SEER-based study. Eur Urol 2015;67:3-6. [Crossref] [PubMed]
2. Satkunasivam R, Kim AE, Desai M, et al. Radical Prostatectomy or External Beam Radiation Therapy vs No Local Therapy for Survival Benefit in Metastatic Prostate Cancer: A SEER-Medicare Analysis. J Urol 2015;194:378-85. [Crossref] [PubMed]
3. Yildirim BA, Onal C, Kose F, et al. Outcome of loco-regional radiotherapy in metastatic castration-resistant prostate cancer patients treated with abiraterone acetate. Strahlenther Onkol 2019;195:872-81. [Crossref] [PubMed]
4. Parker CC, James ND, Brawley CD, et al. Radiotherapy to the primary tumour for newly diagnosed, metastatic prostate cancer (STAMPEDE): a randomised controlled phase 3 trial. Lancet 2018;392:2353-66. [Crossref] [PubMed]
5. Boevé LMS, Hulshof MCCM, Vis AN, et al. Effect on Survival of Androgen Deprivation Therapy Alone Compared to Androgen Deprivation Therapy Combined with Concurrent Radiation Therapy to the Prostate in Patients with Primary Bone Metastatic Prostate Cancer in a Prospective Randomised Clinical Trial: Data from the HORRAD Trial. Eur Urol 2019;75:410-8. [Crossref] [PubMed]
6. Sweeney CJ, Chen YH, Carducci M, et al. Chemohormonal Therapy in Metastatic Hormone-Sensitive Prostate Cancer. N Engl J Med 2015;373:737-46. [Crossref] [PubMed]
7. Burdett S, Boeve LM, Ingleby FC, et al. Prostate Radiotherapy for Metastatic Hormone-sensitive Prostate Cancer: A STOPCAP Systematic Review and Meta-analysis. Eur Urol 2019;76:115-24. [Crossref] [PubMed]
8. Lecouvet FE, Geukens D, Stainier A, et al. Magnetic resonance imaging of the axial skeleton for detecting bone metastases in patients with high-risk prostate cancer: diagnostic and cost-effectiveness and comparison with current detection strategies. J Clin Oncol 2007;25:3281-7. [Crossref] [PubMed]
9. Uprimny C, Kroiss AS, Decristoforo C, et al. (68)Ga-PSMA-11 PET/CT in primary staging of prostate cancer: PSA and Gleason score predict the intensity of tracer accumulation in the primary tumour. Eur J Nucl Med Mol Imaging 2017;44:941-9. [Crossref] [PubMed]
10. Carroll PH, Mohler JL. NCCN Guidelines Updates: Prostate Cancer and Prostate Cancer Early Detection. J Natl Compr Canc Netw 2018;16:620-3. [Crossref] [PubMed]