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转移性肾细胞癌靶向药物治疗长期疗效观察 被引量:6

Long-term efficacy of the targeted therapies for metastatic renal cell carcinoma
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摘要 目的分子靶向药物具有抗血管生成及抗肿瘤的双重作用,文中旨在探讨靶向药物舒尼替尼对转移性肾细胞癌(metastatic renal cell carcinoma,mRCC)的长期疗效和不良反应。方法选择2007年11月至2013年3月收治的281例mRCC患者并根据是否自愿进行治疗分为2组。实验组(接受舒尼替尼50 mg/d口服)102例,比较实验组舒尼替尼治疗前后疼痛评分、转移可测量病灶的变化等,进行疗效评估及不良反应分析。对照组(拒绝接受该方案而采用免疫治疗)179例。比较2组临床资料差异,Kaplan-Meier绘制生存曲线,采用Cox回归模型进行多因素分析。结果实验组透明细胞癌患者缓解率29.4%,稳定率53.8%,总有效率83.2%;乳头状肾癌15例,治疗后缓解率33.3%,稳定率46.7%,总有效率80.0%;集合管肾癌9例治疗后缓解率22.2%,稳定率55.6%,总有效率77.8%。1个周期治疗方案骨扫描显示,进展2例(10.5%),缓解5例(26.3%),稳定例数为12例(63.2%),骨转移治疗总有效率89.5%、实验组1个周期治疗结束后,肺转移有效率81.7%;肝转移患者总有效率60.0%;淋巴结转移患者总有效率72.8%。实验组中位总生存期为28.9个月,对照组为20.7个月,组间差异有统计学意义(P﹤0.05)。Cox回归分析显示年龄、肿瘤分型和肝、肺、骨及淋巴结转移是影响mRCC的预后独立因素。不良反应主要为白细胞、血小板减少,中性粒细胞减少,低蛋白血症。结论靶向药物舒尼替尼使患者转移灶减少或缩小、疼痛减轻,改善生活质量,抑制mRCC的进展,总生存期延长。 Objective Molecular targeted drugs have anti-angiogenesis and anti-tumor effects.The study was to investigate the role of sunitinib on treating metastatic renal cell carcinoma ( mRCC) and its long-term efficacy and adverse reactions. Methods From November 2007 to March 2013, 281 mRCC patients were divided into two groups according to their own willingness.102 patients in the experimental group received sunitinib 50 mg per day.Pain score, metastatic focuses before and after targeted therapies were compared.179 patients in control group was treated by immunotherapy.Kaplan-Meier survival analysis was used to draw the survival curves and Cox regression model was applied in multivariate analysis. Results There was no difference between the two groups on baseline (P〉0.05).In the experimental group, 78 cases were clear cell carcinoma, with remission rate 29.4%, stablity rate 53.8%and total effective rate 83.2%after treatment;15 cases were papillary renal cell carcinoma, with remission rate 33.3%, stablity ratio 46.7%and total effective rate 80.0% after treatment;9 cases were collecting duct carcinoma, with the remission rate 22.2%, the stablity ratio 55.6% and the total effective rate 77.8% after treatment.The bone scan after 1 cycle of treatment showed 2 cases progressed(10.5%), 5 cases relieved(26.3%) and 12 cases sta-blized(63.2%), the total effective rate of bone metastasis amounting to 89.5%, the effective rate of lung metastasis 81.7%, the effective rate of liver metastasis 60.0%and the effective rate of lymph node metastasis 72.8%.The median overall survival in the experimental group was 28.9 months, 20.7 months in control group(P〈0.05).Cox regression analysis showed age, tumor classification, liver, lung, bone and lymph node metastasis were prognostic factors influencing mRCC.The common averse events were white blood cells, thrombocytopenia, neutropenia and hypoalbuminemia. Conclusion Sunitinib for the treatment of mRCC can diminish the metastatic focuses , ease the pain , improve the quality of life, delay the progression of the disease, and prolong the overall survival.
出处 《医学研究生学报》 CAS 北大核心 2015年第7期737-740,共4页 Journal of Medical Postgraduates
关键词 转移性肾癌 靶向治疗 舒尼替尼 Metastatic renal cell carcinoma Targeted therapy Sunitinib
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参考文献15

