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Expansion of the Milan criteria without any sacrifice: combination of the Hangzhou criteria with the pre-transplant platelet-to-lymphocyte ratio
BMC Cancer volume 17, Article number: 14 (2017)
The Hangzhou criteria expand the Milan criteria safely and effectively in selecting hepatocellular carcinoma (HCC) candidates for liver transplantation (LT), but some patients exceeding the Milan but fulfilling the Hangzhou criteria still show poor outcomes due to early tumor recurrence. In this study, the platelet-to-lymphocyte ratio (PLR) was employed to differentiate high-risk tumor recurrence recipients, and a new method combining PLR and the Hangzhou criteria was established.
The clinical data of 343 LT for HCC were retrospectively analyzed. Receiver operating characteristic (ROC) analysis was used to determine the PLR cut-off value to stratify patients exceeding the Milan but fulfilling the Hangzhou criteria. The recurrence-free survival (RFS) of recipients was compared after stratification. The Hangzhou criteria & PLR method was proposed and its feasibility was validated by ROC analysis.
PLR 120 was the most significant cut-off value when comparing RFS of patients exceeding the Milan but fulfilling the Hangzhou criteria. After stratification, the 1-, 3-, and 5-year RFS of patients exceeding the Milan but fulfilling the Hangzhou criteria with PLR < 120 were 84.2%, 73.3%, and 73.3%, respectively, comparable with 85.7%, 73.9%, and 72.8%, respectively, in patients fulfilling the Milan criteria (P = 0.885). Patients exceeding the Milan but fulfilling the Hangzhou criteria with PLR ≥ 120 showed poor outcomes, which were similar in patients exceeding the Hangzhou criteria; 1-, 3-, and 5-year RFS were only 37.5%, 12.5%, and 12.5% vs. 32.3%, 17.6%, and 15.1%, respectively (P = 0.887). ROC analysis demonstrated that the ROC area of the Hangzhou criteria & PLR method was 0.768 for RFS. Multivariate analysis confirmed that PLR ≥ 120 was independently associated with RFS of patients exceeding the Milan but fulfilling the Hangzhou criteria.
The Hangzhou criteria combined with the pre-transplant PLR can accurately exclude high-risk tumor recurrence recipients; this approach expands the Milan criteria effectively without any sacrifice.
Hepatocellular carcinoma (HCC) ranks fifth in morbidity, and third in mortality of cancer in the world . In 2012, the estimated number of new liver malignancy and deaths were 782,500 and 745,500, respectively. Unfortunately, about half of the new cases and deaths of liver cancer happened in China . Liver transplantation (LT) provides the best prognosis for well-selected HCC patients by removing both the tumor and the underlying carcinogenic liver. In the early period, the outcome of LT for HCC was disappointing because of the high tumor recurrence rate of about 30–40% [3, 4]. This situation has changed dramatically since the introduction of the Milan criteria (a solitary HCC nodule 5.0 cm or less in diameter or no more than 3 tumor nodules and each 3.0 cm or less in diameter, without tumor invasion of blood vessels or lymph nodes) . In subsequent studies, it was shown that the selection criteria should not be as restrictive as the Milan criteria, and a number of extended criteria have been proposed, such as the University of California San Francisco (UCSF) criteria by Yao et al. in 2001 , the Hangzhou criteria (total tumor diameter ≤ 8 cm; or total tumor diameter > 8 cm, with histopathologic grade I or II and pre-operative AFP level ≤ 400 ng/mL, simultaneously) by Zheng et al. in 2008 , and the up-to-seven criteria by Mazzaferro et al. in 2009 , respectively. After expansion, increased numbers of eligible HCC patients were provided the chance to be transplanted, with an increase of 16.3% by the UCSF criteria and up to 51.5% by the Hangzhou criteria in the Chinese population . Although there is no statistically significant difference in post-transplant survival between the expanded criteria and the Milan criteria, a mathematic decrease in survival rates was shown in patients exceeding the Milan but fulfilling the expanded criteria compared with those fulfilling the Milan criteria [6, 7, 9]. This situation indicates that there are always exceptional patients exceeding the Milan but fulfilling the expanded criteria who will not benefit from LT, so it is important to differentiate these high-risk tumor recurrence patients from the waiting list.
