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MRI-based Focal Intraprostatic Simultaneous Integrated Boost (SIB) Intensification With De-escalated Adaptive-risk SBRT for Patients With Low to Intermediate Risk Prostate Cancer (MIDAS)

19 août 2026 mis à jour par: Georgetown University

A Phase II Study of MRI-based Focal Intraprostatic SIB (Simultaneous Integrated Boost) Intensification With De-escalated Adaptive-risk SBRT for Patients With Low to Intermediate Risk Prostate Cancer

The goal of this clinical trial is to determine the safety of stereotactic body radiation therapy (SBRT) microboost technique in patients with low to intermediate risk prostate cancer. The main question it aims to answer is: Is microboost SBRT with whole gland de-escalation both safe and effective in managing patients with low to intermediate-risk prostate cancer while maintaining acceptable toxicity levels? All patients will receive microboost SBRT at a dose of 45 Gy delivered in 5 fractions in up to 4 MRI-defined lesions. Patients (Arm 1) with highest grade disease in the microboost target lesion in the absence of GG2-3 beyond the microboost target (only GG1 disease can be present outside of the microboost region) will receive whole gland de-escalation at a dose of 30 Gy delivered in 5 fractions. Patients (Arm 2) with highest grade disease outside of the target lesion will receive whole gland de-escalation at a dose of 35 Gy delivered in 5 fractions. Participants will be treated every other day over a two week period and then follow up after radiation treament for up to 5 years. Participants will be asked to complete questionnaires and provide blood and urine samples for research purposes.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

58

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • District of Columbia
      • Washington D.C., District of Columbia, États-Unis, 20007
        • Recrutement
        • Lombardi Comprehensive Cancer Center, Georgetown University
        • Chercheur principal:
          • Jonathan Lischalk, MD
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  1. Patients age 18 or older.
  2. Patients with an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
  3. Patients with histologically confirmed adenocarcinoma of the prostate who have not received prior pelvic radiation therapy or prostatectomy.
  4. Patients with low to intermediate risk group defined by the NCCN (National Comprehensive Cancer Network) guidelines as follows:

    • Low risk prostate cancer:

      • cT1-cT2a (AJCC; 8TH edition, 2017)
      • Grade Group 1 (GG1)
      • PSA <10 ng/mL
    • Intermediate risk prostate cancer:

      • cT2b-cT2c (AJCC; 8TH edition, 2017)
      • Grade Group 2 (GG2) or Grade Group 3 (GG3)
      • PSA 10-20 ng/mL
  5. Patients with unfavorable intermediate risk prostate cancer defined by the NCCN guidelines are recommended to undergo a PSMA (Prostate-Specific Membrane Antigen) PET, then the PSMA PET must show localized disease.
  6. Patients must have preferably undergone a standard of care pretreatment MRI fusion biopsy* to identify visible intraprostatic lesions and confirm the absence of regional or distant metastatic disease, with criteria as follows:

    • Ability to undergo an MRI fusion biopsy;
    • Prostate size <100 cc on any diagnostic MRI;
    • Presence of a visible prostatic lesion:

      • PIRADS (Prostate Imaging-Reporting and Data System) 4+ lesion, and/or
      • PIRADS 3 lesion with evidence of grade group 2-3
    • Less than or equal to 4 lesions in total allowed;
    • Lesion may contact the capsular edge, "possible" extracapsular extension (ECE) permitted; *MRI fusion biopsy is preferred but if the positive core is in the same region as the target on the MRI based on a systemic biopsy, the patient can be included.
  7. Genitourinary function with a baseline score ≤20 as defined by any pre-treatment IPSS questionnaire.
  8. Patients are mandated to get a fiducial placement. Optional proper rectal spacer placement is recommended as determined by the treating radiation oncologist based upon whether there is overt rectal wall invasion from the hydrogel spacer or if there is minimal to no separation of the prostate-rectal interface measured at the prostate mid-gland.
  9. Patients with a life expectancy of greater than 5 years as assessment by the investigator. Life expectancy can be estimated using any 1 of the following tools:

    • The Social Security Administration tables: https://www.ssa.gov/OACT/STATS/table4c6.html
    • The WHO's Life Tables by country: https://apps.who.int/gho/data/view.main.60000?lang=en
    • The Memorial Sloan Kettering Male Life Expectancy tool: https://www.mskcc.org/nomograms/prostate
    • If using a life expectancy table, life expectancy should be adjusted using the clinician's assessment of overall health as follows: best quartile of health - add 50%; worst quartile of health - subtract 50%; and middle two quartiles of health - no adjustment. See the NCCN Prostate Cancer Guidelines for more information.
  10. Patients who agree to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures, and agree to refrain from donating sperm, as defined below:

