Tumour Biology Team, Breakthrough Breast Cancer Research Centre, The Institute of Cancer Research, London SW3 6JB, UK.
Br J Cancer. 2013 Sep 3;109(5):1230-42. doi: 10.1038/bjc.2013.429. Epub 2013 Aug 6.
We examine how changes in a surrogate marker of tumour vessel density correlate with response and resistance to anti-angiogenic therapy.
In metastatic renal cancer patients treated with anti-angiogenic tyrosine kinase inhibitors, arterial phase contrast-enhanced computed tomography was used to simultaneously measure changes in: (a) tumour size, and (b) tumour enhancement (a surrogate marker of tumour vessel density) within individual lesions.
No correlation between baseline tumour enhancement and lesion shrinkage was observed, but a reduction in tumour enhancement on treatment was strongly correlated with reduction in lesion size (r=0.654, P<0.0001). However, close examination of individual metastases revealed different types of response: (1) good vascular response with significant tumour shrinkage, (2) good vascular response with stabilisation of disease, (3) poor vascular response with stabilisation of disease and (4) poor vascular response with progression. Moreover, contrasting responses between different lesions within the same patient were observed. We also assessed rebound vascularisation in tumours that acquired resistance to treatment. The amplitude of rebound vascularisation was greater in lesions that had a better initial response to therapy (P=0.008).
Changes in a surrogate marker of tumour vessel density correlate with response and resistance to anti-angiogenic therapy. The data provide insight into the mechanisms that underlie response and resistance to this class of agent.
我们研究了肿瘤血管密度的替代标志物的变化如何与抗血管生成治疗的反应和耐药性相关。
在接受抗血管生成酪氨酸激酶抑制剂治疗的转移性肾细胞癌患者中,使用动脉期增强 CT 同时测量以下两种变化:(a)肿瘤大小;(b)肿瘤强化(肿瘤血管密度的替代标志物)在单个病变内。
基线肿瘤强化与病变缩小之间无相关性,但治疗中肿瘤强化的降低与病变大小的缩小呈强烈相关(r=0.654,P<0.0001)。然而,对个别转移灶的仔细检查显示出不同类型的反应:(1)肿瘤明显缩小,血管反应良好;(2)肿瘤稳定,血管反应良好;(3)疾病稳定,血管反应不佳;(4)疾病进展,血管反应不佳。此外,还观察到同一患者不同病变之间的反应不一致。我们还评估了对治疗产生耐药性的肿瘤中血管再激活的情况。对治疗反应更好的病变中,血管再激活的幅度更大(P=0.008)。
肿瘤血管密度替代标志物的变化与抗血管生成治疗的反应和耐药性相关。这些数据为理解此类药物的作用机制提供了线索。