- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07801664
Short Course ADT for High Risk Low/Intermediate Risk ARTERA Prostate Cancer
31. august 2026 oppdatert av: NYU Langone Health
A Phase II Prospective Trial Utilizing Short Course Androgen Deprivation Therapy In Conjunction With Ultra-Hypofractionated SBRT For High Risk Nccn Prostate Cancer With Lower Risk Artera Scores
For this study, high risk prostate cancer patients with lower risk ARTERA scores will be treated with 6 months of Androgen Deprivation Therapy (ADT) in conjunction with dose escalated radiotherapy to the prostate and nodes.
Specifically, patients enrolled in this study will undergo one of several dose-escalated forms of radiotherapy which would include SBRT with or without a brachytherapy boost.
Studieoversikt
Status
Rekruttering
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
90
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Nina Yang, RN
- Telefonnummer: 646-830-4743
- E-post: Nina.Yang@nyulangone.org
Studiesteder
-
-
New York
-
New York, New York, Forente stater, 10016
- Rekruttering
- NYU Langone Health
-
-
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:
- Ability to understand and willingness to sign a written informed consent document
- 18 years of age or older male participants
- Biopsy proven prostate cancer meeting at least one of the following high-risk criteria: Gleason score 8-10 OR; Baseline PSA >20 up to and including 40 ng/ml OR; Patients with Gleason score 6-7 remain eligible if the PSA criterion (>20 ng/mL) is met OR; MRI Radiographic stage T1-T3 disease without evidence of nodal involvement
- No imaging evidence of nodal metastases on baseline MRI/ CT of the pelvis and PET-PSMA scans
- Low risk or intermediate risk ARTERA AI scores
- Serum testosterone ≥ 120 ng/dL determined prior to ADT start
- At least 4 weeks must have elapsed from major surgery
- Karnofsky Performance Status (KPS) > 80
- Prostate size < 90 cc
- MRI findings: Lesion may have extracapsular extension (ECE)
- International Prostate Symptom Score (IPSS) < 22
- Satisfy all MRI screening criteria and be willing to fill out the standard MRI screening form
Exclusion Criteria:
- Gleason score 6 or 7 in the absence of PSA >20 ng/mL
- PSA >40 ng/mL
- Prior or concurrent androgen deprivation therapy for prostate cancer of >3 months duration
- High Risk ARTERA scores
- MRI findings: suspicious nodal metastases
- Evidence of regional lymphadenopathy or metastatic disease on MRI/CT or PSMA PET scan
- Metallic implant or device in the pelvis that might distort the local magnetic field and compromise quality of mp-MRI
- Contra-indications to receiving gadolinium contrast
- KPS < 80
- Pelvic or Prostate MRI or CT (MRI preferred) evidence of radiographic T4, or N1 disease or bone disease
- Prior treatment for prostate cancer, including history of chemotherapy or surgery for prostate cancer (except for prior [transurethral resection of prostate] TURP or greenlight [photo selective vaporization of prostate] PVP which would be allowed)
- History of another malignancy within the previous 2 years except for the following: adequately treated basal cell or squamous cell skin cancer, superficial bladder cancer, currently in complete remission, or any other cancer that has been in complete remission for at least 3 years. Patients with Crohn's disease or ulcerative colitis
- IPSS > 22
- Currently on any ARPis (including but not limited to: enzalutamide, apalutamide, darolutamide, or abiraterone)
- Prior pharmacologic androgen deprivation therapy (ADT) for prostate cancer is permitted under the following (2) conditions: 1) Participants meeting this criterion will be assigned to a separate stratum within each primary treatment cohort. 2) Patients remain eligible for enrollment provided they have received no more than 3 months of ADT in total, regardless of whether ADT was initiated before screening or registration.
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: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: High-Risk Prostate Cancer Patients with Lower-Risk ARTERA Scores
Patients will be treated with 6 months of Androgen Deprivation Therapy (ADT) in conjunction with dose escalated radiotherapy to the prostate and nodes.
|
ADT will be delivered with monthly Degarelix, or Leuprolide injections or daily Relugolix pills which are all standard ADT interventions.
Andre navn:
Dose-escalated radiotherapy.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
5-Year Cumulative Incidence of Distant Metastases
Tidsramme: Up to Year 5
|
Incidence of distant metastases (DM).