  • 1Reeves DJ, Liu CY. Treatment of metastatic renal cell carcinoma [J]. Cancer Chemother Pharmacol, 2009, 64(9) : 11-25.
  • 2Motzer RJ, Hutson TE, Tomczak P, et al. Over all survival and updated results for sunitinib compared with interferon alfa in pa- tients with metastastic renal cell caicinoma [ J ]. Clin Oncol, 2009, 27(17): 3584-3590.
  • 3Keefe DM, Bateman EH. Tumor control versus adverse events with targeted anticancer therapies [ J ]. Nat Rev Clin Oncol,2011,9(12):98-109.
  • 4孔春泽,孔祥波,汪朔,等.肾细胞癌诊断治疗指南[M]2014版.北京:人民卫生出版社,2014:34.
  • 5Escudier B, Eisen T, Stdler WM, et al. Sorafenib for treatment of renal cell carcinoma: final efficacy and safety results of the phase Ill treatment approaches in renal cancer global evaluation trial[J]. J Clin Oncol, 2009, 27(3) : 3312-3318.
  • 6Singer EA, Gupta GN, Srinivasan R. Update on targeted thera- pies for clear cell renal cell carcinoma [ J ]. Curr Opin Oncol, 2011,23(45): 283-289.
  • 7吉蘅山,朱虹.应用PET/CT与单光子发射型计算机断层仪诊断骨转移瘤的研究进展[J].医学研究生学报,2013,26(3):310-313. 被引量:8
  • 8吴楠蝶,魏嘉,刘宝瑞.胃癌分子靶向治疗的研究进展[J].医学研究生学报,2014,27(12):1318-1322. 被引量:25
  • 9郭刚,张帆,杜青山,冯丹,张旭.舒尼替尼在晚期肾细胞癌二线序贯治疗中的临床应用研究[J].临床泌尿外科杂志,2014,29(1):61-64. 被引量:2
  • 10洪雅萍,姚旭东,朱耀,张世林,戴波,张海梁,沈益君,朱一平,马春光,肖文军,秦晓健,林国文,叶定伟.舒尼替尼治疗晚期肾癌患者的血液学毒性[J].中华医学杂志,2013,93(12):902-905. 被引量:6

