中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

甲胎蛋白应答评价索拉非尼联合卡瑞利珠单抗治疗晚期肝细胞癌的效果分析

王星 张韬

引用本文:
Citation:

甲胎蛋白应答评价索拉非尼联合卡瑞利珠单抗治疗晚期肝细胞癌的效果分析

DOI: 10.3969/j.issn.1001-5256.2023.04.015
基金项目: 

新疆维吾尔自治区自然科学基金 (2021D01C322)

伦理学声明:本研究方案经由新疆医科大学第一附属医院伦理委员会审批,批号:K202212-10,所纳入患者均签署知情同意书。
利益冲突声明:本研究不存在研究者、伦理委员会成员、受试者监护人以及公开研究成果有关的利益冲突。
作者贡献声明:王星负责课题设计,资料分析,撰写论文;张韬负责指导撰写文章并最后定稿。
详细信息
    通信作者:

    张韬, zhang1tao3@163.com (ORCID: 0000-0003-1272-675X)

Value of alpha-fetoprotein response in evaluating the efficacy of sorafenib combined with camrelizumab in treatment of advanced hepatocellular carcinoma

Research funding: 

Natural Science Foundation of Xinjiang Uygur Autonomous Region (2021D01C322)

More Information
  • 摘要:   目的  探讨甲胎蛋白(AFP)应答在索拉非尼联合卡瑞利珠单抗治疗晚期肝细胞癌中的临床疗效及安全性。  方法  选取2020年9月—2022年2月于新疆医科大学第一附属医院接受索拉非尼联合卡瑞利珠单抗治疗的48例晚期肝细胞癌患者的临床资料,按照治疗后AFP应答水平进行分组:应答组(治疗6~8个月时,与基础AFP比较,AFP下降率>20%,n=32);无应答组(治疗6~8个月时,与基础AFP比较,AFP下降率≤20%, n=16)。计量资料组间比较采用Mann-Whitney U检验;计数资料组间比较采用χ2检验。绘制生存曲线,行Cox单因素/多因素回归分析得到与OS相关的独立危险因素。比较两组患者无进展生存时间、总生存期与治疗效果。  结果  两组患者中均未观察到达到临床缓解的病例。AFP应答组的客观有效率(21.88% vs 0)和疾病控制率(84.38% vs 43.75%) 均高于无应答组(χ2值分别为2.530、6.668,P值分别为0.112、0.010)。应答组无进展生存期(9.9个月)、总生存期(13.8个月)均高于无应答组(6.8个月、11.1个月)。AFP早期无应答(HR=2.624,95%CI:1.097~6.277,P=0.030)及肝外转移(HR=0.392,95%CI:0.157~0.978,P=0.045)与较短的无进展生存期独立相关。未出现因不良反应导致停药事件的发生。  结论  AFP早期应答在预测索拉非尼联合卡瑞利珠单抗治疗晚期肝细胞癌患者疗效及预后方面具有较高的临床价值。

     

  • 图  1  AFP早期应答组和无应答组的PFS和OS曲线

    注:a, PFS; b, OS。

    Figure  1.  PFS and OS curves in the AFP early responder and non-responder groups

