Molecular-based targeted therapies in patients with hepatocellular carcinoma and hepato-cholangiocarcinoma refractory to atezolizumab/bevacizumab

被引:23
|
作者
Limousin, Wendy [1 ]
Laurent-Puig, Pierre [2 ,3 ,4 ]
Ziol, Marianne [1 ,5 ,6 ]
Ganne-Carrie, Nathalie [1 ,7 ]
Nahon, Pierre [1 ]
Ait-Omar, Amal [8 ]
Seror, Olivier [1 ,9 ]
Sidali, Sabrina [10 ]
Campani, Claudia [1 ,11 ]
Blanc, Pierre [3 ]
Lermine, Alban [3 ]
Marisa, Laetitia [3 ]
Zucman-Rossi, Jessica [1 ]
Nault, Jean-Charles [1 ,7 ,12 ]
机构
[1] Sorbonne Univ, Univ Paris, Cordeliers Res Ctr,Inserm,Labex OncoImmunol, Funct Genom Solid Tumors,Equipe Labellisee Ligue N, F-75006 Paris, France
[2] Sorbonne Univ, Univ Paris Cite, Cordeliers Res Ctr, INSERM,CNRS SNC 5096, Paris, France
[3] Multis Med Biol Lab SeqOIA, Paris, France
[4] Hop Europeen Georges Pompidou, AP HP, Inst Canc Paris CARPEM, Paris, France
[5] Hop Univ Paris Seine St, APHP, Denis Avicenne Avicenne Hosp, Pathol Dept, Bobigny, France
[6] Hop Univ Paris Seine St, APHP, Denis Avicenne Avicenne Hosp, F-00027 Bobigny, France
[7] Avicenne Hosp, APHP, Liver Unit, Bobigny, France
[8] Avicenne Hosp, APHP, Gastroenterol Unit, Bobigny, France
[9] Avicenne Hosp, APHP, Intervent Radiol Unit, Bobigny, France
[10] Paris Cite Univ, APHP, Beaujon Hosp, Liver Unit,DMU DIGEST, Clichy, France
[11] Univ Florence, Dept Expt & Clin Med, Internal Med & Hepatol Unit, Florence, Italy
[12] Avicenne Hosp, AP HP, Hepatol unit, 125 rue Stalingrad, F-93000 Bobigny, France
关键词
hepatocellular carcinoma; hepatocholangiocarcinoma; next generation sequencing; precision medicine; targeted therapy;
D O I
10.1016/j.jhep.2023.08.017
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The "French Medicine Genomic program 2025" has been designed to give patients with cancers that are refractory to systemic treatments access to off-label therapies adapted to their specific genomic profile. Herein, we reported the results of this program in patients with advanced hepatocellular carcinoma (HCC) and hepato-cholangiocarcinoma (H-CCK). Methods: In one center, all patients with HCC or H-CCK who progressed under atezolizumab/bevacizumab with available tumor frozen samples benefited from whole-genome/-exome and RNA sequencing. Targeted therapies were matched to genomic alterations following the recommendations of a molecular tumor board and radiological response and overall survival were assessed. Results: Among 135 patients with HCC and H-CCK treated by atezolizumab/bevacizumab, 20 patients benefited from genomic analysis after progression (16 HCC; 4 H-CCK). Nineteen patients had analyzable data, 70% were male, median age was 57 years, 65% had metastatic disease and 45% had vascular invasion. Among these 19 patients, 14 patients (76%) harbored at least one actionable genomic alteration and 9/14 received an adapted targeted therapy (45%). One patient with H-CCK showing CDK4 amplification was treated with palbociclib and achieved a partial radiological response for 16 months. Another patient with H-CCK, high HER2 overexpression and a high homologous recombination score was treated with trastuzumab/olaparib and had stable disease. One patient with an HCC and bi-allelic inactivation of TSC2 achieved a complete radiological response under everolimus. The remaining six treated patients (all HCC) had progressive disease, including three patients treated with trametinib, two with everolimus and one with olaparib. Conclusion: Molecular-based guided therapy is feasible in patients with HCC/H-CCK progressing under atezolizumab/bevacizumab and may be useful in a small subset of patients.(c) 2023 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1450 / 1458
页数:10
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