Yokoyama I, Carr B, Saitsu H, Iwatsuki S, Starzl T E
Department of Surgery, University Health Center of Pittsburgh, University of Pittsburgh, PA 15213.
Cancer. 1991 Nov 15;68(10):2095-100. doi: 10.1002/1097-0142(19911115)68:10<2095::aid-cncr2820681002>3.0.co;2-y.
The growth rates of recurrent hepatocellular carcinoma (HCC) after orthotopic liver transplantation (OLTX) were estimated by calculating the tumor doubling time (TDT) in 20 patients. The mean TDT, calculated by multiple measurement of tumor size, was 44.3 +/- 11.3 days (mean +/- standard error) in 12 patients with pulmonary metastasis (range, 10 to 161 days) and 37.6 +/- 8.9 days (range, 7 to 65 days) in 5 patients with liver allograft recurrence. The TDT as estimated by serum alpha-fetoprotein (AFP) levels in 6 patients was 37.3 +/- 10.0 days (range, 12 to 84 days). The mean TDT obtained from 5 control subjects with HCC who were treated with liver resection (without immunosuppression) was 273.8 +/- 79.1 days (range, 82 to 560 days). The disease-free period and survival time after OLTX both correlated well with the TDT (r = 0.546 and r = 0.701, respectively). The patients with fibrolamellar HCC had a greater TDT and a longer survival time than those with nonfibrolamellar HCC. Despite a wide range of TDT in patients who received transplants, their recurrent HCC tumors grew significantly faster than those of patients with the same disease who did not receive transplants. The factors involved in this accelerated growth rate may include the use of immunosuppressive drugs and the consequent suppression of host immunity against the growth of micrometastasis.
通过计算20例患者的肿瘤倍增时间(TDT),评估原位肝移植(OLTX)后复发性肝细胞癌(HCC)的生长速率。通过多次测量肿瘤大小计算得出的平均TDT,在12例发生肺转移的患者中为44.3±11.3天(平均值±标准误差)(范围为10至161天),在5例肝移植复发患者中为37.6±8.9天(范围为7至65天)。6例患者通过血清甲胎蛋白(AFP)水平估算的TDT为37.3±10.0天(范围为12至84天)。5例接受肝切除治疗(未进行免疫抑制)的HCC对照患者的平均TDT为273.8±79.1天(范围为82至560天)。OLTX后的无病生存期和生存时间均与TDT密切相关(分别为r = 0.546和r = 0.701)。纤维板层型HCC患者的TDT更长,生存时间也比非纤维板层型HCC患者更长。尽管接受移植患者的TDT范围很广,但他们复发性HCC肿瘤的生长明显快于未接受移植的同病患者。这种加速生长速率涉及的因素可能包括使用免疫抑制药物以及随之而来的宿主对微转移生长的免疫抑制。