- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT07698535
Measuring Circulating Tumor Deoxyribonucleic Acid Tumor Fraction to Guide Early 177Lu-PSMA-617 Treatment Discontinuation in Patients With Metastatic Castration-Resistant Prostate Cancer, DYNAMO Trial
Dynamic Assessments of Molecular Response to Guide Early 177Lu-PSMA-617 Treatment Discontinuation: The DYNAMO Study
Tutkimuksen yleiskatsaus
Tila
Ehdot
Yksityiskohtainen kuvaus
OUTLINE:
CYCLES 1 AND 2: Patients receive 177Lu-PSMA-617 intravenously (IV) over 20-30 minutes on day 1 of each cycle. Cycles repeat every 6 weeks for up to 2 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection with ctDNA TF testing at baseline and C2D1. Patients with undetectable ctDNA TF (< 3%) on C2D1 continue to receive 177Lu-PSMA-617 as above in the absence of disease progression or unacceptable toxicity. Patients with detectable ctDNA TF (≥ 3%) on C2D1 are randomized to 1 of 2 arms.
CYCLE 3+ ARM I: Starting with cycle 3, patients receive 177Lu-PSMA-617 IV over 20-30 minutes on day 1 of each cycle. Cycles repeat every 6 weeks in the absence of disease progression or unacceptable toxicity.
CYCLE 3+ ARM II: Starting with cycle 3, patients receive docetaxel IV on day 1 of each cycle. Cycles repeat every 3 weeks in the absence of disease progression or unacceptable toxicity.
Additionally, all patients undergo PSMA positron emission tomography (PET) during screening, single photon emission computed tomography (SPECT)/computed tomography (CT) on study, and additional blood sample collection as well as CT throughout the study.
After completion of study treatment, patients are followed up every 12 weeks for up to 1 year.
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Vaihe
- Vaihe 2
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Michael Schweizer, MD
- Puhelinnumero: 206-606-6252
- Sähköposti: schweize@uw.edu
Opiskelupaikat
-
-
Washington
-
Seattle, Washington, Yhdysvallat, 98109
- Rekrytointi
- Fred Hutch/University of Washington Cancer Consortium
-
Päätutkija:
- Michael Schweizer, MD
-
Ottaa yhteyttä:
- Michael Schweizer, MD
- Puhelinnumero: 206-606-6252
- Sähköposti: schweize@uw.edu
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Kuvaus
Inclusion Criteria:
- Willing and able to provide informed consent
- Adult males ≥ 18 years age
- History of histologically confirmed adenocarcinoma of the prostate without evidence of neuroendocrine or small cell differentiation. If histology is not available, patients must have metastatic disease typical of prostate cancer (i.e., involving bone or pelvic lymph nodes or para-aortic lymph nodes)
- Evidence of metastatic disease on bone scan or CT scan
Patient must have evidence of castration- resistant prostate cancer as evidenced by PSA progression (per Prostate Cancer Working Group 3 [PCWG3] criteria) and a castrate serum testosterone level (i.e., ≤ 50 mg/dL)
- Serum/plasma PSA progression defined as 2 consecutive increases in PSA over a previous reference value measured at least 1 week prior. The minimal start value is 2.0 ng/mL
- Eastern Cooperative Oncology Group (ECOG) performance status 0-2
- Prior treatment and progression on at least one androgen receptor pathway inhibitor (ARPI), in either castration-sensitive or castration-resistant setting
- Eligible for treatment with either 177Lu-PSMA-617 or docetaxel as per their respective Food and Drug Administration (FDA) labels
- Absolute neutrophil count ≥ 1.5 x 10^9/L
- Platelet count ≥ 100 x 10^9/L
- Hemoglobin ≥ 9 g/dL
- Creatinine clearance ≥ 50 ml/min (calculated by Cockcroft-Gault formula)
- Total bilirubin ≤ 1.5 x upper limit of normal (ULN) except for patients with known Gilbert's syndrome (direct bilirubin ≤ 1.5 x ULN)
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN, unless liver metastases are present in which case they must be ≤ 5 x ULN. For patients with known Gilbert's Syndrome they must be ≤ 3 x ULN
- Able to comply with study requirements including provision of peripheral blood samples at specified time points for correlative studies
Exclusion Criteria:
- Evidence of serious and/or unstable pre-existing medical, psychiatric or other condition that could interfere with patient safety or provision of informed consent to participate in this study
- Evidence of metastatic neuroendocrine/small cell prostate cancer (NEPC). Note: baseline biopsy is not required
- Patients receiving any systemic therapy (aside from a luteinizing hormone-releasing hormone [LHRH] analogue) or radiotherapy within 2 weeks prior to study treatment
