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Open Access 05.07.2020 | Original Article

Current status of surgery for clinical stage IA lung cancer in Japan: analysis of the national clinical database

verfasst von: Norihiko Ikeda, Shunsuke Endo, Eriko Fukuchi, Jun Nakajima, Kohei Yokoi, Masayuki Chida, Hiroshi Date, Akinori Iwasaki, Hiroyasu Yokomise, Masami Sato, Meinoshin Okumura, Hiroyuki Yamamoto, Hiroaki Miyata, Takashi Kondo

Erschienen in: Surgery Today | Ausgabe 12/2020

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Abstract

Purpose

As the number of cases of early lung cancer in Japan grows, an analysis of the present status of surgical treatments for clinical stage IA lung cancer using a nationwide database with web-based data entry is warranted.

Methods

The operative and perioperative data from 47,921 patients who underwent surgery for clinical stage IA lung cancer in 2014 and 2015 were obtained from the National Clinical Database (NCD) of Japan. Clinicopathological characteristics, surgical procedure, mortality, and morbidity were analyzed, and thoracotomy and video-assisted thoracic surgery (VATS) were compared.

Results

The patients comprised 27,208 men (56.8%) and 20,713 women (43.2%); mean age, 69.3 years. Lobectomy was performed in 64.8%, segmentectomy in 15.2%, and wedge resection in 19.8%. The surgical procedures were thoracotomy in 12,194 patients (25.4%) and a minimally invasive approach (MIA) in 35,727 patients (74.6%). MIA was divided into VATS + mini-thoracotomy (n = 13,422, 28.0%) and complete VATS (n = 22,305, 46.5%). The overall postoperative mortality rate was 0.4%, being significantly lower in the MIA group than in the thoracotomy group (0.3% vs 0.8%, P < 0.001).

Conclusions

Our analysis of data from the NCD indicates that MIA has become the new standard treatment for clinical stage IA lung cancer.
Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1007/​s00595-020-02063-x) contains supplementary material, which is available to authorized users.

Publisher's Note

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

Introduction

Lung cancer is the leading cause of cancer-related deaths across the world. The 5-year survival rate of stage IA lung cancer patients is 86.8% [1]; therefore, curative treatment in the early stage is indicative of a favorable prognosis. Video-assisted thoracic surgery (VATS) is used widely for the treatment of stage IA lung cancer. In Japan, 28,568 lung cancer operations were performed using VATS in 2016, accounting for 67.8% of the total operations (n = 42,107) [2]. Thus, an assessment of the surgical treatments for stage I lung cancer will be very useful for clarifying the present status of chest surgery and VATS.
The National Clinical Database (NCD) of Japan is a nationwide web-based surgical patient registration system that enables the collection of data on surgical procedures and perioperative factors as part of the surgical specialization by the Japanese Surgical Board Certification System [3, 4]. In 2014, the data on 1.6 million surgical procedures from more than 4000 hospitals were collected [3]. A committee authorized by the NCD evaluates and compares the reliability of samples and the web-based data from the NCD. The results indicate a high percentage of data correctness (> 94%) even in the initial year of data collection [5]. To ensure the accuracy and traceability of data, the NCD continuously tracks authorized persons responsible for data entry through the web-based data management system in combination with random site visits.
The NCD for chest surgery requires the input of detailed data on patient characteristics, operative information, and postoperative events (Supplemental Table 1) [5]. The NCD was used to analyze cases of stage IA lung cancer (UICC-TNM version 7) to obtain a representative picture of the surgical treatments for early stage lung cancer in Japan, as well as to compare thoracotomy and minimally invasive approach (MIA) surgery with extensive use of VATS.

