Hardavella Georgia, Magouliotis Dimitrios E, Chalela Roberto, Januszewski Adam, Dennstaedt Fabio, Putora Paul Martin, So Alfred, Bhowmik Angshu
4th-9th Department of Respiratory Medicine, 'Sotiria' Athens' Chest Diseases Hospital, Athens, Greece.
Department of Cardiothoracic Surgery, University of Thessaly, Larissa, Greece.
Breathe (Sheff). 2024 Aug 27;20(2):230219. doi: 10.1183/20734735.0219-2023. eCollection 2024 Jun.
Chest radiography, computed tomography (CT) and positron emission tomography (PET)-CT are required for staging nonsmall cell lung cancers. Stage I cancers may be up to 4 cm in maximal diameter, with stage IA tumours being up to 3 cm and stage IB up to 4 cm. A lung cancer becomes stage II if the tumour is between 4 and ≤5 cm (stage IIA), or it spreads to ipsilateral peribronchial or hilar lymph nodes (stage IIB). Stage IA tumours should be surgically resected, ideally using minimally invasive methods. Lobectomy is usually performed, although some studies have shown good outcomes for sublobar resections. If surgery is not possible, stereotactic body radiotherapy is a good alternative. This involves delivering a few high-dose radiation treatments at very high precision. For stage IB to IIB disease, combinations of surgery, chemotherapy or immunotherapy and radiotherapy are used. There is evidence that neoadjuvant treatment (immunotherapy with nivolumab and chemotherapy for stage IB and II) optimises outcomes. Adjuvant chemotherapy with a platinum-based doublet (typically cisplatin+vinorelbine) should be offered for resected stage IIB tumours and considered for resected IIA tumours. Adjuvant pembrolizumab is used for stage IB-IIIA following resection and adjuvant platinum-based chemotherapy. Osimertinib may be used for resected stage IB to IIIA cancers which have relevant mutations (epidermal growth factor receptor exon 19 deletions or exon 21 (L858R) substitution). There are no fixed guidelines for follow-up, but most centres recommend 6-monthly CT scanning for the first 2-3 years after definitive treatment, followed by annual scans.
非小细胞肺癌分期需要进行胸部X线摄影、计算机断层扫描(CT)和正电子发射断层扫描(PET)-CT检查。I期癌症的最大直径可达4 cm,其中IA期肿瘤最大直径可达3 cm,IB期可达4 cm。如果肿瘤直径在4至≤5 cm之间(IIA期),或者扩散到同侧支气管周围或肺门淋巴结(IIB期),则肺癌为II期。IA期肿瘤应进行手术切除,理想情况下采用微创方法。通常进行肺叶切除术,不过一些研究表明亚肺叶切除术也有良好的效果。如果无法进行手术,立体定向体部放疗是一个不错的选择。这包括以非常高的精度进行几次高剂量放射治疗。对于IB期至IIB期疾病,采用手术、化疗或免疫治疗与放疗相结合的方法。有证据表明新辅助治疗(IB期和II期使用纳武单抗免疫治疗和化疗)可优化治疗效果。对于切除的IIB期肿瘤应提供以铂类为基础的双联辅助化疗(通常为顺铂+长春瑞滨),对于切除的IIA期肿瘤可考虑使用。辅助派姆单抗用于切除术后的IB期至IIIA期以及辅助铂类化疗后。奥希替尼可用于切除的IB期至IIIA期且有相关突变(表皮生长因子受体外显子19缺失或外显子21(L858R)替代)的癌症。随访没有固定的指南,但大多数中心建议在确定性治疗后的前2至3年每6个月进行一次CT扫描,之后每年进行一次扫描。