PDF

J Cancer 2021; 12(6):1708-1714. doi:10.7150/jca.49683 This issue Cite

Research Paper

Segmentectomy or Wedge Resection in Stage IA Lung Squamous Cell Carcinoma and Adenocarcinoma?

Guoshu Li^1#, Shuanshuan Xie^1#, Feng Hu^2#, Min Tan¹, Lihong Fan¹ , Changhui Wang¹

1. Department of Respiratory Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200072, China.
2. Tongren Hospital, Shanghai Jiao Tong University School of Medicine, 1111 XianXia Road, Shanghai 200336, China.
#These authors have contributed equally to this work.

✉ Corresponding author: Lihong Fan, Changhui Wang. Department of Respiratory Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301, Yanchang Middle Road, Jing'an District, Shanghai 200072, People's Republic of China. E-mail: fan-li-hongcom; wang-chang-huicom; Fax number: 86-021-66301685; Telephone: 86-021-66301685. More

Abstract

Objectives: We performed this study to compare survival outcomes of segmentectomy (SG) and wedge resection (WR) in stage IA lung squamous cell carcinoma (SQCC) and lung adenocarcinoma (AD).

Methods: Using the Surveillance, Epidemiology, and End Results registry (SEER), we identified 1529 and 4070 patients with stage IA SQCC and AD, respectively, who had complete clinical information between 2004 and 2015. We used Kaplan-Meier analysis to determine the propensity score for patients with limited resection based on the preoperative characteristics of patients. Lung cancer-specific survival (LCSS) was compared in patients treated with WR and SG after adjusting, stratifying, or matching lung cancer patients according to propensity score.

Results: Kaplan-Meier analysis demonstrated that there was a statistically significant difference in survival curves (log rank P=0.01) for patients with stage IA SQCC between SG and WR. But there was no statistically significant difference in survival curves (log rank P>0.05) in patients with stage IA AD between the two limited resections. Compared with the WR, The hazard ratios (95% confidence intervals) of SG were 0.689 (0.519-0.914) and 0.896 (0.752-1.067) in patients with stage IA SQCC and AD, respectively.

Conclusion: This study suggests that SG can yield superior survival outcome compared with WR in patients with stage IA SQCC. However, the survival outcomes of SG and WR are generally equivalent in patients with stage IA AD.

Keywords: SEER, segmentectomy, wedge resection, non-small cell lung cancer, survival

Introduction

Lung cancer is a serious threat to human health, and its incidence has risen rapidly in recent years. Patients with advanced non-small cell lung cancer (NSCLC) have a poor prognosis, but those with stage IA NSCLC have relatively good long-term outcomes after appropriate treatment [1]. Some studies have reported that the 5-year overall survival rate of patients with stage IA NSCLC after surgery is more than 70%, and the prognosis is even better for patients with tumor sizes ≤2 cm [2-5]. Although most patients with NSCLC are diagnosed at an advanced stage, 10%-15% of them are diagnosed with stage IA NSCLC [1]. Moreover, with the introduction of high-resolution computed tomography (CT) and low-dose helical CT screening for lung cancer, the number of patients diagnosed with early-stage lung cancer has increased [6]. Surgery is one of the most important treatment methods for stage IA NSCLC. Currently, lobectomy remains the standard surgical treatment for patients with NSCLC. However, limited resection is commonly used to treat patients who are unable to undergo total lobectomy due to older age, severe impairment of lung function, or other comorbidities [7]. In recent years, many studies have shown that the survival rate of patients with stage IA NSCLC who undergo limited resection is similar to that of patients who undergo lobectomy [8-13]. In addition, patients who undergo limited resection have less resected lung tissue and greater retention of lung function than those who undergo conventional lobectomy, which provides an opportunity for subsequent surgery if a second primary lung cancer occurs [14]. Therefore, limited resection has become an important treatment for patients with stage IA NSCLC.

Limited resection methods include wedge resection (WR) and segmentectomy (SG). SG, as an anatomic resection, has been thought as a preferred approach compared to WR in patients with stage IA NSCLC [15]. However, due to the quality of life in patients receiving SG was not as good as patients undergoing WR [16, 17], the option of WR or SG should be more cautious for patients. Previous studies have compared survival rates between the two types of limited resection primarily based on variables such as tumor size, differentiation grade, age, and so on, but less on the pathology subtypes of NSCLC. This study was to compare survival outcomes of WR and SG by comparing with lung cancer-specific survival (LCSS) in patients with stage IA lung squamous cell carcinoma (SQCC) or lung adenocarcinoma (AD), the major pathology subtypes of NSCLC.