Methods

The study population was derived from the NCD data on patients who underwent surgery for primary lung cancer between January 1, 2014 and December 31, 2015, at 887 surgical units. Records with incomplete data or unspecified patient status within 30 days after surgery were excluded. A total of 78,594 patients who underwent lung cancer resection, with complete data, were registered. Patients with clinical stage IB-IV (N = 30,590) and those who underwent robotic surgery (N = 83) were excluded. Finally, 47,921 patients with surgically treated clinical stage IA lung cancer were selected for analysis.
The NCD registry required the selection of either thoracotomy or VATS as the surgical approach for each lung cancer operation. Herein, we reclassified the surgical approach used in registered cases into thoracotomy or MIA. MIA was divided into complete VATS and VATS with mini-thoracotomy of 8 cm or less (VATS + mini-thoracotomy) [6] according to the definition of Swanson et al. [7]. The presence or absence of rib-spreading is not yet specified in the NCD registry.
Accordingly, the comorbidities should be entered in accordance with the established criteria [5]. The surgical characteristics were analyzed in terms of procedure, type of nodal dissection, blood loss, number of staples applied, maximum wound length, conversion to thoracotomy, and number of access ports [5]. Postoperative major morbidity was defined in accordance with the Society of Thoracic Surgeons risk model [6, 8, 9].

Statistical analysis

The Chi-square test and Fisher’s exact test were used to compare categorical data and their distributions, as appropriate. All P values were two-sided, and P < 0.05 was considered to indicate a statistically significant difference. For continuous data, Student’s t test was performed for the comparison of two groups, and one-way ANOVA followed by Bonferroni analysis was performed for the comparison of three groups. For non-normally distributed continuous data, we used the Wilcoxon rank-sum test and the Kruskal–Wallis test, as appropriate. Statistical analysis was performed using the SPSS statistical software package (Version 24.0; SPSS Inc., Chicago, IL) and STATA 16 software (Stata, College Station, Texas). This study was approved by the Ethics Committee of Tokyo Medical University (T2018-0018).

Results

Table 1 summarizes the clinical characteristics of the registered patients. There were 27,208 men (56.8%) and 20,713 women (43.2%); mean age, 69.3 years. The disease was classified as clinical T1a (62%) or T1b (38%). The surgical approach was thoracotomy in 12,194 patients (25.4%) and MIA in 35,727 patients (74.6%). MIA was divided into VATS + mini-thoracotomy (n = 13,422, 28.0%) and complete VATS (n = 22,305, 46.5%).
Table 1
Clinical characteristics of the patients
 
Total
Thoracotomy
MIA
P value (Thoracotomy vs MIA)
MIA
VATS  + mini-thoracotomy
Complete VATS
No. of patients
47,921
12,194 (25.4%)
35,727 (74.6%)
 
13,422 (28.0%)
22,305 (46.5%)
Age (years) Mean ± SD
69.3 ± 9.3
69.6 ± 8.8
69.2 ± 9.5
 < 0.001
69.4 ± 9.5
69.0 ± 9.6
Sex
(Male/Female)
27,208 (56.8%)/20,713(43.2%)
7614 (62.4%)/4580 (37.6%)
19,594 (54.8%)/16,133 (45.2%)
 < 0.001
7378 (55.0%)/6044 (45.0%)
12,216 (54.8%)/10,089 (45.2%)
clinical T status
 < 0.001
  
 cT1a
29,670 (61.9%)
6847 (56.2%)
22,823 (63.9%)
 
8442 (62.9%)
14,381 (64.5%)
 cT1b
18,250 (38.1%)
5347 (43.8%)
12,903 (36.1%)
 
4980 (37.1%)
7923 (35.5%)
 cTis
1 (0.0%)
0 (0.0%)
1 (0.0%)
   