Recently, systemic inflammation has been shown to be related to a poor prognosis and increased tumor progression. As a marker of the systemic inflammatory response, the platelet-to-lymphocyte ratio (PLR) has been shown to be a prognostic factor for various tumors [10, 11]. Our previous study also identified that an elevated PLR predicted increased HCC recurrence rates after LT . In this study, we aimed to investigate the value of PLR in differentiating those high-risk tumor recurrence candidates who exceed the Milan but fulfill the Hangzhou criteria and further establish a new method combining the Hangzhou criteria and pre-transplant PLR to precisely select HCC patients for LT.
A total of 343 patients who received LT for HCC were enrolled in this retrospective study, and all the HCC developed on the background of liver cirrhosis, which was confirmed by pathology of the explanted liver. The exclusion criteria were (1) recipient age less than 18 years, (2) patients who died during the first month after LT, (3) recipients without clinical data and follow-up data, and (4) patients with pre-transplant sepsis, hypersplenism, or massive gastrointestinal tract bleeding. All the LT were performed at the first affiliated hospital, School of Medicine, Zhejiang University, between January 2003 and December 2013.
Ethical approval was obtained from the Committee of Ethics in Biomedical Research of Zhejiang University and conformed to the ethical guidelines of the Declaration of Helsinki. Written informed consent was obtained from all participants.
Study design and data collection
The complete blood count was performed every week or as necessary before LT; the PLR was calculated as the ratio of the platelet count to the lymphocyte count according to the complete blood count performed within one month before LT; if more than one set of measurements were available for a given patient, only the lowest PLR value was used.
The diagnosis of HCC and tumor-related characteristics including tumor number, tumor size, macrovascular invasion, microvascular invasion, and tumor cell differentiation grading were evaluated based on the pathological findings. The judgment regarding fulfillment of the Milan or the Hangzhou criteria was based on a pathological examination of explanted livers.
The recipients’ clinical data including age, gender, model of end-stage liver disease (MELD) score, hepatitis B virus (HBV) infection status, and transplantation type (living donor liver transplantation [LDLT] or deceased donor liver transplantation [DDLT]) were collected. Pre-transplant treatment for HCC was also recorded, i.e. surgical resection and interventional therapies including transarterial chemoembolization, thermal ablation, and percutaneous ethanol injection.
All transplanted recipients were followed up. Screening for tumor recurrence was performed by α-fetoprotein (AFP) measurement and ultrasonography every month during the first six months and performed every two months during the second six months. In subsequent years, the patients received examinations every three to six months or when necessary. Thoracoabdominal computed tomography was performed every six months or when necessary. Bone scan or positron emission tomography was carried out in cases of suspected HCC recurrence. The date of tumor recurrence was defined as the time at which the tumor recurrence was confirmed by radiological examination or AFP measurement. The recurrence-free survival (RFS) of patients was recorded.
Data are summarized as the mean with standard deviation (SD) for continuous variables and percentages for discrete variables. Student’s t test and the Mann–Whitney U test were used for the comparison of continuous variables with a normal distribution and non-normal distribution, respectively. The chi-squared test was used for categorical variables. Survival analysis was performed using the Kaplan-Meier method and compared using the log-rank test. Receiver operating characteristic (ROC) analysis was used to determine the PLR cut-off value with the most significance in terms of predicting tumor recurrence after LT; the optimal PLR cut-off value was considered when the highest Youden index (sensitivity + specificity - 1) was presented. Cox proportional hazards regression was used to evaluate the risk factors of survival rates. Data were analyzed using SPSS 16.0 (SPSS Inc. Chicago, CA, USA). A P value <0.05 was considered statistically significant.
