Skip to main content

Prognostic significance of 4R lymph node dissection in patients with right primary non-small cell lung cancer

Abstract

Background

To investigate the prognostic significance of station 4R lymph node (LN) dissection in patients who underwent operations for right primary non-small cell lung cancer (NSCLC).

Methods

We performed a retrospective study involving patients with right primary NSCLC who received lobotomy or pneumonectomy with mediastinal LN dissection between January 2011 and December 2017. Propensity score matching was performed. Disease-free survival (DFS) and overall survival (OS) were compared between patients with and without station 4R dissection.

Results

Our study included 2070 patients, with 207 patients having no station 4R dissection (S4RD− group) and 1863 patients having station 4R dissection (S4RD+ group). The 4R LN metastasis rate was 13.4% (142/1748), higher than that for other mediastinal LN metastases. Compared with the S4RD− group, the S4RD+ group had higher 5-year DFS (48.1% vs. 39.1%, P = 0.009) and OS (54.4% vs. 42.8%, P = 0.025). Station 4R dissection was an independent risk factor for DFS (odds ratio, OR, 1.28, 95% confidence interval, CI, 1.08–1.64, P = 0.007) and OS (OR 1.31, 95% CI 1.04–1.63, P = 0.018). Patients with adjuvant chemotherapy had a better prognosis after station 4R dissection than those without adjuvant chemotherapy (57.4% vs. 52.3%, P = 0.006). The 5-year OS in the station 4R metastasis group was lower than that in the station 4R non-metastasis group (26.9% vs. 44.3%, P = 0.006) among N2 patients. The 5-year OS of the single-station 4R metastasis group was lower than that of the single-station 7 metastasis group (15.7% vs. 51.6%, P = 0.002).

Conclusions

Station 4R metastasis was the highest among all the mediastinal station metastases in right primary NSCLC patients. Station 4R dissection can improve the prognosis and should be recommended as a routine procedure for these patients.

Background

Lung cancer is the leading cause of cancer-related deaths worldwide [1]. Non-small cell lung cancer (NSCLC) is the most common type of lung cancer [2]. The mainstay treatment for NSCLC is surgical resection [3]. During the operation, it is essential to remove the tumor as well as involved lymph nodes (LNs). However, preoperative imaging determination of mediastinal LN metastasis can be difficult, with a sensitivity and specificity of only 57% and 82%, respectively [4, 5]. Therefore, mediastinal lymph node dissection (MLND) was proposed as an essential step during the surgical treatment of NSCLC. MLND can provide important prognostic and therapeutic value for patients with NSCLC. Current guideline recommends that MLND should remove at least three mediastinal nodal stations, including station 7 [6]. However, the application of MLND in clinical practice remains controversial, since some studies reported increased operating time, prolonged hospital stays, and potentially high mortality with the procedure [7].

In the mediastinum, station 4R LNs are surrounded by complicated structures, such as the trachea, bronchus, pulmonary arteries, superior vena cava, and azygos. Studies have found that the station 4R LN metastasis rate was high but the resection rates varied between 64.5 and 87.1% [8,9,10,11]. Few studies have been conducted to study the association between station 4R LN dissection and patient prognosis. Therefore, we performed the present study to investigate station 4R metastasis and its association with the prognosis in patients with right primary NSCLC.

Methods

Study design and participants

We performed a retrospective study and reviewed the data for patients with right primary NSCLC who visited Tianjin Medical University Cancer Institute and Hospital, China, between January 2011 and December 2017. The study protocol was approved by the hospital ethics committee.

Patients were included if they had right primary NSCLC and received lobectomy or pneumonectomy with MLND. They were excluded if they (1) had metastatic lung cancer, (2) received pulmonary segment or pulmonary wedge resection, (3) received LN dissection but did not meet the criteria for MLND [6], (4) received preoperative neoadjuvant chemotherapy or radiotherapy, or (5) had incomplete medical records.

