Profound tumor response to combined CTLA-4 and PD-1 inhibition in systemic fourth line therapy observed in a patient with hepatocellular carcinoma harboring SETD2 and LRP1B mutations.

Profundes Tumoransprechen unter kombinierter CTLA-4 und PD-1 Inhibition in systemischer Viertlinie bei einem Patienten mit Hepatozellulärem Karzinom und Nachweis von SETD2 und LRP1B Mutationen.

Journal

Zeitschrift fur Gastroenterologie
ISSN: 1439-7803
Titre abrégé: Z Gastroenterol
Pays: Germany
ID NLM: 0033370

Informations de publication

Date de publication:
Jan 2023
Historique:
pubmed: 16 11 2022
medline: 12 1 2023
entrez: 15 11 2022
Statut: ppublish

Résumé

Immunotherapy has become the standard of care in advanced HCC but is only approved in first- or second-line treatment. We report a patient with HCC refractory to several lines of tyrosine kinase inhibitors, who was treated with Ipilimumab and Nivolumab (Ipi/Nivo) as the fourth line. The tumor responded profoundly to Ipi/Nivo. Established biomarker-predicting responses to immunotherapy, such as a high PD-L1 staining, a high combined-positive score, microsatellite instability or a high tumor mutational burden, were not detected. Potential negative predictive markers for response to immunotherapy such as CTNNB1 and TERT were present. This constellation puts the spotlight on two mutations observed here in the SET domain-containing 2 (SETD2) and low-density lipoprotein receptor-related protein 1b (LRP1B) genes, which may explain the outstanding response. Our case demonstrates that immunotherapy can be efficient in a late-line scenario, resulting in long-term survival. Further studies should prospectively evaluate the value of SETD2 and LRP1B alterations as predictors for the success of immunotherapy in HCC. Die Immuntherapie wurde der Therapiestandard für die Behandlung des fortgeschrittenen HCC, ist allerdings nur in der Erst- oder Zweitlinie zugelassen. Wir berichten hier über einen Patienten mit HCC, der in einer TKI-refraktären Situation mit Ipi/Nivo in der Viertlinie therapiert wurde. Der Tumor sprach profunde auf die Therapie mit Ipi/Nivo an. Etablierte Biomarker, die ein Ansprechen auf eine Immuntherapie voraussagen können, wie eine hohe PD-L1-Expression, ein hoher

Autres résumés

Type: Publisher (ger)
Die Immuntherapie wurde der Therapiestandard für die Behandlung des fortgeschrittenen HCC, ist allerdings nur in der Erst- oder Zweitlinie zugelassen. Wir berichten hier über einen Patienten mit HCC, der in einer TKI-refraktären Situation mit Ipi/Nivo in der Viertlinie therapiert wurde. Der Tumor sprach profunde auf die Therapie mit Ipi/Nivo an. Etablierte Biomarker, die ein Ansprechen auf eine Immuntherapie voraussagen können, wie eine hohe PD-L1-Expression, ein hoher

Identifiants

pubmed: 36379463
doi: 10.1055/a-1952-1233
doi:

Substances chimiques

CTLA-4 Antigen 0
Ipilimumab 0
LRP1B protein, human 0
Nivolumab 31YO63LBSN
Programmed Cell Death 1 Receptor 0
Receptors, LDL 0
SETD2 protein, human EC 2.1.1.43

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

71-75

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

F.P.R. has received honoraria for lectures and travel support from the Falk Foundation, Gilead, Ipsen and Novartis. A.S. Advisory Board/Speaker’s Bureau: AGCT, Aignostics, Astra Zeneca, Bayer, BMS, Eli Lilly, Illumina, Incyte, Janssen, MSD, Novartis, Pfizer, Roche, Seattle Genetics, Takeda, Thermo Fisher Grants: Bayer, BMS, Chugai, Incyte A.G. has received honoraria for lectures, teaching, advisory activities and travel support from AbbVie, Alexion, Bayer, BMS, CSL Behring, Eisai, Gilead, Intercept, Falk, Ipsen, MSD, Merz, Novartis, Pfizer, Roche, Sanofi-Aventis, Sequana and has received research support from Intercept und Falk (NAFLD CSG) and Novartis.

Auteurs

Florian P Reiter (FP)

Division of Hepatology, Department of Medicine II, University Hospital Würzburg, Würzburg, Germany.
Partner site - German Alliance for Liver Cancer (GALC).

Monika Rau (M)

Division of Hepatology, Department of Medicine II, University Hospital Würzburg, Würzburg, Germany.

Volker Kunzmann (V)

Division of Oncology, Department of Medicine II, University Hospital Würzburg, Würzburg, Germany.

Ralph Kickuth (R)

Department of Diagnostic & Interventional Radiology, University Hospital Würzburg, Würzburg, Germany.

Ingo Klein (I)

Department of General, Visceral, Transplantation, Vascular and Pediatric Surgery, University Hospital Würzburg, Würzburg, Germany.

Olaf Neumann (O)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Partner site - German Alliance for Liver Cancer (GALC).

Albrecht Stenzinger (A)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Partner site - German Alliance for Liver Cancer (GALC).

Peter Schirmacher (P)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Partner site - German Alliance for Liver Cancer (GALC).

Andreas Geier (A)

Division of Hepatology, Department of Medicine II, University Hospital Würzburg, Würzburg, Germany.
Partner site - German Alliance for Liver Cancer (GALC).

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Classifications MeSH