Tumor diameter (cm) Mean ± SD
1.85 ± 0.61
1.94 ± 0.60
1.82 ± 0.61
 < 0.001
1.84 ± 0.60
1.81 ± 0.61
Comorbidities
 Diabetes mellitusa
6566 (13.7%)
1707 (14.0%)
4859 (13.6%)
0.272
1782 (13.3%)
3077 (13.8%)
 Ischemic heart diseaseb
2569 (5.4%)
657 (5.4%)
1912 (5.4%)
0.872
670 (5.0%)
1242 (5.6%)
 Arrhythmiac
1719 (3.6%)
450 (3.7%)
1269 (3.6%)
0.482
426 (3.2%)
843 (3.8%)
 Interstitial pneumoniad
1757 (3.7%)
524 (4.3%)
1233 (3.5%)
 < 0.001
449 (3.3%)
784 (3.5%)
 Cerebral nervous disordere
2714 (5.7%)
675 (5.5%)
2039 (5.7%)
0.496
755 (5.6%)
1284 (5.8%)
 Liver dysfunctionf
221 (0.46%)
50 (0.41%)
171 (0.48%)
0.353
71 (0.53%)
100 (0.45%)
MIA minimally invasive approach
aRequired treatment or supplementary explanation
bRequired treatment or had previous treatment
cRequired treatment
dInterstitial pneumonia shadow on chest computed tomography
eRequired treatment or had previous treatment
fChild-Turcotte classification B or C
The tumor diameter (mean ± standard deviation) was 1.85 ± 0.61 cm overall, 1.94 ± 0.60 cm in the thoracotomy group, and 1.82 ± 0.61 cm in the MIA group (P < 0.001). The comorbidities included diabetes mellitus (13.7%), cerebral nervous system disorders (5.7%), ischemic heart disease (5.4%), and interstitial pneumonitis (3.7%). The rates of preoperative comorbidities, apart from interstitial pneumonitis, were not significantly different between the thoracotomy group and the MIA group.
Table 2 shows the results of pathological examination. Adenocarcinoma was the most frequent histologic type (76.3%), followed by squamous cell carcinoma (13.8%). Pathological IA cancer was observed more frequently in the MIA group (79.2%) than in the thoracotomy group (73.1%); however, pathological II and IIIA disease (up-staging) was more frequent in the thoracotomy group. Among the 393 patients with stage IV disease, 359 were diagnosed as having M1a with pleural dissemination and/or pulmonary metastasis which could not be detected preoperatively.
Table 2
Pathological characteristics of the patients
 
Total
Thoracotomy
MIA
P value (Thoracotomy vs MIA)
MIA
VATS  + mini-thoracotomy
Complete VATS
Histology
 < 0.001
 
 Adenocarcinoma
36,570 (76.3%)
8848 (72.6%)
27,722 (77.6%)
 
10,370 (77.3%)
17,352 (77.8%)
 Squamous cell carcinoma
6603 (13.8%)
1974 (16.2%)
4629 (13.0%)
 
1778 (13.2%)
2851 (12.8%)
 Large cell carcinoma
743 (1.6%)
232 (1.9%)
511 (1.4%)
 
179 (1.3%)
332 (1.5%)
 Small cell carcinoma
785 (1.6%)
244 (2.0%)
541 (1.5%)
 
219 (1.6%)
322 (1.4%)
 Adenosquamous carcinoma
500 (1.0%)
148 (1.2%)
352 (1.0%)
 
134 (1.0%)
218 (1.0%)
 Others
2720 (5.7%)
748 (6.1%)
1972 (5.5%)
 
742 (5.5%)
1230 (5.5%)
Pathological stage
 < 0.001
 
 0
519 (1.1%)
77 (0.6%)
442 (1.2%)
 
164 (1.2%)
278 (1.2%)
 IA
37,195 (77.6%)
8909 (73.1%)
28,286 (79.2%)
 
10,561 (78.7%)
17,725 (79.5%)
 IB
5639 (11.8%)
1638 (13.4%)
4001 (11.2%)
 
1537 (11.5%)
2464 (11.0%)
 IIA
1728 (3.6%)
624 (5.1%)
1104 (3.1%)
 
405 (3.0%)
699 (3.1%)
 IIB
589 (1.2%)
206 (1.7%)
383 (1.1%)
 
169 (1.3%)
214 (1.0%)
 IIIA
1714 (3.6%)
608 (5.0%)
1106 (3.1%)
 
435 (3.2%)
671 (3.0%)
 IIIB
20 (0.04%)
7 (0.06%)
13 (0.04%)
 
5 (0.04%)
8 (0.04%)
 IV
393 (0.8%)
99 (0.8%)
294 (0.8%)
 
