eprintid: 1469793 rev_number: 35 eprint_status: archive userid: 608 dir: disk0/01/46/97/93 datestamp: 2015-07-08 14:29:22 lastmod: 2021-10-18 00:24:07 status_changed: 2015-07-08 14:29:22 type: article metadata_visibility: show item_issues_count: 0 creators_name: Rodríguez-Perálvarez, M creators_name: De la Mata, M creators_name: Burroughs, AK title: Liver transplantation ispublished: pub divisions: UCL divisions: B02 divisions: C10 note: This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. https://creativecommons.org/licenses/by-nc-nd/3.0/ abstract: Purpose of review: Long-term survival of liver transplant recipients is threatened by increased rates of de-novo malignancy and recurrence of hepatocellular carcinoma (HCC), both events tightly related to immunosuppression. Recent findings: There is accumulating evidence linking increased exposure to immunosuppressants and carcinogenesis, particularly concerning calcineurin inhibitors (CNIs), azathioprine and antilymphocyte agents. A recent study including 219 HCC transplanted patients showed that HCC recurrence rates were halved if a minimization of CNIs was applied within the first month after liver transplant. With mammalian target of rapamycin (mTOR) inhibitors as approved immunosuppressants for liver transplant patients, pooled data from several retrospective studies have suggested their possible benefit for reducing HCC recurrence. Summary: Randomized controlled trials with sufficiently long follow-up are needed to evaluate the influence of different immunosuppression protocols in preventing malignancy after LT. Currently, early minimization of CNIs with or without mTOR inhibitors or mycophenolate seems a rational strategy for patients with risk factors for de-novo malignancy or recurrence of HCC after liver transplant. A deeper understanding of the immunological pathways of rejection and cancer would allow for designing more specific and safer drugs, and thus to prevent cancer after liver transplant. date: 2014-06 official_url: http://dx.doi.org/10.1097/MOT.0000000000000069 oa_status: green full_text_type: pub language: eng primo: open primo_central: open_green verified: verified_manual elements_source: crossref elements_id: 1041756 doi: 10.1097/MOT.0000000000000069 lyricists_name: Burroughs, Andrew lyricists_id: AKBUR15 full_text_status: public publication: Current Opinion in Organ Transplantation volume: 19 number: 3 pagerange: 253 - 260 issn: 1087-2418 citation: Rodríguez-Perálvarez, M; De la Mata, M; Burroughs, AK; (2014) Liver transplantation. Current Opinion in Organ Transplantation , 19 (3) 253 - 260. 10.1097/MOT.0000000000000069 <https://doi.org/10.1097/MOT.0000000000000069>. Green open access document_url: https://discovery.ucl.ac.uk/id/eprint/1469793/1/Liver_transplantation___immunosuppression_and.8.pdf