• Users Online: 1658
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Contacts Login 

 Table of Contents  
ORIGINAL ARTICLE
Year : 2017  |  Volume : 37  |  Issue : 2  |  Page : 37-43

Sublobar resection for clinical stage I nonsmall cell lung cancers


Division of Thoracic Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, ROC

Date of Web Publication21-Apr-2017

Correspondence Address:
Dr. Tsai-Wang Huang
Department of Surgery, Division of Thoracic Surgery, Tri-Service General Hospital, 325, Section 2, Cheng-Kung Road, Taipei 114, Taiwan
ROC
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1011-4564.204985

Rights and Permissions
  Abstract 

Aim: We investigated outcomes of sublobar resection in patients with clinical early-stage nonsmall cell lung cancers. Patients and Methods: Patients who underwent surgical resection between January 2002 and June 2013 were reviewed. The clinical data, surgical approach, and outcome were analyzed with mean follow-up of 108 months. Results: Of 597 patients, 108 (18.1%) underwent sublobar resection. The 5-year overall survival (OS) and disease-free survival rate for this group were 76.2% and 70.3%, respectively, compared with 79.7% and 73.0% for those undergoing anatomic resection (P = 0.709 and 0.618). After stratifying for tumor size <2 cm, 233 patients with T1a lesions were enrolled in this study. The 5-year OS and disease-free survival rate for 69 patients who underwent sublobar resection were 96% and 87%, respectively, compared with 93.4% and 89.7% for those undergoing anatomic resection (P = 0.760 and 0.868). The local recurrence rate was 3% in the sublobar resection group and 8.5% in the anatomic resection group. There were no significant differences in age, gender, histopathology type, maximum standard uptake value, lymphovascular space invasion, visceral pleural invasion, and epidermal growth factor receptor status, except in the grade of tumor differentiation and numbers of dissected lymph nodes: 13.16 ± 6.62 in the anatomic resection group and 7.34 ± 4.91 in the sublobar resection group (P < 0.01). In the sublobar resection group, 28 patients underwent segmentectomy without local recurrence during follow-up. Conclusions: The oncologic outcomes of sublobar resection were similar to anatomic resection in these patients; lymph node sampling might not compromise surgical outcomes. Further large-scale studies are necessary to clarify the difference in clinical outcome between segmentectomy and wedge resection.

Keywords: Lung cancer, prognosis, surgery


How to cite this article:
Huang TW, Chen YH, Huang KH, Chang H, Lee SC. Sublobar resection for clinical stage I nonsmall cell lung cancers. J Med Sci 2017;37:37-43

How to cite this URL:
Huang TW, Chen YH, Huang KH, Chang H, Lee SC. Sublobar resection for clinical stage I nonsmall cell lung cancers. J Med Sci [serial online] 2017 [cited 2019 Oct 19];37:37-43. Available from: http://www.jmedscindmc.com/text.asp?2017/37/2/37/204985


  Introduction Top


Anatomic lobectomy and mediastinal lymph node dissection are standard operations in patients with nonsmall cell lung cancer (NSCLC).[1] Lobectomy results in loss of pulmonary function and is prohibitive for patients with compromised cardiopulmonary functions. Ginsberg and Rubinstein [2] reported a randomized trial of sublobar resection for patients with clinical stage T1a NSCLC, showing that a high locoregional recurrence was associated with limited resection. Sublobar resection was considered a compromised operation in the past. With the increasing use of chest computed tomography (CT) scans, low-dose CT was more sensitive in detecting early-stage lung cancers.[3] Some retrospective studies reported sublobar resection in patients with early-stage lung cancers with similar oncologic outcomes.[4],[5] The theoretical advantage of limited resection includes preservation of pulmonary function, decreased perioperative morbidity, and the ability of patients to survive the second operation. It promotes the vigorous development of sublobar resection in patients with an early-stage NSCLC. However, there are no robust data from randomized trials that document better long-term outcomes following sublobar resection or on the role of lymph node dissection. In one meta-analysis from the National Cancer Database, sublobar resection for patients with clinical Stage 1A lung cancers led to worse overall survival (OS) than did anatomic resection.[6] Inadequate positive tumor margins are the main complications involved in attempting sublobar resection. Most mortality following surgical resection is associated with tumor recurrence. The adoption of minimally invasive techniques for sublobar resection has been one of the most important advances in thoracic surgery. Thus, video-assisted thoracoscopic surgery (VATS) segmentectomy is a safe and oncologically proven technique for patients with an early-stage NSCLC.[7] That study evaluated the VATS procedure compared with open surgery. Most studies have focused on the oncological outcomes of sublobar resection for patients with clinical T1a lesions. However, this can involve selection bias and raises ethical problems in terms of performing randomized studies. The intraoperative evaluation of lymph nodes might determine the surgeon's decision to do anatomic or sublobar resection. There are still controversies on the methods for carrying out sublobar resection, such as wedge resection versus segmentectomy and lymph node dissection versus lymph node sampling. Here, we investigated the surgical outcomes of sublobar resection for patients with clinical early-stage NSCLC using a VATS procedure and discuss the role of lymph node dissection.


