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酪氨酸激酶抑制剂治疗儿科肉瘤:肺转移空洞的预后意义。

Tyrosine kinase inhibitor therapy in pediatric sarcoma: Prognostic implications of pulmonary metastatic cavitation.

机构信息

Department of Radiology, Molecular Imaging Program at Stanford, Stanford University, Stanford, California, USA.

Department of Radiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

出版信息

Pediatr Blood Cancer. 2023 Nov;70(11):e30629. doi: 10.1002/pbc.30629. Epub 2023 Aug 14.

Abstract

PURPOSES

This study aims to ascertain the prevalence of cavitations in pulmonary metastases among pediatric and young adult patients with sarcoma undergoing tyrosine kinase inhibitor (TKI) therapy, and assess whether cavitation can predict clinical response and survival outcomes.

METHODS

In a single-center retrospective analysis, we examined chest computed tomography (CT) scans of 17 patients (median age 16 years; age range: 4-25 years) with histopathologically confirmed bone (n = 10) or soft tissue (n = 7) sarcoma who underwent TKI treatment for lung metastases. The interval between TKI initiation and the onset of lung nodule cavitation and tumor regrowth were assessed. The combination of all imaging studies and clinical data served as the reference standard for clinical responses. Progression-free survival (PFS) was compared between patients with cavitating and solid nodules using Kaplan-Meier survival analysis and log-rank test.

RESULTS

Five out of 17 patients (29%) exhibited cavitation of pulmonary nodules during TKI therapy. The median time from TKI initiation to the first observed cavitation was 79 days (range: 46-261 days). At the time of cavitation, all patients demonstrated stable disease. When the cavities began to fill with solid tumor, 60% (3/5) of patients exhibited progression in other pulmonary nodules. The median PFS for patients with cavitated pulmonary nodules after TKI treatment (6.7 months) was significantly longer compared to patients without cavitated nodules (3.8 months; log-rank p-value = .03).

CONCLUSIONS

Cavitation of metastatic pulmonary nodules in sarcoma patients undergoing TKI treatment is indicative of non-progressive disease, and significantly correlates with PFS.

摘要

目的

本研究旨在确定接受酪氨酸激酶抑制剂(TKI)治疗的儿童和青年肉瘤患者肺部转移瘤中存在空洞的比例,并评估空洞是否可以预测临床反应和生存结果。

方法

在单中心回顾性分析中,我们检查了 17 名经组织病理学证实患有骨(n=10)或软组织(n=7)肉瘤且接受 TKI 治疗肺转移瘤的患者的胸部计算机断层扫描(CT)。评估了 TKI 开始与肺部结节空洞形成和肿瘤复发之间的间隔。所有影像学研究和临床数据的组合作为临床反应的参考标准。使用 Kaplan-Meier 生存分析和对数秩检验比较有空洞和实性结节的患者之间的无进展生存期(PFS)。

结果

17 名患者中有 5 名(29%)在 TKI 治疗期间出现肺部结节空洞。从 TKI 开始到首次观察到空洞的中位时间为 79 天(范围:46-261 天)。在出现空洞时,所有患者均表现为疾病稳定。当空洞开始充满实性肿瘤时,60%(3/5)的患者其他肺部结节出现进展。TKI 治疗后有空洞的肺部结节患者的中位 PFS(6.7 个月)明显长于无空洞结节患者(3.8 个月;对数秩 p 值=0.03)。

结论

接受 TKI 治疗的肉瘤患者肺部转移瘤空洞化表明疾病无进展,与 PFS 显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1917/10947454/6e516517941e/nihms-1965146-f0001.jpg

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