    • With a female partner of childbearing potential who is not pregnant, men who are not surgically sterile must remain abstinent or use a condom plus an additional contraceptive method, which together result in a failure rate of < 1% per year, during the treatment period and for 1 year after treatment per local and institutional guidelines. Men must refrain from donating sperm during this same period.
    • With a pregnant female partner, men must remain abstinent or use a condom during the treatment period per local and institutional guidelines to avoid potential exposure to the embryo.
    • The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or post-ovulation methods) and withdrawal are not adequate methods of contraception.
  11. Patients who are able to give informed consent.

Exclusion Criteria:

  1. Patients with evidence of disease Grade Group 4 (GG4) or higher.
  2. Patients with PSA >20 ng/mL.
  3. Patients with evidence of clinical stage T3a+ or gross extracapsular extension on the diagnostic MRI.
  4. Patients who received prior or concurrent androgen deprivation therapy for prostate cancer.
  5. Patients with more than 4 disease foci identifiable on MRI.
  6. Patients with evidence of metastatic disease on imaging (e.g., bone scan, PSMA PET scan, or MRI/CT scan).
  7. Patients with ineligibility to undergo an MRI due to:

    • The presence of a cardiac pacemaker, defibrillator, or other implanted metallic or electronic device which is considered MRI unsafe;
    • Severe claustrophobia;
    • Inability to lie flat for the duration of the study;
    • Metallic implant or device in the pelvis that might distort the local magnetic field and compromise quality of MRI;
    • Any other reason as determined by the investigator or treating physician.
  8. Patients with an I-PSS score >20 as defined by any pre-treatment IPSS questionnaire.
  9. Patients with a prior history of transurethral resection of the prostate, TURP, Urolift, or other similar trans-urethral LUTS management procedure within the last 6 months.
  10. Patients with a prior history of severe urethral stricture.
  11. Patients with a prior history of pelvic irradiation.
  12. Patients unable to meet dosimetric constraints
  13. Patients with a prior history of non-cutaneous solid malignancy within the last 5 years.
  14. Patients with a history of active and uncontrolled inflammatory bowel disease.
  15. Patients who are unable to comply with follow-up visits and treatment plans.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Arm 1- Low Risk
Patients enrolled to arm 1 will have low risk prostate cancer without Grade Group 2-3 (GG2-3) outside of the microboost target(s). Patients in arm 1 will receive microboost SBRT at a dose of 45 Gy delivered in 5 fractions in up to 4 MRI-defined lesions plus whole gland de-escalation at a dose of 30 Gy delivered in 5 fractions.
Microboost SBRT at a dose of 45 Gy for 5 fractions
Whole gland de-escalation at a dose of 30 Gy delivered in 5 fractions.
Expérimental: Arm 2- Intermidiate Risk
Patients enrolled to arm 2 will have intermidiate risk prostate cancer with grade group 2-3 disease outside of the microboost target(s). Patients in arm 2 will receive microboost SBRT at a dose of 45 Gy delivered in 5 fractions in up to 4 MRI-defined lesions plus whole gland de-escalation at a dose of 35 Gy delivered in 5 fractions.
Microboost SBRT at a dose of 45 Gy for 5 fractions
Whole gland de-escalation at a dose of 35 Gy delivered in 5 fractions

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Incidence of acute grade 2 or higher genitourinary toxicity
Délai: during treatment through 90 days after radiation treatment
Safety of the microboost technique will be determined based on the incidence of acute grade 2 or higher genitourinary adverse events (AEs). AEs will be assessed and graded according to the current version of the Common Terminology Criteria for Adverse Events (CTCAE) or severity grade when CTCAE grading does not exist. Grade 1 to 5 will be used to characterize the severity of the AE. If CTCAE grading does not exist for an AE, the severity of mild, moderate, severe, life-threatening and death due to the AE, corresponding respectively to Grades 1 - 5, will be used.
during treatment through 90 days after radiation treatment

