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Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers

Chemosaturation (CS; CHEMOSAT®, Delcath Systems Inc.) temporarily administers melphalan into the liver by percutaneous hepatic perfusion (PHP). CS-PHP can effectively control growth in liver tumors, but efficacy and tolerability of sequential treatments are unclear. We analyzed outcomes of sequentia...

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Autores principales: Veelken, Rhea, Maiwald, Bettina, Strocka, Steffen, Petersen, Tim-Ole, Moche, Michael, Ebel, Sebastian, Denecke, Timm, Rehak, Matus, Struck, Manuel Florian, Forstmeyer, Dirk, Rademacher, Sebastian, Seehofer, Daniel, Berg, Thomas, van Bömmel, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555734/
https://www.ncbi.nlm.nih.gov/pubmed/34716470
http://dx.doi.org/10.1007/s00270-021-02983-2
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author Veelken, Rhea
Maiwald, Bettina
Strocka, Steffen
Petersen, Tim-Ole
Moche, Michael
Ebel, Sebastian
Denecke, Timm
Rehak, Matus
Struck, Manuel Florian
Forstmeyer, Dirk
Rademacher, Sebastian
Seehofer, Daniel
Berg, Thomas
van Bömmel, Florian
author_facet Veelken, Rhea
Maiwald, Bettina
Strocka, Steffen
Petersen, Tim-Ole
Moche, Michael
Ebel, Sebastian
Denecke, Timm
Rehak, Matus
Struck, Manuel Florian
Forstmeyer, Dirk
Rademacher, Sebastian
Seehofer, Daniel
Berg, Thomas
van Bömmel, Florian
author_sort Veelken, Rhea
collection PubMed
description Chemosaturation (CS; CHEMOSAT®, Delcath Systems Inc.) temporarily administers melphalan into the liver by percutaneous hepatic perfusion (PHP). CS-PHP can effectively control growth in liver tumors, but efficacy and tolerability of sequential treatments are unclear. We analyzed outcomes of sequential CS-PHP treatment. Patients with either unresectable intrahepatic metastases of ocular melanoma (OM, n = 9), cholangiocarcinoma (CCA, n = 3), or hepatocellular carcinoma (HCC, n = 1) were recruited retrospectively. Response was assessed by tomography imaging. Ten patients (mean age 60 years) with more than one CS-PHP treatment were included. CS-PHP was administered 2–6 times in the OM patients, 3 times in the CCA, and the HCC patient received 6 treatments. Overall response rate (ORR) to CS-PHP was 80%, and stable disease was achieved in one patient. Median hepatic progression-free survival (hPFS) was 336 days (range 0–354) for OM, 251 days for the CCA patient, and 256 days for the HCC patient. At the end of observation (153–701 days after first CS-PHP), 6/10 patients were still alive (5/9 with OM, 0 with CCA, and 1 with HCC). Death cases were not related to CS-PHP. Adverse events were mostly hematologic, grade I-IV, and self-resolving. The liver function was not deteriorated by CS-PHP. We conclude that repeated CS-PHP treatments were effective and well tolerated in the long term. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00270-021-02983-2.
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spelling pubmed-85557342021-11-01 Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers Veelken, Rhea Maiwald, Bettina Strocka, Steffen Petersen, Tim-Ole Moche, Michael Ebel, Sebastian Denecke, Timm Rehak, Matus Struck, Manuel Florian Forstmeyer, Dirk Rademacher, Sebastian Seehofer, Daniel Berg, Thomas van Bömmel, Florian Cardiovasc Intervent Radiol Short Communication Chemosaturation (CS; CHEMOSAT®, Delcath Systems Inc.) temporarily administers melphalan into the liver by percutaneous hepatic perfusion (PHP). CS-PHP can effectively control growth in liver tumors, but efficacy and tolerability of sequential treatments are unclear. We analyzed outcomes of sequential CS-PHP treatment. Patients with either unresectable intrahepatic metastases of ocular melanoma (OM, n = 9), cholangiocarcinoma (CCA, n = 3), or hepatocellular carcinoma (HCC, n = 1) were recruited retrospectively. Response was assessed by tomography imaging. Ten patients (mean age 60 years) with more than one CS-PHP treatment were included. CS-PHP was administered 2–6 times in the OM patients, 3 times in the CCA, and the HCC patient received 6 treatments. Overall response rate (ORR) to CS-PHP was 80%, and stable disease was achieved in one patient. Median hepatic progression-free survival (hPFS) was 336 days (range 0–354) for OM, 251 days for the CCA patient, and 256 days for the HCC patient. At the end of observation (153–701 days after first CS-PHP), 6/10 patients were still alive (5/9 with OM, 0 with CCA, and 1 with HCC). Death cases were not related to CS-PHP. Adverse events were mostly hematologic, grade I-IV, and self-resolving. The liver function was not deteriorated by CS-PHP. We conclude that repeated CS-PHP treatments were effective and well tolerated in the long term. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00270-021-02983-2. Springer US 2021-10-29 2022 /pmc/articles/PMC8555734/ /pubmed/34716470 http://dx.doi.org/10.1007/s00270-021-02983-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Short Communication
Veelken, Rhea
Maiwald, Bettina
Strocka, Steffen
Petersen, Tim-Ole
Moche, Michael
Ebel, Sebastian
Denecke, Timm
Rehak, Matus
Struck, Manuel Florian
Forstmeyer, Dirk
Rademacher, Sebastian
Seehofer, Daniel
Berg, Thomas
van Bömmel, Florian
Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers
title Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers
title_full Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers
title_fullStr Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers
title_full_unstemmed Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers
title_short Repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers
title_sort repeated percutaneous hepatic perfusion with melphalan can maintain long-term response in patients with liver cancers
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555734/
https://www.ncbi.nlm.nih.gov/pubmed/34716470
http://dx.doi.org/10.1007/s00270-021-02983-2
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