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采用乐伐替尼或凡德他尼治疗的晚期甲状腺癌患者的个体化管理:多模式方法的作用

Tailored management of advanced thyroid cancer patients treated with lenvatinib or vandetanib: the role of a multimodal approach.

作者信息

Nervo Alice, Ferrari Matteo, Vaccaro Elisa, Migliore Enrica, Gruosso Giovanni, Roux Anna, Piovesan Alessandro, Arvat Emanuela

机构信息

Oncological Endocrinology Unit, Department of Medical Sciences, Città Della Salute e Della Scienza Hospital, University of Turin, Turin, Italy.

Cancer Epidemiology Unit, Department of Medical Sciences, Città Della Salute e Della Scienza Hospital, University of Turin, Turin, Italy.

出版信息

Endocrine. 2025 Feb;87(2):724-733. doi: 10.1007/s12020-024-04061-2. Epub 2024 Oct 2.

Abstract

BACKGROUND

In differentiated/poorly differentiated (DTC/PDTC) or medullary thyroid cancer (MTC) treated with kinase inhibitors (KIs), additional treatments (ATs) can be performed in selected cases.

METHODS

We retrospectively analysed all the ATs performed in our center in KI-treated TC patients, evaluating the subsequent KI modulation, the local PD in case of loco-regional procedure (LRP) and the AT-related complications. DTC/PDTC patients with or without progressive disease before the first AT (PD and NO PD GROUP, respectively) were analysed separately.

RESULTS

In our center, 32 ATs (30 LRPs and 2 radioactive iodine treatments) were performed in 14 DTC/PDTC patients and 4 MTC subjects after the start of systemic therapy with lenvatinib or vandetanib (27 and 5 ATs, respectively). Brain was the most treated site (11/30 LRPs) and external beam radiation was the most employed LRP (18/30 LRPs). KIs dose reduction or discontinuation of KI therapy (at least transient) was performed after 50% of ATs in DTC/PDTC NO PD GROUP. The KI was maintained at the same dosage after 75% and 50% of the ATs performed in DTC/PDTC PD GROUP and MTC, respectively. During the follow-up, local PD was detected after 14 LRPs. Local progression-free survival (LPFS) was significantly shorter in DTC/PDTC PD GROUP in comparison to NO PD GROUP (12 month-LPFS 91.7% versus 15.2%); in patients with MTC, 12 month-LPFS was 50%. AT-related AEs were mostly G1-G2.

CONCLUSIONS

In selected DTC/PDTC without previous PD and treated with a multimodal strategy, local disease control is generally maintained regardless the KI dose modulation. In DTC/PDTC patients with previous limited PD and in MTC subjects, the choice of performing a LRP and continue the ongoing KI therapy must consider the risk of early local progression. AT-related AEs in KI treated patients were mild in most cases.

摘要

背景

在用激酶抑制剂(KIs)治疗的分化型/低分化型(DTC/PDTC)或甲状腺髓样癌(MTC)中,部分病例可进行额外治疗(ATs)。

方法

我们回顾性分析了本中心对接受KIs治疗的甲状腺癌患者进行的所有ATs,评估后续KIs调整、局部区域手术(LRP)时的局部进展以及与AT相关的并发症。分别分析了首次AT前有或无疾病进展的DTC/PDTC患者(分别为疾病进展组和无疾病进展组)。

结果

在本中心,14例DTC/PDTC患者和4例MTC患者在开始使用乐伐替尼或凡德他尼进行全身治疗后进行了32次ATs(30次LRP和2次放射性碘治疗)(分别为27次和5次ATs)。脑部是接受治疗最多的部位(11/30次LRP),外照射是最常用的LRP(18/30次LRP)。在DTC/PDTC无疾病进展组中,50%的ATs后进行了KIs剂量降低或KI治疗中断(至少是暂时中断)。在DTC/PDTC疾病进展组和MTC中,分别有75%和50%的ATs后KI维持相同剂量。随访期间,14次LRP后检测到局部进展。与无疾病进展组相比,DTC/PDTC疾病进展组的局部无进展生存期(LPFS)显著缩短(12个月LPFS为91.7%对15.2%);在MTC患者中,12个月LPFS为50%。与AT相关的不良事件大多为1-2级。

结论

在采用多模式策略治疗且之前无疾病进展的特定DTC/PDTC中,无论KI剂量如何调整,通常都能维持局部疾病控制。在之前有局限性疾病进展的DTC/PDTC患者和MTC患者中,进行LRP并继续当前KI治疗的选择必须考虑早期局部进展的风险。在接受KI治疗的患者中,与AT相关的不良事件在大多数情况下较轻。

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