116 (0.9%)
178 (0.8%)
 Other
124 (0.3%)
26 (0.2%)
98 (0.3%)
 
30 (0.2%)
68 (0.3%)
MIA minimally invasive approach
Table 3 summarizes the surgical procedures. Lobectomy was performed in 64.8% of patients, segmentectomy in 15.2%, and wedge resection in 19.8%. Lobectomy was performed more frequently in the thoracotomy group (71.3%) than in the MIA group (62.6%) (P < 0.001). Sleeve lobectomy was performed in 25 patients and primary lesions were considered central type tumors (19 and 4 for pathological stages I and II; 12 and 6 for squamous cell carcinoma and carcinoid, respectively). Pneumonectomy was performed in 49 patients, including 10 (20.4%) with pathological stages III and IV disease and 4 (8.2%) with injury of the pulmonary artery (data not shown). The operation time (mean ± standard deviation) for all patients was 184 ± 83 min. It was significantly shorter in the MIA group (177 ± 81 min) than in the thoracotomy group (206 ± 84 min) (P < 0.001). The intraoperative blood loss (median) was 30 ml, being 55 ml in the thoracotomy group and 20 ml in the MIA group (P < 0.001). The number of staples used was 5.3 ± 2.3 overall, being 5.3 ± 2.3 in both the thoracotomy and MIA groups. MIA was converted to thoracotomy in 350 of 35,727 patients (1.0%), from VATS + mini-thoracotomy in 287 (2.1%) and from complete VATS in 63 (0.3%). The median postoperative hospital stay was 9 days in the thoracotomy group and 8 days in the MIA group (P < 0.001). Details about postoperative pain medication and the length of ICU stay were not registered in the NCD.
Table 3
Surgical characteristics
 
Total
Thoracotomy
MIA
P value (Thora cotomy vs MIA)
MIA
VATS + mini thoracotomy
Complete VATS
Surgical procedure
 < 0.001
 
 Wedge resection
9502 (19.8%)
1309 (10.7%)
8193 (23.0%)
 
2885 (21.5%)
5308 (23.8%)
 Segmentectomy
7287 (15.2%)
2121 (17.4%)
5166 (14.5%)
 
2142 (16.0%)
3024 (13.6%)
 Lobectomy
31,058 (64.8%)
8699 (71.3%)
22,359 (62.6%)
 
8389 (62.5%)
13,970 (62.6%)
 Sleeve resection
25 (0.05%)
20 (0.16%)
5 (0.01%)
 
4 (0.03%)
1 (0.004%)
 Pneumonectomy
49 (0.1%)
45 (0.37%)
4 (0.01%)
 
2 (0.01%)
2 (0.009%)
 Postoperative hospital stay (day) median, IQR
8 (6–12)
9 (7–13)
8 (6–11)
 < 0.001
9 (7–12)
8 (6–11)
 Ope time (min) mean ± SD
184 ± 83
206 ± 84
177 ± 81
 < 0.001
174 ± 77
179 ± 83
 Blood loss (ml) median, IQR
30 (10–99)
55 (20–143)
20 (10–75)
 < 0.001
27 (10–75)
20 (10–75)
 No. of staples mean ± SD
5.3 ± 2.3
5.3 ± 2.3
5.3 ± 2.3
0.316
5.2 ± 2.2
5.4 ± 2.3
 Maximum length of wound (cm) mean ± SD
NA
12.8 ± 4.3
4.6 ± 2.0
 < 0.001
6.2 ± 1.8
3.5 ± 1.2
 Conversion to thoracotomy
NA
NA
350 (1.0%)
 