DM is defined as the first occurrence of radiographic or biopsy-confirmed distant metastatic disease.
|
Up to Year 5
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Distant Metastasis-Free Survival (DMFS)
Tidsramme: Up to Year 5
|
Defined as the time from study enrollment to the first occurrence of distant metastasis or death from any cause, whichever occurs first.
|
Up to Year 5
|
|
Time to Biochemical Failure
Tidsramme: Up to Year 5
|
Time to biochemical failure will be measured from study enrollment to the date when the Phoenix criterion (PSA nadir + 2 ng/mL) is first met.
|
Up to Year 5
|
|
Overall Survival (OS)
Tidsramme: Up to Year 5
|
Defined as the time from study enrollment to death from any cause.
|
Up to Year 5
|
|
Change in Expanded Prostate Cancer Index Composite-26 (EPIC-26) Score
Tidsramme: Baseline, Year 2
|
26-item survey assessing prostate cancer-related symptom domains.
Each item is rated on a Likert score.
The raw score is the sum of responses and is converted to a standard score from 0-100, where higher scores indicate greater quality of life.
|
Baseline, Year 2
|
|
Change in International Prostate Symptom Score (IPSS) Score
Tidsramme: Baseline, Year 2
|
7-item assessment of the severity of lower urinary tract symptoms linked to benign prostatic hyperplasia (BPH).
Each item is rated on a Likert scale.
The total score is the sum of responses and ranges from 0-35; lower scores indicate milder symptoms.
|
Baseline, Year 2
|
|
Change in Short-Form-12 (SF-12) Score
Tidsramme: Baseline, Year 2
|
12-item assessment of health and quality of life.
Each item is rated on a Likert scale.
The raw score is the sum of responses and is converted to a standard score between 0-100; higher scores indicate better quality of life.
|
Baseline, Year 2
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Michael Zelefsky, MD, NYU Langone Health
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 (Faktiske)
6. august 2026
Primær fullføring (Antatt)
1. august 2028
Studiet fullført (Antatt)
1. august 2029
Datoer for studieregistrering
Først innsendt
31. august 2026
Først innsendt som oppfylte QC-kriteriene
31. august 2026
Først lagt ut (Faktiske)
3. september 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
3. september 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
31. august 2026
Sist bekreftet
1. august 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Urogenitale sykdommer
- Kjønnssykdommer
- Genitale neoplasmer, hanner
- Urogenitale neoplasmer
- Neoplasmer etter nettsted
- Neoplasmer
- Kjønnssykdommer, mannlige
- Prostata sykdommer
- Mannlige urogenitale sykdommer
- Prostatiske neoplasmer
- Fysiologiske effekter av legemidler
- Hormoner
- Hormoner, hormonsubstitutter og hormonantagonister
- Hormonantagonister
- Humofyshormonfrigjørende hormoner
- Hypotalamiske hormoner
- Peptidhormoner
- Nevropeptider
- Peptider
- Aminosyrer, peptider og proteiner
- Oligopeptider
- Nervevevsproteiner
- Proteiner
- Terapeutikk
- Farmakologiske handlinger
- Kjemiske handlinger og bruk
- Gonadotropinfrigjørende hormon
- Leuprolid
- Androgenantagonister
- Acetyl-2-naftylalanyl-3-klorfenylalanyl-1-oksoheksadecyl-seryyl-4-aminophenylalanyl (hydroorotyl) -4-aminophenylalanyl (karbamoyl) -leucyl-ilys-prolyl-alaninamid
- Relugolix
- Strålebehandling
Andre studie-ID-numre
- 26-00056
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
JA
IPD-planbeskrivelse
The de-identified participant data from the final research dataset will be shared with researchers who provide a methodologically sound proposal immediately following publication.
The protocol and statistical analysis plan will be posted on Clinicaltrials.gov
only as required by federal regulation or supporting awards and agreements.
Proposals may be submitted up to 36 months following article publication.
After 36 months the data will be available in our University's data warehouse but without investigator support other than deposited metadata.
IPD-delingstidsramme
Immediately following publication.
No end date.
Tilgangskriterier for IPD-deling
Researchers must provide a methodologically sound proposal.
Proposals may be submitted up to 36 months following article publication.
After 36 months the data will be available in our University's data warehouse but without investigator support other than deposited metadata.
IPD-deling Støtteinformasjonstype
- STUDY_PROTOCOL
- SEVJE
- ICF
- ANALYTIC_CODE
- CSR
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Ja
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
produkt produsert i og eksportert fra USA
Ja
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. .