- Persistent toxicities (CTCAE grade > 2) from prior cancer therapy, excluding alopecia and stable neuropathy
- Patients considered a poor medical risk due to a serious, uncontrolled medical disorder or active, uncontrolled infection. Examples include, but are not limited to uncontrolled seizure disorder, unstable spinal cord compression, superior vena cava syndrome, or any psychiatric disorder that prohibits obtaining informed consent
- Patients who are known to be serologically positive for human immunodeficiency virus (HIV) and a CD4 count < 200
- Patients with known active hepatitis (i.e. hepatitis B or C). Prior hepatitis C infection is allowed as long as polymerase chain reaction (PCR) is negative
- Major surgery within 2 weeks of starting study treatment and patients must have recovered from any effects of any major surgery
- Serious cardiac disorder, including but not limited to uncontrolled ventricular arrhythmia, recent (within 12 months) myocardial infarction, resting electrocardiogram (ECG) indicating Fridericia's corrected QT interval prolongation > 500ms, or congenital long QT syndrome
- Prior systemic chemotherapy with taxane chemotherapy, including in hormone sensitive setting (e.g. docetaxel or cabazitaxel)
Brain metastases or active epidural disease (treated epidural disease is permitted)
- Note: baseline brain imaging is not required
- Contraindication to prednisone therapy including poorly controlled diabetes mellitus
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Peräkkäinen tehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Muut: Cycles 1 and 2 (177Lu-PSMA-617, ctDNA testing)
Patients receive 177Lu-PSMA-617 IV over 20-30 minutes on day 1 of each cycle.
Cycles repeat every 6 weeks for up to 2 cycles in the absence of disease progression or unacceptable toxicity.
Patients also undergo blood sample collection with ctDNA TF testing at baseline and C2D1.
Patients with undetectable ctDNA TF (< 3%) on C2D1 continue to receive 177Lu-PSMA-617 as above in the absence of disease progression or unacceptable toxicity.
Patients with detectable ctDNA TF (≥ 3%) on C2D1 are randomized to 1 of 2 arms.
Additionally, patients undergo PSMA PET during screening, SPECT/CT on study, and additional blood sample collection as well as CT throughout the study.
|
Suorita CT
Muut nimet:
Suorita verinäytteiden otto
Muut nimet:
Käy läpi PSMA PET
Muut nimet:
Koska IV
Muut nimet:
Suorita SPECT/CT
Muut nimet:
Undergo ctDNA TF testing
Muut nimet:
|
|
Active Comparator: Cycle 3+ Arm I (177Lu-PSMA-617)
Starting with cycle 3, patients receive 177Lu-PSMA-617 IV over 20-30 minutes on day 1 of each cycle.
Cycles repeat every 6 weeks in the absence of disease progression or unacceptable toxicity.
Additionally, patients undergo PSMA PET during screening, SPECT/CT on study, and additional blood sample collection as well as CT throughout the study.
|
Suorita CT
Muut nimet:
Suorita verinäytteiden otto
Muut nimet:
Käy läpi PSMA PET
Muut nimet:
Koska IV
Muut nimet:
Suorita SPECT/CT
Muut nimet:
|
|
Active Comparator: Cycle 3+ Arm II (docetaxel)
Starting with cycle 3, patients receive docetaxel IV on day 1 of each cycle.
Cycles repeat every 3 weeks in the absence of disease progression or unacceptable toxicity.
Additionally, patients undergo PSMA PET during screening, SPECT/CT on study, and additional blood sample collection as well as CT throughout the study.
|
Koska IV
Muut nimet:
Suorita CT
Muut nimet:
Suorita verinäytteiden otto
Muut nimet:
Käy läpi PSMA PET
Muut nimet:
Suorita SPECT/CT
Muut nimet:
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Number and proportion among those recruited with detectable circulating tumor deoxyribonucleic acid (ctDNA) tumor fraction who undergo randomization
Aikaikkuna: Up to 2 cycles (Cycle length = 6 weeks)
|
Will be analyzed descriptively.
Among patients who initiate lutetium Lu 177 vipivotide tetraxetan and undergo cycle (C) 2 day (D) 1 ctDNA tumor fraction assessment, the number (and proportion among those recruited) with detectable ctDNA tumor fraction who undergo randomization will be reported with a two-sided 95% Wilson confidence interval.
|
Up to 2 cycles (Cycle length = 6 weeks)
|
|
Number of patients screened, enrolled, evaluable for C2D1 ctDNA tumor fraction and for who cycle 3 is administered
Aikaikkuna: Up to cycle 3 administration (Cycle length = 6 weeks)
|
Will report the number of patients screened, enrolled, evaluable for C2D1 (week 13) ctDNA tumor fraction, classified as having detectable versus undetectable ctDNA tumor fraction, and for who cycle 3 is administered.
