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An External Control Arm Study Comparing Survival Among Metastatic Castration-Resistant Prostate Cancer (mCRPC) Patients Treated With 177Lu-PSMA-617 vs Androgen Receptor Pathway Inhibitor (ARPI) Switch in Routine Care
Comparing the Lutetium (177Lu) Vipivotide Tetraxetan Arm of the PSMAfore Clinical Trial to a Switch in Androgen Receptor Pathway Inhibitor (ARPI) as External Control Arm (ECA) Using a Real-world Data Source for Patients With Metastatic Castration-Resistant Prostate Cancer (mCRPC) After Progression on Prior ARPI
The aim of this study is to assess the effectiveness of 177Lu-PSMA-617 (lutetium (177Lu) vipivotide tetraxetan) on survival in patients randomized to receive treatment following progression on one ARPI from the PSMAfore trial compared to the effectiveness of a change in ARPI treatment on survival in a real-world setting in patients with mCRPC who are taxane-naive but have progressed after a switch in ARPI.
Studie Overzicht
Toestand
Conditie
Studietype
Inschrijving (Werkelijk)
Contacten en locaties
Studie Locaties
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Basel, Zwitserland, CH-4056
- Novartis
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
PSMAfore trial patients with mCRPC who progressed once after treatment with an ARPI and were taxane-naive, and real-world data (RWD) mCRPC patients from the United States (US)-based health research database who were taxane-naive and had evidence of treatment with a change in ARPI immediately following progression.
Beschrijving
Inclusion criteria:
- Had an International Classification of Diseases, 9th or 10th Revision, Clinical Modification (ICD-9-CM or ICD-10-CM) diagnosis of prostate cancer (PC) (ICD-9-CM 185x or ICD-10-CM C61x).
- Had at least two documented clinical visits, on different days, occurring on or after 01 Jan 2013.
- Included in probabilistic sample of patients queued for review via abstraction.
- Had diagnosis of metastatic disease on or after 01 Jan 2013.
- Histology was confirmed as adenocarcinoma of the prostate.
- Had confirmed mCRPC diagnosis.
- Treated with an ARPI-containing line of therapy (LOT; i.e., index therapy) in the mCRPC setting immediately after progression on one previous ARPI-containing line (in any setting, Hormone Sensitive PC or castration-resistant PC), as defined per the health research database's LOT rules and confirmed via abstraction.
- 18 years of age or older at the start of index therapy.
- Had an Eastern Cooperative Oncology Group Performance Score (ECOG PS) of 0-1 within 30 days before or up to 7 days after index date, or unknown ECOG PS.
Exclusion criteria:
- Female sex.
- Had evidence of untreated brain metastases.
- Had history of cardiac comorbidities, infection with hepatitis B or C, or spinal cord compression that would indicate significant risk to PSMAfore trial participation.
- Diagnosis of an active additional malignancy (i.e., other than prostate cancer).
- Evidence of biomarker status that would indicate eligibility for treatment other than ARPI, or better prognosis.
- Evidence of prior treatment with therapies that potentially affect study outcomes (e.g., radiopharmaceuticals, taxane, immunotherapy or biological therapy, clinical study drug (CSD), or 177Lu-PSMA-617).
- Had evidence of inadequate organ function.
- Had evidence of low levels of albumin (< 2.5 g/dL).
- Had evidence of a negative PSMA-PET scan.
Other protocol-defined inclusion/exclusion criteria may apply.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Observatiemodellen: COHORT
- Tijdsperspectieven: RETROSPECTIVE
Cohorten en interventies
Groep / Cohort |
|---|
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External Control Arm (ECA)
RWD patients with mCRPC who were treated with a change in ARPI after progression on prior ARPI and before taxane treatment. |
|
PSMAfore Trial Treatment Arm (TTA)
PSMAfore trial patients with mCRPC who were treated with 177Lu-PSMA-617 after progression on one ARPI. |
|
PSMAfore Trial Control Arm (TCA)
PSMAfore trial patients with mCRPC who switched to a subsequent ARPI after progression on a prior ARPI. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Overall Survival (OS) of the TTA Group
Tijdsspanne: Up to approximately 3 years and 6 months
|
OS defined as time from randomization to death due to any cause. |
Up to approximately 3 years and 6 months
|
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Real-world Overall Survival (rwOS) of the ECA Group (for the Primary Measure)
Tijdsspanne: Up to approximately 7 years
|
rwOS is defined as the time from initiation of the index ARPI to death due to any cause. |
Up to approximately 7 years
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
OS of the TCA Group
Tijdsspanne: Up to approximately 3 years and 6 months
|
Up to approximately 3 years and 6 months
|
|
rwOS of the ECA Group (for the Secondary Measure)
Tijdsspanne: Up to approximately 7 years
|
Up to approximately 7 years
|
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie directeur: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Publicaties en nuttige links
Nuttige links
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- CAAA617A12004
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
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