Methods

Data source

This retrospective study was conducted to assess the relationship between two types of limited resection and the survival rate in patients with IA stage SQCC or AD, using data from the Surveillance, Epidemiology, and End Results (SEER) database. The SEER project is maintained by the National Cancer Institute in the United States (US). SEER includes a population-based cancer registry, established in 1973, which accounts for approximately 10% of the US population [18].

Study population

We limited the cohort to patients with stage IA SQCC or AD (≤3 cm in tumor size) diagnosed between 2004 and 2015. All included patients underwent WR or SG; the complete information of all included patients was available in the SEER database. Figure 1 shows a flow chart of the literature search for analyses based on the SEER database. Initially, 68,282 patients with IA stage lung cancer were identified. A total 66,312 patients with NSCLC were included, after excluding the following patients: 1,185 patients with small cell lung cancer, 66 with carcinoma not otherwise specified (NOS), 179 with large cell carcinoma, 371 with adenosquamous carcinoma and 169 patients with other cancers. We included 21,385 patients with NSCLC who were treated surgically, after excluding the following patients: 191 patients who underwent unknown surgery; 23,493 with no surgery; 9 with local tumor destruction or excision NOS; 120 with surgery NOS; 509 with laser ablation, cryosurgery, or radiofrequency ablation; 20,459 who underwent lobectomy with mediastinal lymph node dissection, plus pleura or diaphragm; and 146 patients with excision or resection of less than one lobe NOS. Finally, a total of 5,599 patients with stage IA SQCC or AD who were treated with limited resection were included in the analysis, after excluding 15,786 patients with NA not the first tumor.

Clinicopathological data

According to histologic type, histologic codes were classified as follows: (1) SQCC: 8052, 8070-8075, 8083, 8084, 8123, (2) AD: 8244, 8245, 8250-8255, 8260, 8290, 8310, 8323, 8333, 8480, 8481, 8490, 8507, 8550, 8570, 8571, 8574, and 8576. Based on information of the SEER site-specific surgical variables, all 5,599 included patients with stage IA SQCC or AD were classified as having undergone WR (SEER surgical code 21) or SG (SEER surgical code 22).

Statistical analyses

Classification variables were compared using the Pearson's chi-squared test. Kaplan-Meier analysis and the log-rank test were used to compare survival between the WR group and the SG group. Propensity score methods were used to control the potential differences in baseline characteristics of the included patients. Cox regression was performed to assess whether the baseline covariates of the two groups were balanced after adjusting for the estimated propensity scores. Statistical significance was set at a two-tailed P value <0.05. Data were analyzed using IBM SPSS version 20.0 (IBM Corp, Armonk, NY, USA).

Results

Study cohort characteristics

We identified 5,599 limited resection patients with stage IA SQCC or AD, of whom 4,394 (78.5%) and 1,205 (21.5%) underwent WR and SG, respectively, as a primary treatment from 2004 to 2015. Table 1 shows the baseline characteristics of all patients. Kaplan-Meier analyses demonstrated that there were no statistically significant differences in LCSS with regard to tumor location (P=0.996), marital status (P=0.482), laterality (P=0.854) and high school education (P=0.079) between the two groups. However, significant differences in LCSS were found with respect to age (P<0.001), sex (P<0.001), tumor size (P<0.001), differentiation grade (P<0.001), histologic type (P<0.001), radiotherapy (P<0.001), and chemotherapy (P<0.001) (Table 1).

Subsequent analysis using a Cox model, which included above seven significant covariates, showed that there were no statistically significant differences for histologic type (P=0.263) in patients with stage IA SQCC or AD. However, there were statistically significant differences for age (P<0.001), sex (P<0.001), tumor size (P<0.001), differentiation grade (P<0.001), radiotherapy (P<0.001), chemotherapy (P<0.001), and resection (P=0.013) (Table 2). These outcomes demonstrate that the prognoses of patients with stage IA SQCC or AD are related to the followed factors: age, sex, tumor size, differentiation grade, radiotherapy, chemotherapy, and limited resection, but are not related to these factors: tumor location, marital status and laterality.

Table 3 shows the hazard ratio (HR) and 95% confidence interval (CI) between the WR and SG. Compared with the WR group, the HR (95%CI, P) of the SG group were 0.823 (0.710-0.955, P=0.01) in total patients. The HR (95%CI, P) of the SG group were 0.689 (0.519-0.914, P=0.01), 0.896 (0.752-1.067, P=0.217) comparing with the WR group in patients with SQCC and AD, respectively. These outcomes demonstrate that the comparative results of WR and SG are different in pathology subtypes of NSCLC: the SG yields better survival outcome than the WR in patients with stage IA SQCC, but the survival outcomes of SG and WR are generally equivalent in patients with stage IA AD.