二级参考文献75

  • 1常林凤,卢光明,朱虹,王中秋,吴江,胡裕效,秦利萍,王玲.正电子发射型计算机断层扫描/计算机体层扫描对原发性肺癌的诊断价值[J].医学研究生学报,2006,19(12):1081-1084. 被引量:17
  • 2EISEN T, BUKOWSKI R M, STAEHLER M, et al. Randomized phase Ⅲ trial of sorafenib in advanced renal cell carcinoma (RCC) : Impact of crossover on survival[J]. J Clin Oncol, 2006, 24(18S) :4524.
  • 3MOTZER R J, HUSTON T E, TOMCZAK P, et al. Phase Ⅲ randomized trial of sunitinib malate (SUl1248) versus interferon-alfa as first-line systemic therapy for patients with metastatic renal cell carcinoma[J]. Proc Am Soc Clin Oncol, 2006, 24 (2s) : Abstract LBA3.
  • 4吴书其,刘建军,宋少莉,等.^18FDG-PET和^99Tc^m-MDP骨扫描诊断骨转移瘤的比较分析[J].放射实践学,2008,23(11):1273-1277.
  • 5Nakai T, Okuyama C, Kubota T, et al. Pitfalls of FDG-PET for the diagnosis of osteoblastic bone metastases in patients with breast cancer[ J ]. Eur J Nucl Med Mol, Imaging, 2005,32 ( 11 ) : 1253 -1258.
  • 6Even-Sapir E, Metser U, Mishani E, et al. The detection of bone metastases in patients with high-risk prostate cancer:^99m Tc-MDP planar bone scintigraphy, single and muti-field-of-view SPECT, ^18 F-Fluoride PET and lS F-Fluoride PET/CT [ J ]. J Nucl Med, 2006,47 ( 2 ) :287-297.
  • 7Min JW, Um SW, Yim JJ, et al. The role of whole-body FDG PET/CT, Tc 99m MDP bone scintigTaphy, and serum alkaline phosphatase in detecting bone metastasis in patients with newly diagnosed lung cancer [ J ]. J Korean Med Sci,2009,24 (2) :275- 280.
  • 8Shinji I, Katasuhiko K, Mitsuru I, et al. Comparison of ^18F- FDG PET and bone scintigraphy in detection of bone metastases of thyroid cancer [ J ]. J Nucl Med, 2007, 48 (6) : S89-S95.
  • 9Fogelman I, Cook G, Israel O, et al. positron emission tomo- graphy and bone metastases [ J ]. Semin Nucl Meal,2005,35 (2) : 135-142.
  • 10Kruger S, Buck AK, Mottaghy FM, et al. Detection of bone me- tastases in patients with lung cancer:^99m Tc-MDP planar bone scintigraphy, ^18F-fluoride PET or^18 F-FDG PET/CT [ J]. Eur Nucl Med Mol Imaging ,2009,36 ( 11 ) : 1807-1812.

共引文献45

同被引文献73

  • 1熊奎,况建荣,李超,王道梅,马玉芳.三维适形技术在射频消融治疗原发性肝癌中的应用[J].肿瘤防治研究,2005,32(8):513-514. 被引量:9
  • 2刘德华,华阳,王少雷,李森,罗娅红.肝动脉栓塞化疗与灌注化疗介入治疗结肠癌肝转移瘤的临床研究[J].中国全科医学,2006,9(3):211-212. 被引量:6
  • 3Pastore AL, Palleschi G, Silvestri L, et al. Serum and urine bio- markers for human renal cell carcinoma[ J]. Dis Markers, 2015, 2015:251403.
  • 4Chu S J, Zhang J, Zhang R, et al. Evolution and functions of stanuiocalcins in cancer [ J ]. Int J Immunopathol Pha_nnacol, 2015, 28(1) :14-20.
  • 5Arigami T, Uenosono Y, Ishigami S. et al. Expression of stan- niocalcinl as a potential biomarker of gastric cancer[ J ]. Oncolo- gy, 2012, 83(3) :158-164.
  • 6Meyer HA, T5lle A, Jung M, et al. Identification of stanniocal- cin2 as prognostic marker in renal cell carcinoma[J]. Eur Urol, 2009, 55(3) :669-678.
  • 7Zhang ZH, Wu YG, Qin CK, et al. Stanniocalcin 2 expression predicts poor prognosis of hepatoeellular carcinoma [ J ]. Oncol Lett, 2014, 8(5) :2160-2164.
  • 8Shen X J, Gu K, Shi JP, et al. Increased expression of stannio- ealcin2 is associated with tumor progression after radiotherapy in patients with cervical carcinoma [ J ]. Int J Clin Exp Pathol, 2014, 7(12) :8770-8776.
  • 9Kanellis J, Bick R, Garcia G, et al. Stanniocalcin-1, an inhibi- tor of maerophage chemotaxis and chemokinesis [ J ]. Am J Physi-ol Renal Physiol, 2004, 286 (2) : F356-362.
  • 10Ma X, Gu L, Li H, et al. Hypoxia-induced overexpression of stanniocalcin-1 is associated with the metastasis of early stage clear cell renal cell carcinoma [ J]. J Transl Med, 2015, 13 ( 1 ) :56-70.

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