Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Université Paris Saclay, Villejuif, France.
Endocrinology Unit, Department of Experimental and Clinical Biomedical Sciences 'Mario Serio', University of Florence, Florence, Italy.
Endocr Relat Cancer. 2021 Jan;28(1):15-26. doi: 10.1530/ERC-20-0106.
Anaplastic thyroid cancer (ATC) is a rare lethal disease. Lenvatinib is an off-label therapeutic option for ATC in most countries, except in Japan. The aim of this multicenter retrospective survey was to analyze the efficacy and the toxicity profile of off-label lenvatinib treatment in all adults advanced ATC patients, in France. Of the 23 patients analysed (14 males; mean age 64 years), 15 were pure ATC and 8 were mixed tumors (i.e. with a differentiated or poorly differentiated component). Prior treatments included neck external beam irradiation in 74%, at least one line of chemotherapy in 22 cases, two lines of chemotherapy in 11 patients, other TKI in 4 cases. A central RECIST assessment was performed. Since lenvatinib initiation, median PFS was 2.7 months (95% CI; 1.9-3.5) and median OS was 3.1 months (95% CI; 0.6-5.5). OS was significantly longer in case of mixed tumors compared with pure ATC (6.3 vs 2.7 months, P = 0.026). Best tumor response was partial response in two cases and stable disease in seven. Clinical improvement was achieved in seven patients. Lethal adverse events occurred in three patients, consisting in haemoptysis in two cases and pneumothorax in one case. Among long-surviving ATC patients (>6 months), four underwent biopsy of distant metastasis, revealing poorly differentiated histology; three of them had initial mixed ATC histology. Efficacy of lenvatinib appears limited, although pure vs mixed ATC disclose differences in disease aggressiveness and treatment response. Long-surviving ATC patients might benefit from biopsy of persistent disease, searching for histological transition or molecular target.
间变性甲状腺癌(ATC)是一种罕见的致命疾病。在大多数国家,除日本外,仑伐替尼是 ATC 的一种超适应证治疗选择。本多中心回顾性调查的目的是分析法国所有晚期 ATC 成人患者使用仑伐替尼的治疗效果和毒性特征。在分析的 23 名患者中(男性 14 例;平均年龄 64 岁),15 例为纯 ATC,8 例为混合肿瘤(即有分化或低分化成分)。既往治疗包括 74%的颈部外照射,22 例至少接受过一线化疗,11 例接受过二线化疗,4 例接受过其他 TKI。进行了中央 RECIST 评估。自仑伐替尼开始治疗以来,中位无进展生存期(PFS)为 2.7 个月(95%CI;1.9-3.5),中位总生存期(OS)为 3.1 个月(95%CI;0.6-5.5)。混合肿瘤的 OS 明显长于纯 ATC(6.3 个月 vs 2.7 个月,P=0.026)。最佳肿瘤反应为 2 例部分缓解,7 例稳定疾病。7 例患者出现临床改善。3 例患者出现致死性不良事件,包括 2 例咯血和 1 例气胸。在生存时间超过 6 个月的 ATC 患者中,4 例对远处转移灶进行了活检,发现为低分化组织学;其中 3 例最初为混合 ATC 组织学。尽管纯 ATC 和混合 ATC 在疾病侵袭性和治疗反应方面存在差异,但仑伐替尼的疗效似乎有限。对于生存时间较长的 ATC 患者,可能需要对持续性疾病进行活检,以寻找组织学转化或分子靶点。