  Patients and Methods Top


All patients who underwent anatomic resection for clinical Stage I or II NSCLC at Tri-Service General Hospital, Taiwan, between January 2002 and June 2013 were reviewed retrospectively. This study was approved by the Institutional Review Board of our hospital (TSGHIRB 2-103-05-119). The patients underwent preoperative staging workups, including chest CT scans, positron emission tomography (PET), and abdominal ultrasonography. PET was performed for the assessment of mediastinal lymph node or bone metastases. We excluded patients who had received neoadjuvant chemotherapy, those with synchronous lung cancers, or those who underwent open surgery. Determinations of cancer stage were based on the tumor-node-metastasis classification (7th edition) of the American Joint Committee on Cancer.[8] In all, 597 patients with NSCLC underwent surgical resection and mediastinal lymph node dissection after evaluation of resectability and operability. Postoperative surveillance included contrast-enhanced CT and measurements of serum carcinoembryonic antigen. CT scans were performed for tumor assessment every 4–6 months. Magnetic resonance imaging of the brain was performed as indicated clinically. Relapse (including locoregional recurrence or distant metastasis) was documented either with imaging or histopathology diagnosis for all patients.

Statistical analysis

Descriptive data are expressed as the mean ± standard deviation. Student's t-test was used to investigate continuous variables, and the Chi-square test was used to compare categorical variables between groups. Survival from the date of surgery was calculated using Kaplan–Meier survival analysis. SPSS version 18.0 software (SPSS, Inc., Chicago, IL, USA) was used for all analyses, and statistical significance was defined as P< 0.05.


  Results Top


Of 630 patients with lung cancer who underwent surgical resection, 33 were excluded as having had neoadjuvant chemotherapy, synchronous lung cancers, or open surgery, so 597 patients were enrolled finally. Of these, 108 patients (18.1%) underwent sublobar resection, and 489 underwent anatomic resection (including pneumonectomy in 5 patients, lobectomy in 476 patients, and bilobectomy in 8 patients). There was no 30-day mortality. In the anatomic resection group, there were high rates of advanced tumor stages (Stage II 33.2%; Stage III 12.9%) compared with the sublobar resection group (Stage II 15.7%; Stage III 13.9%). Of the 108 patients who underwent sublobar resection, 75% had Stage I tumors. Some of these patients underwent sublobar resection because of comorbidity and old age. The characteristics of tumors in the anatomic resection group were poorer differentiation of tumors, central location, larger tumor size, and higher maximum standard uptake value (SUVmax) of fluorodeoxyglucose compared with the sublobar resection group [Table 1] and [Table 2]. The results showed poorer outcome with lower OS rate and a higher incidence of relapse in the anatomic resection group. The mean numbers of dissected lymph nodes in the anatomic resection group (13.38 ± 6.93) were greater than in the sublobar resection group (7.58 ± 5.89; P< 0.001). The 5-year OS was 76.2% for patients in the sublobar resection group and 79.7% for the anatomic resection group [P = 0.709; [Figure 1]a. The 5-year disease-free survival (DFS) was 70.3% for patients in the sublobar resection group and 73.0% for the anatomic resection group patients [P = 0.618, [Figure 1]b.
Table 1: Characteristics of patients with or without tumor recurrence after resection for clinical Stage I nonsmall cell lung cancer

Click here to view
Table 2: Characteristics of patients with or without recurrence after surgical resection for clinical Stage I nonsmall cell lung cancer

Click here to view
Figure 1: (a) Overall patient survival curves following anatomic or sublobar resection. (b) Disease-free patient survival curves following anatomic or sublobar resection

