Department of Transplantation/Pediatric Surgery, Postgraduate School of Life Science, Kumamoto University, Kumamoto 8603-8556, Japan.
Correspondence Address: Dr. Yasuhiko Sugawara, Department of Transplantation/Pediatric Surgery, Postgraduate School of Life Science, Kumamoto University, 1-1-1 Honjo, Chuo-ku, Kumamoto 8603-8556, Japan. E-mail: firstname.lastname@example.org
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Liver transplantation has now been an established treatment for hepatocellular carcinoma and cirrhosis. The Milan criteria have been accepted and applied widely in the world as an indication for deceased donor liver transplant. Due to the severe organ shortage, however, living donor liver transplant (LDLT) has accounted for the majority of transplantations in Japan and the other Asian countries/regions. LDLT cannot be limited by the restrictions imposed by the allocation system but depends on institutional criterion or case-by-case considerations. Accumulating data from a nationwide survey and each center experience have indicated that extending the Milan criteria is warranted.
Liver transplantation, living donor, hepatocellular carcinoma
Liver transplantation has now become a standard therapy for patients with hepatocellular carcinoma (HCC) in the early-stage. Liver transplantation can treat both the tumors and the underlying liver disease. Therefore patients who receive transplants theoretically have higher chance of cure than the other treatments for HCC.
Early outcome following liver transplantation was poor, associated with high incidence of HCC recurrence after transplantation. However, Mazzaferro et al. proposed the criteria to restrict liver transplantation to only those patients with HCC of a single tumor ≤ 5 cm or two or three tumors ≤ 3 cm without major vessel invasion or extrahepatic tumor spread based on the imagings. They showed a 4-year patient survival of 75% and a recurrence-free survival of 83% of the patients who meet these criteria. Many centers worldwide have now adopted the criteria for deceased donor liver transplantation and also living donor liver transplantation (LDLT). However, the criteria have been sometimes estimated as being too strict to include many patients in the transplant list.
In Asian countries/regions, unlike the Western countries, LDLT has accounted for the majority of transplantations[6,7]. LDLT can be thought to be a private issue among the patients and the families. Therefore the selection criteria of the patients from the view point of tumor status can be considered on a case-by-case basis. Also the grafts are not always restricted by the system of the public organ allocation. It should be taken into account how high the recurrence rate and the chance of survival are and how firm the will to donate the part of the liver is. Many high-volume transplantation centers have performed LDLT for patients with HCC based on the criteria extending Milan to include patients with slightly larger tumors as transplant candidates and such an expansion of criteria did not result in a significantly higher rate of disease recurrence after transplantation. The review described the current status of liver transplantation for HCC in Japan and the other Asian countries/regions.
In Japan, the serious shortage of deceased donor livers has still continued despite the approval of the Japanese Organ Transplantation Act in 1997 and its revision in 2006. According to a report from the Japanese Liver Transplantation Society Registry, by the end of 2016, 378 liver transplantations were performed using deceased donor grafts while 8825 LDLTs were performed during the same period. Of these, 1598 were indicated for HCC. The 1-, 3-, 5-, 10-, 15- and 20-year survival rates of LDLT for HCC were 85%, 75%, 70%, 62%, 55%, and 54%, respectively.
The insuring system of the Japanese Ministry of Health, Labor, and Welfare covered the patients who undergo transplantation only when the tumor status is within the Milan criteria. The tumors should be diagnosed to be HCC by computed tomography or magnetic resonance imagings obtained within one month before transplantation. The tumors must be diagnosed on the dynamic computed tomography to be low density in plain, high in arterial phase, and low in portal phase. Local treatment for HCC must be done at least 3 months before transplantation is planned. Only the patients with tumors within the Milan criteria can be listed for and undergo deceased donor liver transplantation. In LDLT, however, many Japanese institutions have their own criteria beyond the Milan.
A survey was done using a database consisting of the 653 patients who underwent LDLT for HCC in Japan between 1990 and 2005. On the preoperative imagings, 62% were within the Milan criteria while 38% were beyond. The overall patient survival was 83%, 73%, and 69%. The disease-free survival was 77%, 65%, and 61%, at 1, 3, and 5 years, respectively. The 5-year recurrence free survival was 90% and 61% for those within and beyond the Milan, respectively (P < 0.001). HCC recurred in the 92 (14%) recipients, with a rate at 1, 3, and 5 years of 9%, 20%, and 22%, respectively. The multivariate analysis revealed that preoperative alpha-feto-protein and des-gamma carboxyprothrombin (DCP) levels were independent factors for HCC recurrence.
The Kyoto group proposed that the criteria should be “tumors ≤ 5 cm and the numbers are 10 or less than 10, and DCP levels < 400 mAU/mL”. One hundred ninety-eight patients underwent LDLT for HCC between 1999 and 2011. Of these, the 147 (76%) patients met the Milan criteria. The 5-year survival rate of those within the criteria was 82% and that of those beyond was 42% (P < 0.001). The 5-year recurrence rate for those within the Kyoto criteria was less than that for patients beyond them (4% vs. 51%, P < 0.001).
