Segmentectomy versus lobectomy for ground-glass opacity dominant cT1N0 invasive lung adenocarcinoma.

IF 4 2区 医学 Q2 ONCOLOGY Translational lung cancer research Pub Date : 2024-06-30 Epub Date: 2024-06-22 DOI:10.21037/tlcr-24-191
Zelin Ma, Yang Zhang, Han Han, Shengping Wang, Yuan Li, Haiquan Chen
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Abstract

Background: The Japan Clinical Oncology Group (JCOG) 1211 suggested that segmentectomy should be considered as standard treatment for clinical T1N0 (cT1N0) ground glass opacity (GGO). However, over half of patients in JCOG1211 had pre-/minimal invasive adenocarcinoma. This study aims to retrospectively investigate the long-term survival of GGO featured cT1N0 invasive lung adenocarcinoma undergoing segmentectomy or lobectomy.

Methods: This study screened patients with primary cT1N0 lung adenocarcinoma who received segmentectomy or lobectomy from 2010-2020. Prior computed tomography (CT) scans before surgery of all patients were reviewed and the inclusion was confirmed according to tumor diameter and consolidation tumor ratio (CTR). GGO nodules between 2-3 cm with CTR ≤0.5 or ≤2 cm with CTR between 0.25-0.5 were finally included. Patients with pathologically diagnosed pre-/minimally invasive lung adenocarcinoma were excluded. Long-term survivals between segmentectomy group and lobectomy group were compared after propensity score matching (PSM). Recurrence and postoperative complication events were also analyzed.

Results: In total, 617 patients were enrolled, 159 received segmentectomy and 458 received lobectomy. Clinicopathological characteristics were well distributed between two groups. With a median follow-up time of 61.1 months (IQR: 42.3-71.7 months), after PSM, the 5-year overall survival rate was 98.8% (97.9-99.6%) for lobectomy and 99.3% (98.2-99.8%) for segmentectomy (P=0.42), the 5-year relapse-free survival rate was 95.3% (92.2-97.6%) for lobectomy and 95.2% for segmentectomy (92.3-98.7%) (P=0.81). The proportion of recurrence was 4.1% for lobectomy and 4.4% for segmentectomy (P=0.89). The proportion of grade 2 and above early postoperative complications was 9.6% for lobectomy and 8.8% for segmentectomy (P=0.86).

Conclusions: For cT1N0 GGO featured invasive lung adenocarcinoma (2 cm < tumor diameter ≤3 cm, CTR ≤0.5 or tumor diameter ≤2 cm, 0.25< CTR ≤0.5), postoperative outcomes between segmentectomy group and lobectomy group were comparable. Concerning minimally invasive surgical strategy, segmentectomy should be confirmed as the standard surgical approach.

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分段切除术与肺叶切除术治疗磨玻璃不明显的 cT1N0 浸润性肺腺癌。
背景:日本临床肿瘤学小组(JCOG)1211 建议,临床 T1N0(cT1N0)磨玻璃不透明(GGO)的标准治疗应考虑分段切除术。然而,JCOG1211 中超过半数的患者患有前/微小浸润性腺癌。本研究旨在回顾性调查以GGO为特征的cT1N0浸润性肺腺癌患者接受肺段切除术或肺叶切除术后的长期生存情况:本研究筛选了2010-2020年间接受分段切除术或肺叶切除术的原发性cT1N0肺腺癌患者。对所有患者术前的计算机断层扫描(CT)进行审查,并根据肿瘤直径和合并肿瘤比率(CTR)确认是否纳入。CTR≤0.5的2-3厘米GGO结节或CTR在0.25-0.5之间的≤2厘米GGO结节最终被纳入其中。病理诊断为前/微小浸润性肺腺癌的患者被排除在外。经过倾向评分匹配(PSM)后,比较了分段切除术组和肺叶切除术组的长期生存率。此外,还对复发和术后并发症事件进行了分析:共有617名患者入组,其中159人接受了分段切除术,458人接受了肺叶切除术。两组患者的临床病理特征分布良好。中位随访时间为61.1个月(IQR:42.3-71.7个月),PSM术后,肺叶切除术的5年总生存率为98.8%(97.9-99.6%),肺段切除术的5年无复发生存率为99.3%(98.2-99.8%)(P=0.42),肺叶切除术的5年无复发生存率为95.3%(92.2-97.6%),肺段切除术的5年无复发生存率为95.2%(92.3-98.7%)(P=0.81)。肺叶切除术的复发比例为 4.1%,肺段切除术为 4.4%(P=0.89)。2级及以上早期术后并发症的比例为:肺叶切除术9.6%,肺段切除术8.8%(P=0.86):结论:对于cT1N0 GGO特征性浸润性肺腺癌(2厘米<肿瘤直径≤3厘米,CTR≤0.5或肿瘤直径≤2厘米,0.25<CTR≤0.5),分段切除组与肺叶切除组的术后效果相当。关于微创手术策略,应将分段切除术确定为标准手术方法。
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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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