Click here to view


After stratifying patients according to T1a lesions (tumor size <2 cm), 233 were included in the study; 164 (70.4%) underwent anatomic resection and 69 (29.6%) underwent sublobar resection after intraoperative node examination with free metastases. Three patients with preoperative PET–CT-negative N status had lymph node involvement, and this finding changed the operation (sublobar resections were converted to anatomic resections). There were no significant differences in age, gender balance, tumor histopathology type, SUVmax of tumor, lymphovascular space invasion (LVSI), visceral pleural invasion, or epidermal growth factor receptor gene mutation status, except in terms of the grade of tumor differentiation and the numbers of dissected lymph node [Table 3] and [Table 4]. In the sublobar resection group, 74% of the patients had well-differentiated tumors, compared with 53.0% in the anatomic resection group (P = 0.015). There were more dissected lymph nodes in the anatomic resection group (13.16 ± 6.62) than in the sublobar resection group (7.34 ± 4.91; P< 0.001). The 5-year OS and DFS were 96% and 87% for the 69 patients who underwent sublobar resection versus 93.4% and 89.7% for the anatomic resection group (P = 0.760 and 0.868, respectively; [Figure 2]a and [Figure 2]b. One local recurrence was found in 2 of the 69 patients with sublobar resection (3%) and in 14 of the 164 patients who underwent anatomic resection (8.5%). In the sublobar resection group, 28 patients underwent VATS-aided segmentectomy without any local recurrence [Figure 3]. The 5-year OS and DFS of segmentectomy patients had trends of better oncologic outcomes in the short-term follow-up.
Table 3: Characteristics of patients with or without tumor recurrence after resection for clinical T1a nonsmall cell lung cancer

Click here to view
Table 4: Characteristics of patients with or without recurrence after surgical resection for clinical T1a nonsmall cell lung cancer

Click here to view
Figure 2: (a) Overall survival curves of patients with T1a lesions following anatomic or sublobar resection. (b) Disease-free patients with T1a lesions survival curves following anatomic or sublobar resection

Click here to view
Figure 3: (a) Overall survival curves of patients with T1a lesions according to the surgical procedure used. (b) Disease-free patient survival curves of patients with T1a lesions according to the surgical procedure used

Click here to view



  Discussion Top


Lung cancer remains the leading cause of cancer-related death. Despite advances in molecular markers and new drugs, long-term survival is unsatisfactory. Anatomic lobectomy is the gold standard in surgical treatment of patients with a resectable NSCLC. Mortality following surgical resection is most often associated with tumor relapse.[8],[9] In our previous study, tumor differentiation and LVSI were independent factors for postoperative relapse after surgical resection for patients with clinical Stage I NSCLC; 17 of 261 patients (6.5%) developed a local recurrence. Anatomic or sublobar resection did not affect the recurrence rate.[10]

The oncologic outcome of sublobar resection remains a controversial issue. This approach including wedge resection and segmentectomy had a trend for equal OS and DFS.[11] That study focused on T1a lesions (tumor size <2 cm). However, sublobar resection has been found to be an independent predictor of locoregional recurrence.[12] Bando et al.[13] reported that a higher recurrence rate was associated with sublobar resection in patients with tumors >2 cm (locoregional recurrence rate of 1.9% for tumors <2 cm compared with 33% in patients with tumors >2 cm). Regarding anatomic or sublobar resection approaches, the tumor size is important for postoperative outcome. In our study, the 5-year OS and DFS were no different between the two groups [Figure 1]a and [Figure 1]b. Although this was the retrospective study, some patients underwent sublobar resections because of comorbidity and old age in early period of this study. The recurrence rate was 13% in the whole cohort of sublobar resection. The recurrence rate was still lower than in a previous report.[13] After stratifying for a tumor size <2 cm, there were still no differences between the groups in terms of the 5-year OS and DFS [Figure 2]a and [Figure 2]b. The surgical outcome was better for patients with T1a lesions; the postoperative recurrence rate was 3% in the sublobar resection group versus 8.5% for patients who underwent anatomic resection.

Cerfolio et al. reported that a high SUVmax was correlated with tumor stage and with recurrence and survival rates.[14] A SUVmax of ≥10 was an independent predictor of DFS and OS. In published study, a SUVmax of ≥4.5 was found to be an independent predictor of recurrence after resection, with an odds ratio of 5.45 in 310 patients with Stages I and II disease.[15] The metabolic activity of tumors has been shown to contribute significant information in terms of prognosis. However, the cutoff values of SUVmax measurements vary widely, making their clinical application difficult. In the present study, there was no significant difference of SUVmax between the two groups after we stratified the tumor size to <2 cm. A SUVmax cutoff of 3.3 based on our previous study [16] did not show statistical significance in predicting postoperative recurrence. The SUVmax as a parameter used in determining the decision to apply anatomic or sublobar resection has not been evaluated rigorously and here we showed that it was not a prognostic factor for T1a lesions.

