Thoracic Oncology Unit, Instituto Nacional de Cancerología, Mexico City, Mexico
Department of Nuclear Medicine and Molecular Imagenology, Instituto Nacional de Cancerología, Mexico City, Mexico.
J Nucl Med. 2018 Mar;59(3):403-409. doi: 10.2967/jnumed.117.192393. Epub 2017 Aug 17.
Nintedanib is an oral angiokinase inhibitor used as second-line treatment for non-small cell lung cancer. New radiotracers, such as Ga-DOTA-E-[c(RGDfK)], that target αβ integrin might have an impact as a noninvasive method for assessing angiogenesis inhibitors. From July 2011 through October 2015, 38 patients received second-line nintedanib plus docetaxel. All patients underwent PET/CT with Ga-DOTA-E-[c(RGDfK)] radiotracer and blood-sample tests to quantify angiogenesis factors (fibroblast growth factor, vascular endothelial growth factor, and platelet-derived growth factor AB) before and after completing 2 therapy cycles. Of the 38 patients, 31 had available baseline and follow-up PET/CT. Baseline lung tumor volume addressed with Ga-DOTA-E-[c(RGDfK)] PET/CT correlated with serum vascular endothelial growth factor levels, whereas baseline lung/liver SUV index correlated with platelet-derived growth factor AB. After treatment, the overall response rate and disease control rate were 7.9% and 47.3%, respectively. A greater decrease in lung tumor volume (-37.2% vs. -27.6%) was associated with a better disease control rate in patients ( = 0.005). Median progression-free survival was 3.7 mo. Nonsmokers and patients with a higher baseline lung tumor volume were more likely to have a higher progression-free survival (6.4 vs. 3.74 [ = 0.023] and 6.4 vs. 2.1 [ = 0.003], respectively). Overall survival was not reached. Patients with a greater decrease in lung SUV (not reached vs. 7.1 mo; = 0.016) and a greater decrease in the lung/spleen SUV index (not reached vs. 7.1; = 0.043) were more likely to have a longer overall survival. Ga-DOTA-E-[c(RGDfK)] PET/CT is a potentially useful tool for assessing responses to angiogenesis inhibitors. Further analysis and novel studies are warranted to identify patients who might benefit from this therapy.
尼达尼布是一种口服血管激酶抑制剂,用于非小细胞肺癌的二线治疗。新型放射性示踪剂,如靶向 αβ 整合素的 Ga-DOTA-E-[c(RGDfK)],可能作为评估血管生成抑制剂的非侵入性方法具有重要意义。从 2011 年 7 月至 2015 年 10 月,38 例患者接受了二线尼达尼布加多西他赛治疗。所有患者在完成 2 个治疗周期前后均接受了 Ga-DOTA-E-[c(RGDfK)]放射性示踪剂和血样检测,以定量评估血管生成因子(成纤维细胞生长因子、血管内皮生长因子和血小板衍生生长因子 AB)。在 38 例患者中,有 31 例有基线和随访的 Ga-DOTA-E-[c(RGDfK)] PET/CT。Ga-DOTA-E-[c(RGDfK)] PET/CT 检测的基线肺部肿瘤体积与血清血管内皮生长因子水平相关,而基线肺/肝 SUV 指数与血小板衍生生长因子 AB 相关。治疗后,总缓解率和疾病控制率分别为 7.9%和 47.3%。与疾病控制率较好的患者相比,肺肿瘤体积的总体下降幅度更大(-37.2%比-27.6%)( = 0.005)。中位无进展生存期为 3.7 个月。不吸烟者和基线肺部肿瘤体积较高的患者更有可能获得更长的无进展生存期(6.4 比 3.74 [ = 0.023] 和 6.4 比 2.1 [ = 0.003])。总生存期未达到。肺部 SUV 下降更大的患者(未达到比 7.1 个月; = 0.016)和肺部/脾脏 SUV 指数下降更大的患者(未达到比 7.1 个月; = 0.043)更有可能获得更长的总生存期。Ga-DOTA-E-[c(RGDfK)] PET/CT 是评估血管生成抑制剂反应的一种潜在有用的工具。需要进一步分析和新的研究来确定可能受益于这种治疗的患者。