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Yttrium-90 Transarterial Radioembolization for Chemotherapy-Refractory Intrahepatic Cholangiocarcinoma: A Prospective, Observational Study.
White, Judith; Carolan-Rees, Grace; Dale, Megan; Patrick, Hannah E; See, Teik Choon; Bell, Jon K; Manas, Derek M; Crellin, Adrian; Slevin, Nicholas J; Sharma, Ricky A.
Affiliation
  • White J; Cedar, Cardiff & Vale University Health Board, Cardiff Medicentre, Heath Park, Cardiff, United Kingdom.
  • Carolan-Rees G; Cedar, Cardiff & Vale University Health Board, Cardiff Medicentre, Heath Park, Cardiff, United Kingdom.
  • Dale M; Cedar, Cardiff & Vale University Health Board, Cardiff Medicentre, Heath Park, Cardiff, United Kingdom.
  • Patrick HE; Centre for Health Technology Evaluation, National Institute for Health and Care Excellence, London, United Kingdom.
  • See TC; Cambridge University Hospitals National Health Service (NHS) Foundation Trust, Cambridge, United Kingdom.
  • Bell JK; Department of Radiology, Manchester, United Kingdom.
  • Manas DM; Liver Unit, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
  • Crellin A; Institute of Oncology, NHS England, Leeds, United Kingdom.
  • Slevin NJ; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Sharma RA; University College London (UCL) Cancer Institute, National Institute for Health Research UCL Hospitals Biomedical Research Centre, University College London, 72 Huntley Street, London WC1E 6DD, United Kingdom. Electronic address: ricky.sharma@ucl.ac.uk.
J Vasc Interv Radiol ; 30(8): 1185-1192, 2019 Aug.
Article in En | MEDLINE | ID: mdl-31255499
ABSTRACT

PURPOSE:

To evaluate the safety and efficacy of yttrium-90 transarterial radioembolization (TARE) for the treatment of unresectable, chemotherapy-refractory intrahepatic cholangiocarcinoma (ICC).

METHODS:

A prospective, observational study was carried out in 10 centers between 2013 and 2017. TARE plus standard care was delivered to patients with unresectable, chemotherapy-refractory or chemotherapy-intolerant ICC. Primary outcome was overall survival. Secondary outcomes included safety, progression-free survival (PFS), and liver-specific progression-free survival (LPFS).

RESULTS:

Sixty-one patients were treated with TARE. Patients were 53% male; median age was 64 years; 91% had performance status 0/1; 92% had received prior chemotherapy; and 59% had no extrahepatic disease. Median follow-up was 13.9 months (95% confidence interval [CI], 9.6-18.1). Overall survival was 8.7 months (95% CI, 5.3-12.1), and 37% of patients survived to 12 months. PFS was 2.8 months (95% CI, 2.6-3.1), and LPFS was 3.1 months (95% CI, 1.3-4.8). One severe complication (abdominal pain) occurred at the time of the TARE procedure. Thirty patients experienced a total of 49 adverse events, of which 8% were grade ≥3; most common were grade 1-2 fatigue and abdominal pain. A total of 77 abnormal laboratory value events were recorded, of which 4% were grade ≥3.

CONCLUSIONS:

Patients with advanced ICC have limited therapeutic options and a poor prognosis. This prospective study examined the survival of patients with unresectable, chemotherapy-refractory primary ICC treated with TARE in real-world practice. The results demonstrate that this treatment merits further investigation in this patient cohort in a larger study, including collection of patient-reported outcomes.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Yttrium Radioisotopes / Bile Duct Neoplasms / Cholangiocarcinoma / Drug Resistance, Neoplasm / Radiopharmaceuticals / Embolization, Therapeutic Type of study: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Yttrium Radioisotopes / Bile Duct Neoplasms / Cholangiocarcinoma / Drug Resistance, Neoplasm / Radiopharmaceuticals / Embolization, Therapeutic Type of study: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Year: 2019 Type: Article