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Completed

NCT Number: NCT07489729

Hypo Fractionated Versus Conventional IMRT in Unfavorable Intermediate- and High-Risk Prostate Cancer

The aim of the study is

1. Statistical evaluation of patients' characteristics who have intermediate & high risk localized prostate cancer. 2. Statistical analysis of treatment efficacy of combined hormonal therapy & hypo fractionated intensity modulated radiotherapy compared with conventionally fractionated radiotherapy plus hormonal treatment as regard biochemical failure, disease free survival & overall survival. 3. Evaluation of acute as well as late toxic side effects after radiotherapy.

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Key information

Age range

50 year–80 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Tanta University

Tanta, Egypt

About this study

The incidence rate of prostate cancer is rapidly increasing, and it has become the most prevalent solid tumor diagnosed in men.

In most cases the prostate cancer is organ-confined at the time of initial diagnosis . Radical prostatectomy and radiotherapy, either given as a seed implant or external beam radiation therapy, are the accepted standard options for treating the primary tumor itself, and androgen deprivation may be added selectively for certain cases with an intermediate or high risk of dissemination based on clinical and pathologic features evident at the time of diagnosis.

Regarding the specific option of external beam radiotherapy, the current widely accepted standard regimen for organ-confined prostate cancer involves approximately eight weeks of fractionated treatments with a daily dose of 1.8-2.0 Gy to a total dose in the range of 70-80 Gy .

Over the last decade, there have been three major advances in the use of external RT for the management of clinically localized prostate cancer: (a) androgen deprivation therapy ; (b) image-guided ration therapy with three-dimensional conformal radiotherapy and intensity modulated radiotherapy , and particularly c) radiation dose escalation schedules compared with conventional 70-80 Gy (2 Gy per fraction), which has been shown to improve biochemical and distant metastases control with minimum toxicity, but not overall survival .

The rapid dose gradients, which are able to be generated with Intensity Modulated Radiation Therapy have been demonstrated to reduce OAR dose relative to three-dimensional conformal radiotherapy resulting in well-established reductions in toxicity in the conventionally fractionated, dose escalated prostate cancer radiotherapy setting .

The use of conventional fractionated radiation therapy with a single 1.8-2 Gy fraction/day is related to more radiation therapy sessions and longer treatments; therefore, influencing the decision-making and patient non-adherence, since longer treatments can affect their financial situation (by not being able to work during radiotherapy) or cause a disruption in their daily life .

Hypofractionated Radiation Therapy and conventional fractionated radiation therapy schedules have been shown to be isoeffective in terms of incidence of biochemical control or late complications in several phase III trials .

The aim of the study is

  • Statistical evaluation of patients' characteristics who have intermediate & high risk localized prostate cancer.
  • Statistical analysis of treatment efficacy of combined hormonal therapy & hypo fractionated intensity modulated radiotherapy compared with conventionally fractionated radiotherapy plus hormonal treatment as regard biochemical failure, disease free survival & overall survival.
  • Evaluation of acute as well as late toxic side effects after radiotherapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Biopsy proven prostate adenocarcinoma
  • Patient has been classified as intermediate or high risk according to the National Comprehensive Cancer Network v2018 .
  • Clinically localized stage (cT2-T3b N0M0, using the AJCC 8th TNM classification) .
  • Eastern Cooperative Oncology Group performance status ranged from 0-1 . - Mean age was 65 years (range: 50-80 years).
  • a prostate-specific antigen test at the time of diagnosis ≥10 ng/ml.
  • Gleason scores range from 7 to 10.
  • The patient must not receive any cytotoxic anticancer therapy for prostate cancer prior to randomization.
  • Adequate hematological, hepatic, renal function tests

Exclusion criteria

  • Patients with a history of other malignancies, except: non-melanoma skin cancer.
  • Patients with any contraindication to pelvic radiotherapy: including, previous pelvic radiotherapy, inflammatory bowel disease or severe bladder irritability.
  • Patients who had prior surgical treatment for carcinoma of the prostate apart from trans-urethral resection,
  • Nodal or distant metastasis proven by a computed tomography pelvis or bone scan,
  • Co-morbidities as Congestive heart failure, recent myocardial infarction.

Treatment and study plan

Hypofractionated Intensity-Modulated Radiation Therapy

Radiation

Moderately hypofractionated schedule include 60 Gy in 20fx (3 Gy/fx) over 4 weeks (5 fractions/week).

The prostate will be prescribed 60 Gy in 20 fx (3 Gy/fx). Proximal seminal vesicles will be prescribed 48-50 Gy in 2.4-2.5 Gy/fx, Entire seminal vesicles will be prescribed full dose (60 Gy) in case of evidence of seminal vesicle invasion on multi parametric MRI.

If treating the elective pelvic LNs (risk of involvement >20% according to roach formula), prescribed dose will be 44 Gy in 2.2 Gy/fx.

A simultaneous integrated boost technique will be utilized with moderate hypo fractionation).

Conventional Intensity-Modulated Radiation Therapy

Radiation

Conventional fractionation of 76 Gy in 38 fractions (5 fractions/week) at 2.0 Gy/fraction over 8 weeks.

The prostate will be prescribed 76 Gy in 38 fractions (2 Gy/fx). Proximal seminal vesicles will be prescribed 54-66Gy (2Gy/fx), paying attention to bowel toxicity.

Entire seminal vesicle will be prescribed full dose (76 Gy) in case of evident seminal vesicle invasion on MRI.

If treating elective pelvic lymph nodes (risk of involvement >20% according to roach formula), prescribed dose will be 45-50 Gy.

Primary outcomes

  1. Tumor response

    Time frame: Three monthly the first year after radiation, 4 months the second and third year.

    Evaluation of tumor response will be performed by digital rectal examination, prostate-specific antigen, testosterone levels and Magnetic resonance imaging abdomen & pelvis with contrast 3-monthly the first year after radiation therapy, 4-monthly the second and third year.

Secondary outcomes

  1. Overall survival

    Time frame: 3 years

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Official study title

Hypo Fractionated Versus Conventional IMRT in Unfavorable Intermediate- and High-Risk Prostate Cancer: A Phase II Comparative Study of PSA Kinetics and Dosimetric Outcomes

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Mar 24, 2026
Registry last updated
Mar 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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