All patients underwent routine preoperative evaluations. Lobectomy or pneumonectomy with MLND was performed with thoracotomy or thoracoscopy by experienced thoracic surgeons. Based on the recommended LN clearance criteria during the radical surgical resection of lung cancer proposed by the International Association for the Study of Lung Cancer (IASLC) and the relevant guidelines [6, 12], at least three mediastinal LN stations, including the subcarinal LNs, as well as stations 10, 11, and 12 LNs, were routinely removed. The station 13 and 14 LNs were also removed along with the adjacent lung tissue but no pathologic examinations were performed on the tissues. The resected lung cancer tissue and LNs were evaluated by two experienced pathologists. All patients were staged according to the 8th edition TNM criteria [13].

Postoperative follow-up evaluations

All patients were followed up postoperatively. The follow-up outcomes were obtained from the hospital medical records. Patients received a chest X-ray or computed tomography (CT) scan 3–4 months after the surgery. Afterward, they were followed-up in the clinic every 4–6 months for the first 2 years and every 6–12 months for the next 3–5 years. After 5 years, patients were followed-up once a year. During the follow-up visits, patients received routine examinations, including laboratory tests, computed tomography (CT), magnetic resonance imaging (MRI), or positron emission tomography–computed tomography (PET/CT) scans when necessary.

The primary end point was the overall survival (OS) from the time of surgery to death or December 31, 2020. The secondary end point was the disease-free survival (DFS) from the time of surgery to cancer recurrence, metastasis, or the end of the study.

Propensity score matching

Propensity score matching (PSM) was performed to minimize the influence from confounding variables [14]. The propensity score was calculated for each patient based on a propensity score model that included every possible covariate, such as age, gender, smoking history, surgical approaches, tumor location, adjuvant chemotherapy, histological type, pT stage, and pN stage. The patients were matched with the Nearest Neighbor method with caliper restrictions in R (version 4.0.4) using the Matchit package (Version 4.1.0).

Statistical analysis

Patients were assigned to either the S4RD− group (without 4R dissection) or the S4RD+ group (with 4R dissection). The categorical variables were compared with the chi-square test. A multivariate logistic regression model was constructed to evaluate the relationship between station 4R metastasis and risk variables. The reverse Kaplan-Meier method was used to calculate the median follow-up time. Survival outcomes were evaluated with the Kaplan-Meier method and compared using the Log-Rank test. Multivariate Cox proportional hazards regression analysis was performed with statistically significant variables in the univariate analyses to assess the relationships between different variables and DFS or OS. The hazard ratios (HRs) and corresponding 95% confidence intervals (95%CI) were reported. All the statistical analyses were performed in R (version 4.0.4). P < 0.05 was considered statistically significant in a two-tailed test.

Results

Baseline characteristics

A total of 2070 patients met the selection criteria, including 207 patients in the S4RD− group and 1863 patients in the S4RD+ group. All patients were followed up in the clinic; however, 312 patients (15.1%) were lost during the follow-up period (36 patients, 17.4%, in the S4RD− group and 276 patients, 14.8%, in the S4RD+ group).

There were statistically significant differences in the baseline smoking history (P < 0.001) and tumor location (P = 0.025) between the S4RD− and S4RD+ groups (Table 1). After the PSM, the score gap between the two groups decreased (Fig. 1). The smoking history (P = 0.926) and tumor location (P = 0.710) were also similar between the two groups (Table 1). Finally, the data for 1004 patients (205 in the S4RD− group and 799 in the S4RD+ group) were included in the outcome analysis.

Table 1 Baseline characteristics before and after propensity score matching
Fig. 1
figure 1

Density maps of propensity score of entire cohort (A) and propensity score matching (B)

