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Exploring Auger-Enhanced PSMA-Targeted Radioligand Therapy: A First-in-Taiwan Clinical Study of 161Tb-PSMA-I&T
Exploring Auger-Enhanced PSMA-Targeted Radioligand Therapy: A First-in-Taiwan Clinical Study of 161Tb-PSMA-I&T in Patients With Metastatic Castration-Resistant Prostate Cancer
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
Metastatic castration-resistant prostate cancer (mCRPC) represents the most advanced and treatment-refractory form of prostate cancer, where disease progression continues despite hormone-suppressing therapies and multiple lines of systemic treatment. Radioligand therapy (RLT) targeting prostate-specific membrane antigen (PSMA) has emerged as a promising treatment strategy, delivering targeted radiation to cancer cells using PSMA-binding ligands labeled with therapeutic radioisotopes. While Lutetium-177 (177Lu)-labeled compounds such as 177Lu-PSMA-617 have demonstrated meaningful clinical benefit, their effectiveness may be limited in cases of micrometastatic disease or heterogeneous PSMA expression, due to the physical characteristics of longer-range β particle radiation.
Terbium-161 (161Tb) is a next-generation radionuclide that emits not only β particles but also short-range, high-linear energy transfer Auger electrons. This dual emission profile enables more effective cell killing in small or poorly perfused tumor sites, with potentially enhanced tumor-to-normal tissue selectivity. Preclinical studies and early case reports suggest that 161Tb-labeled PSMA agents may offer superior tumor dosimetry and cytotoxicity compared to 177Lu analogs. Most notably, the recently published VIOLET Phase I/II trial-the largest clinical experience with 161Tb-PSMA-I&T to date-demonstrated favorable safety across escalating doses (up to 7.4 GBq) and promising therapeutic activity. These findings confirm that 161Tb-PSMA RLT is both safe and clinically active, even in patients previously treated with 177Lu-based agents.
Building on this foundation, our study aims to establish a standardized GMP-grade production process for 161Tb-PSMA-I&T and to evaluate its pharmacokinetics, biodistribution, and radiation dosimetry in a small cohort of Taiwanese patients with mCRPC. These pilot data will generate critical clinical insight and infrastructure, directly informing the design of future Phase Ib/II trials and accelerating national readiness for next-generation PSMA-targeted therapies, especially emphasizing on three specific aims: (1) to establish a GMP-compliant manufacturing process for clinical-grade 161Tb-PSMA-I&T suitable for clinical application in Taiwan; (2) to characterize 161Tb-PSMA-I&T focusing on its pharmacokinetics, biodistribution, and radiation dosimetry; (3) to explore preliminary safety data of 161Tb-PSMA-I&T using potential treatment doses in Asian population.
Studietype
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studiecontact
- Naam: Pei-Ju Chuang
- Telefoonnummer: 237966 +886-2-2322-0322
- E-mail: pjchuang.ntucc@gmail.com
Studie Contact Back-up
- Naam: Ching-Chu Lu
- Telefoonnummer: 265477 +886-2-2312-3456
- E-mail: kelvinlu@ntuh.gov.tw
Studie Locaties
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Taipei, Taiwan
- Werving
- National Taiwan University Hospital
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Contact:
- Dr. Lu
- Telefoonnummer: 265477 +886-2-2312-3456
- E-mail: kelvinlu@ntuh.gov.tw
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Taipei, Taiwan
- Werving
- National Taiwan University Cancer Center
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Contact:
- Dr. Chuang
- Telefoonnummer: 237966 +886-2-2322-0322
- E-mail: pjchuang.ntucc@gmail.com
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Age ≥ 20 years, ability to understand and willingness to sign informed consent, cooperate with all study-related procedures and assessments including blood tests and imaging
- Histologically confirmed adenocarcinoma of the prostate with evidence of metastatic castration-resistant prostate cancer (mCRPC)
- Prior surgical orchiectomy or chemical castration maintained on luteinizing hormone-releasing hormone analog, with a serum testosterone level <50 ng/dL (castrate range)
