Association between number of dissected lymph nodes and survival in stage IA non-small cell lung cancer: a propensity score matching analysis

Lung cancer is one of the most aggressive malignancies worldwide. In 2019, lung cancer accounted for 13% of all estimated new cancer cases and one-quarter of all estimated cancer deaths in adults [1]. Patients with stage IA (according to 8^th American Joint Committee on Cancer [AJCC] Staging Manual) non-small-cell lung cancer (NSCLC) may undergo different surgical treatments, such as wedge resection, segmental resection, lobectomy, or pneumonectomy; however, their 5-year overall survival rate remains around 73–90% [2]. Lobectomy along with mediastinal lymph nodes (LNs) resection has been considered the standard surgical treatment for early-stage NSCLC for more than 2 decades [3]. LNs’ dissection is widely used to determine the accurate pathologic staging of NSCLC and to provide guidance regarding the prognosis and additional treatments. Multiple studies have indicated that LN resection conferred benefit in terms of the survival outcomes of patients with stage T1-4N0M0 NSCLC [4‐8]. Furthermore, it seems that the dissection of more number of LNs may result in a clearer TNM classification and improve the survival outcomes of patients [9, 10].

Whereas with the popularization of computed tomography (CT)-based screening and application of some CT features, the predictive ability to distinguish benign and malignant lesions of small pulmonary nodules has significantly improved [11‐13]. Patients with clinical stage I NSCLC commonly undergo lung cancer screening by CT, which helps detect the pulmonary nodules. Recently, the results of JCOG0804 demonstrated that for patients who were found with a lesion with a diameter ≤ 2 cm and a solid component ≤ 25%, the 5-year disease-free survival rate of those patients with sub-lobectomy was 99.7% [14]. Therefore, surgeons and patients might consider sub-lobar resection, including wedge resection, and segmental resection as a preferred treatment approach to protect more healthy tissues in the lung. However, with increased sub-lobar resection, the decision to include LN dissection remains controversial. In addition, few studies have investigated the relationship between LN resection and the survival outcomes of patients with clinical stage IA (8th AJCC) NSCLC with tumor size ≤ 2 cm who underwent different types of lung surgery (wedge resection, segmental resection, lobectomy, pneumonectomy) [7].

Therefore, we aimed to investigate whether resection of more LNs resulted in better survival outcomes among patients with clinical stage IA NSCLC with tumor size ≤ 2 cm and to determine the effects of the number of removed lymph nodes (NLNs) on conferring survival benefit to patients who underwent wedge resection, segmental resection, lobectomy, or pneumonectomy.

This study examined the relationship between NLNs and the survival outcomes of patients with stage IA NSCLC ≤ 2 cm in size who underwent different types of lung surgeries. Kaplan–Meier analysis and log-rank test demonstrated that patients with more than 5 LNs dissected showed significantly better CSS and OS in the unmatched and matched patients, which indicates that dissection of more LNs might result in better survival. In addition, both univariable and multivariable analyses revealed that NLNs served as a protective prognostic predictor for CSS and OS in the unmatched and matched patients. Further, according to our subgroup study, patients who underwent wedge resection, segmental resection, or lobectomy rather than pneumonectomy, together with resection of more than 5 LNs, had statistically better survival outcomes. To sum up, patients with stage IA NSCLC ≤ 2 cm in size who undergo wedge resection, segmental resection, or lobectomy may have better survival outcomes after undergoing incremental NLNs.