Clinical characteristics of 343 patients received LT for HCC
A total of 500 LT for HCC were performed, and 343 HCC patients were enrolled in this study after exclusion (Fig. 1). The mean age of recipients was 49.4 (19.0–71.0) years, and 308 (89.8%) cases were males and 35 (10.2%) were females. Of these patients, 320 (93.3%) were HBV infected, the pre-transplant MELD score was 13.0 ± 6.0, and LDLT was performed in 41 (12.0%) patients. Before LT, 52 (15.2%) patients received surgical tumor resections and 170 (49.6%) received interventional therapies. The mean follow-up period was 57.7 months, ranging from 33.5–156.0 months.
Outcomes of patients divided according to the Milan and Hangzhou criteria
Of these patients, 144 (42.0%) patients were within the Milan criteria (in-Milan group), 49 (14.3%) were beyond the Milan but within the Hangzhou criteria (Milan ~ Hangzhou group), and the remaining 150 patients (43.7%) were beyond the Hangzhou criteria (out-Hangzhou group). The 1-, 3-, and 5-year RFS of patients in the out-Hangzhou group were 32.3%, 17.6%, and 15.1%, respectively, significantly worse than the other two groups. The 1-, 3-, and 5-year RFS of the Milan ~ Hangzhou group were 76.1%, 62.6%, and 62.6%, respectively, less than the 85.1%, 73.4%, and 72.2% of the in-Milan group, respectively, but no statistically significant difference was presented (Fig. 2).
Stratification of patients in the Milan ~ Hangzhou group by pre-transplant PLR values
The stratification analysis of patients in the Milan ~ Hangzhou group was performed using different PLR values. As described previously , we used the ROC curve to determine the PLR cut-off value with the most significance in predicting tumor recurrence after LT; the Youden index was highest when the PLR was 120 with a sensitivity and specificity of 61.6% and 62.7%, respectively. Therefore, we considered PLR = 120 as the optimal cut-off. After stratification, the 49 patients in the Milan ~ Hangzhou group were divided into the Milan ~ Hangzhou and PLR < 120 group (40 patients) and the Milan ~ Hangzhou and PLR ≥ 120 group (9 patients).
Comparison of survival rates after stratification by PLR
As shown in Fig. 3, there were significant differences between the RFS of the two sub-groups divided according to PLR 120 (P = 0.000). The 1-, 3-, and 5-year RFS of the Milan ~ Hangzhou and PLR < 120 group were 84.2%, 73.3%, and 73.3%, respectively, comparable with 85.7%, 73.9%, and 72.8%, respectively, of the in-Milan group (P = 0.885). To our surprise, the Milan ~ Hangzhou and PLR ≥ 120 group showed very poor outcomes which were similar to those of the out-Hangzhou group, i.e. the 1-, 3-, and 5-year RFS were 37.5%, 12.5%, and 12.5% vs. 32.3%, 17.6%, and 15.1%, respectively (P = 0.887).
We further stratified the patients fulfilling the Milan criteria or exceeding the Hangzhou criteria using PLR 120, but we could not find significant differences in RFS in either the in-Milan (Fig. 4a) or out-Hangzhou group (Fig. 4b). In addition, we also used different PLR cut-off values (90, 100, 110, 130, and 140) to do the survival analysis, but we failed to find any differentiate value of PLR in HCC patients fulfilling the Milan criteria (Additional file 1: Figure S1), or exceeding the Hangzhou criteria (Additional file 2: Figure S2).
Establishment of the Hangzhou criteria & PLR method
Based on our present study, we developed the so-called “Hangzhou criteria & PLR method”: patients exceeding the Milan but fulfilling the Hangzhou criteria with PLR < 120, together with those fulfilling the Milan criteria, were regarded as fulfilling the Hangzhou criteria & PLR method, while patients exceeding the Milan but fulfilling the Hangzhou criteria with PLR ≥ 120 as well as patients exceeding the Hangzhou criteria should be regarded as exceeding the Hangzhou criteria & PLR method.
Using the Hangzhou criteria & PLR method, the ROC analysis showed that the ROC area was 0.768 for RFS, higher than that of the current selection criteria including the Milan, UCSF, up-to-seven, and Hangzhou criteria (Fig. 5a).