287 (2.1%)
63 (0.3%)
 No. of ports
NA
NA
3.0 ± 0.84
 
2.4 ± 0.79
3.3 ± 0.70
MIA minimally invasive approach, IQR interquartile range, Ope time operation time
* vs **: P < 0.001
Table 4 lists the intraoperative injuries and postoperative complications. Pulmonary artery injury occurred in 409 patients (0.85%): in 1.9% of those undergoing thoracotomy and 0.48% of those undergoing MIA (P < 0.001). The most frequent postoperative complications were prolonged air leakage (3.6%), pneumonia (1.4%), and arrhythmia (1.3%). Postoperative acute exacerbation of interstitial pneumonia occurred in 180 patients (0.38%), after thoracotomy in 0.57%, and after MIA in 0.31%. Major morbidity was observed in 1978 patients (4.1%): 741 (6.1%) from the thoracotomy group and 1237 (3.5%) from the MIA group (P < 0.001). Operative mortality was 0.4%, being significantly higher in the thoracotomy group (0.8%) than in the MIA group (0.3%) (P < 0.001).
Table 4
Major complications and mortality
 
Total
Thoracotomy
MIA
p value (Thoracotomy
vs MIA)
MIA
VATS + mini-thoracotomy
Complete VATS
Intraoperative injury
      
 Aorta
6 (0.01%)
4 (0.03%)
2 (0.006%)
0.040
0 (0%)
2 (0.009%)
 Pulmonary artery
409 (0.85%)
236 (1.9%)
173 (0.48%)
 < 0.001
74 (0.55%)
99 (0.44%)
 Pulmonary vein
75 (0.16%)
41 (0.34%)
34 (0.10%)
 < 0.001
12 (0.09%)
22 (0.10%)
 Superior vena cava
10 (0.02%)
5 (0.04%)
5 (0.01%)
0.136
0 (0%)
5 (0.02%)
Postoperative complications
      
 Respiratory failurea
154 (0.3%)
72 (0.6%)
82 (0.2%)
 < 0.001
41 (0.31%)
41 (0.18%)
 Pneumonia
671 (1.4%)
292 (2.4%)
379 (1.1%)
 < 0.001
124 (0.92%)
273 (1.2%)
 Acute exacerbation of interstitial pneumonia
180 (0.38%)
70 (0.57%)
110 (0.31%)
 < 0.001
47 (0.35%)
63 (0.28%)
 Prolonged air leakageb
1720 (3.6%)
523 (4.3%)
1197 (3.4%)
 < 0.001
422 (3.1%)
775 (3.5%)
 Pyothorax
258 (0.5%)
92 (0.8%)
166 (0.5%)
 < 0.001
71 (0.52%)
95 (0.43%)
 Broncho pleural fistula
74 (0.15%)
26 (0.2%)
48 (0.1%)
0.058
12 (0.09%)
36 (0.2%)
 Pulmonary embolus
30 (0.06%)
12 (0.1%)
18 (0.05%)
0.090
3 (0.02%)
15 (0.07%)
 Cardiac failurec
63 (0.13%)
31 (0.25%)
32 (0.09%)
 < 0.001
18 (0.13%)
14 (0.06%)
 Arrhythmiad
619 (1.3%)
222 (1.8%)
397 (1.1%)
 < 0.001
124 (0.9%)
273 (1.2%)
 Myocardial infarction
17 (0.04%)
8 (0.07%)
9 (0.03%)
0.051
3 (0.02%)
6 (0.03%)
 Cerebral infarction, hemorrhage
148 (0.31%)
48 (0.39%)
100 (0.28%)
0.056
38 (0.28%)
62 (0.28%)
 Chylothorax
268 (0.56%)
69 (0.57%)
199 (0.56%)
0.893
71 (0.51%)
128 (0.57%)
 Re-operatione
73 (0.15%)
23 (0.19%)
50 (0.14%)
0.228
25 (0.19%)
25 (0.11%)
Mortality
      
