P3, N=92, Active, not recruiting, Boston Scientific Corporation | Recruiting --> Active, not recruiting | Trial primary completion date: Jun 2025 --> Dec 2025
Careful patient selection, including consideration of the prognostic factors ECOG, baseline CEA, and KRAS status, sets outcome expectations in patients with colorectal liver metastases suitable for TARE/Chemo as second-line treatment (Trial Registry Number: NCT01483027).
P1, N=2, Terminated, Northwestern University | Trial completion date: Dec 2022 --> Oct 2023 | Active, not recruiting --> Terminated | Trial primary completion date: Dec 2022 --> Oct 2023; Lack of funding
9 months ago
Trial completion date • Trial termination • Trial primary completion date
P1, N=12, Recruiting, Boston Scientific Corporation | Trial completion date: Jun 2024 --> Jun 2025 | Trial primary completion date: Jan 2024 --> Jun 2024
11 months ago
Trial completion date • Trial primary completion date
A panel of Human HCC cell lines (HepG2 and PLC/PRF/5 characterized by high expression of hepatocyte and liver progenitor genes, and SNU-449 and SNU-423, characterized by high expression of stem cell and epithelial-mesenchymal transition genes) and a selected tumoroid were treated at escalating activities (0-20 MBq/ml) of glass Y-90 microspheres (Therasphere, Boston Scientific) for 10 days in vitro... HCC cell lines and tumoroids demonstrate heterogenous sensitivity to Y-90 microsphere treatment in vitro, potentially reflected by underlying transcriptomic profiles. Establishing patient derived HCC tumoroids for in vitro Y-90 microsphere treatment screens is feasible and serves as a powerful platform to assess biological underpinnings of Y-90-RE response with the advantage of being linked to clinical metadata.
1 year ago
Preclinical
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KEAP1 (Kelch Like ECH Associated Protein 1) • AXIN1 (Axin 1)
P=N/A, N=5, Recruiting, Boston Scientific Corporation | Trial completion date: May 2023 --> Aug 2023 | Trial primary completion date: May 2023 --> Aug 2023
over 1 year ago
Trial completion date • Trial primary completion date
First-line treatment of ICC with radioembolization showed promising OS and minimal toxicity, especially in patients with solitary tumor. Radioembolization may be considered as the first line treatment of unresectable ICC.
Real-world data confirmed a significant association between TAD and OR, TAD and OS, and TAD and AFP response. No association was found between ≥ grade 3 hyperbilirubinemia and NTAD.
P2, N=150, Not yet recruiting, Boston Scientific Corporation | Trial completion date: Jun 2025 --> Mar 2026 | Trial primary completion date: Jun 2025 --> Mar 2026
over 2 years ago
Trial completion date • Trial primary completion date
At the 3-month follow-up the radiographic objective response rate was 46.6% and disease control rate was 70%. The treatment of patients with liver-dominant chemotherapy-refractory breast cancer metastases with TARE using yttrium-90 labeled glass microspheres is safe and led to promising hepatic disease control and OS especially in patients with ER+ tumors and in patients without extrahepatic extraosseous metastases.