    表  1  基线特征的比较

    Table  1.   Comparison of baseline characteristics

    变量 应答组(n=32) 无应答组(n=16) 统计值 P
    性别[例(%)] χ2=1.497 0.239
      男 23(71.80) 15(93.80)
      女 9(28.00) 1(6.30)
    年龄[例(%)] χ2=0.381 0.573
      ≥60岁 13(40.60) 8(50.00)
      <60岁 19(59.40) 8(50.00)
    基线AFP(ng/mL) 353.31(113.10~1 015.87) 1 616.89(92.08~2 000.00) Z=-2.203 0.088
    AST(U/L) 49.10(37.26~97.53) 63.56(42.36~91.18) Z=-0.787 0.331
    ALT(U/L) 48.89(36.42~68.00) 39.73(30.73~68.11) Z=-0.437 0.662
    TBil(mol/L) 20.85(17.51~30.61) 17.69(15.46~19.48) Z=-3.040 0.002
    Alb(g/L) 38.59(31.32~41.34) 36.19(33.53~37.88) Z=-0.262 0.793
    PLT(×109/L) 112.00(60.25~163.25) 141.50(100.50~191.25) Z=-1.488 0.137
    Hb(g/L) 138.00(125.25~147.75) 123.50(107.50~146.00) Z=-1.969 0.049
    PT(s) 13.20(12.60~14.50) 13.20(12.00~13.85) Z=-0.941 0.347
    INR 1.16(1.11~1.25) 1.15(1.06~1.20) Z=-0.733 0.463
    病因[例(%)] χ2=0.034 0.854
      HBV 30(93.80) 14(87.50)
      HCV 2(6.30) 2(12.50)
    ECOG评分[例(%)] χ2=0.671 0.413
      0 16(50.0) 6(37.50)
      1 16(50.0) 10(62.50)
    肝硬化[例(%)] 26(81.25) 15(93.75) χ2=0.523 0.470
    腹水[例(%)] 27(84.38) 14(87.50) χ2=0.000 1.000
    远处转移[例(%)] 7(21.88) 5(68.75) χ2=0.125 0.480
    门静脉癌栓[例(%)] 8(25.00) 8(25.00) χ2=3.000 0.083
    下载: 导出CSV

    表  2  AFP早期应答组和无应答组的临床疗效比较

    Table  2.   Comparison of clinical outcomes between the early responders and non-responders of AFP

    临床疗效 应答组(n=32) 无应答组(n=16)
    CR(例) 0 0
    PR(例) 7 0
    SD(例) 20 7
    PD(例) 5 9
    ORR 21.88% 0
    DCR 84.38% 43.75%
    下载: 导出CSV

    表  3  PFS相关的单因素和多因素分析

    Table  3.   PFS-related univariate and multifactorial analyses

    变量 单因素分析 多因素分析
    HR(95%CI) P HR(95%CI) P
    年龄(≥60岁vs<60岁) 1.152(0.479~2.771) 0.751
    AFP(早期无应答vs有应答) 2.751(1.162~6.517) 0.021 2.624(1.097~6.277) 0.030
    腹水(有vs无) 0.588(0.193~1.796) 0.351
    HBsAg(阳性vs阴性) 0.750(0.171~3.282) 0.702
    肝外转移(有vs无) 2.715(1.102~6.690) 0.030 0.392(0.157~0.978) 0.045
    门静脉癌栓(有vs无) 1.791(0.748~4.289) 0.191
    ECOG评分(0 vs 1) 0.228(0.701~4.423) 0.228
    Child-Pugh分级(A级vs B级) 0.275(0.326~2.440) 0.275
    下载: 导出CSV

    表  4  OS相关的单因素和多因素分析

    Table  4.   OS-related univariate and multifactorial analyses

    变量 单因素分析 多因素分析
    HR(95%CI) P HR(95%CI) P
    年龄(≥60岁vs<60岁) 1.138(0.467~2.772) 0.776
    AFP(早期无应答vs有应答) 2.639(1.113~6.260) 0.028 2.364(0.957~5.835) 0.062
    腹水(有vs无) 0.587(0.191~1.800) 0.351
    HBsAg(阳性vs阴性) 0.596(0.133~2.669) 0.498
    肝外转移(有vs无) 2.921(1.129~7.235) 0.021
    门静脉癌栓(有vs无) 1.941(0.810~4.651) 0.137 2.940(1.152~7.506) 0.024
    ECOG评分(1 vs 0) 3.050(1.118~8.318) 0.029 3.000(1.045~8.608) 0.041
    Child-Pugh分级(A级vs B级) 0.325(0.053~2.487) 0.279
    下载: 导出CSV
  • [1] BRAY F, FERLAY J, SOERJOMATARAM I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin, 2018, 68(6): 394-424. DOI: 10.3322/caac.21492.
    [2] WU T, CHEN L. New advances in the precision diagnosis and treatment of liver cancer[J]. J Clin Hepatol, 2022, 38(3): 497-498. DOI: 10.3969/j.issn.1001-5256.2022.03.001.