 Major morbidity
1978 (4.1%)
741 (6.1%)
1237 (3.5%)
 < 0.001
459 (3.4%)
778 (3.5%)
 Operative death (in hospital or within 30 days postop)
206 (0.4%)
94 (0.8%)
112 (0.3%)
 < 0.001
49 (0.37%)
63 (0.28%)
 Operative death or major morbidity
2048 (4.3%)
773 (6.3%)
1275 (3.6%)
 < 0.001
479 (3.6%)
796 (3.6%)
MIA: Minimally invasive approach
aRequired ventilation support > 48 h
bAir leakage > 6 days or required treatment
cRequired treatment
dRequired treatment (Detailed definitions are found in Ref. 5)
eRedo surgery within 24 h after the initial surgery
Table 5 analyzes the patients who underwent lobectomy. Of the total 31,058 patients who underwent lobectomy, 8699 (28.0%) underwent thoracotomy, 8389 (27.0%) underwent VATS + mini-thoracotomy, and 13,970 (45.0%) underwent complete VATS. The mean operation time for thoracotomy (214 ± 82 min) was significantly longer than that for VATS + mini-thoracotomy (195 ± 71 min) and that for complete VATS (208 ± 70 min) (both P < 0.001). The rate of conversion to thoracotomy was significantly lower in complete VATS (0.31%) than in VATS + mini-thoracotomy (2.3%) (P < 0.001). The number of staples used during the operation was 5.6 ± 2.0 in VATS + mini-thoracotomy and 5.9 ± 2.2 in complete VATS, the latter number being significantly greater than that in thoracotomy (5.5 ± 2.2, P < 0.001).
Table 5
Surgical characteristics of lobectomy cases
 
Thoracotomy
n = 8699, 28%
VATS
 + mini-thoracotomy
n = 8389, 27%
Complete VATS
n = 13,970, 45%
P value (ANOVA or Kruskal–Wallis test)
P value* (Thoracotomy vs VATS + mini-thoracotomy)
P value* (Thoracotomy vs complete VATS)
Tumor diameter (cm)
mean ± SD
2.02 ± 0.57
1.98 ± 0.57
1.97 ± 0.57
 < 0.001
p < 0.001
p < 0.001
Ope time (min) mean ± SD
214 ± 82
195 ± 71
208 ± 70
 < 0.001
p < 0.001
p < 0.001
Postoperative Hospital stay
(day) median, IQR
9 (7–13)
9 (7–12)
8 (6–11)
 < 0.001
 < 0.001
 < 0.001
Blood loss (ml) median, IQR
67 (25–156)
45 (10–100)
50 (10–100)
 < 0.001
 < 0.004
p < 0.001
No. of staplers
5.5 ± 2.2
5.6 ± 2.0
5.9 ± 2.2
 < 0.001
0.057
p < 0.001
Conversion to thoracotomy
NA
192 (2.3%)
44 (0.31%)
 < 0.001**
  
IQR Interquartile range, Ope time operation time
*Post hoc test by multiple comparison with Bonferroni correction
**Fisher’s exact test
Table 6 lists the post-lobectomy complications. The incidence of respiratory failure was lower in the complete VATS group (0.2%) than in the thoracotomy (0.6%) or the VATS + mini-thoracotomy (0.3%) groups. Prolonged air leakage and arrhythmia occurred significantly less in the VATS + mini-thoracotomy group (3.3%, 1.2%) than in the thoracotomy group (4.4%, 2.0%) or the complete VATS group (4.3%, 1.6%). The operative mortality rates in the complete VATS group (0.3%) and the VATS + mini-thoracotomy group (0.4%) were significantly lower than that in the thoracotomy group (0.8%) (P < 0.001, P < 0.002).
Table 6
Major complications of lobectomy
 