Involvements of mediastinal LN

The resection rate and metastasis rate of each LN station for all patients are shown in Fig. 2. All the station 7 LNs and 90.0% (1863/2070) of station 4R LNs were removed. The metastasis rate of station 4R was 13.4% (250/1863), which was significantly higher than the rates for all other stations, namely station 7 (10.9%, 225/2070, P = 0.034), station 3 (10.7%, 152/1414, P = 0.046), station 2 (7.4%, 129/1748, P < 0.001), station 8 (5.3%, 42/786, P < 0.001), and station 9 (4.6%, 55/1198, P < 0.001). In the S4RD+ group, subgroup analyses were performed based on the LN metastasis in stations 4 and 7 in patients with N2 diseases (Fig. 2C, D). The results showed that the metastatic rate of station 2 in patients with station 4R metastasis was significantly higher than that in patients without station 4R metastasis (38.2% vs. 25.0%, P = 0.017). The metastasis rate of station 7 in patients with station 4R metastasis was significantly lower than that in patients without station 4R metastasis (42.0% vs. 68.5%, P = 0.002). The metastasis rates of station 2, station 3, and station 4 in patients with station 7 metastasis were lower than those in patients without station 7 metastasis (23.6% vs. 43.1%, P = 0.008, 41.0% vs. 55.4%, P = 0.020, and 50.7% vs. 75.5%, P < 0.001, respectively). In addition, in N2 patients with station 10 metastasis, the metastasis rate of station 4R (60.0%) was statistically significantly higher than that of station 2 (34.3%, P < 0.001), station 3 (44.7%, P = 0.018), station 7 (52.9%, P = 0.252), station 8 (33.3%, P < 0.001), and station 9 (18.0%, P < 0.001).

Fig. 2
figure 2

Dissection rate (A) and metastasis rate (B) of each lymph node station. Distribution of lymph node involvements in patients with N2 disease and station 4R (C) or 7 (D) metastasis. Chi-square analysis was used to compare the dissection or metastasis rates between subgroups. *P < 0.05, **P < 0.01, ***P < 0.001

Variables associated with station 4R metastasis

Univariate and multivariate analysis demonstrated that tumor location (P = 0.013) and pT stage (P < 0.001) were significantly associated with station 4R metastasis, whereas gender, age, smoking history, surgical approaches, and pathological types had no relationship with station 4R metastasis (Table 2). In addition, station 2 (P < 0.001), station 3 (P < 0.001), station 7 (P < 0.001), and station 11 (P < 0.001) metastases were associated with station 4R metastasis, whereas station 8 (P = 0.432) and 9 (P = 0.355) metastases were not associated with station 4R metastasis.

Table 2 Univariate and multivariate analyses of variables associated with station 4R lymph node metastasis

Survival outcomes

There were 1004 patients included in the survival analysis after PSM. In the end, 157 patients (15.6%) were lost during the follow-up period, including 36 patients (17.6%) in the S4RD− group and 121 patients (15.1%) in the S4RD+ group. The median follow-up periods were 64.9 and 59.7 months in the S4RD− and S4RD+ groups, respectively (P = 0.39). The 5-year DFS was 48.1% in the S4RD+ group and 49.1% in the S4RD− group. The 5-year OS was 54.4% in the S4RD+ group and 42.8% in the S4RD− group. The DFS and OS of patients with station 4R dissection were significantly higher than the values for those without 4R dissection (P = 0.009 and 0.025, respectively (Fig. 3A, B). Univariate analysis showed that station 4R dissection, pT stage, pN stage, histological type, and pTNM stage were related to the DFS and OS (Table 3). Multivariate analysis showed that station 4R dissection was an independent risk factor for DFS (HR 1.33, 95%CI 1.08–1.64, P = 0.007) and OS (HR 1.31, 95%CI 1.04–1.63, P = 0.018) (Table 3). After excluding patients with no station 4R dissection, further analysis of patients with N2 LN metastasis showed that the 5-year OS of the group with station 4R metastasis was significantly lower than that of the group without station 4R metastasis (250 vs.149 patients; 29.1% vs. 42.1%, P = 0.032; Fig. 3C). The 5-year OS of the single-station 4R metastasis group was significantly lower than that of the single-station 7 metastasis group (44 vs. 64 patients; 15.7% vs. 51.6%, P = 0.002, Fig. 3D). After re-performing PSM based on chemotherapy in patients with 4R station dissection, the analysis results showed that the prognosis of patients who received adjuvant chemotherapy was better than that of patients who did not (546 vs. 546 patients; 57.4 % vs. 52.3%, P = 0.006, Fig. 3E).