    吴彤, 陈磊. 肝癌精准诊疗新进展[J]. 临床肝胆病杂志, 2022, 38(3): 497-498. DOI: 10.3969/j.issn.1001-5256.2022.03.001.
    [3] RUMGAY H, ARNOLD M, FERLAY J, et al. Global burden of primary liver cancer in 2020 and predictions to 2040[J]. J Hepatol, 2022, 77(6): 1598-1606. DOI: 10.1016/j.jhep.2022.08.021.
    [4] European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma[J]. J Hepatol, 2018, 69(1): 182-236. DOI: 10.1016/j.jhep.2018.03.019.
    [5] WILHELM SM, CARTER C, TANG L, et al. BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis[J]. Cancer Res, 2004, 64(19): 7099-7109. DOI: 10.1158/0008-5472.CAN-04-1443.
    [6] GAO R, KALATHUR R, COTO-LLERENA M, et al. YAP/TAZ and ATF4 drive resistance to Sorafenib in hepatocellular carcinoma by preventing ferroptosis[J]. EMBO Mol Med, 2021, 13(12): e14351. DOI: 10.15252/emmm.202114351.
    [7] ZHOU YY, ZHAO XX, CHEN YY, et al. Tumor immune checkpoint inhibitor and its combination research progress of combination therapy[J]. China pharmacy, 2020, 31(7): 890-896. DOI: 10.6039/j.issn.1001-0408.2020.07.24.

    周姚邑, 赵新新, 陈沅沅, 等. 肿瘤免疫检查点抑制剂及其联合疗法的研究进展[J]. 中国药房, 2020, 31(7): 890-896. DOI: 10.6039/j.issn.1001-0408.2020.07.24.
    [8] QIN S, REN Z, MENG Z, et al. Camrelizumab in patients with previously treated advanced hepatocellular carcinoma: a multicentre, open-label, parallel-group, randomised, phase 2 trial[J]. Lancet Oncol, 2020, 21(4): 571-580. DOI: 10.1016/S1470-2045(20)30011-5.
    [9] KUDO M. Immune checkpoint blockade in hepatocellular carcinoma: 2017 update[J]. Liver Cancer, 2016, 6(1): 1-12. DOI: 10.1159/000449342.
    [10] ZHAO X, CHEN Q, LIU W, et al. Codelivery of doxorubicin and curcumin with lipid nanoparticles results in improved efficacy of chemotherapy in liver cancer[J]. Int J Nanomedicine, 2014, 10: 257-270. DOI: 10.2147/IJN.S73322.
    [11] GAO YX, YANG TW, YIN JM, et al. Progress and prospects of biomarkers in primary liver cancer (Review)[J]. Int J Oncol, 2020, 57(1): 54-66. DOI: 10.3892/ijo.2020.5035.
    [12] HAO X, FAN R, HOU JL. Early warning and accurate screening for the high-risk population of hepatocellular carcinoma[J]. J Clin Hepatol, 2022, 38(3): 499-504. DOI: 10.3969/j.issn.1001-5256.2022.03.002.

    郝新, 樊蓉, 侯金林. 原发性肝癌高危人群的早期预警和精准筛查[J]. 临床肝胆病杂志, 2022, 38(3): 499-504. DOI: 10.3969/j.issn.1001-5256.2022.03.002.
    [13] LENCIONI R, LLOVET JM. Modified RECIST (mRECIST) assessment for hepatocellular carcinoma[J]. Semin Liver Dis, 2010, 30(1): 52-60. DOI: 10.1055/s-0030-1247132.
    [14] SHIBA S, OKUSAKA T, IKEDA M, et al. Characteristics of 18 patients with hepatocellular carcinoma who obtained a complete response after treatment with sorafenib[J]. Hepatol Res, 2014, 44(13): 1268-1276. DOI: 10.1111/hepr.12297.
    [15] LIU YC, CHENG TC, BIAN ZL. Progress and challenges of combined immune checkpoint inhibitors in the treatment of hepatocellular carcinoma[J/OL]. Chin J Immunol, 2023. [Online ahead of print]

