- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07843758
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.
Studieoversikt
Status
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
-
-
-
Basel, Sveits, CH-4056
- Novartis
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
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.
Beskrivelse
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.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Observasjonsmodeller: COHORT
- Tidsperspektiver: RETROSPECTIVE
Kohorter og intervensjoner
Gruppe / Kohort |
|---|
|
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. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Overall Survival (OS) of the TTA Group
Tidsramme: 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
|
|
Real-world Overall Survival (rwOS) of the ECA Group (for the Primary Measure)
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
OS of the TCA Group
Tidsramme: 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)
Tidsramme: Up to approximately 7 years
|
Up to approximately 7 years
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Studieleder: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Publikasjoner og nyttige lenker
Hjelpsomme linker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- CAAA617A12004
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
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