In our cohort, compared to the Milan criteria, the UCSF, up-to-seven, Hangzhou criteria provided an expansion of 15.3% (n = 22), 17.4% (n = 25), and 34.0% (n = 49), respectively. The expansion of Hangzhou criteria & PLR method was 27.8% (n = 40), lower than that of Hangzhou criteria, but higher than that of UCSF and up-to-seven criteria (Fig. 5b).
Tumor-related characteristics and clinical data in the Milan ~ Hangzhou and PLR < 120 and Milan ~ Hangzhou and PLR ≥ 120 groups
In order to identify an explanation for the poor outcomes in the Milan ~ Hangzhou and PLR ≥ 120 group, we evaluated the distribution of tumor-related characteristics and clinical data between the PLR ≥ 120 and < 120 groups of patients exceeding the Milan but fulfilling the Hangzhou criteria. As shown in Table 1, we found that a high proportion of patients with PLR ≥ 120 had a large tumor size of ≥ 7 cm, pre-transplant partial hepatectomy and interventional therapies. There was no difference in terms of recipient age, gender, MELD score, AFP level, HBV infection status, LDLT, microvascular invasion, tumor lesion number, or tumor differentiation. This result indicates that patients with PLR ≥ 120 tended to be associated with a large tumor size, pre-transplant partial hepatectomy and interventional therapies. These disparities may be an explanation for the poor prognosis of patients with PLR ≥ 120.
Univariate and multivariate analysis of risk factors for RFS of patients in Milan ~ Hangzhou group
The univariate Cox regression analysis showed that pre-transplant PLR ≥ 120, AFP ≥ 200 ng/ml and pre-LT surgical resection were risk factors of RFS of patients in Milan ~ Hangzhou group. Based on multivariate Cox regression analysis, pre-transplant PLR ≥ 120 (hazard ratio [HR] = 5.194, P = 0.020) and AFP ≥ 200 ng/ml (HR = 4.313, P = 0.004) were confirmed as independent risk factors of RFS of HCC patients in Milan ~ Hangzhou group (Table 2).
Since the induction of the Milan criteria by Mazzaferro et al. in 1996, excellent clinical outcomes after LT have been achieved for HCC patients fulfilling the Milan criteria [5, 13]. In the following decades, the selection criteria were expanded effectively and safely [6, 7]. The current selection criteria are based solely or mainly on a pre-transplant radiological examination, which places no consideration on tumor biological behavior and is limited in detecting small tumor lesions. Radiological imaging has been reported to be insufficiently accurate and always underestimates the real tumor status . To avoid the bias caused by radiological imaging, many studies have been performed to identify biological markers which can be used in combination with the current selection criteria, including AFP , matrix metalloproteinase-9 , osteopontin , and albumin mRNA . For example, Sieghart et al. indicated that serum osteopontin is an independent predictor of RFS in patients beyond the Milan criteria, and the authors suggested that osteopontin staining in liver biopsies should be performed at the time of LT, especially for the candidates exceeding the Milan criteria . Recently, Xu et al. studied a large cohort of Chinese HCC patients and stratified patients fulfilling the Hangzhou criteria into type A (tumor burden ≤8 cm or tumor burden >8 cm, but with AFP ≤100 ng/mL and well to moderate differentiation) and type B (tumor burden >8 cm, but AFP between 100 and 400 ng/mL and well to moderate differentiation). These authors found that Hangzhou type B was associated with a relatively poor prognosis, and suggested that Hangzhou type B should be regarded as a relative contraindication for LT considering the shortage of organs .