The principle criteria I have adopted for LDLT for HCC in University of Tokyo is “tumor numbers ≤ 5 cm and number of the tumors ≤ 5” (5-5 rule). Of the 125 HCC patients, 118 (94%) were within the 5-5 rule and 109 (87%) were within the Milan criteria. Overall survival was 88%, 82%, and 76% at 1, 3, and 5 years, respectively. Eleven patients (9%) developed the recurrence of HCC with a rate of 6%, 9%, and 11% at 1, 3, and 5 years, respectively. Multivariate analysis showed that the tumor status beyond the 5-5 rule, alpha-feto-protein level > 400 ng/mL, and DCP level > 200 mAU/mL were independent risk factors for recurrence of HCC.
The Kyushu University proposed the extended criteria which is “tumor size ≤ 5 cm (no restrictions on the numbers) and DCP level ≤ 300 mAU/mL”. One hundred nine HCC patients underwent LDLT. Of these, 103 patients (94%) were within the criteria while 55 (50%) met the Milan criteria. The 5-year recurrence free survival of the patients who met the criteria was 71%, while all the 6 patients beyond the criteria developed recurrence of HCC within 2 years after transplantation. Totally 90 patients within the criteria were prospectively analyzed. The 5-year recurrence-free survival of the within-Milan and that of beyond were 90% and 80%, respectively with no significant difference (P = 0.22).
In Asian countries/regions other than Japan, the majority of liver transplantation for HCC patients are also LDLT. Apart from the predominance of hepatitis B related HCC[8,16], therefore, the situation in other Asian countries/regions is similar to that in Japan. The Taiwan group adopted the Milan criteria in LDLT. The 1-, 3-, and 5-year survivals were 98%, 96%, and 90%, respectively. The Asan medical center in South Korea, like Japanese institutions, advocates their own criteria, stressing “the tumor numbers ≤ 6 and the maximum diameter of the tumor size ≤ 5 cm”. The overall 5-year patient survival rates were 76.3%. The Hong Kong group has changed the criteria. Before 2002, the radiological Milan criteria were used. From 2002 till 2005, the selection criteria were expanded to match the radiological University of California, San Francisco criteria (1 tumor ≤ 6.5 cm, or 2-3 tumors ≤ 4.5 cm and total tumor diameter ≤ 8 cm). From 2006 onwards, the selected patients with more advanced HCC were enrolled for LDLT according to the following exclusion criteria: (1) no evidence of gross vascular tumor invasion, (2) no evidence of distant metastases and (3) no evidence of diffuse HCC.
Notably, most expanded criteria in the Asian countries/regions restrict the tumor ≤ 5 cm as the indication for LDLT. In contrast there is a large discrepancy regarding the limitation for the numbers. Previous studies indicated that tumors > 5 cm have a high recurrence rate after transplantation. There may be an association between tumor size, vascular invasion and poor differentiation. Microscopic vascular invasion was present in the 20% of tumors ≤ 2 cm, 30% to 60% of those of 2-5 cm, and up to 60% to 90% for those > 5 cm.
In Japan, the incidence of hepatitis-associated HCC is high (~90%) and the antiviral therapy for patients undergoing liver transplantation for hepatocellular carcinoma is mandatory. The combination of long-term antiviral and low-dose hepatitis B immune globulin can effectively prevent hepatitis B virus recurrence in more than 90% of transplant recipients. As to hepatitis C, now direct antiviral agents (DAA) have enabled us effective treatment for patients who underwent liver transplantation for hepatitis C virus related cirrhosis. The currently available direct antiviral agents achieve a satisfactory sustained viral response in post-liver transplantation patients. Optimal timing of the DAA treatment is not yet established, but it may be appropriate to consider DAA treatment after the patients’ condition and graft function become stable.
As the number of the deceased donors was scarce in Japan, unique indications and strategies in liver transplantation have been developed. LDLT will continue to be a mainstay treatment for patients with HCC and cirrhosis. The indication of transplantation in patients with HCC still continues to be under debate in Japan.
Designed the study: Yamamoto H, Hibi T
Wrote the draft of the manuscript: Sugawara YAvailability of data and materials
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All authors declare that there are no conflicts of interest.Ethical approval and consent to participate
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© The Author(s) 2018.