Comparison of survival curves between WR and SG

According to Kaplan-Meier analysis, the survival curves were compared between WR and SG groups (Figure 2). The survival curve of the SG group is better than the WR group (log rank P=0.01) in total patients (Figure 2A). Similarly, the survival curve of the SG group is better (log rank P=0.01) than the WR group in patients with stage IA SQCC (Figure 2B). However, in patients with stage IA AD, the survival curves (log rank P=0.217) show no statistically significant difference between the WR and SG groups (Figure 2C). This outcome also demonstrates that the SG can yield better survival outcome than WR in patients with stage IA SQCC, but the SG and WR yield generally equivalent survival outcomes in patients with stage IA AD.

Comparison of lung cancer-specific mortality between the WR and SG groups

The lung cancer-specific mortality was 21.4 (940/4394) for WR group, and 17.8% (214/1205) for SG group in patients with stage IA NSCLC. The lung cancer-specific mortalities were 26.0% (320/1231) and 19.10% (249/1304) for the WR and SG groups in patients with stage IA SQCC, respectively. In patients with stage IA AD, The lung cancer-specific mortalities were 19.6% (620/3163) and 17.3% (157/907) for the WR and SG groups, respectively (Table 4). The outcomes indicate that the lung cancer-specific mortality of SG group is superior to WR group in stage IA SQCC, but this advantage decreases obviously in stage IA AD.

 Figure 1 

Study flow diagram. Abbreviations: NSCLC, non-small cell lung cancer; NOS, not otherwise specified; RFA, radiofrequency ablation.

 Figure 2 

Comparison of survival curves between WR and SG. (A) Comparison of survival curves (P=0.01) in patients with stage IA NSCLC; (B) Comparison of survival curves (P=0.01) in patients with stage IA SQCC; (C) Comparison of survival curves (P>0.05) in patients with stage IA AD. Abbreviations: LCSS, lung cancer-specific survival; NSCLC, non-small cell lung cancer; SQCC, squamous cell carcinoma; AD, adenocarcinoma.

Table 4 also shows the median survival time and the mean survival time of WR and SG groups in different histologic types. In total NSCLC patients, the median survival time and the mean survival time were 38.0 months and 44.56 months for WR group, and 37.00 months and 45.02 months for SG group. In SQCC patients, the median survival time and the mean survival time were 34.00 months and 41.11 months for WR group, and 34.00 months and 44.24 months for SG group. In AD patients, the median survival time and the mean survival time were 39.00 months and 45.90 months for WR group, and 38.00 months and 45.28 months for SG group. The datum demonstrated that the difference of mean survival time is more obvious in SQCC than AD between WR and SG groups.

Discussion

Currently, with advances in radiology and the emergence of lung cancer screening programs, a higher incidence of early stage NSCLC has been observed. In this scenario, limited resection has been adopted as an effective treatment for stage IA NSCLC patients, especially in the elderly and patients with pulmonary insufficiency. Over the past decade, SG has become more common and played an increasingly important role in the treatment of pulmonary metastases. It is technically difficult for anatomic SG which not only demands a thorough understanding of the pulmonary anatomy, but also requires in-depth tomographic study of the location of the pulmonary nodules. Persistent pneumothorax (over five days) is the most common complication of SG, which occurs between 8% and 10% [19]. Therefore, the nodules must be well positioned to ensure safe resection. WR has been considered "inferior" cancer operation for nearly two decades, but much of the contemporary literature is contradictory and inconclusive. Several recent studies have shown that WR is even equivalent to lobectomy [20-22]. There is enough controversy to avoid overly dogmatic statements about the poor quality of WR in the absence of modern large-scale prospective trials. Instead, the surgeon should place the emphasis on the quality of the operation and ensure the most possible excision of margin when WR is required. Performed well, WR is maybe an appropriate surgical option.

