Department of Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Dermatology, National Center for Tumor Diseases (NCT), Heidelberg, Germany.
Sci Rep. 2019 Jul 5;9(1):9728. doi: 10.1038/s41598-019-46189-6.
Immunotherapies demand for predictive biomarkers to avoid unnecessary adverse effects and costs. Analytic morphomics is the technique to use body composition measures as imaging biomarkers for underlying pathophysiology to predict prognosis or outcome to therapy. We investigated different body composition measures to predict response to immunotherapy. This IRB approved retrospective analysis encompassed 147 patients with ipilimumab therapy. Degree of macroangiopathy was quantified with the newly defined total plaque index (TPI), i.e. the body height corrected sum of the soft and hard plaque volume of the infrarenal aorta on portalvenous CT scans. Furthermore, mean psoas density (MPD), different adipose tissue parameters as well as degree of cerebral microangiopathy were extracted from the imaging data. Subsequent multivariate Cox regression analysis encompassed TPI, MPD, serum LDH, S100B, age, gender, number of immunotherapy cycles as well as extent of distant metastases. TPI and MPD correlated positively with PFS in multivariate analysis (p = 0.03 and p = 0.001, respectively). Furthermore, single visceral organ and/or soft tissue involvement significantly decreased progression risk (p = 0.01), whereas increased S100B level showed a trend towards PFS shortening (p = 0.05). In conclusion, degree of macroangiopathy and sarcopenia were independent predictors for outcome to immunotherapy and of equivalent significance compared to other clinical biomarkers.
免疫疗法需要预测性生物标志物,以避免不必要的不良反应和费用。分析形态计量学是一种将人体成分测量用作成像生物标志物的技术,用于预测潜在病理生理学,以预测对治疗的预后或结果。我们研究了不同的身体成分测量来预测对免疫疗法的反应。这项经机构审查委员会批准的回顾性分析包括 147 名接受依匹单抗治疗的患者。宏观血管病变的程度通过新定义的总斑块指数(TPI)来量化,即门静脉 CT 扫描下肾下主动脉的软斑块和硬斑块体积之和的身体高度校正。此外,从影像数据中提取了平均竖脊肌密度(MPD)、不同的脂肪组织参数以及脑微血管病变的程度。随后的多变量 Cox 回归分析包括 TPI、MPD、血清 LDH、S100B、年龄、性别、免疫治疗周期数以及远处转移的程度。TPI 和 MPD 在多变量分析中与 PFS 呈正相关(p=0.03 和 p=0.001)。此外,单一内脏器官和/或软组织受累显著降低了进展风险(p=0.01),而 S100B 水平升高则提示 PFS 缩短(p=0.05)。总之,宏观血管病变和肌肉减少症是免疫治疗结果的独立预测因素,与其他临床生物标志物具有同等重要性。