Endocrinology Service, Memorial Sloan Kettering Cancer Center, Weill-Cornell College of Medicine, New York, New York, USA.
Head and Neck Medical Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, Weill-Cornell College of Medicine, New York, New York, USA.
Thyroid. 2020 Aug;30(8):1112-1119. doi: 10.1089/thy.2019.0579. Epub 2020 Apr 20.
To evaluate the impact of structural disease progression of metastatic lesions after initial surgery on overall survival (OS) of patients presenting with metastatic medullary thyroid cancer (MTC). We used tumor volume doubling time (TVDT) as a marker of structural disease progression and aimed to correlate the average structural tumor volume doubling time (midDT) with OS in MTC patients after initial surgery. In this retrospective study, we examined the clinical characteristics; average tumor volume doubling times of neck, lung, and liver metastasis; and disease-specific survival of patients with metastatic MTC. Tumor growth is constant in MTC metastasis, irrespective of location of the metastasis. The median correlation coefficient () and the coefficient of determination () were similar in lung metastasis ( = 0.91, = 0.95) and liver metastasis ( = 0.88, = 0.94), and comparable in neck metastasis ( = 0.73, = 0.85). Patients with metastatic MTC with a midDT ≤1 year have a worse prognosis than those with higher midDT ( = 0.002). Those with midDT ≤1 year had a median OS of 11.1 years [confidence interval (CI) 7.4-14.8 years]. In contrast, patients with midDT 1-3 years had a median OS of 16.5 years [CI 10.3-22.6 years]. All patients with midDT ≥3 survived by the end of the follow-up period. Preliminary results suggest that measurement of midDT can predict response to molecular targeted therapies. In conclusion, TVDT is a strong predictor of OS in patients with recurrent or metastatic MTC, can be used as a marker of progression, and potentially can help select patients who may benefit from molecular targeted therapy.
评估初始手术后转移性病变结构疾病进展对有转移性甲状腺髓样癌 (MTC) 患者总生存期 (OS) 的影响。我们使用肿瘤体积倍增时间 (TVDT) 作为结构疾病进展的标志物,并旨在将初始手术后 MTC 患者的平均结构性肿瘤体积倍增时间 (midDT) 与 OS 相关联。 在这项回顾性研究中,我们检查了转移性 MTC 患者的临床特征;颈部、肺部和肝脏转移的平均肿瘤体积倍增时间;以及疾病特异性生存情况。 MTC 转移中的肿瘤生长是恒定的,与转移部位无关。肺转移中的中位相关系数 () 和决定系数 () 相似 ( = 0.91, = 0.95) 和肝转移 ( = 0.88, = 0.94),与颈部转移相当 ( = 0.73, = 0.85)。 midDT ≤1 年的转移性 MTC 患者预后比 midDT 较高的患者差 ( = 0.002)。 midDT ≤1 年的患者中位 OS 为 11.1 年 [置信区间 (CI) 7.4-14.8 年]。相比之下,midDT 1-3 年的患者中位 OS 为 16.5 年 [CI 10.3-22.6 年]。所有 midDT ≥3 的患者在随访结束时均存活。初步结果表明,midDT 的测量可以预测分子靶向治疗的反应。 总之,TVDT 是预测有复发性或转移性 MTC 患者 OS 的强有力指标,可以作为进展的标志物,并有可能帮助选择可能受益于分子靶向治疗的患者。