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Incidence of acute grade 2 or higher gastrointestinal (GI) toxicity
Délai: Up to 5 years
The incidence of acute grade 2 or higher gastrointestinal AEs will be assessed and graded according to the current version of the Common Terminology Criteria for Adverse Events (CTCAE) or severity grade when CTCAE grading does not exist. Grade 1 to 5 will be used to characterize the severity of the AE. If CTCAE grading does not exist for an AE, the severity of mild, moderate, severe, life-threatening and death due to the AE, corresponding respectively to Grades 1 - 5, will be used.
Up to 5 years
Incidence of late grade 2 or higher genitourinary (GU) or gastrointestinal (GI) toxicity
Délai: Up to 5 years
The incidence of late grade 2 or higher genitourinary or gastrointestinal AEs will be assessed and graded according to the current version of the Common Terminology Criteria for Adverse Events (CTCAE) or severity grade when CTCAE grading does not exist. Grade 1 to 5 will be used to characterize the severity of the AE. If CTCAE grading does not exist for an AE, the severity of mild, moderate, severe, life-threatening and death due to the AE, corresponding respectively to Grades 1 - 5, will be used.
Up to 5 years
Incidence of late grade 3 or higher genitourinary or gastrointestinal toxicity
Délai: Up to 5 years
The cumulative incidence of late grade 3 or higher genitourinary or gastrointestinal AEs will be assessed and graded according to the current version of the Common Terminology Criteria for Adverse Events (CTCAE) or severity grade when CTCAE grading does not exist. Grade 1 to 5 will be used to characterize the severity of the AE. If CTCAE grading does not exist for an AE, the severity of mild, moderate, severe, life-threatening and death due to the AE, corresponding respectively to Grades 1 - 5, will be used
Up to 5 years
PSA (Prostate-specific antigen) nadir
Délai: at 2 years and 5 years
PSA nadir is defined as the lowest PSA achieved at the time of follow up as determined by the treating physician. The PSA nadir will be determined by denoting the lowest value by 2- and 5-years of follow up.
at 2 years and 5 years
Biochemical failure (BF)
Délai: at 2 years and 5 years
Biochemical failure is defined as a PSA rise of at least 2.0 n/g/mL above the patient's PSA nadir following radiation treatment by the Phoenix definition and as determined by the treating physician.
at 2 years and 5 years
Biochemical failure free survival (BFFS)
Délai: up to 5 years
Biochemical failure free survival (BFFS) is defined as the length of time from radiation completion to the first documented evidence of biochemical failure of prostate cancer or death, whichever occurs first. Patients who are alive and free from biochemical failure will be censored at the date of last follow-up for BFFS.
up to 5 years
Disease-free survival (DFS)
Délai: up to 5 years
Defined as the length of time from radiation completion to the first evidence of biochemical or clinical recurrence of prostate cancer or death, whichever occurs first. Patients who are alive and free from disease recurrence will be censored at the date of last follow-up for DFS.
up to 5 years
Patient-reported QoL (Quality of life) outcomes- Expanded Prostate Index Composite (EPIC)-26
Délai: up to 5 years

Patient-reported QoL as measured by EPIC-26 questionnaire which measures health related quality of life. Scores range from 0 to 100 with higher scores indicating a better quality of life.

The EPIC-26 instrument includes sub-scales like urinary function, bowel habits, and sexual function, which will be used to measure the changes in the GU (Genitourinary), GI (gastrointestinal), and sexual domains, respectively.

up to 5 years
Patient-reported QoL outcomes- International Prostate Symptom Score (I-PSS)
Délai: up to 5 years
The I-PSS is based on the answers to 7 questions concerning Urinary symptoms. Scores range from 0 to 35, with 0 being asymptomatic to 35 being very symptomatic.
up to 5 years
Patient-reported QoL outcomes- International Index of Erectile Dysfunction (IIEF-5)
Délai: up to 5 years
The IIEF-5 is a 5 question questionnaire which evaluates erectile dysfunction. Scores range from 5 to 25, 5-7 being severe erectile dysfunction and 22-25 being no erectile dysfunction.
up to 5 years
Patient-reported QoL outcomes- Health Questionnaire (EQ-5D-5L)
Délai: up to 5 years
EQ-5D-5L questionnaire will have participants evaluate their quality of life across 5 Dimensions including Mobility, Self-care, Usual activities, Pain/discomfort, Anxiety/depression. Index scores range from -0.59 to 1, where 1 is the best possible health state.
up to 5 years

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 septembre 2026

Achèvement primaire (Estimé)

1 janvier 2028

Achèvement de l'étude (Estimé)

1 janvier 2035

Dates d'inscription aux études

Première soumission

28 mai 2026

Première soumission répondant aux critères de contrôle qualité

8 juin 2026

Première publication (Réel)

12 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

20 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

19 août 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

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Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

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Étudie un produit d'appareil réglementé par la FDA américaine

Oui

produit fabriqué et exporté des États-Unis.

Non

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