1. Bruix J, Reig M, Sherman M. Evidence-based diagnosis, staging, and treatment of patients with hepatocellular carcinoma. Gastroenterology 2016;150:835-53.DOIPubMed
2. El-Serag HB, Kanwal F. Epidemiology of hepatocellular carcinoma in the United States: where are we? Where do we go? Hepatology 2014;60:1767-75.DOIPubMed PMC
3. Penn I, Starzl TE. Malignant tumors arising de novo in immunosuppressed organ transplant recipients. Transplantation 1972;14:407-17.DOIPubMed PMC
4. Mazzaferro V, Regalia E, Doci R, Andreola S, Pulvirenti A, Bozzetti F, Montalto F, Ammatuna M, Morabito A, Gennari L. Liver transplantation for the treatment of small hepatocellular carcinomas in patients with cirrhosis. N Engl J Med 1996;334:693-9.DOIPubMed
5. Mancuso A, Perricone G. Hepatocellular carcinoma and liver transplantation: state of the art. J Clin Transl Hepatol 2014;2:176-81.PubMed PMC
6. de Villa V, Lo CM. Liver transplantation for hepatocellular carcinoma in Asia. Oncologist 2007;12:1321-31.DOIPubMed
7. Hwang S, Moon DB, Lee SG. Liver transplantation and conventional surgery for advanced hepatocellular carcinoma. Transpl Int 2010;23:723-7.DOIPubMed
8. Chan SC. Liver transplantation for hepatocellular carcinoma. Liver Cancer 2013;2:338-44.DOIPubMed PMC
9. Umeshita K, Inomata Y, Furukawa H, Kasahara M, Kawasaki S, Kobayashi E, Kokudo N, Sakisaka S, Shimada M, Tanaka E, Uemoto S, Japanese Liver Transplantation Society. Liver transplantation in Japan: Registry by the Japanese Liver Transplantation Society. Hepatol Res 2016;46:1171-86.DOIPubMed
10. Tamura S, Sugawara Y, Kokudo N. Living donor liver transplantation for hepatocellular carcinoma: the Japanese experience. Oncology 2011:111-5.DOIPubMed
11. Todo S, Furukawa H, Tada M. Extending indication: role of living donor liver transplantation for hepatocellular carcinoma. Liver Transpl 2007;13:S48-54.DOIPubMed
12. Kaido T, Mori A, Ogura Y, Hata K, Yoshizawa A, Iida T, Yagi S, Uemoto S. Living donor liver transplantation for recurrent hepatocellular carcinoma after liver resection. Surgery 2012;151:55-60.DOIPubMed
13. Sugawara Y, Tamura S, Makuuchi M. Living donor liver transplantation for hepatocellular carcinoma: Tokyo University series. Dig Dis 2007;25:310-2.DOIPubMed
14. Shirabe K, Taketomi A, Morita K, Soejima Y, Uchiyama H, Kayashima H, Ninomiya M, Toshima T, Maehara Y. Comparative evaluation of expanded criteria for patients with hepatocellular carcinoma beyond the Milan criteria undergoing living-related donor liver transplantation. Clin Transplant 2011;25:E491-8.DOIPubMed
15. Uchiyama H, Itoh S, Yoshizumi T, Ikegami T, Harimoto N, Soejima Y, Harada N, Morita K, Toshima T, Motomura T, Maehara Y. Living donor liver transplantation for hepatocellular carcinoma: results of prospective patient selection by Kyushu University Criteria in 7 years. HPB (Oxford) 2017;19:1082-90.DOIPubMed
16. Lee SG, Moon DB, Shin H, Kim KH, Ahn CS, Ha TY, Song GW, Jung DH, Park GC. Living donor liver transplantation for hepatocellular carcinoma: current status in Korea. Transplant Proc 2012;44:520-2.DOIPubMed
17. Concejero A, Chen CL, Wang CC, Wang SH, Lin CC, Liu YW, Yang CH, Yong CC, Lin TS, Jawan B, Huang TL, Cheng YF, Eng HL. Living donor liver transplantation for hepatocellular carcinoma: a single-center experience in Taiwan. Transplantation 2008;85:398-406.PubMed
18. Lee S, Ahn C, Ha T, Moon D, Choi K, Song G, Chung D, Park G, Yu Y, Choi N, Kim K, Kim K, Hwang S. Liver transplantation for hepatocellular carcinoma: Korean experience. J Hepatobiliary Pancreat Sci 2010;17:539-47.DOIPubMed
19. Ng KK, Lo CM, Chan SC, Chok KS, Cheung TT, Fan ST. Liver transplantation for hepatocellular carcinoma: the Hong Kong experience. J Hepatobiliary Pancreat Sci 2010;17:548-54.DOIPubMed
20. Klintmalm GB. Liver transplantation for hepatocellular carcinoma: a registry report of the impact of tumor characteristics on outcome. Ann Surg 1998;228:479-90.DOIPubMed PMC
21. Ravaioli M, Grazi GL, Vetrone G, Kimura T, Zanello M, Ercolani G, Cescon M, Varotti G, Del Gaudio M, Tuci F, Cucchetti A, La Barba G, Vivarelli M, Lauro A, Ramacciato G, Pinna AD. A new liver transplant priority for patients with hepatocellular carcinoma. Hepatogastroenterology 2008;55:1742-5.PubMed
22. Roche B, Samuel D. Prevention of hepatitis B virus reinfection in liver transplant recipients. Intervirology 2014;57:196-201.DOIPubMed
23. Chen T, Terrault NA. Perspectives on treating hepatitis C infection in the liver transplantation setting. Curr Opin Organ Transplant 2016;21:111-9.DOIPubMed
24. Sugawara Y, Hibi T. Direct-acting agents for hepatitis C virus before and after liver transplantation. Biosci Trends 2018;11:606-11.DOIPubMed
Sugawara Y, Yamamoto H, Hibi T. Living donor liver transplantation for patients with hepatocellular carcinoma in Japan. Hepatoma Res 2018;4:33. http://dx.doi.org/10.20517/2394-5079.2018.69