Proton therapy for high‐risk prostate cancer: Results from the Proton Collaborative Group PCG 001‐09 prospective registry trial

Author:

Hasan Shaakir1,Lazarev Stanislav2,Garg Madhur3,Gozland Rachel4ORCID,Chang John5,Hartsell William6,Chen Jonathan7,Tsai Henry8,Vargas Carlos9,Simone Charles B.1,Gorovets Daniel10

Affiliation:

1. New York Proton Center New York New York USA

2. Department of Radiation Oncology Mount Sinai Medical Center New York New York USA

3. Department of Radiation Oncology Montefiore Medical Center Bronx New York USA

4. Albert Einstein College of Medicine Bronx New York USA

5. Department of Radiation Oncology Oklahoma Proton Center Oklahoma City Oklahoma USA

6. Department of Radiation Oncology Northwestern University Chicago Illinois USA

7. Department of Radiation Oncology University of Washington Seattle Washington USA

8. ProCure Proton Therapy Center Somerset New Jersey USA

9. Department of Radiation Oncology Mayo Clinic Arizona Phoenix Arizona USA

10. Department of Radiation Oncology Memorial Sloan Kettering Cancer Center New York New York USA

Abstract

AbstractBackgroundData for proton therapy in high‐risk prostate cancer (HRPC) are limited. Using the Proton Collaborative Group prospective registry, we evaluated outcomes for HRPC patients treated with proton therapy.MethodsA totsl of 605 men with localized HRPC treated with proton therapy from 8/2009 to 3/2019 at nine institutions were selected. Outcomes examined included freedom from progression (FFP), metastasis free survival (MFS), overall survival (OS), and toxicity. Multivariable cox/binomial regression models were used to assess predictors of FFP and toxicity.ResultsMedian age was 71 years. Gleason grade groups 4 (49.4%) and 5 (31.7%) were most common, as were clinical stage T1c (46.1%) and cT2 (41.3%). The median pretreatment prostate specific antigen (PSA) was 9.18 and median International Prostate Symptom Score (IPSS) was 6. Androgen deprivation therapy was given in 63.6%. Median dose was 79.2 GyE in 44 fractions. Pelvic lymph nodes were treated in 58.2% of cases. Pencil beam scanning was used in 54.5%, uniform scanning in 38.8%, and a rectal spacer in 14.2%. At a median followup of 22 months, the 3‐ and 5‐year FFP were 90.7% and 81.4%, respectively. Five‐year MFS and OS were 92.8% and 95.9%, respectively. Independent correlates of FFP included Gleason ≥8, PSA > 10, and cT2 (all p < 0.05). No grade 4 or 5 adverse events were reported. There were 23 (5%) grade 2 and 0 grade 3 gastrointestinal events. Prevalence of late grade 3, late grade 2, acute grade 3, and acute grade 2 genitourinary toxicity was 1.7%, 5.8%, 0%, and 21.8%, respectively. Prevalence of grade 2 and 3 erectile dysfunction at 2 years was 48.4% and 8.4%, respectively.ConclusionsIn the largest series published to date, our results suggest early outcomes using proton therapy for HRPC are encouraging for both safety and efficacy. Further evaluation is needed to determine if an advantage exists to use protons over other radiation techniques in this population.

Publisher

Wiley

Subject

Urology,Oncology

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