Main Session
Sep 28
PQA 02 - Lung Cancer/Thoracic Malignancies, Patient Reported Outcomes/QoL/Survivorship, Pediatric Cancer

2376 - Patient-Reported Outcomes (PROs) in Prostate Cancer Patients Undergoing IMRT vs. IMRT with Brachytherapy

04:45pm - 06:00pm PT
Hall F
Screen: 23
POSTER

Presenter(s)

Emily Hanus, BS - University of Kansas School of Medicine, Kansas City, KS

E. Hanus1, R. C. Chen2, J. C. Shiao2, Y. Cao2, and X. Shen2; 1University of Kansas Medical Center, Kansas City, KS, 2Department of Radiation Oncology, University of Kansas Medical Center, Kansas City, KS

Purpose/Objective(s): For patients with high-risk prostate cancer, the ASCENDE-RT trial showed that adding brachytherapy (BT) to intensity modulated radiation therapy (IMRT) improves cancer control over IMRT alone but significantly increases toxicity. However, real-time brachytherapy (compared to pre-planning as was done in ASCENDE-RT) may better spare organs at risk and thereby decrease toxicity. We compare prospectively collected PROs of consecutive patients treated at our institution.

Materials/Methods: As part of our clinical workflow, the International Prostate Symptom Score (IPSS) and Expanded Prostate Cancer Index Composite-Clinical Practice (EPIC-CP) are collected at pre-treatment and then prospectively for all patients. We analyzed patients treated from 2021-2024, and compared outcomes between patients treated with IMRT vs IMRT/BT at 0-6, 6-12, and 12-24 months. Minimally important differences (MID) were defined based on published literature as a change of 3 points for IPSS and 1 point for EPIC-CP. Statistical tests were performed using SAS v9.4.

Results: 112 patients were analyzed (IMRT: n=50; IMRT/BT: n=62), median age 67. Both groups significantly increased IPSS from baseline to 0-6 months (+5.0 vs +7.0, NS). IMRT group returned to baseline for IPSS, whereas IMRT/BT group had persistently elevated symptoms at 6-12 months (-1.0 vs + 1.0, p = 0.02) and 12-24 months (+0.0 vs + 3.0, p = 0.18). The EPIC-CP measure showed similar findings, with urinary QOL for IMRT patients recovering to baseline, while IMRT/BT patients had persistently elevated urinary incontinence (0.0 vs +1.0, p=0.05) and urinary irritation (0.0 vs +1.0, p=0.02) at 12-24 months. However, only a subset of the IMRT/BT group had elevated symptoms meeting the MID in IPSS (26%), EPIC-CP urinary irritation (21%), and urinary incontinence (18%). Bowel function remained stable across groups.

On multivariable analysis that adjusted for race, baseline IPSS, and use of pelvic radiation, IMRT/BT was associated with higher odds of increasing urinary incontinence that met the MID threshold (OR=18.79, p=0.02). There was no difference between IMRT and IMRT/BT patients in IPSS or urinary irritation.

Conclusion: Both IMRT alone and IMRT/BT result in post-treatment QOL declines. IMRT patients recovered by 6-12 months, whereas IMRT/BT patients had mild but persistent urinary QOL declines at 12-24 months, with 1-2 points increases compared to baseline. These data inform patient decision-making balancing the disease control benefit vs mild increased urinary symptoms from adding BT.

Abstract 2376 - Table 1: Median IPSS and EPIC-CP scores (higher score = worse symptoms)

IMRT vs IMRT/BT

Domain

Baseline

0-6 Months

6-12 Months

12-24 Months

IPSS

6.5 vs 7.0

16.5 vs 16.0

5.0 vs 10.0

7.0 vs 9.0

Urinary Incontinence

1.0 vs 0.0

2.0 vs 2.0

0.0 vs 1.0

0.0 vs 1.0

Urinary Irritation

2.0 vs 2.0

5.0 vs 5.0

1.0 vs 2.0

1.0 vs 3.0

Bowel

0.0 vs 0.0

2.0 vs 2.0

0.0 vs 0.0

0.0 vs 0.0