Fig. 3
figure 3

Kaplan–Meier curves for DFS (A) and OS (B) between propensity-matched N2 patients with or without station 4R dissection. C OS of patients without or with station 4R metastasis. D OS of patients with single-station 4R or station 7 metastasis. E OS of patients with adjuvant chemotherapy and station 4R dissection (S4RD+ AC) or not (S4RD− AC)

Table 3 Univariate and multivariate Cox regression analyses of prognostic factors in propensity-matched patients

Discussion

Mediastinal LN dissection is an essential step during lung cancer surgical treatment. It plays an important role in the therapeutic and postoperative staging of lung cancer. Evaluation of metastasis in the mediastinal LN can also provide information on the prognosis of patients, as well as guide further treatment [15, 16]. However, at the present time, there is no conclusive evidence to support the dissection of station 4R during right lung cancer treatment [17,18,19]. The relevant guidelines also do not provide any recommendations on the extent of dissection [6]. In a previous study in patients who received lobectomy with MLND due to primary non-small cell lung cancer with a diameter smaller than 3 cm, the station 4R resection rates were 69%, 63%, and 61% in patients with the upper, middle, and lower lobe lesions, respectively [10]. Liu et al. reported a station 4R resection rate of 87% in patients who underwent lobectomy with MLND [8]. A Canadian survey of 86 thoracic surgeons found that 5 to 30% of surgeons did not consider that the station 4R dissection was necessary for different tumor sites [9]. In another study on patients with the lobe-specific lymph node dissection, the resection rate of station 4R in patients with right upper lobe lung cancer was only 70%, even if the station 4R metastasis rate was high up to 21% [11]. All this evidence suggested that a significant number of patients with the station 4R metastases might not be managed properly. Their managements could be delayed due to the errors in the pathological staging. The station 4R metastasis rate was the highest, or second only to that of station 7, in patients with right primary NSCLC [8, 10]. Therefore, we performed this retrospective study to explore the prognostic significance of station 4R dissection in patients with right primary NSCLC.

The results of our study suggested that the most common mediastinal LN station with metastasis was station 4R. We further analyzed LN metastasis in N2 patients with station 4R dissection in the subgroup of patients with and without station 4R or station 7 metastasis. The results indicated that the metastatic rate of station 2 was significantly higher in the group with station 4R metastasis than in the group without station 4R metastasis, whereas the metastasis rate of station 7 was lower in the group with station 4R metastasis than in the group without station 4R metastasis. The metastatic rates of stations 2, 3, and 4 were significantly lower in the group with station 7 metastasis than in the group without station 7 metastasis. There were no statistically significant differences in the metastasis rates among stations 8, 9, 11, and 12 in the subgroup analyses. N2 patients with station 10 metastasis had the highest station 4R metastasis rate, suggesting a positive correlation between the metastases of station 10 and station 4R. The anatomical associations among stations 2, 3, 4, and 10 might contribute to the difference in the metastases rates among the above subgroups. Univariate analysis suggested that the tumor location, surgical approaches, pT stage, and other LN station metastases were associated with station 4R metastasis. Multivariate analysis showed that the tumor location, pT stage, and stations 2, 3, 7, 10, and 11 metastases were independent risk factors for station 4R metastasis. The anatomical interactions among these LNs might contribute to the close association of metastases among them. When there was metastasis in stations 2, 3, 7, 10, and 11, the cancer cells could migrate to station 4 through the lymphatic duct, resulting in metastasis to the other station [20]. Riquet et al. [21] proposed that stations 2, 4, and 10 had the same drainage pathway and that tracheoesophageal LNs in station 3 were closely associated with the right paratracheal LNs. Zheng et al. [22] suggested that the 3A LN participated in the mediastinal lymphatic drainage system due to an extensive communication network among stations 4R, 2R, and 10R. Our study also suggested that stations 7 and 11 were independently associated with station 4R metastasis, although there was no strong evidence to support an anatomical connection among these stations. We also found that the tumor location was an independent risk factor for station 4R metastasis. The risk of station 4R metastasis was higher with upper lobe tumors than with middle and lower lobe tumors, which was consistent with many previous studies. Upper lobe NSCLCs are more likely to metastasize to the mediastinal LN, which is the underlying theory for dedicated lung lymphadenectomy [10, 23, 24]. Our results also suggested that the pT stage was a risk factor for station 4R metastasis, which was in agreement with other studies showing a relationship between tumor size and mediastinal LN metastasis [25, 26]. Zhang et al. suggested that systematic LN dissection should be performed, since tumor size was an independent risk factor for LN metastasis in patients even with pT1 stage lung adenocarcinoma [27]. Similarly, Jia et al. proposed that the tumor volume, but not the maximum diameter, could be the indicator of the tumor burden. A larger tumor usually correlated with a high risk of LN metastasis [28]. Other studies have indicated that the preoperative carcinoembryonic antigen [29], platelet count [30], and plasma D-dimer level [31] could be used to predict LN metastatic status in patients with operable NSCLC, suggesting that surgeons should carefully review the imaging and laboratory results and make comprehensive preoperative evaluations on the possibility of LN metastasis in NSCLS patients.

