A follow-up analysis of the pattern and predictors of dropout from the waiting list for liver transplantation in patients with hepatocellular carcinoma: Implications for the current organ allocation policy

被引:239
作者
Yao, FY
Bass, NM
Nikolai, B
Merriman, R
Davern, TJ
Kerlan, R
Ascher, NL
Roberts, AP
机构
[1] Univ Calif San Francisco, Dept Med, Div Gastroenterol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Surg, Div Transplantat, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA
关键词
D O I
10.1053/jlts.2003.50147
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Since our interim report of the intention-to-treat outcome of orthotopic liver transplantation (OLT) for hepatocellular carcinoma (HCC), we have performed a follow-up analysis of an expanded cohort of 70 patients to further assess whether the observed pattern and predictors of dropout are consistent with the rationale behind current HCC-adjusted Model for End Stage Liver Disease (MELD) organ allocation scheme. All except one patient had prctransplantation staging meeting our proposed expanded criteria-a single lesion less than or equal to6.5 cm, or three or fewer lesions none >4.5 cm and total tumor diameter less than or equal to8 cm. Thirty-eight patients received OLT. The cumulative probabilities of dropout at 6, 12, and 18 months were 7.2%, 37.8%, and 55.1%, respectively. The respective dropout probabilities would have been 11.0%, 57.4%, and 68.7% if the United Network for Organ Sharing (UNOS) criteria for exclusion (single lesion :55 cm or three or fewer lesions none >3 cm) were applied. Predictors of dropout with either criteria included three tumor nodules and a single lesion >3 cm at initial presentation, whereas preoperative chemoembolization or ablation therapies were associated with a lower risk for dropout only when applying the UNOS criteria for patient exclusion. In the subgroup with two or three lesions or a solitary tumor >3 cm, the cumulative probabilities of dropout were nine-fold higher than those with a single lesion less than or equal to3cm (P = .004). In conclusion, the low dropout rate in the first 6 months and the differing dropout risks based on tumor characteristics support further refinements in the HCC-adjusted MELD organ allocation scheme.
引用
收藏
页码:684 / 692
页数:9
相关论文
共 34 条
[1]
Domino liver transplants for metabolic disorders: Experience with familial amyloidotic polyneuropathy [J].
Azoulay, D ;
Samuel, D ;
Castaing, D ;
Adam, R ;
Adams, D ;
Said, G ;
Bismuth, H .
JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 1999, 189 (06) :584-593
[2]
NATURAL-HISTORY OF SMALL UNTREATED HEPATOCELLULAR-CARCINOMA IN CIRRHOSIS - A MULTIVARIATE-ANALYSIS OF PROGNOSTIC FACTORS OF TUMOR-GROWTH RATE AND PATIENT SURVIVAL [J].
BARBARA, L ;
BENZI, G ;
GAIANI, S ;
FUSCONI, F ;
ZIRONI, G ;
SIRINGO, S ;
RIGAMONTI, A ;
BARBARA, C ;
GRIGIONI, W ;
MAZZIOTTI, A ;
BOLONDI, L .
HEPATOLOGY, 1992, 16 (01) :132-137
[3]
Hepatocellular carcinoma: Diagnosis and treatment [J].
Befeler, AS ;
Di Bisceglie, AM .
GASTROENTEROLOGY, 2002, 122 (06) :1609-1619
[4]
Liver transplantation for hepatocellular carcinoma [J].
Bismuth, H ;
Majno, PE ;
Adam, R .
SEMINARS IN LIVER DISEASE, 1999, 19 (03) :311-322
[5]
Prognostic prediction and treatment strategy in hepatocellular carcinoma [J].
Bruix, J ;
Llovet, JM .
HEPATOLOGY, 2002, 35 (03) :519-524
[6]
Predicting the probability of progression-free survival in patients with small hepatocellular carcinoma [J].
Cheng, SJ ;
Freeman, RB ;
Wong, JB .
LIVER TRANSPLANTATION, 2002, 8 (04) :323-328
[7]
NATURAL-HISTORY OF MINUTE HEPATOCELLULAR-CARCINOMA SMALLER THAN .3. CENTIMETERS COMPLICATING CIRRHOSIS - A STUDY IN 22 PATIENTS [J].
EBARA, M ;
OHTO, M ;
SHINAGAWA, T ;
SUGIURA, N ;
KIMURA, K ;
MATSUTANI, S ;
MORITA, M ;
SAISHO, H ;
TSUCHIYA, Y ;
OKUDA, K .
GASTROENTEROLOGY, 1986, 90 (02) :289-298
[8]
Edmondson H, 1954, CANCER, V1, P462
[9]
Rising incidence of hepatocellular carcinoma in the United States [J].
El-Serag, HB ;
Mason, AC .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (10) :745-750
[10]
Eng Sue C, 2002, Gastroenterology, V122, P579, DOI 10.1016/S0016-5085(02)80327-4