Reasons for failure to undergo C1D28 ctDNA assessment or randomization will be tabulated.
|
Up to cycle 3 administration (Cycle length = 6 weeks)
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Radiographic progression free survival (PFS)
Aikaikkuna: From randomization to disease progression, clinical progression, or death, whichever occurs first, assessed up to 1 year
|
Will be estimated in the subset of patients who undergo randomization.
Disease progression assessed per modified Response Evaluation Criteria in Solid Tumors criteria or the Prostate Cancer Working Group 3 criteria for bone lesions.
Clinical progression as determined by the treating physician.
Will be estimated using the Kaplan-Meier method.
Differences between groups will be evaluated using the log-rank test and the hazard ratio from a Cox regression model with treatment group as the predictor variable following assessment of proportional hazards.
Will also visualize PFS point estimates and 95% confidence interval (CI) bands over time and report median and 95% CIs of PFS for each group.
|
From randomization to disease progression, clinical progression, or death, whichever occurs first, assessed up to 1 year
|
|
Overall survival
Aikaikkuna: From the start of treatment until death from any cause, assessed up to 1 year
|
Will be estimated in the subset of patients who undergo randomization.
Will be estimated using the Kaplan-Meier method.
Differences between groups will be evaluated using the log-rank test and the hazard ratio from a Cox regression model with treatment group as the predictor variable following assessment of proportional hazards.
|
From the start of treatment until death from any cause, assessed up to 1 year
|
|
Prostate-specific antigen (PSA) PFS
Aikaikkuna: From the start of treatment until PSA progression, assessed up to 1 year
|
Will be estimated in the subset of patients who undergo randomization.
Will be estimated using the Kaplan-Meier method.
Differences between groups will be evaluated using the log-rank test and the hazard ratio from a Cox regression model with treatment group as the predictor variable following assessment of proportional hazards.
|
From the start of treatment until PSA progression, assessed up to 1 year
|
|
Proportion of patients with a ≥ 50% decline in PSA from baseline (PSA50) response rate
Aikaikkuna: Up to 1 year
|
Will be estimated in the subset of patients who undergo randomization.
Will be reported as a percentage with 95% CI calculated using Wilson's method.
Changes in PSA from baseline, with patients achieving PSA50, may be visualized using waterfall plots.
|
Up to 1 year
|
|
Duration of response
Aikaikkuna: From the time measurement criteria are met for complete response or partial response (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented, assessed up to 1 year
|
Will be estimated in the subset of patients who undergo randomization.
|
From the time measurement criteria are met for complete response or partial response (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented, assessed up to 1 year
|
Yhteistyökumppanit ja tutkijat
Sponsori
Yhteistyökumppanit
Tutkijat
- Päätutkija: Michael Schweizer, MD, Fred Hutch/University of Washington Cancer Consortium
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Ensisijainen valmistuminen (Arvioitu)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
- Urogenitaaliset sairaudet
- Sukuelinten sairaudet
- Sukuelinten kasvaimet, mies
- Urogenitaaliset kasvaimet
- Neoplasmat sivustoittain
- Neoplasmat
- Sukuelinten sairaudet, mies
- Eturauhasen sairaudet
- Miesten urogenitaaliset sairaudet
- Eturauhasen kasvaimet
- Orgaaniset kemikaalit
- Tutkintatekniikat
- Kliiniset laboratoriotekniikat
- Diagnostiikkatekniikat ja menettelyt
- Diagnoosi
- Hiilivety
- Sykloparaffiinit
- Hiilivedyt, aliisykliset
- Hiilivedyt, sykliset
- Terpeenit
- Hydrolaasit
- Entsyymit
- Entsyymit ja koentsyymit
- Taksoidit
- Syklodekaanit
- Diterpeenit
- Peptidihydrolaasit
- Metalloproteases
- Karboksipeptidaasit
- Eksopeptidaasit
- Metalloexopeptidaasit
- Doketakseli
- Pluvicto
- Näytteenkäsittely
- Glutamaatin karboksipeptidaasi II
Muut tutkimustunnusnumerot
- RG1126448
- NCI-2026-03971 (Rekisterin tunniste: CTRP (Clinical Trial Reporting Program))
- FHIRB0021269 (Muu tunniste: Fred Hutch/University of Washington Cancer Consortium)
Yksittäisten osallistujien tietojen suunnitelma (IPD)
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