The results of survival analysis showed that DFS and OS in the S4RD+ group were significantly higher than those in the S4RD− group. Multivariate analysis suggested the status of station 4R dissection was an independent risk factor for DFS and OS. The station 4R metastasis rate was the highest among all mediastinal LN stations. Patients without station 4R dissection could have lower postoperative pathological staging and therefore might receive inadequate postoperative treatments. MLND could increase the accuracy of staging by improving the detection of occult N2 disease [17, 32]. Thorough MLND could improve the survival chances of patients. In addition, station 4R dissection could facilitate the clearance of potential LN micrometastases and thus block the development of LN metastases at an early stage [33]. These were consistent with previous studies on the single LN station [8, 34]. In other studies on the number of LN dissection, the researchers also believed that a high number of LN dissection was associated with improved OS and DFS [35, 36]. More LN dissections could make a higher accurate TNM staging and would be more likely to remove occult metastasis. A small number of dissected LN could make the N staging difficult [37]. A high accurate TNM staging is essential to determine the appropriate adjuvant therapy strategies and improve the survival chance. The number of LN removed and examined is determined by the different surgical operative approaches. A meta-analysis reported that, compared with the thoracoscope surgery, the thoracotomy could remove more numbers of total LN and N2 LN, although both surgery approaches removed similar numbers of N1 LN [38]. Our current study did not show a difference between different approaches. Future higher quality and large-scale randomized controlled trials are required to confirm this.

We further performed subgroup survival analyses after excluding patients without station 4R dissection. Patients were assigned into two subgroups based on the status of station 4R metastasis, single-station 4R metastasis, or single-station 7 metastasis. The results showed that the prognosis was worse in the group with station 4R metastases than in the group without station 4R metastases. The prognosis of the single-station 4R metastasis group was worse than that of the single-station 7 metastasis group. Of note, our univariate analysis did not support an association between adjuvant chemotherapy and the outcomes in 1004 PSM patients. This might be due to the imbalanced baseline characteristics, pT stage, and pN stage between patients with and without chemotherapy. When we analyzed this association in all the enrolled PSM patients, patients who received chemotherapy had a higher OS compared to patients who did not. Adjuvant chemotherapy was a risk factor for the treatment prognosis in patients with station 4R dissection.

In summary, we demonstrated the importance of station 4R LNs based on studies on LN metastasis and patient prognosis. Station 4R dissection should be a required step during the MLND in patients with right NSCLC. In clinical practice, patients were more likely to receive station 7, but not station 4R, dissection. Our results suggested that station 4R was more important than station 7 in terms of patient outcomes. Recent advances in endoscopic and robotic techniques could facilitate the dissection and removal of station 4R with complex anatomical structures. Finally, we recommend that station 4R dissection should be a routine procedure during MLND for patients with right lung cancer.

Our present study showed that the LN dissection was correlated with the outcomes in patients with NSCLC. LN metastasis and dissection in different locations could also have different impacts on the survivals. A recent study proposed a nomogram that could predict the survival in patients with stage III N2 small cell lung cancer. The nomogram also included the LN metastasis [39]. Whether different locations of the LN metastasis could have different influences on the survivals in patients with small cell lung cancer requires further studies.

The limitations of the current study included its retrospective and single-center design, which could introduce selection bias in the analysis. We performed PSM during the analyses for all enrolled patients, but not in the subgroup due to a relatively small number of patients. This might fail to reduce the data bias and confounding variables, resulting in systemic bias. In addition, a total of 312 (15.1%) patients were lost during the follow-up period, which might cause bias in survival analysis. Therefore, further multicenter randomized clinical trials are required to confirm our study results.

