Pelvic Nodes Ultra-Hypo vs Conventionally Fractionated IMRT With HDR Boost in Prostate Cancer.

Last updated: September 7, 2025
Sponsor: CHU de Quebec-Universite Laval
Overall Status: Suspended

Phase

N/A

Condition

Urologic Cancer

Prostate Cancer, Early, Recurrent

Prostate Cancer

Treatment

Report and compare changes in a non-inferiority analysis of the toxicities reported according to the Common Terminology Criteria for Adverse Events (CTCAE)

Report and compare the biochemical disease free survival (bDFS)

Report and compare the overall survival (OS)

Clinical Study ID

NCT05820633
MP-20-2023-6396: PCS XI
  • Ages 18-95
  • Male

Study Summary

Randomized Phase III study, comparing pelvic ultra-hypo fractionated radiotherapy (UHF: 5Gy/fraction) to a standard or moderate hypo-fractionation (1.8-2.15Gy/fraction), both associated to an HDR prostate +/- adjacent seminal vesicles brachytherapy boost (HDR-BT)+ ADT according to NCCN guidelines. Considering that the calculated bio-equivalent doses to the tumor are similar for all treatment options, the UHF technique is deemed to be non-inferior to the standard approach. Treatment acceptability, tolerance and adverse events will be reported and compared for non-inferiority as the primary objective. Secondary objectives are biochemical control, metastasis-free, disease specific and overall survival.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Histopathologically confirmed adenocarcinoma of the prostate.

  • All clinical stages with lymph node involvement risk needing pelvis RT.

  • Stage Mx or M0.

  • Unfavorable Intermediate, high or very high-risk disease according to NCCNguidelines.

  • Having the ability to give free and informed consent.

Exclusion

Exclusion Criteria:

  • Clinical stage M1.

  • IPSS Score > 20 with alpha-blocking medication.

  • Prior pelvic radiotherapy,

  • History of active collagenosis (Lupus, Scleroderma, Dermatomyositis).

  • Past history of Inflammatory Bowell Disease.

  • Bilateral hip prosthesis.

Study Design

Total Participants: 500
Treatment Group(s): 8
Primary Treatment: Report and compare changes in a non-inferiority analysis of the toxicities reported according to the Common Terminology Criteria for Adverse Events (CTCAE)
Phase:
Study Start date:
September 01, 2022
Estimated Completion Date:
December 31, 2035

Study Description

Prostate cancer is the most common non-skin cancer in North American men. In 2020, an estimated 23 300 Canadian men will be diagnosed with prostate cancer of which, 4200 will die. Fortunately, with an early screening, most will have a localized disease at diagnosis. Despite this, high risk disease affects a growing portion of the population and this according to age (29.3%, 39.1%, 60.4%, et 90.6% respectively at 55-59, 65-69, 75-79, & 85-89 years of age). Gleason score 8 to 10 tumors follow the same pattern (16.5%, 23.4%, 37.2%, and 59.9% at respective ages). Those patients are at risk for harboring lymph nodes metastasis.

Multiple therapeutic options, with similar biochemical disease-free survival (bDFS) are available: surgery +/- salvage radiotherapy +/- androgen deprivation therapy (ADT) or radiotherapy (RT) +/- HDR-BT +/- ADT. For men with high-risk disease, the combined approach of RT + HDR-BT + ADT might even offer higher cancer specific survival (CSS) rates when compared to surgery.

HDR-BT allows for the delivery of a very high (ablative) dose of radiation while giving a lower dose to the nearby organs at risk (OARs). Recently published literature showed that pelvic RT plus HDR-BT significantly increased bDFS (84 vs 77%).

Pelvic RT is generally given on a daily basis (5 days/week) over a period of 4-5 weeks, with 1,8-2,15Gy per fraction. This requires a substantial time investment from patients undergoing treatment. Many studies have shown that prostate cancer offers a radiation cell kill ratio (α/β) of 0.9-1.5 Gy. Furthermore, the most commonly used α/β value for prostate cancer is 1,5 Gy (range 0,8 - 2,2). This low α/β ratio offers a more efficient cell kill with hypo-fractionated doses, offering a better tumor control with a lower cumulative dose, given in a shorter time span. Recently, a multicentric randomized phase III study has shown similar late toxicity and oncologic control outcomes between UHF (>/= 5 Gy/fraction) and conventionally fractionated RT. However, until now, no phase III study has compared combined UHF pelvic RT to standard fractionation combined with an HDR-BT in this population.

The proposed experimental fractionation scheme for whole pelvic RT in this study will be 5Gy administered every other day over 2 weeks (UHF). It will be compared to standard pelvic RT (1.8-2.15Gy/working day) given over 4 to 5 weeks. Both will be combined with a single 15 Gy fraction of HDR-BT and ADT (goserelin). The UHF treatment modality significantly reduces the overall treatment time, freeing machine-time and allowing more patients to be treated. Given its low α/β ratio, prostate cancer is readily amenable to UHF fractionation. The bio-equivalent dose calculations were done based on published litterature. Neo-adjuvant and adjuvant ADT (goserelin) will be administered for a duration according to NCCN guidelines.