In our study, the pre-transplant PLR was employed in combination with Hangzhou criteria to select HCC candidates for LT. In recent years, studies have confirmed that elevated systemic inflammation predicts poor prognosis in various kinds of cancers, including HCC . The tumor can stimulate the inflammatory process, and inflammatory cells can promote angiogenesis, tumor proliferation, and metastasis by complicated molecular mechanisms [20, 21]. Various indices have been used to evaluate systemic inflammation, including the PLR, neutrophil-to-lymphocyte ratio , and modified Glasgow prognostic score . All these indices can be easily calculated based on routinely performed blood tests in the clinical work-up. For PLR, it can be used to predict the prognosis of HCC patients receiving transarterial chemoembolization , thermal ablation , or partial hepatectomy . Our previous work also confirmed that pre-transplant elevated PLR was associated with a high proportion of multiple tumors, large tumor size, micro- and macrovascular invasion, and predicted post-transplant tumor recurrence .
Our present study identified that HCC patients exceeding the Milan but fulfilling the Hangzhou criteria could be stratified effectively by the pre-transplant PLR value. After stratification, the patients exceeding the Milan but fulfilling the Hangzhou criteria with PLR ≥ 120 showed poor outcomes, which were very similar to those of patients exceeding the Hangzhou criteria, indicating that PLR ≥ 120 effectively excludes high-risk tumor recurrence patients from candidates exceeding the Milan but fulfilling the Hangzhou criteria. The prognosis of patients exceeding the Milan but fulfilling the Hangzhou criteria with PLR < 120 was almost the same as patients fulfilling the Milan criteria. Furthermore, the multivariate analysis confirmed that PLR ≥ 120 was an independent risk factor of RFS of HCC patients exceeding the Milan but fulfilling the Hangzhou criteria. Consistent with previous studies , PLR failed to predict post-transplant tumor recurrence for patients fulfilling the Milan criteria. Our results show that patients fulfilling the Milan criteria can obtain satisfactory outcomes whether elevated pre-transplant PLR is present or not. In line with our estimation, patients exceeding the Hangzhou criteria were associated with poor prognosis regardless of their PLR status.
According to this study, we propose the Hangzhou criteria & PLR method. In this method, patients exceeding the Milan but fulfilling the Hangzhou criteria with PLR < 120 should be regarded homogenously as those fulfilling the Milan criteria; similarly, patients exceeding the Hangzhou criteria, and patients who exceed the Milan but fulfill the Hangzhou criteria with PLR ≥ 120 should be regarded as contraindicated for LT. The ROC analysis confirmed the feasibility of this new method and demonstrated its superiority to other selection criteria. Compared to the Milan criteria, 40 (27.8%) more patients were provided the option of LT by the Hangzhou criteria & PLR method without any sacrifice in prognosis.
One limitation of our study was the small number of enrolled patients, and all these recipients were Chinese citizens and majority of them were hepatitis B virus infected. Further studies based on a larger, multi-center cohort need to be carried out to verify our conclusions. The advantage of our study was that the PLR value we used can be obtained easily and conveniently from the routinely performed complete blood count, in contrast to other molecular or genetic markers or complicated mathematical predictive models.
In order to maximize recipient benefit and make full use of scarce liver grafts, we suggest that pre-transplant PLR can be combined with the Hangzhou criteria to select LT candidates more carefully. The Hangzhou criteria combined with the pre-transplant PLR can accurately exclude high-risk tumor recurrence recipients; this approach expands the Milan criteria effectively without any sacrifice.
deceased donor liver transplantation
hepatitis B virus
living donor liver transplantation
model of end-stage liver disease
platelet to lymphocyte ratio
receiver operating characteristic
University of California San Francisco
El-Serag HB. Hepatocellular carcinoma. N Engl J Med. 2011;365(12):1118–27.
Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-Tieulent J, Jemal A. Global cancer statistics, 2012. CA Cancer J Clin. 2015;65(2):87–108.
Iwatsuki S, Gordon RD, Shaw Jr BW, Starzl TE. Role of liver transplantation in cancer therapy. Ann Surg. 1985;202(4):401–7.
O'Grady JG, Polson RJ, Rolles K, Calne RY, Williams R, Liver transplantation for malignant disease. Results in 93 consecutive patients. Ann Surg. 1988;207(4):373–9.
