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

L

Laval University

Status

Enrolling

Conditions

Radiotherapy Side Effect
Node; Prostate
Prostate Cancer

Treatments

Radiation: Report and compare changes in a non-inferiority analysis of the Sexual Health Inventory for Men (SHIM)
Radiation: Report and compare the overall survival (OS)
Radiation: Report and compare changes in a non-inferiority analysis of the International Prostate Symptom Score (I-PSS)
Radiation: Report and compare changes in a non-inferiority analysis of the expanded prostate cancer index composite" (EPIC-26):
Radiation: Report and compare the biochemical disease free survival (bDFS)
Radiation: Report and compare the metastase free survival (MFS)
Radiation: Report and compare the disease free survival (DFS)
Radiation: Report and compare changes in a non-inferiority analysis of the toxicities reported according to the Common Terminology Criteria for Adverse Events (CTCAE)

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT05820633
MP-20-2023-6396: PCS XI

Details and patient eligibility

About

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.

Full 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.

Enrollment

500 estimated patients

Sex

Male

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

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 NCCN guidelines.
  • Having the ability to give free and informed consent.

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

500 participants in 2 patient groups

ultra hypo fractionation radiation therapy (UHF)
Experimental group
Description:
5 radiation treatments (5 Gy per fraction) to the prostate, seminal vesicle and pelvic nodes given every other day over 2 weeks for a total of 25 Gy.
Treatment:
Radiation: Report and compare the metastase free survival (MFS)
Radiation: Report and compare the overall survival (OS)
Radiation: Report and compare the biochemical disease free survival (bDFS)
Radiation: Report and compare changes in a non-inferiority analysis of the toxicities reported according to the Common Terminology Criteria for Adverse Events (CTCAE)
Radiation: Report and compare changes in a non-inferiority analysis of the International Prostate Symptom Score (I-PSS)
Radiation: Report and compare changes in a non-inferiority analysis of the Sexual Health Inventory for Men (SHIM)
Radiation: Report and compare the disease free survival (DFS)
Radiation: Report and compare changes in a non-inferiority analysis of the expanded prostate cancer index composite" (EPIC-26):
standard of care fractionation (SOC)
Active Comparator group
Description:
20-25 radiation treatments (range: 1,8 to 2,15 Gy per fraction) to the prostate, seminal vesicle and pelvic nodes given in 20-25 working day treatments over 4-5 weeks for a total of 43 Gy to 46 Gy.
Treatment:
Radiation: Report and compare the metastase free survival (MFS)
Radiation: Report and compare the overall survival (OS)
Radiation: Report and compare the biochemical disease free survival (bDFS)
Radiation: Report and compare changes in a non-inferiority analysis of the toxicities reported according to the Common Terminology Criteria for Adverse Events (CTCAE)
Radiation: Report and compare changes in a non-inferiority analysis of the International Prostate Symptom Score (I-PSS)
Radiation: Report and compare changes in a non-inferiority analysis of the Sexual Health Inventory for Men (SHIM)
Radiation: Report and compare the disease free survival (DFS)
Radiation: Report and compare changes in a non-inferiority analysis of the expanded prostate cancer index composite" (EPIC-26):

Trial contacts and locations

11

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Central trial contact

Andre-Guy Martin, MD MSc FRCPC; Josee Allard

Data sourced from clinicaltrials.gov

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