NARA Discovery
Article Details
← Back to Search Results
Journal Article

New perspectives in unresectable cholangiocarcinoma? Evaluation of chemosaturation with percutaneous hepatic perfusion as a palliative treatment option

Cornelia L. A. Dewald; Lena S. Becker; Timo C. Meine; Sabine K. Maschke; Frank K. Wacker; Anna Saborowski; Arndt Vogel; Jan B. Hinrichs
Clinical & Experimental Metastasis · Vol. 40, Issue 1 · pp. 95-104 · 2023

Abstract

Cholangiocarcinoma (CCA) are the second most common primary liver tumors and carry a dismal prognosis. Chemosaturation with percutaneous hepatic perfusion (PHP) is a palliative, intra-arterial therapeutic approach that provides a high dose chemotherapy of the liver with reduced systemic exposure. Aim of this retrospective, monocentric study was to analyze PHP as a palliative treatment for unresectable CCA. Toxicity, adverse events and complications were classified using the Common Terminology Criteria for Adverse Events (CTCAE v5.0). Overall response rate (ORR) and disease control rate (DCR) were evaluated according to the Response Evaluation Criteria in Solid Tumors (RECIST1.1). Median overall survival (mOS), median progression-free survival (mPFS) and hepatic mPFS (mhPFS) were computed using Kaplan–Meier estimation. In total 17 patients were treated with 42 PHP between 10/2014 and 09/2020. No significant complications occurred during the interventions. mOS was 27.6 (interquartile range (IQR) 16.5–37) months from first diagnosis and 9.9 (IQR 3.8–21) months from first PHP. mPFS was 4 (IQR 2–7) and mhPFS was 4 (IQR 3–10) months. ORR was 25% and DCR 75%. Significant, but transient hematotoxicity was frequent with grade 3/4 thrombopenia after 50%, leukopenia after 26% and anaemia after 21% of the interventions. An increase of transaminases (AST increase after 21% and ALT increase after 14% of the PHP) developed more often than a deterioration of the liver synthesis capacity. Salvage treatment with PHP has the potential to prolong life in selected patients with unresectable, refractory cholangiocarcinoma. The interventional procedure is safe. Post-interventional toxicity is frequent but manageable.

Bibliographic Information

JournalClinical & Experimental Metastasis
PublisherSpringer
Publication Date2023-02-01
Publication Year2023
Volume40
Issue1
Pages95-104
Document TypeJournal Article
eISSN1573-7276
DOI10.1007/s10585-022-10193-4

Access Information

NARA Access Coverage1983-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10585
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.