Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Wuhan Mental Health Center, Wuhan, China.
Medicine (Baltimore). 2024 Aug 2;103(31):e38679. doi: 10.1097/MD.0000000000038679.
The poor prognosis of anaplastic thyroid cancer (ATC) patients is associated with limited effective therapeutic strategies. Multiple antiangiogenesis tyrosine kinase inhibitors (TKIs) have been applied in later-line treatment of ATC; however, the results reported in clinical trials were controversial. In this study, we reconstructed the patient-level data to pooled-analyze the survival data, responses, and adverse events.
Online databases (PubMed, Web of Science, Embase, and Cochrane CENTRAL) were searched on September 03, 2023. R software combined with the "metaSurvival" and "meta" packages were used to reconstruct the survival curves and summarize the response rates. The primary endpoints were progression-free survival (PFS) and overall survival (OS). The secondary endpoints were survival rate, objective response rate (ORR), disease control rate (DCR), and treatment-related adverse events.
Six prospective clinical trials involving 140 ATC patients were enrolled. Four types of TKIs (imatinib, pazopanib, sorafenib, and lenvatinib) were included. When advanced ATC patients were treated with the TKIs, the median OS was 4.8 months and the median PFS was 2.6 months. The pooled ORR and DCR were 9% and 53%. Hypertension, decreased appetite, rash, and lymphopenia were the most common grade ≥ 3 treatment-related adverse events.
Mono-anitangiogenesis TKI therapy showed limited improvements in treating advanced ATC patients. Combining antiangiogenesis TKI therapy with chemotherapy, radiotherapy, or immunotherapy could be the direction of future studies.
间变性甲状腺癌(ATC)患者的预后较差,这与有限的有效治疗策略有关。多种抗血管生成酪氨酸激酶抑制剂(TKI)已被应用于 ATC 的后线治疗;然而,临床试验报告的结果存在争议。在这项研究中,我们重建了患者水平的数据,以汇总分析生存数据、反应和不良事件。
于 2023 年 9 月 03 日在线检索了 PubMed、Web of Science、Embase 和 Cochrane CENTRAL 数据库。R 软件结合“metaSurvival”和“meta”包用于重建生存曲线并总结反应率。主要终点为无进展生存期(PFS)和总生存期(OS)。次要终点为生存率、客观缓解率(ORR)、疾病控制率(DCR)和治疗相关的不良事件。
纳入了 6 项涉及 140 例 ATC 患者的前瞻性临床试验。包括 4 种 TKI(伊马替尼、帕唑帕尼、索拉非尼和仑伐替尼)。当晚期 ATC 患者接受 TKI 治疗时,中位 OS 为 4.8 个月,中位 PFS 为 2.6 个月。汇总的 ORR 和 DCR 分别为 9%和 53%。高血压、食欲下降、皮疹和淋巴细胞减少是最常见的≥3 级治疗相关不良事件。
单一抗血管生成 TKI 治疗对晚期 ATC 患者的治疗效果有限。将抗血管生成 TKI 治疗与化疗、放疗或免疫治疗相结合可能是未来研究的方向。