Conclusion

Station 4R had the highest metastasis rate among all the mediastinal stations in patients with right primary NSCLC. These patients could benefit from station 4R dissection to have a better survival chance. Routine station 4R dissection should be recommended during surgical treatment for these patients.

Availability of data and materials

The datasets generated and analyzed during the current study are not publicly available due to none of the data types requiring uploading to a public repository but are available from the corresponding author on reasonable request.

Abbreviations

NSCLC:

Non-small cell lung cancer

DFS:

Disease-free survival

OS:

Overall survival

S4RD− group:

Patients having no station 4R dissection

S4RD+ group:

Patients having station 4R dissection

MLND:

Mediastinal lymph node dissection

LNs:

Lymph nodes

IASLC:

International Association for the Study of Lung Cancer

CT:

Computed tomography

MRI:

Magnetic resonance imaging

PET/CT:

Positron emission tomography–computed tomography

PSM:

Propensity score matching

HRs:

Hazard ratios

95%CI:

95% confidence intervals

References

  1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71:209–49.

    PubMed  Google Scholar 

  2. Clark SB, Alsubait S. Non small cell lung cancer. Treasure Island: StatPearls; 2021.

    Google Scholar 

  3. Zappa C, Mousa SA. Non-small cell lung cancer: current treatment and future advances. Transl Lung Cancer Res. 2016;5:288–300.

    Article  CAS  Google Scholar 

  4. Toloza EM, Harpole L, McCrory DC. Noninvasive staging of non-small cell lung cancer: a review of the current evidence. Chest. 2003;123:137S–46S.

    Article  Google Scholar 

  5. Schmidt-Hansen M, Baldwin DR, Hasler E, Zamora J, Abraira V, Roque IFM. PET-CT for assessing mediastinal lymph node involvement in patients with suspected resectable non-small cell lung cancer. Cochrane Database Syst Rev. 2014;2014(11):CD009519.

    PubMed Central  Google Scholar 

  6. National Comprehensive Cancer Network. NCCN clinical practice guidelines in oncology: non-small cell lung cancer (version 3.2020). 2020.

    Google Scholar 

  7. Deslauriers J. Mediastinal lymph nodes: ignore? sample? dissect? The role of mediastinal node dissection in the surgical management of primary lung cancer. Gen Thorac Cardiovasc Surg. 2012;60:724–34.

    Article  Google Scholar 

  8. Liu C, Wei S, Guo C, Mei J, Pu Q, Liu L. Clinical significance of station 3A lymph node dissection in patients with right-side non-small-cell lung cancer: a retrospective propensity-matched analysis. Ann Surg Oncol. 2021;28:194–202.

    Article  Google Scholar 

  9. Turner SR, Seyednejad N, Nasir BS. Patterns of practice in mediastinal lymph node staging for non-small cell lung cancer in Canada. Ann Thorac Surg. 2018;106:428–34.

    Article  Google Scholar 

  10. Yang MZ, Hou X, Liang RB, Lai RC, Yang J, Li S, et al. The incidence and distribution of mediastinal lymph node metastasis and its impact on survival in patients with non-small-cell lung cancers 3 cm or less: data from 2292 cases. Eur J Cardiothorac Surg. 2019;56:159–66.

    Article  Google Scholar 

  11. Liang RB, Yang J, Zeng TS, Long H, Fu JH, Zhang LJ, et al. Incidence and distribution of lobe-specific mediastinal lymph node metastasis in non-small cell lung cancer: data from 4511 resected cases. Ann Surg Oncol. 2018;25:3300–7.

    Article  Google Scholar 

  12. Rusch VW, Asamura H, Watanabe H, Giroux DJ, Rami-Porta R, Goldstraw P. The IASLC lung cancer staging project: a proposal for a new international lymph node map in the forthcoming seventh edition of the TNM classification for lung cancer. J Thorac Oncol. 2009;4:568–77.

    Article  Google Scholar 

  13. Goldstraw P, Chansky K, Crowley J, Rami-Porta R, Asamura H, Eberhardt WE, et al. The IASLC lung cancer staging project: proposals for revision of the TNM stage groupings in the forthcoming (eighth) edition of the TNM classification for lung cancer. J Thorac Oncol. 2016;11:39–51.