Mazzaferro V, Regalia E, Doci R, Andreola S, Pulvirenti A, Bozzetti F, et al. Liver transplantation for the treatment of small hepatocellular carcinomas in patients with cirrhosis. N Engl J Med. 1996;334(11):693–9.
Yao FY, Ferrell L, Bass NM, Watson JJ, Bacchetti P, Venook A, et al. Liver transplantation for hepatocellular carcinoma: expansion of the tumor size limits does not adversely impact survival. Hepatology. 2001;33(6):1394–403.
Zheng SS, Xu X, Wu J, Chen J, Wang WL, Zhang M, et al. Liver transplantation for hepatocellular carcinoma: Hangzhou experiences. Transplantation. 2008;85(12):1726–32.
Mazzaferro V, Llovet JM, Miceli R, Bhoori S, Schiavo M, Mariani L, et al. Predicting survival after liver transplantation in patients with hepatocellular carcinoma beyond the Milan criteria: a retrospective, exploratory analysis. Lancet Oncol. 2009;10(1):35–43.
Xu X, Lu D, Ling Q, Wei X, Wu J, Zhou L, et al. Liver transplantation for hepatocellular carcinoma beyond the Milan criteria. Gut. 2016;65(6):1035–41.
Kilincalp S, Coban S, Akinci H, Hamamci M, Karaahmet F, Coskun Y, et al. Neutrophil/lymphocyte ratio, platelet/lymphocyte ratio, and mean platelet volume as potential biomarkers for early detection and monitoring of colorectal adenocarcinoma. Eur J Cancer Prev. 2015;24(4):328–33.
Neofytou K, Smyth EC, Giakoustidis A, Khan AZ, Cunningham D, Mudan S. Elevated platelet to lymphocyte ratio predicts poor prognosis after hepatectomy for liver-only colorectal metastases, and it is superior to neutrophil to lymphocyte ratio as an adverse prognostic factor. Med Oncol. 2014;31(10):239.
Xia W, Ke Q, Wang Y, Wang W, Zhang M, Shen Y, et al. Predictive value of pre-transplant platelet to lymphocyte ratio for hepatocellular carcinoma recurrence after liver transplantation. World J Surg Oncol. 2015;13:60.
Hemming AW, Cattral MS, Reed AI, Van Der Werf WJ, Greig PD, Howard RJ. Liver transplantation for hepatocellular carcinoma. Ann Surg. 2001;233(5):652–9.
Freeman RB, Mithoefer A, Ruthazer R, Nguyen K, Schore A, Harper A, Edwards E. Optimizing staging for hepatocellular carcinoma before liver transplantation: A retrospective analysis of the UNOS/OPTN database. Liver Transpl. 2006;12(10):1504–11.
Vibert E, Azoulay D, Hoti E, Iacopinelli S, Samuel D, Salloum C, et al. Progression of alphafetoprotein before liver transplantation for hepatocellular carcinoma in cirrhotic patients: a critical factor. Am J Transplant. 2010;10(1):129–37.
Nart D, Yaman B, Yilmaz F, Zeytunlu M, Karasu Z, Kilic M. Expression of matrix metalloproteinase-9 in predicting prognosis of hepatocellular carcinoma after liver transplantation. Liver Transpl. 2010;16(5):621–30.
Sieghart W, Wang X, Schmid K, Pinter M, Konig F, Bodingbauer M, et al. Osteopontin expression predicts overall survival after liver transplantation for hepatocellular carcinoma in patients beyond the Milan criteria. J Hepatol. 2011;54(1):89–97.
Cheung ST, Fan ST, Lee YT, Chow JP, Ng IO, Fong DY, Lo CM. Albumin mRNA in plasma predicts post-transplant recurrence of patients with hepatocellular carcinoma. Transplantation. 2008;85(1):81–7.
Zhou X, Du Y, Huang Z, Xu J, Qiu T, Wang J, et al. Prognostic value of PLR in various cancers: a meta-analysis. PLoS One. 2014;9(6), e101119.
Coussens LM, Werb Z. Inflammation and cancer. Nature. 2002;420(6917):860–7.
