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18-FDG PET/CT assessment of basal cell carcinoma with vismodegib

机译:vismodegib 18-FDG PET / CT对基底细胞癌的评估

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摘要

The use of 18-fluorodeoxyglucose (FDG) positron emission tomography with computed tomography (PET/CT) in subjects with advanced basal cell carcinoma (BCC) has not been fully explored due to the rarity of disease presentation. This study evaluated PET/CTs from subjects with advanced BCC participating in a phase I dose-escalation clinical trial of vismodegib. Fourteen subjects with BCC were imaged with 18-FDG PET/CT for lesion identification and response categorizing (European Organisation for Research and Treatment for Cancer [EORTC] and PET response criteria in solid tumors [PERCIST] 1.0). Several parameters including metabolic activity of target lesions, site of disease presentation and spread, treatment response, and prognostic significance of metabolic activity following therapy were evaluated. All subjects exhibited at least one hypermetabolic lesion. Most subjects had only four organ systems involved at study enrollment: skin–muscle (93%), lung (57%), lymph nodes (29%), and bone (21%). SUVmax measured across all lesions decreased (median 33%, SD ± 45%) following therapy with metabolic activity normalizing or disappearing in 42% of lesions. No significant difference was observed between EORTC and PERCIST 1.0. Subjects that demonstrated at least a 33% reduction in SUVmax from baseline had a significantly longer progression-free survival (PFS) (median 17 months, 95% confidence interval [CI] ±4 months vs. 9 months, 95% CI ±5 months, P = 0.038) and overall survival (OS) (median 24 months, 95% CI ±4 months vs. 17 months, 95% CI ±13 months, P = 0.019). BCC lesions are hypermetabolic on 18-FDG PET/CT. A decrease in SUVmax was associated with improved PFS and OS. These results further support the incorporation of 18-FDG PET/CT scans in advanced BCC management.
机译:由于罕见的疾病表现,尚未完全探讨在晚期基底细胞癌(BCC)患者中使用18-氟脱氧葡萄糖(FDG)正电子发射断层显像与计算机断层摄影(PET / CT)。这项研究评估了参加vismodegib的I期剂量递增临床试验的晚期BCC受试者的PET / CT。使用18-FDG PET / CT对14例BCC受试者进行成像,以进行病变识别和反应分类(欧洲癌症研究与治疗组织[EORTC]和实体瘤中PET反应标准[PERCIST] 1.0)。评价了几个参数,包括靶病变的代谢活性,疾病的表现和扩散部位,治疗反应以及治疗后代谢活性的预后意义。所有受试者均表现出至少一种代谢异常。大多数受试者只有四个器官系统参与研究:皮肤肌肉(93%),肺(57%),淋巴结(29%)和骨骼(21%)。治疗后,在所有病变中测得的SUVmax下降(中位数33%,SD±45%),其中代谢活性正常化或消失于42%病变中。在EORTC和PERCIST 1.0之间没有观察到显着差异。 SUVmax较基线降低至少33%的受试者的无进展生存期(PFS)明显更长(中位数17个月,95%置信区间[CI]±4个月,而9个月,95%CI±5个月) ,P = 0.038)和总生存期(OS)(中位24个月,95%CI±4个月,而17个月,95%CI±13个月,P = 0.019)。 BCC病变在18-FDG PET / CT上具有代谢性。 SUVmax的降低与PFS和OS的改善有关。这些结果进一步支持将18-FDG PET / CT扫描并入高级BCC管理中。

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