Systematic Review of Preoperative Prognostic Biomarkers in Perihilar Cholangiocarcinoma

Author:

Pawaskar Rishaan1,Huang Kevin Zhang2,Pham Helen123,Nagrial Adnan45,Wong Mark45,O’Neill Siobhan5,Pleass Henry1234,Yuen Lawrence1234,Lam Vincent W. T.12346,Richardson Arthur123,Pang Tony1234,Nahm Christopher B.1234ORCID

Affiliation:

1. Department of Upper GI Surgery, Westmead Hospital, Sydney, NSW 2145, Australia

2. Westmead Hospital, Sydney, NSW 2145, Australia

3. Surgical Innovations Unit, Westmead Hospital, Sydney, NSW 2145, Australia

4. Westmead Clinical School, Faculty of Medicine and Health Sciences, The University of Sydney, Sydney, NSW 2006, Australia

5. Crown Princess Mary Cancer Centre, Westmead Hospital, Sydney, NSW 2145, Australia

6. Macquarie University Medical School, Macquarie University, Sydney, NSW 2145, Australia

Abstract

Perihilar cholangiocarcinoma (pCCA) is an uncommon malignancy with generally poor prognosis. Surgery is the primary curative treatment; however, the perioperative mortality and morbidity rates are high, with a low 5-year survival rate. Use of preoperative prognostic biomarkers to predict survival outcomes after surgery for pCCA are not well-established currently. This systematic review aimed to identify and summarise preoperative biomarkers associated with survival in pCCA, thereby potentially improving treatment decision-making. The Embase, Medline, and Cochrane databases were searched, and a systematic review was performed using the PRISMA guidelines. English-language studies examining the association between serum and/or tissue-derived biomarkers in pCCA and overall and/or disease-free survival were included. Our systematic review identified 64 biomarkers across 48 relevant studies. Raised serum CA19-9, bilirubin, CEA, neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and tumour MMP9, and low serum albumin were most associated with poorer survival; however, the cutoff values used widely varied. Several promising molecular markers with prognostic significance were also identified, including tumour HMGA2, MUC5AC/6, IDH1, PIWIL2, and DNA index. In conclusion, several biomarkers have been identified in serum and tumour specimens that prognosticate overall and disease-free survival after pCCA resection. These, however, require external validation in large cohort studies and/or in preoperatively obtained specimens, especially tissue biopsy, to recommend their use.

Publisher

MDPI AG

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