Mantovani A, Allavena P, Sica A, Balkwill F. Cancer-related inflammation. Nature. 2008;454(7203):436–44.
Lai Q, Castro Santa E, Rico Juri JM, Pinheiro RS, Lerut J. Neutrophil and platelet-to-lymphocyte ratio as new predictors of dropout and recurrence after liver transplantation for hepatocellular cancer. Transpl Int. 2014;27(1):32–41.
Kinoshita A, Onoda H, Imai N, Iwaku A, Oishi M, Tanaka K, et al. The Glasgow Prognostic Score, an inflammation based prognostic score, predicts survival in patients with hepatocellular carcinoma. BMC Cancer. 2013;13:52.
Xue TC, Jia QA, Ge NL, Zhang BH, Wang YH, Ren ZG, Ye SL. The platelet-to-lymphocyte ratio predicts poor survival in patients with huge hepatocellular carcinoma that received transarterial chemoembolization. Tumour Biol. 2015;36(8):6045–51.
Li X, Han Z, Cheng Z, Yu J, Yu X, Liang P. Clinical significance of preoperative platelet-to-lymphocyte ratio in recurrent hepatocellular carcinoma after thermal ablation: A retrospective analysis. Int J Hyperthermia. 2015;31(7):758–63.
Li C, Wen TF, Yan LN, Li B, Wang WT, Yang JY, Xu MQ. Postoperative neutrophil-to-lymphocyte ratio plus platelet-to-lymphocyte ratio predicts the outcomes of hepatocellular carcinoma. J Surg Res. 2015;198(1):73–9.
Parisi I, Tsochatzis E, Wijewantha H, Rodriguez-Peralvarez M, De Luca L, Manousou P, et al. Inflammation-based scores do not predict post-transplant recurrence of hepatocellular carcinoma in patients within Milan criteria. Liver Transpl. 2014;20(11):1327–35.
We are grateful to Mrs. Lin Zhang and Mrs. Saxiao Tang for their help in follow-up of liver transplant recipients.
This study was supported by the National Natural Science Foundation of China (No. 81300362), Natural Science Foundation of Zhejiang Province (LY12H16011, LY14H160022 and LY14H030003), grant from Science Technology Department of Zhejiang Province (No. 2015C03G2010192) and National S&T Major Project (No. 2012ZX10002017).
Availability of data and materials
All data generated or analysed during this study are included in this published article and its supplementary information files.
All authors fulfill the authorship criteria because of their substantial contributions to the conception, design, analysis and interpretation of the data. WX, QK, and SZ designed the study. WX, QK, and HG were responsible for the acquisition and analysis of data. WX drafted the manuscript. JW, XX, SY, JY, and MZ helped to revise the manuscript. WW, MZ, YS, and SZ did the study supervision. All authors have read and approved the final version of this manuscript.
The authors declare that they have no competing interests.
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Ethics approval and consent to participate
Ethical approval was obtained from the Committee of Ethics in Biomedical Research of Zhejiang University and conformed to the ethical guidelines of the Declaration of Helsinki. Written informed consent was obtained from all participants.
RFS of patients fulfilling the Milan criteria stratified by different pre-transplant PLR values. For patients who fulfilled the Milan criteria, the RFS was comparable after stratification by different PLR cut-off values (90, 100, 110, 130, and 140). (TIF 738 kb)
Differentiate value of PLR for patients exceeding the Hangzhou criteria. There was no significant difference in RFS for patients exceeding the Hangzhou criteria after stratification by different PLR cut-off values (90, 100, 110, 130, and 140). (TIF 52 kb)
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Xia, W., Ke, Q., Guo, H. et al. Expansion of the Milan criteria without any sacrifice: combination of the Hangzhou criteria with the pre-transplant platelet-to-lymphocyte ratio. BMC Cancer 17, 14 (2017) doi:10.1186/s12885-016-3028-0
- Hangzhou criteria
- Liver transplantation
- Hepatocellular carcinoma
- Platelet-to-lymphocyte ratio