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新辅助治疗衔接经皮冠状动脉介入治疗(PCI)与电视辅助胸腔镜(VATS)肺叶切除术:一项回顾性研究。

Neoadjuvant therapy bridging percutaneous coronary intervention (PCI) and video-assisted thoracoscopic (VATS) lobectomy: a retrospective study.

作者信息

Guo Lin, Ou Songlei, Zhang Shaoyan, Li Dong, Ma Xuchen

机构信息

Department of Thoracic Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing, China.

出版信息

Transl Cancer Res. 2024 Jun 30;13(6):2662-2673. doi: 10.21037/tcr-24-132. Epub 2024 Jun 18.

Abstract

BACKGROUND

Currently, there is no unified standard for the treatment of coronary artery disease (CAD) in non-small cell lung cancer (NSCLC), and the treatments have their own advantages and disadvantages. Thus, this study aimed to analyze the safety and feasibility of neoadjuvant therapy during the dual antiplatelet therapy (DAPT) period before surgery in patients with NSCLC coexisting with CAD after percutaneous coronary intervention (PCI) treatment.

METHODS

We retrospectively included 13 patients with T2aN0M0 (stage IB) NSCLC who also had concomitant CAD. After PCI treatment, neoadjuvant targeted or immunotherapy was administered based on the type of lung cancer, and the effects on treatment and impact on surgery were observed.

RESULTS

The objective response rate (ORR) after neoadjuvant treatment in 13 patients was 53.8% [95% confidence interval (CI): 25.1-80.8%], and the disease control rate (DCR) reached 100%. Ten patients (76.9%) experienced adverse events (AEs) ≤ grade 2. All patients underwent standard VATS lobectomy with lymph node dissection. One case (7.7%) required conversion to open thoracotomy, and all cases achieved R0 resection. The median operative time was 150 [interquartile range (IQR) 125-250] minutes, median intraoperative blood loss was 180 (IQR 150-235) mL, median postoperative drainage tube placement time was 4 (IQR 3-5) days, median total drainage volume was 1,310 (IQR 780-1,705) mL, and the median postoperative hospitalization was 7 (IQR 7-8) days. One patient (7.7%) experienced rapid atrial fibrillation. No deaths occurred. Postoperative pathological evaluation in three cases achieved major pathological response (MPR) (23.1%, 95% CI: 5-53.8%), with two cases achieving pathological complete response (pCR) (15.4%, 95% CI: 1.9-45.4%).

CONCLUSIONS

The study presents initial evidence suggesting for the safety and feasibility of performing PCI treatment followed by neoadjuvant therapy during the DAPT period for patients with T2aN0M0 (IB) stage NSCLC coexisting with CAD. This approach presents a potential treatment option to control the disease while eliminating concerns about tumor progression and metastasis.

摘要

背景

目前,非小细胞肺癌(NSCLC)合并冠状动脉疾病(CAD)的治疗尚无统一标准,各种治疗方法都有其优缺点。因此,本研究旨在分析经皮冠状动脉介入治疗(PCI)后,NSCLC合并CAD患者在术前双重抗血小板治疗(DAPT)期间进行新辅助治疗的安全性和可行性。

方法

我们回顾性纳入了13例T2aN0M0(IB期)NSCLC且合并CAD的患者。PCI治疗后,根据肺癌类型给予新辅助靶向治疗或免疫治疗,并观察其对治疗的效果及对手术的影响。

结果

13例患者新辅助治疗后的客观缓解率(ORR)为53.8%[95%置信区间(CI):25.1 - 80.8%],疾病控制率(DCR)达到100%。10例患者(76.9%)发生≤2级不良事件(AE)。所有患者均接受了标准的电视辅助胸腔镜肺叶切除术及淋巴结清扫术。1例患者(7.7%)需转为开胸手术,所有病例均实现R0切除。中位手术时间为150[四分位数间距(IQR)125 - 250]分钟,中位术中出血量为180(IQR 150 - 235)mL,中位术后引流管放置时间为4(IQR 3 - 5)天,中位总引流量为1310(IQR 780 - 1705)mL,中位术后住院时间为7(IQR 7 - 8)天。1例患者(7.7%)发生快速房颤。无死亡病例。3例患者术后病理评估达到主要病理缓解(MPR)(23.1%,95%CI:5 - 53.8%),2例患者达到病理完全缓解(pCR)(15.4%,95%CI:1.9 - 45.4%)。

结论

本研究提供了初步证据,表明对于T2aN0M0(IB)期NSCLC合并CAD的患者,在DAPT期间先进行PCI治疗,然后进行新辅助治疗是安全可行的。这种方法为控制疾病提供了一种潜在的治疗选择,同时消除了对肿瘤进展和转移的担忧。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1029/11231793/79a369120652/tcr-13-06-2662-f1.jpg

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