Department of Gastroenterology and Digestive Oncology, UZ Leuven, Leuven, Belgium.
Department of Internal Medicine, UZ Leuven, Leuven, Belgium.
Clin Colorectal Cancer. 2017 Dec;16(4):377-380. doi: 10.1016/j.clcc.2017.03.017. Epub 2017 Mar 29.
The benefit of regorafenib in colorectal cancer is not very pronounced. At present, there is lack of predictive biological or radiological markers. We studied if density reduction or small changes in size of lung metastases could be a predictive marker.
We retrospectively measured density in size of lung metastases of all patients included in the CORRECT and CONSIGN trials at our center. Contrast-enhanced CT scan at baseline and at week 8 were compared. Data of progressive-free survival and overall survival were collected from the CORRECT and CONSIGN trials.
A significant difference in progressive-free survival was seen in 3 groups: response or stable disease in size (5.36 vs. 3.96 months), response in density (6.03 vs. 2.72 months), and response in corrected density (6.14 vs. 3.08 months). No difference was seen for response in size versus stable disease or progressive disease in size. For overall survival, a difference was observed in the same 3 groups: response or stable disease in size (9.89 vs. 6.44 months), response in density (9.59 vs. 7.04 months), and response in corrected density (9.09 vs. 7.16 months). No difference was seen for response in size versus stable disease or progressive disease in size.
Density reduction in lung metastases might be a good predictive parameter to predict outcome for regorafenib. Early tumor progression might be a negative predictive factor. If further validated, density reduction and early tumor progression might be useful to ameliorate the cost-benefit of regorafenib.
瑞戈非尼在结直肠癌中的获益并不明显。目前,缺乏预测性的生物学或影像学标志物。我们研究了肺转移灶密度降低或体积变化是否可以作为预测标志物。
我们回顾性地测量了本中心参与 CORRECT 和 CONSIGN 试验的所有患者的肺转移灶密度和大小。比较基线和第 8 周的增强 CT 扫描。从 CORRECT 和 CONSIGN 试验中收集无进展生存期和总生存期的数据。
在 3 组中观察到无进展生存期的显著差异:大小方面的缓解或稳定疾病(5.36 与 3.96 个月)、密度方面的缓解(6.03 与 2.72 个月)和校正密度方面的缓解(6.14 与 3.08 个月)。大小方面的缓解与稳定疾病或进展疾病之间无差异。对于总生存期,在相同的 3 组中观察到差异:大小方面的缓解或稳定疾病(9.89 与 6.44 个月)、密度方面的缓解(9.59 与 7.04 个月)和校正密度方面的缓解(9.09 与 7.16 个月)。大小方面的缓解与稳定疾病或进展疾病之间无差异。
肺转移灶密度降低可能是预测瑞戈非尼疗效的良好预测参数。早期肿瘤进展可能是一个负预测因素。如果进一步验证,密度降低和早期肿瘤进展可能有助于改善瑞戈非尼的成本效益。