In this study, the characteristics of tumors in the anatomic resection group were poorer differentiation of tumors, central location, larger tumor size, and higher SUVmax of compared with the sublobar resection group. The study was designed as retrospective study. It was the possible reason why the surgeon preferred the sublobar resection for peripheral lesions. It was easier to get tumor-free margin for peripheral lesions. In anatomic group, the grade of tumor differentiation was high than sublobar resection (both clinical Stage 1 and T1a tumor). We thought that the imaging characteristics of tumors were selective bias when the surgeon performed operation. For solid tumor, the surgeon tended to do anatomic operation. Further prospective study was necessary to clarify this issue.

Accurate staging can help predict the prognosis for patients with NSCLC. The number of lymph nodes dissected is a key factor because it can help improve both DFS and OS.[17],[18] However, the extent of lymph node dissection needed remains controversial.[19] The current staging system for NSCLC is based on the 7th edition of the International Association for the Study of Lung Cancer classification.[20] This focuses on the locations of the involved lymph nodes but not on their number. The role of lymphadenectomy or sampling for early-stage NSCLC is still under debate. In a previous meta-analysis, sublobar resection produced a lower likelihood of having more than three lymph nodes and a significantly lower rate of nodal upstaging.[6] That analysis focused on Stage 1A disease and came to no conclusions on the role of lymph node examination for prognosis. In the present study, there were fewer dissected lymph nodes in the sublobar resection group than in the anatomic resection group. One possible reason was the intraoperative examination of frozen sections of lymph nodes. Attempts at sublobar resection would have been converted to anatomic resection if this proved the presence of lymph node metastasis. The prognosis for the sublobar resection group of patients was no worse than that for the anatomic resection group even though they had fewer dissected lymph nodes. We consider that intraoperative lymph node evaluation is important for the sublobar resection procedure, and the absence of lymph node metastases can reassure the surgeon to proceed in performing anatomic resection. Lymph node sampling did not compromise the prognosis in this situation.

The limitations of this study were in its small sample size and that it was a single-institution retrospective study. More data are needed with a larger number of patients and a longer follow-up. In addition, we did not address the imaging characteristics of the tumor (e.g., “ground-glass” opacity), the classification of adenocarcinomas (preinvasive, minimally invasive, or invasive) in the two groups. Further studies combined with histopathological characteristics of the tumors might provide more convincing results.


  Conclusions Top


The oncologic outcomes of sublobar resection were fair to those of anatomic resection in these patients with clinical T1a NSCLC. Lymph node sampling might not compromise surgical outcomes in such patients. Further large-scale studies are necessary to clarify the difference in clinical outcome between segmentectomy or wedge resection.

Acknowledgments

This research was supported by the Cancer Registry Group, Tri-Service General Hospital. We thank Miss Chia-Ling Yu, who made a significant contribution to analyzing the patient survival data.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
  References Top

1.
Howington JA, Blum MG, Chang AC, Balekian AA, Murthy SC. Treatment of stage I and II non-small cell lung cancer: Diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013;143 5 Suppl:e278S-313S.  Back to cited text no. 1
    
2.
Ginsberg RJ, Rubinstein LV. Randomized trial of lobectomy versus limited resection for T1 N0 non-small cell lung cancer. Lung Cancer Study Group. Ann Thorac Surg 1995;60:615-22.  Back to cited text no. 2
    
3.
Aberle DR, DeMello S, Berg CD, Black WC, Brewer B, Church TR, et al. Results of the two incidence screenings in the National Lung Screening Trial. N Engl J Med 2013;369:920-31.  Back to cited text no. 3
    
4.
Tsutani Y, Miyata Y, Nakayama H, Okumura S, Adachi S, Yoshimura M, 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;146:358-64.  Back to cited text no. 4
    
5.
Kodama K, Higashiyama M, Okami J, Tokunaga T, Imamura F, Nakayama T, et al. Oncologic outcomes of segmentectomy versus lobectomy for clinical T1a N0 M0 non-small cell lung cancer. Ann Thorac Surg 2016;101:504-11.  Back to cited text no. 5
    
6.
Khullar OV, Liu Y, Gillespie T, Higgins KA, Ramalingam S, Lipscomb J, et al. Survival after sublobar resection versus lobectomy for clinical stage IA lung cancer: An analysis from the national cancer data base. J Thorac Oncol 2015;10:1625-33.  Back to cited text no. 6
    