- Prior treated with at least one line of taxane-based chemotherapy unless medically unsuitable, and at least one line of androgen receptor pathway inhibitor (e.g., abiraterone, enzalutamide, apalutamide, or darolutamide)
- Prior treated with 177Lu-labeled PSMA RLT unless medically unsuitable or declined by the patient
- Progressive disease defined according to Prostate Cancer Clinical Trials Working Group 3: Either a PSA progression of more than 2 rising PSA values from baseline with intervals ≥ 1 week, or a soft-tissue progression on images per RECIST 1.1 criteria, or a bone progression on images with more than 2 new lesions
- Evidence of significant PSMA-avid lesions on 68Ga- or 18F-labeled PSMA PET/CT within 12 weeks prior to screening, which defined as 68Ga-PSMA or 18F-PSMA uptake greater than that of liver or spleen parenchyma (depend on the tracer used) in at least one metastatic lesion of any size in any organ system
- A life expectancy of ≥ 6 months and Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- Adequate bone marrow and organ functions 9.1 Hemoglobin ≥ 10 g/dL without RBC transfusion within 4 weeks 9.2 Absolute neutrophil count ≥ 1.5 × 109/L 9.3 Platelet count ≥ 150 × 109/L 9.4 Creatinine clearance ≥ 50 mL/min (Cockcroft-Gault) 9.5 AST and ALT ≤ 3 × ULN, total bilirubin ≤ 1.5 × ULN
- Willingness to comply with the use of medically acceptable forms of barrier contraception if sexually active
Exclusion Criteria:
- History of allergic reaction to PSMA-targeted compounds or radiometals
- Prior radioligand therapy with 223Ra or 177Lu-PSMA within 6 months
- Prior surgery or radiotherapy within 4 weeks prior to first investigational dose
- Prior systemic therapies against prostate cancer within 4 weeks, including androgen receptor pathway inhibitor, chemotherapy, targeted therapy such as PARP inhibitors (PARPi)
- Discordant disease on PET images: FDG-positive disease with minimal PSMA expression
- Urinary tract obstruction causing hydronephrosis unless appropriately treated beforehand
- Known symptomatic brain metastases or leptomeningeal disease, symptomatic or impending cord compression unless appropriately treated beforehand
- Other active malignancy requiring systemic treatment
- Significant cardiovascular disease (e.g., recent myocardial infarction, unstable angina)
- Concurrent severe uncontrolled illness that may jeopardize patient safety, including uncontrolled infections
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Sequentiële toewijzing
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Dose level 1
120 mCi of 161Tb-PSMA-I&T every 6 weeks for 3 cycles
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161Tb-PSMA-I&T for injections, slow intravenous administration, 200 mCi/5 mL/Vial
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Experimenteel: Dose level 2
150 mCi of 161Tb-PSMA-I&T every 6 weeks for 3 cycles
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161Tb-PSMA-I&T for injections, slow intravenous administration, 200 mCi/5 mL/Vial
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Experimenteel: Dose level 3
200 mCi of 161Tb-PSMA-I&T every 6 weeks for 3 cycles
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161Tb-PSMA-I&T for injections, slow intravenous administration, 200 mCi/5 mL/Vial
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Treatment-emergent adverse events
Tijdsspanne: From enrollment to the end of post-treatment surveillance, at least 36 weeks
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Incidence, nature, and severity of treatment-emergent adverse events (TEAEs) graded by CTCAE v5.0 across the entire treatment and 18-week post-treatment surveillance period
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From enrollment to the end of post-treatment surveillance, at least 36 weeks
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Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Ching-Chu Lu, National Taiwan University Hospital
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
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
Andere studie-ID-nummers
- 202507234MINB
Plan Individuele Deelnemersgegevens (IPD)
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Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
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