(S011) Hypofractionated vs Standard Fractionated Proton Beam Therapy for Early-Stage Prostate Cancer: Interim Results of a Randomized Prospective Trial

Publication
Article
OncologyOncology Vol 29 No 4_Suppl_1
Volume 29
Issue 4_Suppl_1

Patients tolerated proton therapy in this randomized trial well, with excellent QoL scores, persistent low IPSS, and no grade ≥ 3 AEs in either arm. Thus far, there is no apparent clinical difference in outcomes with hypofractionated proton beam therapy compared to standard fractionation.

William F. Hartsell, MD, Megan Dunn, PhD, Gary Larson, MD, Carlos Vargas, MD; CDH Proton Center; Proton Collaborative Group; ProCure Proton Center; Mayo Clinic

PURPOSE: After prostate cancer treatment, most adverse event (AE) and quality of life (QoL) changes can be initially identified within the first 2 years. The purpose of this interim analysis is to determine if there are differences in terms of QoL, International Prostate Symptom Score (IPSS), or AEs among prostate cancer patients treated on a randomized prospective trial with either standard fractionation or hypofractionation.

MATERIALS AND METHODS: Eighty-two patients were randomized to 38 Gy(relative biologic effectiveness [RBE]) in 5 treatments (n = 49) vs 79.2 Gy(RBE) in 44 treatments (n = 33). All patients had stage I prostate cancer and were treated with proton therapy using fiducial markers and daily image guidance.

RESULTS: Median follow-up for both groups was 18 months, with 33 patients reaching follow-up of 2 years or more. Patient characteristics for both groups were similar, with most patients being T1c (84%) and all having a Gleason score of 6 and a prostate-specific antigen (PSA) level < 10 ng/mL (median, 5.6 ng/mL). Baseline median IPSS was 5 for the 5-fraction arm (range: 0–15), and median IPSS was also 5 for the 44-fraction arm (range: 0–14). There was no difference between the two groups with regard to Expanded Prostate Index Composite (EPIC) urinary, bowel, or sexual function scores at 3, 6, 9, 12, 18, 24, or 36 months. The only significant difference was the IPSS score at 12 months: 5 for the 44-fraction arm vs 8 for the 5-fraction arm (P = .03), but there was no difference in the IPSS scores at the other time points. No grade ≥ 3 AEs were seen in either arm.

CONCLUSIONS: Patients tolerated proton therapy in this randomized trial well, with excellent QoL scores, persistent low IPSS, and no grade ≥ 3 AEs in either arm. Thus far, there is no apparent clinical difference in outcomes with hypofractionated proton beam therapy compared to standard fractionation.

Proceedings of the 97th Annual Meeting of the American Radium Society - americanradiumsociety.org

Articles in this issue

(P005) Ultrasensitive PSA Identifies Patients With Organ-Confined Prostate Cancer Requiring Postop Radiotherapy
(P001) Disparities in the Local Management of Breast Cancer in the United States According to Health Insurance Status
(P002) Predictors of CNS Disease in Metastatic Melanoma: Desmoplastic Subtype Associated With Higher Risk
(P003) Identification of Somatic Mutations Using Fine Needle Aspiration: Correlation With Clinical Outcomes in Patients With Locally Advanced Pancreatic Cancer
(P004) A Retrospective Study to Assess Disparities in the Utilization of Intensity-Modulated Radiotherapy (IMRT) and Proton Therapy (PT) in the Treatment of Prostate Cancer (PCa)
(S001) Tumor Control and Toxicity Outcomes for Head and Neck Cancer Patients Re-Treated With Intensity-Modulated Radiation Therapy (IMRT)-A Fifteen-Year Experience
(S003) Weekly IGRT Volumetric Response Analysis as a Predictive Tool for Locoregional Control in Head and Neck Cancer Radiotherapy 
(S004) Combination of Radiotherapy and Cetuximab for Aggressive, High-Risk Cutaneous Squamous Cell Cancer of the Head and Neck: A Propensity Score Analysis
(S005) Radiotherapy for Carcinoma of the Hypopharynx Over Five Decades: Experience at a Single Institution
(S002) Prognostic Value of Intraradiation Treatment FDG-PET Parameters in Locally Advanced Oropharyngeal Cancer
(P006) The Role of Sequential Imaging in Cervical Cancer Management
(P008) Pretreatment FDG Uptake of Nontarget Lung Tissue Correlates With Symptomatic Pneumonitis Following Stereotactic Ablative Radiotherapy (SABR)
(P009) Monte Carlo Dosimetry Evaluation of Lung Stereotactic Body Radiosurgery
(P010) Stereotactic Body Radiotherapy for Treatment of Adrenal Gland Metastasis: Toxicity, Outcomes, and Patterns of Failure
(P011) Stereotactic Radiosurgery and BRAF Inhibitor Therapy for Melanoma Brain Metastases Is Associated With Increased Risk for Radiation Necrosis
Recent Videos
Elucidating nonresponses to bispecific T-cell engagers may be an important research consideration in the multiple myeloma field.
Barriers to access and financial toxicities are challenges that must be addressed for CAR T-cell therapies in LBCL, according to Jose Sandoval Sus, MD.
Fixed treatment durations with bispecific antibodies followed by observation may help in mitigating infection-related AEs, according to Shebli Atrash, MD.
Shebli Atrash, MD, stated that MRD should be considered carefully as an end point, given potential recurrence despite MRD negativity.
Data from the phase 3 DeLLphi-304 trial at ASCO 2025 revealed a survival advantage with tarlatamab vs chemotherapy in second-line ES-SCLC.
The FDA approval of tarlatamab in SCLC has received much press attention, according to Daniel R. Carrizosa, MD, MS.
The National ICE-T Conference may inspire future collaboration between community and academic oncologists in the management of different cancers.
One of the largest obstacles to tackle in the kidney cancer landscape will be translating the research on rare kidney cancer subtypes into clinical trials.
Long-term toxicities like infections and secondary primary malignancies remain a concern when sequencing novel agents for those with multiple myeloma.
Zanzalitinib exhibited favorable data when evaluated alone or in combination with anti-PD-1 immune checkpoint inhibition in phase 1 RCC trials.
Related Content