Randomized trial of concomitant hypofractionated IMRT boost versus conventional fractionated IMRT boost for localized high-risk prostate cancer (pHART2-RCT).

Prostate cancer elective pelvic nodal irradiation high-risk hypofractionation

Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
16 Nov 2023
Historique:
received: 07 09 2023
revised: 15 10 2023
accepted: 02 11 2023
medline: 19 11 2023
pubmed: 19 11 2023
entrez: 18 11 2023
Statut: aheadofprint

Résumé

To report on the results of a phase II randomized trial of moderately hypofractionated (MH) versus conventionally fractionated (CF) radiotherapy to the prostate with elective nodal irradiation (ENI). This was a single-centre prospective phase II randomized study. Patients with high-risk disease (cT3, PSA >20 ng/mL, or Gleason score 8-10) were eligible. Patients were randomized to either MH using a simultaneous integrated boost (68 Gy in 25 fractions to prostate; 48 Gy to pelvis) or CF (46 Gy in 23 fractions with a sequential boost to the prostate of 32 Gy in 16 fractions), with long-term androgen deprivation therapy (ADT). The primary endpoint was grade ≥2 acute gastrointestinal (GI) and genitourinary (GU) toxicity (CTCAE v3.0). Secondary endpoints included late GI and GU toxicity, quality of life, and oncologic outcomes. 180 patients enrolled: 90 were randomized to and received MH and 90 to CF. Median follow-up was 67.4 months. Seventy-five (41.7%) patients experienced a grade ≥2 acute GI and/or GU toxicity, including 34 (37.8%) in the MH and 41 (45.6%) in the CF arms, respectively (p=0.29). Late grade ≥2 GI (p=0.07) and GU (p=0.25) toxicity was not significantly different between arms, however, late grade ≥3 GI toxicity was worse in the MH group (p=0.01). There were no statistically significant quality of life differences between the two treatments. There were no statistically significant differences observed in cumulative incidence of biochemical failure (p=0.71) or distant metastasis (p=0.31), and overall survival (p=0.46). MH to the prostate and pelvis with ADT for men with high-risk localized prostate cancer was not significantly different than CF with regards to acute toxicity, quality of life and oncologic efficacy. However, late grade ≥3 late GI toxicity was more common in the MH arm.

Sections du résumé

BACKGROUND BACKGROUND
To report on the results of a phase II randomized trial of moderately hypofractionated (MH) versus conventionally fractionated (CF) radiotherapy to the prostate with elective nodal irradiation (ENI).
MATERIALS AND METHODS METHODS
This was a single-centre prospective phase II randomized study. Patients with high-risk disease (cT3, PSA >20 ng/mL, or Gleason score 8-10) were eligible. Patients were randomized to either MH using a simultaneous integrated boost (68 Gy in 25 fractions to prostate; 48 Gy to pelvis) or CF (46 Gy in 23 fractions with a sequential boost to the prostate of 32 Gy in 16 fractions), with long-term androgen deprivation therapy (ADT). The primary endpoint was grade ≥2 acute gastrointestinal (GI) and genitourinary (GU) toxicity (CTCAE v3.0). Secondary endpoints included late GI and GU toxicity, quality of life, and oncologic outcomes.
RESULTS RESULTS
180 patients enrolled: 90 were randomized to and received MH and 90 to CF. Median follow-up was 67.4 months. Seventy-five (41.7%) patients experienced a grade ≥2 acute GI and/or GU toxicity, including 34 (37.8%) in the MH and 41 (45.6%) in the CF arms, respectively (p=0.29). Late grade ≥2 GI (p=0.07) and GU (p=0.25) toxicity was not significantly different between arms, however, late grade ≥3 GI toxicity was worse in the MH group (p=0.01). There were no statistically significant quality of life differences between the two treatments. There were no statistically significant differences observed in cumulative incidence of biochemical failure (p=0.71) or distant metastasis (p=0.31), and overall survival (p=0.46).
CONCLUSION CONCLUSIONS
MH to the prostate and pelvis with ADT for men with high-risk localized prostate cancer was not significantly different than CF with regards to acute toxicity, quality of life and oncologic efficacy. However, late grade ≥3 late GI toxicity was more common in the MH arm.

Identifiants

pubmed: 37979707
pii: S0360-3016(23)08131-2
doi: 10.1016/j.ijrobp.2023.11.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Auteurs

Rachel M Glicksman (RM)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.

Andrew Loblaw (A)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Gerard Morton (G)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Danny Vesprini (D)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Ewa Szumacher (E)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Hans T Chung (HT)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

William Chu (W)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Stanley K Liu (SK)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Chia-Lin Tseng (CL)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Rohann Correa (R)

London Health Sciences Centre, London, Canada.

Andrea Deabreu (A)

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Alexandre Mamedov (A)

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Liying Zhang (L)

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.

Patrick Cheung (P)

Department of Radiation Oncology, University of Toronto, Toronto, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada. Electronic address: patrick.cheung@sunnybrook.ca.

Classifications MeSH