Propensity score-matched analysis comparing prostate EBRT versus EBRT + HDR brachytherapy
MO-0552
Abstract
Propensity score-matched analysis comparing prostate EBRT versus EBRT + HDR brachytherapy
Authors: Jörg Tamihardja1, Ingulf Lawrenz1, Paul Lutyj1, Johannes Kraft1, Marcus Zimmermann1, Stefan Weick1, Michael Flentje1, Bülent Polat1
1University of Wuerzburg, Department of Radiation Oncology, Wuerzburg, Germany
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Purpose or Objective
Propensity
score-matching (PSM) based long-term outcome and toxicity comparison of EBRT
versus EBRT plus HDR brachytherapy boost (HDR-BT boost).
Material and Methods
744
prostate cancer patients were treated with either EBRT alone (n = 406) or EBRT
plus HDR-BT boost (n=338) between 2002 and 2019 and were retrospectively
compared in this monocentric study. PSM
was performed including age, Gleason score, initial PSA value, tumor stage, use
of ADT, and risk group according to D´Amico. After PSM, 258 patient pairs (n =
516) were included into the final analysis. For EBRT alone, 33 fractions were
applied using VMAT with a simultaneous integrated boost of 60 Gy (D95)
/ 76.23 Gy (Dmean). For combined EBRT and HDR brachytherapy, EBRT
was delivered in 46 Gy (DMean) in conventional fractionation,
followed by two fractions HDR-BT boost with 9 Gy (D90%) two and four
weeks after EBRT. Genitourinary (GU) and gastrointestinal (GI) toxicity was
evaluated utilizing the Common Toxicity Criteria for Adverse Events (version
5.0) and biochemical failure was defined according to the Phoenix definition.
Toxicities were calculated for the total group without PSM. For all statistical
analyses, R software environment for statistical computing and graphics (version
4.1; The R Foundation for Statistical Computing, Vienna, Austria) was used. All
tests were two-sided with a level of significance set at p < 0.05.
Results
The
median follow-up was 95.3 months (range 0.5-230.7 months) in the propensity score-matched
cohort (n = 516). 36 / 190 / 290 patients had low- / intermediate- / high-risk
prostate cancer, respectively. Additive androgen deprivation therapy was given in
52.7% of the patients. Biochemical relapse-free survival (bRFS), metastasis-free
survival (MFS), and overall survival (OS) for both groups were not
statistically different after PSM. The estimated 10-year bRFS was 82.0% versus 76.3%
(p = 0.075) for EBRT versus EBRT + HDR brachytherapy, respectively. The
estimated 10-year MFS was 82.9% versus 87.4% (p = 0.19) and the 10-year OS was
65.7% versus 68.9% (p = 0.30). EBRT, compared to EBRT + HDR-BT boost, showed significantly
higher acute toxicities and higher cumulative 5-year late GI toxicity ≥ grade 2: Acute GU toxicity ≥ grade 2 occurred in 25.9% vs 11.8% (p <
0.001) and acute GI toxicity ≥
grade 2 in 11.8% vs 2.7% (p < 0.001). Cumulative 5‑year late GU ≥
grade 2 toxicities were observed in 23.6% vs 19.2% (p = 0.086) and 5‑year late GI ≥
grade 2 toxicities in 11.1% vs 5.0% of the patients (p = 0.002). Cumulative 5‑year late grade 3 GU toxicity occurred in 4.2%
and 3.6% (p=0.401) and GI toxicity in 1.0% and 0.3% (p=0.249) in both groups.
Conclusion
EBRT
alone and combined EBRT + HDR-BT boost showed no differences in long-term biochemical
relapse-free survival, metastasis-free survival, and overall survival. Acute toxicities
and late gastrointestinal toxicity ≥
grade 2 were lower for the combined treatment.