To date, the relationship between NLNs and survival outcome for patients with stage IA NSCLC ≤ 2 cm in size remains controversial. Dissection of more LNs may result in a clearer TNM classification, a higher possibility to discover, and eradicate occult metastasis, and therefore a better survival outcome [9, 10]. Further, Burdett et al. noted that an increase in NLNs can make the pTNM stage more precise that it is beneficial to decide the strategy of adjuvant therapy [15]. Several retrospective studies based on the SEER database have confirmed the relationship between NLNs and survival outcomes of patients with stage N0 NSCLC and have proposed optimal NLNs for survival outcomes [4, 6‐8]. Furthermore, Osarogiagbon et al. suggested that the resection of 11 to 15 LNs might be associated with better survival [6]. Similarly, Becker et al. observed a consistently increasing survival benefit for patients with 16 to 18 LNs removed [8]. Additionally, several single-center studies also highlighted the relationship. However, a study conducted by Saji et al. determined the optimal minimum NLNs as 8 for patients with stage I NSCLC [16]. Moreover, Wen et al. demonstrated that patients with stage T2N0M0 NSCLC should have at least 12 LNs resected during the surgery [5]. In addition, the minimal NLNs for patients with N0 NSCLC was not clear. Likewise, the NCCN guidelines indicate that N1 and N2 nodes should be dissected, and mapping should be performed; however, it does not specify the minimum NLNs [17]. Conversely, the European Society of Thoracic Surgeons guidelines proposes that at least six LNs from the hilar and mediastinal stations should be removed for accurate nodal staging [10].

Unfortunately, only a few studies have focused on whether NLNs is associated with the survival outcomes of patients with stage IA NSCLC 2 cm or less. Ding et al. demonstrated that 4 to 16 LNs should be examined for patients with NSCLC < 2 cm undergoing wedge resection, and these NLNs could provide a survival advantage to those patients. However, among patients who received segmentectomy, LN resection did not improve survival outcomes [7]. In Ding’s study, there were some stage IB patients, as they did not exclude the patients with pleura invasion. Wolf et al. showed that lobectomy led to superior survival compared to sub-lobar resection in patients with N0 NSCLC ≤ 2 cm; however, the survival outcome was not different from that in patients with LN resection performed together with lobectomy [18]. In contrast, our study revealed that LN resection conferred independent survival benefit to patients with NSCLC ≤ 2 cm, and NLNs contributed to survival benefit for patients who received wedge resection, segmental resection, or lobectomy, but not for patients who received pneumonotomy. Several theories can explain this phenomenon. There were only 45 patients who underwent pneumonectomy in comparison to a larger number of patients who received wedge resection, segmental resection, or lobectomy in our study (n = 1647, 364, 5228, respectively), and a small sample entails a risk of bias. Notably, the patients who received lobectomy or wedge resection and with more than 5 LNs dissected had a significantly better CSS, while there was no effect of dissection of more than 5 LNs with segmental resection, or pneumonectomy on CSS. The smaller sample sizes of patients undergoing segmental resection, or pneumonectomy might be responsible for it. Since p values of segmental resection were both near 0.05 (P = 0.055), and univariable and multivariable studies together with a subgroup study on OS revealed that all the four surgical methods except pneumonectomy together with dissection of more than 5 LNs contributed to better survival outcome, we concluded that patients who underwent wedge resection, segmental resection, or lobectomy had better survival outcome after having incremental NLNs.

There are several limitations to this study. Because of the retrospective nature of the study, the bias in our results was inevitably unremovable. However, the potential selection bias derived from a retrospective study was minimized by performing PSM. Due to the short follow-up period and a low malignancy rate of stage IA NSCLC tumors ≤ 2 cm, the median survival time of all patients was not identified. The exact location of the dissected LNs was unknown due to the statistical limitations. Moreover, our findings did not provide an exact optimal NLNs for LN dissection in clinical practice. Despite these limitations, we believe that our study could be used as a reference for the treatment of patients with stage IA NSCLC ≤ 2 cm in size who undergo wedge resection, segmental resection, or lobectomy.

In conclusion, NLNs was a strong prognosticator for patients who received wedge resection, segmental resection, or lobectomy rather than pneumonectomy. Our study indicates that patients with stage IA NSCLC ≤ 2 cm who undergo wedge resection, segmental resection, or lobectomy should undergo higher NLNs to achieve better OS, but the efficacy of our conclusions should be investigated further by a large-scale, prospective, multi-center study.