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Molecular portraits of patients with intrahepatic cholangiocarcinoma who diverge as rapid progressors or long survivors on chemotherapy

Abstract:
OBJECTIVE: Cytotoxic agents are the cornerstone of treatment for patients with advanced intrahepatic cholangiocarcinoma (iCCA), despite heterogeneous benefit. We hypothesised that the pretreatment molecular profiles of diagnostic biopsies can predict patient benefit from chemotherapy and define molecular bases of innate chemoresistance. DESIGN: We identified a cohort of advanced iCCA patients with comparable baseline characteristics who diverged as extreme outliers on chemotherapy (survival 23 m in long survivors, LS). Diagnostic biopsies were characterised by digital pathology, then subjected to whole-transcriptome profiling of bulk and geospatially macrodissected tissue regions. Spatial transcriptomics of tumour-infiltrating myeloid cells was performed using targeted digital spatial profiling (GeoMx). Transcriptome signatures were evaluated in multiple cohorts of resected cancers. Signatures were also characterised using in vitro cell lines, in vivo mouse models and single cell RNA-sequencing data. RESULTS: Pretreatment transcriptome profiles differentiated patients who would become RPs or LSs on chemotherapy. Biologically, this signature originated from altered tumour-myeloid dynamics, implicating tumour-induced immune tolerogenicity with poor response to chemotherapy. The central role of the liver microenviroment was confrmed by the association of the RPLS transcriptome signature with clinical outcome in iCCA but not extrahepatic CCA, and in liver metastasis from colorectal cancer, but not in the matched primary bowel tumours. CONCLUSIONS: The RPLS signature could be a novel metric of chemotherapy outcome in iCCA. Further development and validation of this transcriptomic signature is warranted to develop precision chemotherapy strategies in these settings
Publication status:
Published
Peer review status:
Peer reviewed

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Author
ORCID:
0000-0002-2224-2663
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Role:
Author
ORCID:
0000-0002-5579-7454
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Role:
Author
ORCID:
0000-0003-4432-6670
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Role:
Author
ORCID:
0000-0001-8570-2519
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Role:
Author
ORCID:
0000-0001-8898-3600


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Funder identifier:
10.13039/501100000589
Grant:
TCS/21/25
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Funder identifier:
10.13039/100020581
Grant:
HUNTER
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Funder identifier:
10.13039/501100004587
Grant:
PI21/01619
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Funder identifier:
10.13039/100010269
Grant:
31038
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Funder identifier:
10.13039/100008392
Grant:
1030-00070B


Publisher:
BMJ Publishing Group
Journal:
Gut More from this journal
Volume:
73
Issue:
3
Pages:
496-508
Publication date:
2023-09-27
Acceptance date:
2023-09-11
DOI:
EISSN:
1468-3288
ISSN:
0017-5749


Language:
English
Keywords:
Pubs id:
1537197
Local pid:
pubs:1537197
Source identifiers:
W4387093069
Deposit date:
2026-05-17
ARK identifier:
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