In these COVID-19 pandemic times, a reduction in the number of patients' visits to the clinic is highly desirable in order to limit the risk of virus transmission. UHF would also lower the socio-economic burden incurred by the patients and their families. It also increases the therapeutic efficiency reducing costs for both, patients and health services. The proposed study aims to demonstrate the non-inferiority of UHF treatment compared to standard of care. If this hypothesis is confirmed, all future patients could benefit from it.

In order to improve the quality of life of men diagnosed with prostate cancer this study aim to demonstrate that combined UHF pelvic RT plus HDR-BT (+ ADT according to NCCN guidelines) is safe and non-inferior to standard fractionation regimens in regard to toxicities and tumor control for prostate cancer patients with risk of nodal involvement. Therefore, 500 men will be recruited, in order to confirm the hypothesis.

Connect with a study center

  • BC Cancer Sindi Ahluwalia centre for the Southern Interior

    Kelowna, British Columbia V1Y 5L3
    Canada

    Site Not Available

  • BC Cancer Sindi Ahluwalia centre for the Southern Interior

    Kelowna 5990579, British Columbia 5909050 V1Y 5L3
    Canada

    Site Not Available

  • Carlo Fidani Peel Regional Cancer Centre

    Mississauga, Ontario L5M 2N1
    Canada

    Site Not Available

  • Lakeridge Health Oshawa Cancer centre

    Oshawa, Ontario L1G 2B9
    Canada

    Site Not Available

  • Carlo Fidani Peel Regional Cancer Centre

    Mississauga 6075357, Ontario 6093943 L5M 2N1
    Canada

    Site Not Available

  • Lakeridge Health Oshawa Cancer centre

    Oshawa 6094578, Ontario 6093943 L1G 2B9
    Canada

    Site Not Available

  • CISSS de l'Outaouais, Hôpital de Gatineau

    Gatineau, Quebec J8P 7H2
    Canada

    Site Not Available

  • CISSS de Laval, Hôpital de la Cité-de-la-Santé

    Laval, Quebec H7M 3L9
    Canada

    Site Not Available

  • CISSS de la Montérégie-Centre, Hôpital Charles-Le Moyne

    Longueuil, Quebec J4V 2H1
    Canada

    Site Not Available

  • CIUSSS du Centre-Ouest-de-l'Île-de-Montréal, Jewish General Hospital

    Montréal, Quebec H3T 1E2
    Canada

    Active - Recruiting

  • Cedars Cancer Centre, McGill University Health Centre (MUHC)

    Montréal, Quebec H4A 3J1
    Canada

    Site Not Available

  • CIUSSS de l'Est-de-l'Île-de-Montréal, Hôpital Maisonneuve-Rosemont

    Montréal-Est, Quebec H1T 2M4
    Canada

    Site Not Available

  • CIUSSS de l'Estrie - Centre Hospitalier Universitaire de Sherbrooke (CHUS)

    Sherbrooke, Quebec
    Canada

    Site Not Available

  • CISSS de l'Outaouais, Hôpital de Gatineau

    Gatineau 5959974, Quebec 6115047 J8P 7H2
    Canada

    Site Not Available

  • CISSS de Laval, Hôpital de la Cité-de-la-Santé

    Laval 6050610, Quebec 6115047 H7M 3L9
    Canada

    Site Not Available

  • CISSS de la Montérégie-Centre, Hôpital Charles-Le Moyne

    Longueuil 6059891, Quebec 6115047 J4V 2H1
    Canada

    Site Not Available

  • CIUSSS du Centre-Ouest-de-l'Île-de-Montréal, Jewish General Hospital

    Montreal 6077243, Quebec 6115047 H3T 1E2
    Canada

    Site Not Available

  • Cedars Cancer Centre, McGill University Health Centre (MUHC)

    Montreal 6077243, Quebec 6115047 H4A 3J1
    Canada

    Site Not Available

  • CIUSSS de l'Est-de-l'Île-de-Montréal, Hôpital Maisonneuve-Rosemont

    Montreal East 6077251, Quebec 6115047 H1T 2M4
    Canada

    Site Not Available

  • CIUSSS de l'Estrie - Centre Hospitalier Universitaire de Sherbrooke (CHUS)

    Sherbrooke 6146143, Quebec 6115047
    Canada

    Site Not Available

  • CHU de Québec - Université Laval

    Quebec, G1R 2J6
    Canada

    Site Not Available

  • CHUdeQuebec

    Quebec, G1R 2J6
    Canada

    Active - Recruiting

  • CHU de Québec - Université Laval

    Québec 6325494, G1R 2J6
    Canada

    Site Not Available

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