Impact of ground-glass component on prognosis in early-stage lung cancer treated with stereotactic body radiotherapy via Helical Tomotherapy.

IF 3.3 2区 医学 Q2 ONCOLOGY Radiation Oncology Pub Date : 2024-12-18 DOI:10.1186/s13014-024-02571-x
Jintao Ma, Shaonan Fan, Wenhan Huang, Xiaohong Xu, Yong Hu, Jian He
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Abstract

Purpose: This study aims to investigate the prognostic impact of ground-glass opacity (GGO)-component in early-stage lung cancer patients treated with stereotactic body radiotherapy (SBRT).

Methods: From January 2013 to December 2022, 239 early-stage lung cancer patients (T1-2N0M0) underwent SBRT. They were categorized into two groups based on the presence of GGO-component: 65 patients in the subsolid group with a consolidation tumor ratio (CTR) between 0.25 and 1 and 174 patients in the solid group with a CTR of 1. Lung cancer-specific survival (LCSS) and progression-free survival (PFS) were analyzed using Cox regression models for both univariate and multivariate analyses to identify prognostic factors. Stabilized inverse probability of treatment weighting (IPTW) was employed for adjusting confounding factors. Recurrence incidence was assessed using competing risk analysis and compared using Gray's test.

Results: In the multivariate analysis, female, peripheral location, and subsolid nodules were favorable prognostic factors for LCSS; peripheral location, subsolid nodules, and adjuvant therapy were favorable prognostic factors for PFS. Between the subsolid (n = 65) and solid groups (n = 174), the median LCSS were not reached (p = 0.003), with 3-, 5-, and 9-year LCSS rates of 94.7% versus 80.3%, 90.9% versus 64.1%, 82.7% versus 53.5%, respectively. The median PFS were 72.5 months and 50.5 months (p = 0.030), with 3-, 5-, and 9-year PFS rates of 75.4% versus 61.2%, 56.6% versus 44.9%, 48.6% versus 23.3%, respectively. After stabilized IPTW (n = 240), the median LCSS were not reached (p = 0.024), with 3-, 5-, and 9-year LCSS rates of 94.0% versus 82.4%, 92.2% versus 67.7%, 85.3% versus 58.2%, respectively. The median PFS were 60.2 months and 50.5 months (p = 0.096), with 3-, 5-, and 9-year PFS rates of 73.8% versus 61.0%, 53.5% versus 46.2%, 46.8% versus 22.4%, respectively. The subsolid group had lower rates of locoregional recurrence (LRR) (10.4% vs. 25.9%, p = 0.035) and distant metastasis (DM) (17.1% vs. 37.9%, p = 0.064) compared to the solid group.

Conclusions: The presence of GGO-component in the lesion is an independent prognostic factor for LCSS and PFS. Subsolid nodules treated with SBRT demonstrated better prognosis, with significantly lower rates of local-regional recurrence. We should highlight GGO-component as a practical indicator for risk stratification of SBRT patients to guide treatment decisions.

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磨玻璃成分对螺旋断层立体定向放射治疗早期肺癌预后的影响。
目的:本研究旨在探讨磨玻璃混浊(GGO)成分对早期肺癌立体定向放射治疗(SBRT)患者预后的影响。方法:2013年1月至2022年12月,239例早期肺癌患者(T1-2N0M0)接受SBRT治疗。根据是否存在ngo -成分将患者分为两组:65例为亚实性组,实性肿瘤比(CTR)在0.25至1之间;174例为实性组,CTR为1。采用Cox回归模型对肺癌特异性生存期(LCSS)和无进展生存期(PFS)进行单因素和多因素分析,以确定预后因素。采用稳定处理加权逆概率法(IPTW)调整混杂因素。使用竞争风险分析评估复发率,并使用Gray检验进行比较。结果:在多因素分析中,女性、外周位置和实下结节是LCSS的有利预后因素;外周位置、实下结节和辅助治疗是PFS的有利预后因素。在亚固体组(n = 65)和固体组(n = 174)之间,未达到中位LCSS (p = 0.003), 3年,5年和9年LCSS率分别为94.7%对80.3%,90.9%对64.1%,82.7%对53.5%。中位PFS分别为72.5个月和50.5个月(p = 0.030), 3年、5年和9年PFS率分别为75.4%对61.2%、56.6%对44.9%、48.6%对23.3%。稳定IPTW (n = 240)后,未达到中位LCSS (p = 0.024), 3年、5年和9年LCSS率分别为94.0%对82.4%、92.2%对67.7%、85.3%对58.2%。中位PFS分别为60.2个月和50.5个月(p = 0.096), 3年、5年和9年PFS率分别为73.8%对61.0%、53.5%对46.2%、46.8%对22.4%。与固体组相比,亚固体组的局部复发(LRR)率(10.4% vs. 25.9%, p = 0.035)和远处转移(DM)率(17.1% vs. 37.9%, p = 0.064)较低。结论:病变中存在的ngo成分是LCSS和PFS的独立预后因素。SBRT治疗的亚实性结节预后较好,局部区域复发率显著降低。我们应该强调ngo成分作为SBRT患者风险分层的实用指标,以指导治疗决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Radiation Oncology
Radiation Oncology ONCOLOGY-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
6.50
自引率
2.80%
发文量
181
审稿时长
3-6 weeks
期刊介绍: Radiation Oncology encompasses all aspects of research that impacts on the treatment of cancer using radiation. It publishes findings in molecular and cellular radiation biology, radiation physics, radiation technology, and clinical oncology.
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