Some researches has focused on which limited resection was better to the survival of NSCLC patients. Many people have reported that SG is superior to WR for NSCLC patients. For example, Dai et al. [23] considered that SG should be recommended for patients with NSCLC in whom lobectomy is unsuitable. Hou et al. [24] reported that SG results in higher survival rates than WR in patients with stage I NSCLC. Reveliotis et al.[25] reported that SG is superior to WR in terms of local recurrence and cancer-related mortality rates, and those authors recommended SG for high-risk patients. However, there were some different sounds about this view. In 2016, Altorki et al. [26] reported a retrospective analysis and concluded that WR maybe ontologically equivalent to anatomic SG for clinical T1a tumors. Sybron Harrison et al. [22] has reported a contemporary prospective randomized trial (ACOSOG Z4032) which supported to the view that WR and SG maybe equivalent methods of sub-lobar resection. In our study, we evaluated the survival outcomes of SG versus WR in patients with stage IA NSCLC. Although we found that SG yielded better survival rate than WR in overall patients, there were different in pathology subtypes of NSCLC. The result shows that SG yields better survival rate than WR in patients with stage IA SQCC, but SG and WR yield generally equivalent survival rate in patients with stage IA AD. In addition, patients underwent SG can obtain more advantageous mean survival time than WR in patients with stage IA SQCC, but this advantage almost lost in patients with stage IA AD. This result may provide patients with stage IA AD a personalized surgical option.

Admittedly, there are some limitations in our study, mainly owing to its retrospective design. For example, the lack of original datum from our own studies as well as validation for main findings and conclusion. In addition, the SEER database does not include some important information, such as the types of therapy, histological subtypes, and gene mutations. This information should be included in future prospective studies. Nevertheless, with the inclusion of 12 variables and nearly 5,600 patients in our cohort, the present study represents a well-balanced analysis of SG and WR surgical methods. Thus, in the absence of data from prospective trials, our findings can provide information that is useful for the management of patients with stage IA SQCC and AD.

In summary, the prognosis of patients with stage IA NSCLC is related to a variety of factors.

According to the development trend of modern medicine, there must be a personalized surgical approach which should take into account the characteristics of each patient, the imaging characteristics of tumor as well as the impact on the quality of life and surgical recovery in the future. This study indicates that SG is superior to WR in patients with stage IA SQCC, but the survival outcomes of SG and WR are generally equivalent in patients with stage IA AD. The result may provide a basis for individualized surgical option for stage IA AD patients.

Abbreviations

NSCLC, non-small cell lung cancer; WR, wedge resection; SG, segmentectomy; SEER, Surveillance, Epidemiology and End Results; LCSS, lung cancer-specific survival; SQCC, squamous cell carcinoma; AD, adenocarcinoma; NOS, not otherwise specified; HR, hazard ratio; CI, confidence interval.

Acknowledgements

We would like to thank all the staff of the National Cancer Institute for their efforts in the SEER program.

Funding

This work was supported by the National Natural Science Foundation of China (No. 81802262) and Shanghai Tenth Hospital's improvement plan for NSFC (No. 04.03.17.032, 04.01.18. 048).

Author Contributions

Conception and design: G.S.L. and S.S.X. Acquisition, statistical analysis or interpretation of the data: all authors. Drafting of the manuscript: L.H.F. and C.H.W. All authors reviewed and approved the final version of the manuscript.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. For this type of study, formal consent is waived.

Competing Interests

The authors have declared that no competing interest exists.

References

1. Spiro SG, Porter JC. Lung cancer-where are we today? Current advances in staging and nonsurgical treatment. Am J Respir Crit Care Med. 2002;166:1166-1196

2. Nesbitt JC, Putnam JB Jr, Walsh GL. et al. Survival in early-stage non-small cell lung cancer. Ann Thorac Surg. 1995;60:466-472

3. Williams DE, Pairolero PC, Davis CS. et al. Survival of patients surgically treated for stage I lung cancer. J Thorac Cardiovasc Surg. 1981;82:70-76

4. Harpole DH Jr, Herndon JE 2nd, Young WG Jr. et al. Stage I non-small cell lung cancer. A multivariate analysis of treatment methods and patterns of recurrence. Cancer. 1995;76:787-796

5. Martini N, Bains MS, Burt ME. et al. Incidence of local recurrence and second primary tumors in resected stage I lung cancer. J Thorac Cardiovasc Surg. 1995;109:120-129

6. Xue W, Duan G, Zhang X. et al. Meta-analysis of segmentectomy versus wedge resection in stage IA non-small-cell lung cancer. Onco Targets Ther. 2018;11:3369-3375

7. Wisnivesky JP, Henschke CI, Swanson S. et al. Limited resection for the treatment of patients with stage IA lung cancer. Ann Surg. 2010;251:550-554

8. Zhong C, Fang W, Mao T. et al. Comparison of thoracoscopic segmentectomy and thoracoscopic lobectomy for small-sized stage IA lung cancer. Ann Thorac Surg. 2012;94:362-367

