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NCT Number: NCT02946008

Neoadjuvant Stereotactic Body Radiotherapy Prior to Radical Prostatectomy for High Risk Prostate Cancer

This is a single-arm prospective non-randomized, non-blinded trial to assess the safety of neoadjuvant stereotactic body radiation therapy (SBRT) before surgery in high risk prostate cancer patients.

Radiation therapy will be delivered over 5 treatment sessions for approximately 1.5 weeks total.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

The University of Michigan Comprehensive Cancer Center

Ann Arbor, Michigan, 48109, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subjects must have biopsy-confirmed adenocarcinoma of the prostate.
  • Subjects must have a negative bone scan.
  • Subjects must have one of the following risk factors:
  • PSA ≥20 and/or
  • Gleason score ≥8 and/or
  • Clinical or radiographic stage ≥T3a per AJCC (American Joint Committee on Cancer) 7th Edition Staging Manual and/or
  • Radiographic pelvic lymph node positive disease and/or
  • At least two out of four of the following: PSA (Prostate Specific Antigen) 10-19.9, GS (Gleason Score) = 3+4, clinical stage = T2b/T2c, ≥50% positive biopsy cores.
  • Subjects must freely sign informed consent to enroll in the study.
  • Subjects must be medically fit to undergo surgery determined by the PI.
  • Age ≥ 18
  • KPS Karnofsky Performance Status (performance status is an attempt to quantify cancer patients' general well-being and activities of daily life, scores range from 0 to 100 where 100 represents perfect health and 0 represents death): ≥70.
  • No prior invasive malignancy in the past 3-years, except non-melanomatous skin cancer unless disease free for a minimum of 2 years. Carcinoma in-situ of the bladder or head and neck region is permissible.
  • Subjects must not have had prior pelvic radiation therapy,
  • Subjects must not have had prior androgen deprivation therapy in the past 6 months.

Exclusion criteria

  • Metastatic disease as demonstrated by bone scan, CT scan or MRI (Magnetic Resonance Imaging) of the pelvis, or chest x-ray.
  • Declared high-risk for anesthesia by attending anesthesiologist, cardiologist, or other physician.
  • History of prior pelvic radiation therapy.
  • History of androgen deprivation therapy within the past 6 months.

Treatment and study plan

Stereotactic Body Radiation Therapy

Radiation

Delivered over 5 treatment sessions for approximately 1.5 weeks total.

radical prostatectomy

Procedure

Open, laparoscopic, or robotic radical prostatectomy and pelvic lymph node dissection to remove the prostate, seminal vesicles, and pelvic lymph nodes.

Primary outcomes

  1. Maximum Tolerated Dose (MTD) of Neoadjuvant SBRT

    Time frame: 6-week post-prostatectomy

    The MTD is defined as the SBRT dose that with radical prostatectomy induces dose-limiting toxicity in 28% of subjects or less.

Secondary outcomes

  1. Incidence of Urinary Incontinence

    Time frame: up to one year post treatment

    Urinary incontinence will be scored according to Common Toxicity Criteria for Adverse Events (CTCAE) v.4.0 (Grade 1 = Occasional, Grade 2 = Spontaneous, pads indicated, Grade 3 = Intervention indicated)

  2. Incidence of Urinary Stricture

    Time frame: up to one year post treatment

    Urinary stricture, according to Common Toxicity Criteria for Adverse Events (CTCAE) v.4.0 (Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = life threatening, Grade 5 = death.)

  3. Incidence of Urinary Bother

    Time frame: up to one year post treatment

    Urinary bother, according to Common Toxicity Criteria for Adverse Events (CTCAE) v.4.0 (Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = life threatening, Grade 5 = death.)

  4. Rectal Toxicity

    Time frame: up to one year post treatment

    Rectal Toxicity, according to Common Toxicity Criteria for Adverse Events (CTCAE) v.4.0 (Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = life threatening, Grade 5 = death.)

  5. Number of Patients with Positive Surgical Margins

    Time frame: 4-10 weeks post radiation therapy

    Surgical specimens will be evaluated by the study pathologist to determine rate of margin positivity.

  6. Number of Patients with Extracapsular Extension

    Time frame: 4-10 weeks post radiation therapy

    Surgical specimens will be evaluated by the study pathologist to determine rate of extracapsular extension.

Sponsors and collaborators

Lead sponsor

University of Michigan Rogel Cancer Center

Other

Registry information

Official study title

A Phase I Trial of Neoadjuvant Stereotactic Body Radiotherapy Prior to Radical Prostatectomy for High Risk Prostate Cancer

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
Oct 26, 2016
Registry last updated
Nov 27, 2019

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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