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A Multi-Center Experience of Direct Acting Anti-Viral Agents in HCV Positive Patients Receiving HCV Positive Livers.

N. Kapila,1 B. Zervos,2 B. Ismail,1 C. Lindenmeyer,3 V. Sanghi,3 K. Menon,3 G. Schnickel,2 J. Rivas,2 D. Reino,2 A. Tzakis.2

1Gastroenterology, Cleveland Clinic, Weston, FL
2Transplant, Cleveland Clinic, Weston, FL
3Gastroenterology, Cleveland Clinic, Cleveland, OH

Meeting: 2017 American Transplant Congress

Abstract number: 149

Keywords: Hepatitis C, Liver, Liver transplantation, Waiting lists

Session Information

Session Name: Concurrent Session: Liver: Viral Hepatitis

Session Type: Concurrent Session

Date: Sunday, April 30, 2017

Session Time: 4:30pm-6:00pm

 Presentation Time: 5:18pm-5:30pm

Location: E271a

Background: HCV cirrhosis is the leading indication for liver transplantation in the U.S. The development of direct acting anti-viral agents (DAAs) has changed the approach to HCV positive grafts. Herein, we present our experience with DAAs in HCV positive patients who receive an HCV positive graft.

Methods: Multi-center, retrospective review of patients from July, 2015 till present. HCV positive patients receiving an HCV positive liver and then treated with DAAs were included.

Results: 20 HCV positive patients received an HCV positive graft. 10 patients have started HCV treatment at the time of this abstract.

Genotype Pre-Treatment Viral Load Treatment Regimen in Weeks Response Adverse Events
1 1a 57100000 Sofosbuvir/Ledipasvir x12 SVR –
2 1a/1b 69100 Sofosbuvir/Ledipasvir x24 SVR –
3 1a 926000 Sofosbuvir/Ledipasvir/Ribavirin x12 ETR Anemia
4 1a 21400000 Sofosbuvir/Ledipasvir x12 ETR Headache
5 1a 1590000 Sofosbuvir/Ledipasvir x12 EVR Fatigue
6 1a 122000 Sofosbuvir/Ledipasvir/Ribavirin x24 EVR –
7 3 939000 Daclatasvir/Sofosbuvir/Ribavirin x12 EVR –
8 1a 20100000 Sofosbuvir/Ledipasvir/Ribavirin x12 EVR –
9 1a 10000000 Sofosbuvir/Ledipasvir/Ribavirin x16 Non-responder –
10 1a 2040000 Sofosbuvir/Ledipasvir x12 EVR –

DAAs were initiated an average of 6 months post OLT. All were on Tacrolimus based immunosupression and none required adjustment.

Discussion: Historically, HCV grafts are more likely to be discarded compared to HCV negative grafts. Our series demonstrates a favorable response to Sofosbuvir based regimens. The patients in our series were given anti-virals regardless of graft fibrosis or viral load. Our series is unique in describing empiric initiation of DAAs in HCV patients receiving a HCV graft. While further studies are required to confirm our experience, the remarkable response to DAAs may shift our approach to HCV positive grafts.

CITATION INFORMATION: Kapila N, Zervos B, Ismail B, Lindenmeyer C, Sanghi V, Menon K, Schnickel G, Rivas J, Reino D, Tzakis A. A Multi-Center Experience of Direct Acting Anti-Viral Agents in HCV Positive Patients Receiving HCV Positive Livers. Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Kapila N, Zervos B, Ismail B, Lindenmeyer C, Sanghi V, Menon K, Schnickel G, Rivas J, Reino D, Tzakis A. A Multi-Center Experience of Direct Acting Anti-Viral Agents in HCV Positive Patients Receiving HCV Positive Livers. [abstract]. Am J Transplant. 2017; 17 (suppl 3). https://atcmeetingabstracts.com/abstract/a-multi-center-experience-of-direct-acting-anti-viral-agents-in-hcv-positive-patients-receiving-hcv-positive-livers/. Accessed May 13, 2025.

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