Abstract | BACKGROUND: The efficacy and safety of prostate SBRT in men with mCRPC is unknown. MATERIALS AND METHODS: A prospective cohort study was conducted with 125 men diagnosed with mCRPC. All patients received ADT plus chemotherapy. Patients were randomly assigned to receive daily prostate SBRT (36-48 Gy in 6-8 fractions). Patients who did not receive SBRT served as controls. RESULTS: The primary endpoints were PFS and OS. After 89 months of total follow-up, the median PFS was 13.8 months in the SBRT group (n = 61) and 12.0 months in the control group (n = 64) (HR, 0.87; 95% CI, 0.61-1.24; P = 0.249). The OS was 25.7 months in the SBRT group and 23.8 months in the control group (HR, 0.93; 95% CI, 0.65-1.33; P = 0.230). A non-significant increase in the PSA response rate (50.8% vs. 43.7%) and time to PSA progression (8.3 months vs. 7.0 months) was observed in the SBRT group compared to the control group; however, the time to symptomatic progression was significantly prolonged in the SBRT group (11.3 months) compared to the control group (8.5 months) (HR, 0.76; 95% CI, 0.53-1.08; P = 0.019). There was an 11.5% incidence of radiation cystitis and radiation rectitis in the SBRT group, and the degree and incidence of hormone-related and chemotherapy-related adverse events were similar between the two groups. CONCLUSION: Adding prostate SBRT significantly prolonged the time to symptomatic progression and non-significantly prolonged PFS and OS among men with mCRPC compared to treatment with ADT plus chemotherapy alone.
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Authors | Jun Li, JunYong Dai, Peng Xian, Lin Xiong, YanPing Song, XianLi Tang, Yuan Li, Yongzhong Wu, Hong Zhou, Nan Liu |
Journal | Cancer treatment and research communications
(Cancer Treat Res Commun)
Vol. 27
Pg. 100368
( 2021)
ISSN: 2468-2942 [Electronic] England |
PMID | 33848805
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2021. Published by Elsevier Ltd. |
Chemical References |
- Docetaxel
- Gonadotropin-Releasing Hormone
- Prostate-Specific Antigen
|
Topics |
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(adverse effects, therapeutic use)
- Cystitis
(etiology)
- Docetaxel
(administration & dosage)
- Dose Fractionation, Radiation
- Follow-Up Studies
- Gonadotropin-Releasing Hormone
(agonists, antagonists & inhibitors)
- Humans
- Male
- Neoplasm Grading
- Orchiectomy
- Proctitis
(etiology)
- Progression-Free Survival
- Prospective Studies
- Prostate-Specific Antigen
(blood)
- Prostatic Neoplasms, Castration-Resistant
(blood, pathology, therapy)
- Radiation Injuries
(etiology)
- Radiosurgery
(adverse effects)
- Random Allocation
- Survival Rate
- Tumor Burden
|