Checkpoint Inhibition Causing Complete Remission of Metastatic Combined Hepatocellular-Cholangiocarcinoma after Hepatic Resection.

Checkpoint inhibition Combined hepatocellular-cholangiocarcinoma Immune-related hepatitis Sorafenib

Journal

Case reports in oncology
ISSN: 1662-6575
Titre abrégé: Case Rep Oncol
Pays: Switzerland
ID NLM: 101517601

Informations de publication

Date de publication:
Historique:
received: 16 03 2020
accepted: 17 03 2020
entrez: 9 6 2020
pubmed: 9 6 2020
medline: 9 6 2020
Statut: epublish

Résumé

Combined hepatocellular-cholangiocarcinoma (CHC) is a rare type of primary liver cancer, speculated to arise from hepatic progenitor cells, and with a worse prognosis than hepatocellular carcinoma (HCC). Serum alpha-fetoprotein (AFP) levels may be one prognostic factor. It has been suggested that checkpoint inhibition might be useful in the treatment of HCC where there is an increased expression of PD-1 and PD-L1 in the microenvironment. Its effect on CHC is unknown. We report a case with a large CHC, which was radically resected, but the 53-year-old female patient subsequently developed pulmonary metastases. Histology demonstrated low-differentiated CHC without microsatellite instability. Treatment with sorafenib was started but was stopped due to angioedema. Under subsequent gemcitabine/cisplatin treatment, the metastatic disease progressed with rising AFP levels. A third-line treatment with pembrolizumab was then started, 2 mg/kg b.w. i.v. every third week for 6 months. This resulted in a radiologically complete remission of the pulmonary metastases and AFP levels were normalized (<10 μg/L) from a level of 1,790 μg/L before treatment. The patient developed immune-related adverse events (AEs) including diarrhea and hepatitis. These AEs were successfully treated with prednisolone and mycophenolate mofetil, and they were eventually resolved. There are no signs of cancer recurrence neither in the liver nor in the lungs at 33 months after the start of the checkpoint inhibition treatment, and the patient is doing well. Further study is urgently needed on the role of checkpoint inhibition therapy in liver cancer.

Identifiants

pubmed: 32508620
doi: 10.1159/000507320
pii: cro-0013-0478
pmc: PMC7250374
doi:

Types de publication

Case Reports

Langues

eng

Pagination

478-484

Informations de copyright

Copyright © 2020 by S. Karger AG, Basel.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

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Auteurs

Magnus Rizell (M)

Transplant Institute, Sahlgrenska University Hospital, Gothenburg, Sweden.

Fredrik Åberg (F)

Transplant Institute, Sahlgrenska University Hospital, Gothenburg, Sweden.

Mats Perman (M)

Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Lars Ny (L)

Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Liselotte Stén (L)

Department of Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Farida Hashimi (F)

Department of Radiology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Joar Svanvik (J)

Transplant Institute, Sahlgrenska University Hospital, Gothenburg, Sweden.

Per Lindnér (P)

Transplant Institute, Sahlgrenska University Hospital, Gothenburg, Sweden.

Classifications MeSH