Patient-derived tumor organoids for personalized medicine in a patient with rare hepatocellular carcinoma with neuroendocrine differentiation: a case report.

Hepatocellular carcinoma

Journal

Communications medicine
ISSN: 2730-664X
Titre abrégé: Commun Med (Lond)
Pays: England
ID NLM: 9918250414506676

Informations de publication

Date de publication:
2022
Historique:
received: 21 09 2021
accepted: 21 06 2022
entrez: 5 7 2022
pubmed: 6 7 2022
medline: 6 7 2022
Statut: epublish

Résumé

Hepatocellular carcinoma with neuroendocrine differentiation (HCC-NED) is a very rare subtype of primary liver cancer. Treatment allocation in these patients therefore remains a challenge. We report the case of a 74-year-old man with a HCC-NED. The tumor was surgically removed in curative intent. Histopathological work-up revealed poorly differentiated hepatocellular carcinoma (Edmondson-Steiner grade IV) with diffuse expression of neuroendocrine markers synaptophysin and chromogranin. Three months after resection, multifocal recurrence of the HCC-NED was observed. In the meantime, tumor organoids have been generated from the resected HCC-NED and extensively characterized. Sensitivity to a number of drugs approved for the treatment of HCC or neuroendocrine carcinomas was tested in vitro. Based on the results of the in vitro drug screening, etoposide and carboplatin are used as first line palliative combination treatment. With genomic analysis revealing a The rapid establishment of patient-derived tumor organoids allows in vitro drug testing and thereby personalized treatment choices, however clinical translation remains a challenge. To the best of our knowledge, this report provides a first proof-of-principle for using organoids for personalized medicine in this rare subtype of primary liver cancer.

Sections du résumé

Background UNASSIGNED
Hepatocellular carcinoma with neuroendocrine differentiation (HCC-NED) is a very rare subtype of primary liver cancer. Treatment allocation in these patients therefore remains a challenge.
Methods UNASSIGNED
We report the case of a 74-year-old man with a HCC-NED. The tumor was surgically removed in curative intent. Histopathological work-up revealed poorly differentiated hepatocellular carcinoma (Edmondson-Steiner grade IV) with diffuse expression of neuroendocrine markers synaptophysin and chromogranin. Three months after resection, multifocal recurrence of the HCC-NED was observed. In the meantime, tumor organoids have been generated from the resected HCC-NED and extensively characterized. Sensitivity to a number of drugs approved for the treatment of HCC or neuroendocrine carcinomas was tested in vitro.
Results UNASSIGNED
Based on the results of the in vitro drug screening, etoposide and carboplatin are used as first line palliative combination treatment. With genomic analysis revealing a
Conclusion UNASSIGNED
The rapid establishment of patient-derived tumor organoids allows in vitro drug testing and thereby personalized treatment choices, however clinical translation remains a challenge. To the best of our knowledge, this report provides a first proof-of-principle for using organoids for personalized medicine in this rare subtype of primary liver cancer.

Identifiants

pubmed: 35789568
doi: 10.1038/s43856-022-00150-3
pii: 150
pmc: PMC9249908
doi:

Types de publication

Journal Article

Langues

eng

Pagination

80

Informations de copyright

© The Author(s) 2022.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare no competing interest.

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Auteurs

Marie-Anne Meier (MA)

Department of Biomedicine, University Hospital and University of Basel, CH-4031 Basel, Switzerland.
Clarunis University Center for Gastrointestinal and Liver Diseases, CH-4002 Basel, Switzerland.

Sandro Nuciforo (S)

Department of Biomedicine, University Hospital and University of Basel, CH-4031 Basel, Switzerland.

Mairene Coto-Llerena (M)

Department of Biomedicine, University Hospital and University of Basel, CH-4031 Basel, Switzerland.
Institute of Medical Genetics and Pathology, University Hospital Basel, CH-4031 Basel, Switzerland.

John Gallon (J)

Department of Biomedicine, University Hospital and University of Basel, CH-4031 Basel, Switzerland.

Matthias S Matter (MS)

Institute of Medical Genetics and Pathology, University Hospital Basel, CH-4031 Basel, Switzerland.

Caner Ercan (C)

Institute of Medical Genetics and Pathology, University Hospital Basel, CH-4031 Basel, Switzerland.

Jürg Vosbeck (J)

Institute of Medical Genetics and Pathology, University Hospital Basel, CH-4031 Basel, Switzerland.

Luigi M Terracciano (LM)

Department of Anatomic Pathology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Humanitas University, Department of Biomedical Sciences, Pieve Emanuele, Milan, Italy.

Savas D Soysal (SD)

Clarunis University Center for Gastrointestinal and Liver Diseases, CH-4002 Basel, Switzerland.

Daniel Boll (D)

Radiology and Nuclear Medicine, University Hospital Basel, CH-4031 Basel, Switzerland.

Otto Kollmar (O)

Clarunis University Center for Gastrointestinal and Liver Diseases, CH-4002 Basel, Switzerland.

Raphaël Delaloye (R)

Department of Oncology, University Hospital Basel, CH-4031 Basel, Switzerland.

Salvatore Piscuoglio (S)

Department of Biomedicine, University Hospital and University of Basel, CH-4031 Basel, Switzerland.
Institute of Medical Genetics and Pathology, University Hospital Basel, CH-4031 Basel, Switzerland.

Markus H Heim (MH)

Department of Biomedicine, University Hospital and University of Basel, CH-4031 Basel, Switzerland.
Clarunis University Center for Gastrointestinal and Liver Diseases, CH-4002 Basel, Switzerland.

Classifications MeSH