期刊文献+

重组人血小板生成素可预防恶性肿瘤化疗后血小板减少 被引量:20

Prophylactic recombinant human thrombopoietin treatment alleviates chemotherapy-induced thrombocytopenia in tumor patients
下载PDF
导出
摘要 目的观察重组人血小板生成素(rhTPO)预防应用治疗恶性肿瘤患者化疗后血小板减少的临床疗效。方法采用随机交叉自身对照研究,24例恶性肿瘤患者随机分为A、B两组,每组12例,接受方案和剂量相同的两个周期化疗。A组:第1个周期(对照周期)不注射rhTPO,第2个周期(用药周期)化疗前3 d开始注射rhTPO;B组:第1个周期(对照周期)不注射rhTPO,第2个周期(用药周期)化疗后6~24 h内注射rhTPO。结果 24例恶性肿瘤患者用药周期与对照周期血小板减少程度和持续时间差异有显著性;A、B两组用药周期与对照周期血小板减少程度和持续时间差异有统计学意义。结论恶性肿瘤患者化疗前提前给予国产rhTPO可明显提高化疗后血小板的最低值,以及缩短化疗后血小板恢复时间。 Objective To assess the efficacy of prophylactic treatment with recombinant human thrombopoietin (rhTPO) on chemotherapy-induced thrombocytopenia in tumor patients. Methods In this randomized cross-over self-controlled clinical trial, 24 patients with malignant neoplasms were randomized group A (12 cases) and group B (12 cases). All the patients underwent two identical cycles of chemotherapy. In group A, RhTPO (1.0μg/kg) was administered subcutaneously on a daily basis 3 days before the second chemotherapy cycle for 7 consecutive days, and in group B, RhTPO was administered daily 6-24 h after the second chemotherapy cycle for 7 days. In both groups, RhTPO was not administered in the first chemotherapy cycle, which served as the control cycle. Results In both the groups, platelet count was significantly higher in the second cycle than in the control cycle, and the duration of thrombocytopenia was significantly shortened in the second cycle. Compared with group B, the patients in group A showed a significantly higher platelet count in the second cycle and a significantly shorter duration of thrombocytopenia in the second cycle. Conclusion Prophylactic administration of rhTPO can significantly reduce the severity and duration of thrombocytopenia and promote platelet recovery in patients undergoing chemotherapy for malignant tumors.
出处 《南方医科大学学报》 CAS CSCD 北大核心 2012年第7期1064-1066,共3页 Journal of Southern Medical University
基金 北京市科技创新苗圃基金(09KMM30)
关键词 重组人血小板生成素 恶性肿瘤 血小板减少症 recombinant human thromopoietin tumor thrombocytopenia
  • 相关文献

参考文献8

二级参考文献46

  • 1王树国,张艳玲.疏血通注射液对冠心病糖尿病病人血浆ET-1,ICAM-1,TNF-α和P-选择素水平的研究[J].中西医结合心脑血管病杂志,2007,5(7):574-575. 被引量:10
  • 2Ridker PM, Rifai N, Pfeffer M, et al. Elevation of tumor necrosis factor-alpha and increased risk of recurrent coronary events after myocardial infaretion[J ]. Circulation, 2000, 101(18): 2149-56.
  • 3Stefan KJ, Paul A, Elliott B, et al. Tropoein and C-reactive protein have different relational to subsequent mortality and myocardial infarction after acute coronary syndrome[J]. J Am Coll Cardiol, 2003, 41(5): 916-24.
  • 4Kozinski M, Kubica J, Sukiermik A, et al. Periprocedural soluble P- and E-selectin levels fail as predictors of clinical restenosis in patients treated with elective coronary stenting [J]. Int J Mol Med, 2007, 19(1): 187-95.
  • 5Seino Y, Ogawa A, Yamashita T, et al. Multi-biomarker approach to acute coronary syndrome[J]. Nippon Rinsho, 2006, 64(4): 691-9.
  • 6Szpalski M, Gunzburg R. The role of surgery in the management of low back pain[J]. Baillieres C/in Rheumatol, 1998, 12(1): 141-59.
  • 7Sairyo K, Biyani A, Goel VK, et al. Lumbar ligamentum flavum hypertrophy is due to accumulation of inflammation-related scar tissue[J]. Spine (Phila Pa 1976), 2007, 32(11): E340-7.
  • 8Sairyo K, Biyani A, Goel VK, et al. Pathomechanism of ligam- entum flavum hypertrophy:a multidisciplinary investigation based on clinical,biomechanical,histologic and biologic assessments [J]. Spine, 2005, 30: 2649-56.
  • 9Yayama T, Kobayashi S, Sato R, et al. Calcium pyrophosphate crystal deposition in the ligamentum flavum of degenerated lumbar spine:histopathological and immunohistological findings [Jl. Clin Rheumatol, 2008, 27(5): 597-604.
  • 10Abbas J, Hamoud K, Masharawi YM, et al. Ligamentum flavum thickness in normal and stenotic lumbar spines[J]. Spine (Phila Pa 1976), 2010, 35(12): 1225-30.

共引文献44

同被引文献252

引证文献20

二级引证文献145

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部