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Clinical Trial Summary

The main purpose of this study is to further assess treatment efficacy and safety after using QuiremSpheres® for the treatment of patients with unresectable primary liver cancer or unresectable liver metastases suitable for SIRT and allocated to this treatment by a multidisciplinary tumor board.


Clinical Trial Description

Liver tumors can be of primary (Hepatocellular Carcinoma, HCC) or metastatic (mainly from colorectal carcinoma, CRC) origin. Both HCC and CRC are common causes of death from cancer worldwide. The overall incidence of HCC and CRC remains high in developing countries and is steadily rising in most industrialized countries. Available treatment options depend on the size, number, and location of tumors, on liver status, overall performance status and comorbidities, on patency of portal vein and presence of extrahepatic metastatic disease. They include surgical (liver resection, liver transplantation), systemic (e.g. chemotherapy, immunotherapy), ablative (thermal ablation, chemical ablation) and intra-arterial (chemoembolization, radioembolization) modalities. Radioembolization, also known as Selective Internal Radiation Therapy (SIRT) with microspheres containing a radiation-emitting isotope (Yttrium-90 or Holmium-166) delivers localized radiation in the vasculature around liver tumors with relatively limited concurrent injury to the surrounding normal/healthy tissue. Yttrium-90 radioembolization is currently included in several guidelines (EASLEORTC, ESMO). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03563274
Study type Observational [Patient Registry]
Source Terumo Europe N.V.
Contact
Status Terminated
Phase
Start date June 21, 2018
Completion date July 31, 2020

See also
  Status Clinical Trial Phase
Completed NCT03239158 - Bioinformation Therapy for Liver Cancer Phase 2/Phase 3
Completed NCT04090645 - TheraSphere & Treatment of Unresectable Primary or Unresectable Secondary Liver Cancer N/A
Recruiting NCT05497453 - A Phase 1/2 Study to Evaluate OTX-2002 in Patients With Hepatocellular Carcinoma and Other Solid Tumor Types Known for Association With the MYC Oncogene Phase 1/Phase 2