    Article  Google Scholar 

  14. Austin PC. Optimal caliper widths for propensity-score matching when estimating differences in means and differences in proportions in observational studies. Pharm Stat. 2011;10:150–61.

    Article  Google Scholar 

  15. Zhong W, Yang X, Bai J, Yang J, Manegold C, Wu Y. Complete mediastinal lymphadenectomy: the core component of the multidisciplinary therapy in resectable non-small cell lung cancer. Eur J Cardiothorac Surg. 2008;34:187–95.

    Article  Google Scholar 

  16. Whitson BA, Groth SS, Maddaus MA. Surgical assessment and intraoperative management of mediastinal lymph nodes in non-small cell lung cancer. Ann Thorac Surg. 2007;84:1059–65.

    Article  Google Scholar 

  17. Darling GE, Allen MS, Decker PA, Ballman K, Malthaner RA, Inculet RI, et al. Randomized trial of mediastinal lymph node sampling versus complete lymphadenectomy during pulmonary resection in the patient with N0 or N1 (less than hilar) non-small cell carcinoma: results of the American College of Surgery Oncology Group Z0030 Trial. J Thorac Cardiovasc Surg. 2011;141:662–70.

    Article  Google Scholar 

  18. Darling GE, Allen MS, Decker PA, Ballman K, Malthaner RA, Inculet RI, et al. Number of lymph nodes harvested from a mediastinal lymphadenectomy: results of the randomized, prospective American College of Surgeons Oncology Group Z0030 trial. Chest. 2011;139:1124–9.

    Article  Google Scholar 

  19. Lardinois D, De Leyn P, Van Schil P, Porta RR, Waller D, Passlick B, et al. ESTS guidelines for intraoperative lymph node staging in non-small cell lung cancer. Eur J Cardiothorac Surg. 2006;30:787–92.

    Article  Google Scholar 

  20. Riquet M. Bronchial arteries and lymphatics of the lung. Thorac Surg Clin. 2007;17:619–38 viii.

    Article  Google Scholar 

  21. Riquet M, Arame A, Foucault C, Le Pimpec BF. Prognostic classifications of lymph node involvement in lung cancer and current International Association for the Study of Lung Cancer descriptive classification in zones. Interact Cardiovasc Thorac Surg. 2010;11:260–4.

    Article  Google Scholar 

  22. Zheng H, Gao W, Fei K, Xie HK, Jiang GN, Ding JA, et al. Prognostic role of station 3A mediastinal nodes for non-small-cell lung cancers. Interact Cardiovasc Thorac Surg. 2013;17:447–54.

    Article  Google Scholar 

  23. Sakao Y, Okumura S, Mingyon M, Uehara H, Ishikawa Y, Nakagawa K. The impact of superior mediastinal lymph node metastases on prognosis in non-small cell lung cancer located in the right middle lobe. J Thorac Oncol. 2011;6:494–9.

    Article  Google Scholar 

  24. GCCB-S. Intraoperative lymph node staging in bronchogenic carcinoma surgery. Consensus report. Arch Bronconeumol. 2001;37:495–503.

    Article  Google Scholar 

  25. Kuzucuoglu M, Gokyer A, Kula O, Yekdes AC, Sunal BS, Karamustafaoglu YA, et al. Relationship between the size and location of the mass and hilar and mediastinal lymph node metastasis in early and locally advanced non-small cell lung cancer. J Coll Physicians Surg Pak. 2020;30:172–6.

    Article  Google Scholar 

  26. Wang L, Zhan C, Gu J, Xi J, Lin Z, Xue L, et al. Role of skip mediastinal lymph node metastasis for patients with resectable non-small-cell lung cancer: a propensity score matching analysis. Clin Lung Cancer. 2019;20:e346–e55.

    Article  Google Scholar 

  27. Zhang YK, Chai ZD, Tan LL, Wang ZY, Chen ZJ, Le HB, et al. Association of lymph node involvement with the prognosis of pathological T1 invasive non-small cell lung cancer. World J Surg Oncol. 2017;15:64.

