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ADT De-escalation in Selected High-Risk Prostate Cancer Patients (ADaPPt Trial) a GROUQ Led PCS Study (PCS XIV)

18. august 2026 oppdatert av: Dr. Tamim Niazi

ADT De-escalation in Selected High-Risk Prostate Cancer Patients (ADaPPt Trial) a GROUQ Led PCS Study: A Phase III Trial Randomized Trial (PCS XIV)

High-risk prostate cancer is usually treated with a combination of radiation therapy and hormone therapy (ADT). Radiation destroys cancer cells, while ADT lowers testosterone, a hormone that prostate cancer cells need to grow. Together, these treatments help control the cancer.

ADT is usually given for 18 to 24 months, but it can cause side effects that may affect quality of life.

Some people with high-risk prostate cancer may do just as well with a shorter course of ADT. This study will identify people who are most likely to benefit from shorter treatment using imaging scans and tumor tests. It will then evaluate whether a shorter course of ADT works as well as the standard treatment while reducing long-term side effects.

Studieoversikt

Status

Har ikke rekruttert ennå

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Antatt)

600

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  • • Able to understand and sign informed consent form (ICF);

    • Males aged ≥ 18 years;
    • Histologically confirmed adenocarcinoma of the prostate;
    • Participants with high-risk prostate cancer according to either of the following:

      a) High-risk disease - at least one of the following: i. T3a ii. Gleason 8 or less iii. PSA ≤ 30 ng/mL

iv. Gleason 9 (4+5) not more than 30% of the biopsy (e.g. a 10-needle biopsy can only have a maximum of 3 x 9 [4+5]);

  • PTEN-proficient tumor confirmed by CLIA-certified immunohistochemistry (IHC);
  • PSMA-PET within 90 days prior to randomization: negative for nodal or distant disease.
  • Candidate for definitive radiation to prostate and pelvis;
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 or Karnofsky performance status of ≥70%;
  • Testosterone ≥150 ng/dL or 5 nmol/L;
  • Adequate hematologic, renal, liver function (Hemoglobin ≥10 g/dL, Absolute Neutrophil Count ≥1.5x10⁹/L, Platelets ≥100x10⁹/L);
  • Judged to be medically fit for ADT and RT;
  • Participants must be accessible for treatment and follow-up. Investigators must assure themselves the participants enrolled on this trial will be available for complete documentation of the treatment, adverse events, and follow-up.
  • Sexually active patients, unless surgically sterile, must agree to use condoms as an effective barrier method and refrain from sperm donation during the study treatment and for 3 months after the end of the study treatment.

Exclusion Criteria:

  • • Prior local or systemic therapy for prostate cancer (e.g. ADT, chemotherapy or novel Androgen Receptor Inhibitors [ARIs]);

    • PSMA-PET positive nodal or distant metastases;
    • PTEN loss or equivocal by IHC (at least more than 50%);
    • Evidence of nodal or distant metastases on conventional imaging;
    • Prior pelvic radiation or prostate surgery interfering with RT (except biopsy/TURP);
    • Life expectancy <5 years regardless of the prostate cancer;
    • Severe concurrent disease, infection, or co-morbidity that would make the patient inappropriate for enrollment (e.g. cardiovascular disease, hypertension, diabetes, etc);
    • Uncontrolled cardiovascular disease including:

      • Myocardial infarction within 6 months;
      • Unstable angina;
      • Congestive Heart Failure: New York Heart Association (NYHA) class III or IV;
      • Severe arrhythmia;
    • Active severe infection or immunocompromised;
    • Active second malignancy within 5 years with the exception of:

      • Non-melanoma skin cancer;
      • Chronic Lymphocytic Leukemia (CLL) that is stable and not actively treated;
    • Any condition compromising adherence to the protocol.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Arm 1 (experimental): 12 months of ADT + Radiotherapy
Zoladex is given for 12 months instead of 24
The purpose of the study is to identify a subset of patient that may benefit to have a shorter Zoladex treatment (12 months vs 24 months)
Aktiv komparator: Arm 2 (standard of care): 24 months of ADT + Radiotherapy
The purpose of the study is to identify a subset of patient that may benefit to have a shorter Zoladex treatment (12 months vs 24 months)

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
5-year biochemical failure-free survival (bFFS)
Tidsramme: 5 years
Time from ADT initiation to time of first occurrence of biochemical failure (per Phoenix definition: PSA nadir + 2 ng/ml)
5 years

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Metastasis-free survival
Tidsramme: 5-8 years
The first occurrence of distant progression or death from ADT initiation
5-8 years
Overall survival
Tidsramme: 5-8 years
The time from ADT initiation to the time of death from any cause.
5-8 years
Prostate cancer-specific mortality
Tidsramme: 5-8 years
The time from ADT initiation to the time of death from prostate cancer
5-8 years
8-year biochemical failure-free survival (bFFS)
Tidsramme: 8 years
Time from ADT initiation to time of first occurrence of biochemical failure (per Phoenix definition: PSA nadir + 2 ng/ml)
8 years
Toxicity - Acute
Tidsramme: 5 years
To determine acute toxicity due to treatment using the Common Terminology Criteria for Adverse Events (CTCAE) version 6.0
5 years
Toxicity - Late
Tidsramme: 8 years
To determine late toxicity due to treatment using the Common Terminology Criteria for Adverse Events (CTCAE) version 6.0
8 years
Quality of Life - General
Tidsramme: 5-8 years
Evaluate the impact of the treatment on the patient's quality of life using the FACT-P questionnaire
5-8 years
Quality of Life - Pain
Tidsramme: 5-8 years
Evaluate the impact of the treatment on the patient's quality of life using the Brief Pain Inventory (BPI) questionnaire
5-8 years
Quality of Life - Fatigue
Tidsramme: 5-8 years
Evaluate the impact of the treatment on the patient's quality of life using the Brief Fatigue Inventory (BFI) questionnaire
5-8 years
Testosterone Recuperation
Tidsramme: 5-8 years
Time from ADT completion to the return of serum-testosterone to non-castrate or normal baseline level
5-8 years

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. oktober 2026

Primær fullføring (Antatt)

1. oktober 2035

Studiet fullført (Antatt)

1. oktober 2040

Datoer for studieregistrering

Først innsendt

22. juli 2026

Først innsendt som oppfylte QC-kriteriene

18. august 2026

Først lagt ut (Faktiske)

20. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

20. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

18. august 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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