9. Watanabe T, Okada A, Imakiire T. et al. Intentional limited resection for small peripheral lung cancer based on intraoperative pathologic exploration. Jpn J Thorac Cardiovasc Surg. 2005;53:29-35

10. Tsutani Y, Miyata Y, Nakayama H. et al. Oncologic outcomes of segmentectomy compared with lobectomy for clinical stage IA lung adenocarcinoma: propensity score-matched analysis in a multicenter study. J Thorac Cardiovasc Surg. 2013;146:358-364

11. Okada M, Koike T, Higashiyama M. et al. Radical sublobar resection for small-sized non-small cell lung cancer: a multicenter study. J Thorac Cardiovasc Surg. 2006;132:769-775

12. Koike T, Yamato Y, Yoshiya K. et al. Intentional limited pulmonary resection for peripheral T1 N0 M0 small-sized lung cancer. J Thorac Cardiovasc Surg. 2003;125:924-928

13. Sugi K, Kobayashi S, Sudou M. et al. Longterm prognosis of video-assisted limited surgery for early lung cancer. Eur J Cardiothorac Surg. 2010;37:456-460

14. Smith CB, Swanson SJ, Mhango G. et al. Survival after segmentectomy and wedge resection in stage I non-small-cell lung cancer. J Thorac Oncol. 2013;8:73-78

15. Sihoe AD, Van Schil P. Non-small cell lung cancer: when to offer sublobar resection. Lung Cancer. 2014;86:115-120

16. Fernando HC, Landreneau RJ, Mandrekar SJ. et al. Analysis of longitudinal quality-of-life data in high-risk operable patients with lung cancer: results from the ACOSOG Z4032 (Alliance) multicenter randomized trial. J Thorac Cardiovasc Surg. 2015;149:718-725 discussion 725-726

17. Chen H, Louie AV. SABR vs. Limited Resection for Non-small Cell Lung Cancer: Are We Closer to an Answer? Curr Treat Options Oncol. 2016;17:27

18. Yang J, Zhang Y, Sun X. et al. The prognostic value of multiorgan metastases in patients with non-small cell lung cancer and its variants: a SEER-based study. J Cancer Res Clin Oncol. 2018;144:1835-1842

19. Zhao K, Mei J, Xia C. et al. Prolonged air leak after video-assisted thoracic surgery lung cancer resection: risk factors and its effect on postoperative clinical recovery. J Thorac Dis. 2017;9:1219-1225

20. Altorki NK, Yip R, Hanaoka T. et al. Sublobar resection is equivalent to lobectomy for clinical stage 1A lung cancer in solid nodules. J Thorac Cardiovasc Surg. 2014;147:754-764

21. Razi SS, Daskalaki D, Burack J. Current trends in lung resection for T1a non-small cell lung cancer: is lobectomy still the answer? J Thorac Dis. 2017;9:E164-E165

22. Harrison S, Stiles B, Altorki N. What is the role of wedge resection for T1a lung cancer? J Thorac Dis. 2018;10(Suppl 10):S1157-S1162

23. Dai C, Shen J, Ren Y. et al. Choice of Surgical Procedure for Patients With Non-Small-Cell Lung Cancer ≤ 1 cm or > 1 to 2 cm Among Lobectomy, Segmentectomy, and Wedge Resection: A Population-Based Study. J Clin Oncol. 2016;34:3175-3182

24. Hou B, Deng XF, Zhou D. et al. Segmentectomy versus wedge resection for the treatment of high-risk operable patients with stage I non-small cell lung cancer: a meta-analysis. Ther Adv Respir Dis. 2016;10:435-443

25. Reveliotis K, Kalavrouziotis G, Skevis K. et al. Wedge resection and segmentectomy in patients with stage I non-small cell lung carcinoma. Oncol Rev. 2014;8:74-81

26. Altorki NK, Kamel MK, Narula N. et al. Anatomical segmentectomy and wedge resections are associated with comparable outcomes for patients with small ct1n0 non-small cell lung cancer. J Thorac Oncol. 2016;11:1984-1992

Author contact

Corresponding author: Lihong Fan, Changhui Wang. Department of Respiratory Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301, Yanchang Middle Road, Jing'an District, Shanghai 200072, People's Republic of China. E-mail: fan-li-hongcom; wang-chang-huicom; Fax number: 86-021-66301685; Telephone: 86-021-66301685.

Received 2020-6-18
Accepted 2020-12-24
Published 2021-1-18

Citation styles

©2024 Ivyspring International Publisher. Terms of use