    Article  Google Scholar 

  28. Jia B, Chen B, Long H, Rong T, Su X. Tumor volume is more reliable to predict nodal metastasis in non-small cell lung cancer of 3.0 cm or less in the greatest tumor diameter. World J Surg Oncol. 2020;18:168.

    Article  Google Scholar 

  29. Ye B, Cheng M, Ge XX, Geng JF, Li W, Feng J, et al. Factors that predict lymph node status in clinical stage T1aN0M0 lung adenocarcinomas. World J Surg Oncol. 2014;12:42.

    Article  Google Scholar 

  30. Liu HB, Gu XL, Ma XQ, Lv TF, Wu Y, Xiao YY, et al. Preoperative platelet count in predicting lymph node metastasis and prognosis in patients with non-small cell lung cancer. Neoplasma. 2013;60:203–8.

    Article  CAS  Google Scholar 

  31. Gao XL, Wang SS, Cao DB, Liu W. The role of plasma D-dimer levels for predicting lymph node and mediastinal lymph node involvement in non-small cell lung cancer. Clin Respir J. 2018;12:2151–6.

    Article  CAS  Google Scholar 

  32. Cerfolio RJ, Bryant AS, Minnich DJ. Complete thoracic mediastinal lymphadenectomy leads to a higher rate of pathologically proven N2 disease in patients with non-small cell lung cancer. Ann Thorac Surg. 2012;94:902–6.

    Article  Google Scholar 

  33. Verhagen AF, Bulten J, Shirango H, Thunnissen FB, van der Drift MA, van der Bruggen W, et al. The clinical value of lymphatic micrometastases in patients with non-small cell lung cancer. J Thorac Oncol. 2010;5:1201–5.

    Article  Google Scholar 

  34. Wang YN, Yao S, Wang CL, Li MS, Sun LN, Yan QN, et al. Clinical significance of 4L lymph node dissection in left lung cancer. J Clin Oncol. 2018;36:2935–42.

    Article  Google Scholar 

  35. Zhai W, Duan F, Zheng Y, Yan Q, Dai S, Chen T, et al. Significance of accurate hilar and intrapulmonary lymph node examination and prognostication in stage IA-IIA non-small cell lung cancer, a retrospective cohort study. World J Surg Oncol. 2020;18:258.

    Article  Google Scholar 

  36. Wu LL, Lai JJ, Liu X, Huang YY, Lin P, Long H, et al. Association between number of dissected lymph nodes and survival in stage IA non-small cell lung cancer: a propensity score matching analysis. World J Surg Oncol. 2020;18:322.

    Article  Google Scholar 

  37. Tamura M, Matsumoto I, Saito D, Yoshida S, Takata M, Takemura H. Lymph node ratio as a prognostic factor in patients with pathological N2 non-small cell lung cancer. World J Surg Oncol. 2016;14:295.

    Article  Google Scholar 

  38. Zhang W, Wei Y, Jiang H, Xu J, Yu D. Thoracotomy is better than thoracoscopic lobectomy in the lymph node dissection of lung cancer: a systematic review and meta-analysis. World J Surg Oncol. 2016;14:290.

    Article  Google Scholar 

  39. Chai Y, Ma Y, Feng W, Lu H, Jin L. Effect of surgery on survival in patients with stage III N2 small cell lung cancer: propensity score matching analysis and nomogram development and validation. World J Surg Oncol. 2021;19:258.

    Article  Google Scholar 

Download references

Acknowledgements

None

Funding

None

Author information

Authors and Affiliations

Authors

Contributions

DZ: conceptualization, data curation, writing—original draft; DY: validation, formal analysis, writing—review and editing; ZZ: resources, validation; PT: data curation, formal analysis; YF: data curation, validation; ZL: formal analysis, methodology; BZ: investigation, project administration; MW: data curation; XZ: methodology; CW: conceptualization, project administration. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Changli Wang.

Ethics declarations

Ethics approval and consent to participate

The study protocol was approved by the hospital ethics committee. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. Written informed consent was obtained from all individual participants included in the study.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhou, D., Yue, D., Zhang, Z. et al. Prognostic significance of 4R lymph node dissection in patients with right primary non-small cell lung cancer. World J Surg Onc 20, 222 (2022). https://doi.org/10.1186/s12957-022-02689-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12957-022-02689-w

Keywords