7.
Ghaly G, Kamel M, Nasar A, Paul S, Lee PC, Port JL, et al. Video-assisted thoracoscopic surgery is a safe and effective alternative to thoracotomy for anatomical segmentectomy in patients with clinical stage I non-small cell lung cancer. Ann Thorac Surg 2016;101:465-72.  Back to cited text no. 7
    
8.
Spira A, Ettinger DS. Multidisciplinary management of lung cancer. N Engl J Med 2004;350:379-92.  Back to cited text no. 8
    
9.
Scott WJ, Howington J, Feigenberg S, Movsas B, Pisters K; American College of Chest Physicians. Treatment of non-small cell lung cancer stage I and stage II: ACCP evidence-based clinical practice guidelines (2nd edition). Chest 2007;132 3 Suppl: 234S-42S.  Back to cited text no. 9
    
10.
Chen YY, Huang TW, Tsai WC, Lin LF, Cheng JB, Chang H, et al. Risk factors of postoperative recurrences in patients with clinical stage I NSCLC. World J Surg Oncol 2014;12:10.  Back to cited text no. 10
    
11.
Yendamuri S, Sharma R, Demmy M, Groman A, Hennon M, Dexter E, et al. Temporal trends in outcomes following sublobar and lobar resections for small (≤2 cm) non-small cell lung cancers – A surveillance epidemiology end results database analysis. J Surg Res 2013;183:27-32.  Back to cited text no. 11
    
12.
Varlotto JM, Recht A, Flickinger JC, Medford-Davis LN, Dyer AM, Decamp MM. Factors associated with local and distant recurrence and survival in patients with resected nonsmall cell lung cancer. Cancer 2009;115:1059-69.  Back to cited text no. 12
    
13.
Bando T, Yamagihara K, Ohtake Y, Miyahara R, Tanaka F, Hasegawa S, et al. A new method of segmental resection for primary lung cancer: Intermediate results. Eur J Cardiothorac Surg 2002;21:894-9.  Back to cited text no. 13
    
14.
Cerfolio RJ, Bryant AS, Ohja B, Bartolucci AA. The maximum standardized uptake values on positron emission tomography of a non-small cell lung cancer predict stage, recurrence, and survival. J Thorac Cardiovasc Surg 2005;130:151-9.  Back to cited text no. 14
    
15.
Koo HK, Jin SM, Lee CH, Lim HJ, Yim JJ, Kim YT, et al. Factors associated with recurrence in patients with curatively resected stage I-II lung cancer. Lung Cancer 2011;73:222-9.  Back to cited text no. 15
    
16.
Huang TW, Hsieh CM, Chang H, Cheng YL, Tzao C, Huang WS, et al. Standard uptake value of positron emission tomography in clinical stage I lung cancer: Clinical application and pathological correlation. Eur J Cardiothorac Surg 2012;41:869-73.  Back to cited text no. 16
    
17.
Doddoli C, Aragon A, Barlesi F, Chetaille B, Robitail S, Giudicelli R, et al. Does the extent of lymph node dissection influence outcome in patients with stage I non-small-cell lung cancer? Eur J Cardiothorac Surg 2005;27:680-5.  Back to cited text no. 17
    
18.
Gajra A, Newman N, Gamble GP, Kohman LJ, Graziano SL. Effect of number of lymph nodes sampled on outcome in patients with stage I non-small-cell lung cancer. J Clin Oncol 2003;21:1029-34.  Back to cited text no. 18
    
19.
Nwogu CE, Groman A, Fahey D, Yendamuri S, Dexter E, Demmy TL, et al. Number of lymph nodes and metastatic lymph node ratio are associated with survival in lung cancer. Ann Thorac Surg 2012;93:1614-9.  Back to cited text no. 19
    
20.
Goldstraw P, Crowley J, Chansky K, Giroux DJ, Groome PA, Rami-Porta R, et al. The IASLC Lung Cancer Staging Project: Proposals for the revision of the TNM stage groupings in the forthcoming (seventh) edition of the TNM Classification of malignant tumours. J Thorac Oncol 2007;2:706-14.  Back to cited text no. 20
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Patients and Methods
Results
Discussion
Conclusions
References
Article Figures
Article Tables

 Article Access Statistics
    Viewed1079    
    Printed18    
    Emailed0    
    PDF Downloaded84    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]