    刘一村, 程苕莼, 卞兆连. 联合免疫检查点抑制剂治疗肝细胞癌的进展与挑战[J/OL]. 中国免疫学杂志, 2023. [网络首发]
    [16] CHANG YS, ADNANE J, TRAIL PA, et al. Sorafenib (BAY 43-9006) inhibits tumor growth and vascularization and induces tumor apoptosis and hypoxia in RCC xenograft models[J]. Cancer Chemother Pharmacol, 2007, 59(5): 561-574. DOI: 10.1007/s00280-006-0393-4.
    [17] FU Y, WEI X, LIN L, et al. Adverse reactions of sorafenib, sunitinib, and imatinib in treating digestive system tumors[J]. Thorac Cancer, 2018, 9(5): 542-547. DOI: 10.1111/1759-7714.12608.
    [18] European Association for the Study of the Liver, European Organisation for Research and Treatment of Cancer. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma[J]. J Hepatol, 2012, 56(4): 908-943. DOI: 10.1016/j.jhep.2011.12.001.
    [19] MOTZER RJ, AGARWAL N, BEARD C, et al. NCCN clinical practice guidelines in oncology: kidney cancer[J]. J Natl Compr Canc Netw, 2009, 7(6): 618-630. DOI: 10.6004/jnccn.2009.0043.
    [20] FINN RS, IKEDA M, ZHU AX, et al. Phase Ib study of lenvatinib plus pembrolizumab in patients with unresectable hepatocellular carcinoma[J]. J Clin Oncol, 2020, 38(26): 2960-2970. DOI: 10.1200/JCO.20.00808.
    [21] FINN RS, QIN S, IKEDA M, et al. Atezolizumab plus bevacizumab in unresectable hepatocellular carcinoma[J]. N Engl J Med, 2020, 382(20): 1894-1905. DOI: 10.1056/NEJMoa1915745.
    [22] KAO WY, CHIOU YY, HUNG HH, et al. Serum alpha-fetoprotein response can predict prognosis in hepatocellular carcinoma patients undergoing radiofrequency ablation therapy[J]. Clin Radiol, 2012, 67(5): 429-436. DOI: 10.1016/j.crad.2011.10.009.
    [23] SHAO YY, LIN ZZ, HSU C, et al. Early alpha-fetoprotein response predicts treatment efficacy of antiangiogenic systemic therapy in patients with advanced hepatocellular carcinoma[J]. Cancer, 2010, 116(19): 4590-4596. DOI: 10.1002/cncr.25257.
    [24] SHAO YY, LIU TH, HSU C, et al. Early alpha-foetoprotein response associated with treatment efficacy of immune checkpoint inhibitors for advanced hepatocellular carcinoma[J]. Liver Int, 2019, 39(11): 2184-2189. DOI: 10.1111/liv.14210.
    [25] PAUL SB, SAHU P, SREENIVAS V, et al. Prognostic role of serial alpha-fetoprotein levels in hepatocellular carcinoma treated with locoregional therapy[J]. Scand J Gastroenterol, 2019, 54(9): 1132-1137. DOI: 10.1080/00365521.2019.1660403.
    [26] SÁNCHEZ A, ROCES LV, GARCÍA IZ, et al. Value of α-fetoprotein as an early biomarker for treatment response to sorafenib therapy in advanced hepatocellular carcinoma[J]. Oncol Lett, 2018, 15(6): 8863-8870. DOI: 10.3892/ol.2018.8400.
    [27] PARK JG. Long-term outcomes of patients with advanced hepatocellular carcinoma who achieved complete remission after sorafenib therapy[J]. Clin Mol Hepatol, 2015, 21(3): 287-294. DOI: 10.3350/cmh.2015.21.3.287.
    [28] LLOVET JM, RICCI S, MAZZAFERRO V, et al. Sorafenib in advanced hepatocellular carcinoma[J]. N Engl J Med, 2008, 359(4): 378-390. DOI: 10.1056/NEJMoa0708857.
    [29] CHEN LT, LIU TW, CHAO Y, et al. alpha-fetoprotein response predicts survival benefits of thalidomide in advanced hepatocellular carcinoma[J]. Aliment Pharmacol Ther, 2005, 22(3): 217-226. DOI: 10.1111/j.1365-2036.2005.02547.x.
  • 加载中
图(1) / 表(4)
计量
  • 文章访问数:  421
  • HTML全文浏览量:  95
  • PDF下载量:  46
  • 被引次数: 0
出版历程
  • 收稿日期:  2022-08-31
  • 录用日期:  2022-10-27
  • 出版日期:  2023-04-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回