Department of Medical Oncology, VU University Medical Center, De Boelelaan 1117, Amsterdam, The Netherlands.
Anticancer Drugs. 2010 Apr;21(4):439-46. doi: 10.1097/CAD.0b013e3283359c79.
Hypertension is a common side effect in cancer patients treated with inhibitors of vascular endothelial growth factor/vascular endothelial growth factor receptor-2 signaling and may represent a marker of clinical benefit. Functional rarefaction (a decrease in perfused microvessels) or structural rarefaction (a reduction in anatomic capillary density) may play an important role in the development of hypertension. We investigated whether sunitinib caused impairment of microvascular function and/or reduction of capillary density in patients with metastatic renal cell cancer (mRCC). Sixteen mRCC patients were treated with sunitinib (50 mg/day). Assessments of 24-h ambulatory blood pressure, microvascular endothelial function by laser Doppler fluxmetry, and capillary density by capillary microscopy were performed at baseline and days 14 and 28. Median blood pressure had increased on day 14 (systolic 10 mmHg, P<0.01 and diastolic blood pressure 8 mmHg, P<0.01). Capillary density had decreased from 69 to 61 capillaries/mm (P<0.01). This decrease was related to the increase in systolic and diastolic blood pressure (r=-0.57, P<0.05 and r=-0.68, P<0.01, respectively). A more pronounced decrease in capillary density was associated with increased visibility of the subpapillary plexus (P=0.041). Preliminary findings indicated that median progression-free survival was significantly prolonged in patients with a greater than 6 capillaries/mm decrease in density as compared with patients with a less pronounced decrease (P=0.044). In conclusion, reduction in skin capillary density is associated with a rise in blood pressure during sunitinib therapy and, by itself, might be useful as a predictive marker of clinical outcome.
高血压是接受血管内皮生长因子/血管内皮生长因子受体-2 信号抑制剂治疗的癌症患者的常见副作用,可能是临床获益的标志。功能稀疏(灌注的微血管减少)或结构稀疏(解剖学毛细血管密度降低)可能在高血压的发展中起重要作用。我们研究了舒尼替尼是否会导致转移性肾细胞癌(mRCC)患者的微血管功能障碍和/或毛细血管密度降低。16 名 mRCC 患者接受舒尼替尼(50mg/天)治疗。在基线和第 14 天和第 28 天进行 24 小时动态血压监测、激光多普勒通量测量的微血管内皮功能评估和毛细血管显微镜检查的毛细血管密度评估。第 14 天血压中位数升高(收缩压 10mmHg,P<0.01 和舒张压 8mmHg,P<0.01)。毛细血管密度从 69 个降至 61 个/毫米(P<0.01)。这种下降与收缩压和舒张压的增加有关(r=-0.57,P<0.05 和 r=-0.68,P<0.01)。毛细血管密度的更明显下降与视乳头下丛的可见度增加相关(P=0.041)。初步研究结果表明,与密度下降较少的患者相比,密度下降大于 6 个/毫米的患者中位无进展生存期显著延长(P=0.044)。总之,舒尼替尼治疗期间皮肤毛细血管密度的降低与血压升高相关,并且本身可能作为临床结果的预测标志物有用。