Tumour response and secondary resectability of colorectal liver metastases following neoadjuvant chemotherapy with cetuximab: the CELIM randomised phase 2 trial

…, F Lordick, JT Hartmann, H Lang, A Frilling… - The lancet …, 2010 - thelancet.com
Background Neoadjuvant chemotherapy for unresectable colorectal liver metastases can
downsize tumours for curative resection. We assessed the effectiveness of cetuximab …

Recommendations for management of patients with neuroendocrine liver metastases

A Frilling, IM Modlin, M Kidd, C Russell… - The lancet …, 2014 - thelancet.com
Many management strategies exist for neuroendocrine liver metastases. These strategies
range from surgery to ablation with various interventional radiology procedures, and include …

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET Mutation …

…, H Gharib, SN Thibodeau, A Lacroix, A Frilling… - Jama, 1996 - jamanetwork.com
Objective. —Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant
disorder. The 3 recognized subtypes include MEN 2A, characterized by medullary thyroid …

A limited set of human MicroRNA is deregulated in follicular thyroid carcinoma

…, RE Teresi, CE Broelsch, A Frilling… - The Journal of …, 2006 - academic.oup.com
Context: Although the pathogenesis of follicular thyroid carcinoma (FTC) and its relation to
follicular adenoma (FA) remains unclear, detailed understanding of FTC carcinogenesis …

Consensus on biomarkers for neuroendocrine tumour disease

…, W De Herder, M Pavel, D Klimstra, A Frilling… - The Lancet …, 2015 - thelancet.com
Management of neuroendocrine neoplasia represents a clinical challenge because of its
late presentation, lack of treatment options, and limitations in present imaging modalities and …

Germline Dinucleotide Mutation in Codon 883 of the RETProto-Oncogene in Multiple Endocrine Neoplasia Type 2B Without Codon 918 Mutation

O Gimm, DJ Marsh, SD Andrew, A Frilling… - The Journal of …, 1997 - academic.oup.com
The autosomal dominant multiple endocrine neoplasia type 2 syndromes (MEN 2) comprise
three clinically distinct entities, MEN 2A, familial medullary thyroid carcinoma and MEN 2B, …

Increased levels of interleukin-10 in serum from patients with hepatocellular carcinoma correlate with profound numerical deficiencies and immature phenotype of …

S Beckebaum, X Zhang, X Chen, Z Yu, A Frilling… - Clinical Cancer …, 2004 - AACR
Increased levels of interleukin (IL)-10 have been described as a negative prognostic
indicator for survival in patients with various types of cancer. IL-10 exerts tolerogenic and …

[HTML][HTML] Neuroendocrine tumor disease: an evolving landscape

A Frilling, G Åkerström, M Falconi… - Endocrine-related …, 2012 - erc.bioscientifica.com
Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) represent a heterogenous
group of tumors arising from a variety of neuroendocrine cell types. The incidence and …

A precision oncology approach to the pharmacological targeting of mechanistic dependencies in neuroendocrine tumors

…, AM Chinnaiyan, T Detre, S Ezzat, A Frilling… - Nature …, 2018 - nature.com
We introduce and validate a new precision oncology framework for the systematic prioritization
of drugs targeting mechanistic tumor dependencies in individual patients. Compounds …

Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene

…, VJ Hyland, BG Robinson, A Frilling… - Human Molecular …, 1994 - academic.oup.com
Mutations of the RET proto-oncogene are the underlying cause of some cases of Hlrschsprung
disease (HSCR) and the Inherited cancer syndromes multiple endocrine neoplasia types …