Thoracotomy
VATS  + mini-thoracotomy
Complete VATS
p value
Thoracotomy vs VATS  + mini-thoracotomy
Thoracotomy vs complete VATS
VATS  + mini-thoracotomy vs complete VATS
Respiratory failure
51 (0.6%)
29 (0.3%)
28 (0.2%)
0.025
 < 0.001
0.039
Pneumonia
214 (2.5%)
101 (1.2%)
155 (1.1%)
 < 0.001
 < 0.001
0.518
Acute exacerbation of interstitial pneumonia
53 (0.6%)
30 (0.4%)
48 (0.3%)
0.018
0.003
0.863
Prolonged air leakage
379 (4.4%)
277 (3.3%)
597 (4.3%)
 < 0.001
0.763
 < 0.001
Pyothorax
62 (0.7%)
52 (0.6%)
78 (0.6%)
0.511
0.162
0.588
Broncho pleural fistula
20 (0.2%)
12 (0.1%)
31 (0.2%)
0.218
0.891
0.212
Pulmonary embolus
11 (0.1%)
1 (0.0%)
14 (0.1%)
0.006
0.546
0.014
Cardiac failure
19 (0.2%)
13 (0.2%)
5 (0.0%)
0.379
 < 0.001
0.005
Arrhythmia
174 (2.0%)
101 (1.2%)
218 (1.6%)
 < 0.001
0.015
0.032
Myocardial infarction
4 (0.0%)
1 (0.0%)
4 (0.0%)
0.375
0.493
0.657
Cerebral infarction, hemorrhage
42 (0.5%)
26 (0.3%)
49 (0.4%)
0.089
0.13
0.632
Chylothorax
65 (0.7%)
69 (0.8%)
121 (0.9%)
0.603
0.364
0.762
Re-operation
14 (0.2%)
16 (0.2%)
22 (0.2%)
0.716
1
0.62
Operative death
68 (0.8%)
34 (0.4%)
48 (0.3%)
0.002
 < 0.001
0.495

Discussion

The number of early lung cancers being diagnosed is increasing with the widespread use of chest computed tomography (CT). Therefore, an analysis of the current status of surgical treatments for stage IA lung cancer based on the NCD data will be highly beneficial. Our analysis of 47,921 clinical stage IA lung cancer patients shows the current status of surgical treatments for early stage lung cancer in Japan. This is because the number of lung cancer operations recorded in the NCD accounts for more than 94% of all cases registered in the Regional Bureau of Health and Welfare in Japan [4, 5]. MIA was the procedure selected for 74.6% of patients, which shows that complete VATS or at least MIA with the use of VATS has become the standard treatment for clinical stage IA lung cancer cases in Japan.
The overall rate of intraoperative injury of the pulmonary artery was 0.85%, occurring in 1.9% of patients who underwent thoracotomy and 0.48% of those who underwent MIA, suggesting the safety of VATS. However, the specific causes of the higher rate of vessel injury in thoracotomy are unclear. We suspect that vessel injuries during MIA and conversion to thoracotomy registered as thoracotomy are underreported.
The definition of “re-operation” in the case report form in the NCD is “redo surgery within 24 h after the initial surgery”. This may account for the smaller number of recorded cases of re-operation than the actual number of cases. An inherent limitation to the current NCD is the lack of a slot for the actual number of cases. Thus, the actual number of redo-operations could not be analyzed.
Although the reasons for MIA conversions to thoracotomy were not stated in the NCD registry, vessel injury, severe adhesion, and incomplete interlobular fissure were suspected. The rates of conversion from VATS + mini-thoracotomy and complete VATS were 2.1% and 0.3%, respectively. There may be a slight difference in the policy of selecting the surgical approach depending on the institution and the surgeon; however, the reasons for the difference in the conversion rates could not be clarified in the current study. In the future, we would like to compare the changes in surgical outcomes over time according to regions, to identify areas for improvement.
The mean operation time was shorter and the mean blood loss was less in the MIA group than in the thoracotomy group. Scott et al. published similar results indicating that the median operation time was significantly shorter in a VATS group than in a thoracotomy group (117.5 min vs. 171.5 min, P < 0.001) in their propensity-matched analysis [10]. A systematic review revealed two types of reports, one showing that VATS lobectomy prolonged the operation time and another showing that the operating time did not significantly differ between the approaches [11]. The mean number of staples used was five for both thoracotomy and MIA. As the NCD does not have entry slots for a rapid pathological diagnostic procedure, the number of staples used for wedge resections for this purpose cannot be identified separately.
The postoperative mortality and morbidity rates were lower in the MIA group than in the thoracotomy group, in accordance with the previous reports [12, 13]; however, the underlying reason remains to be clarified. Gopaldas et al. reported similar postoperative morbidity rates after thoracotomy (n = 12,860) and VATS lobectomy (n = 759) [14]. On the other hand, Scott et al. reported significantly fewer patients with complication in the VATS group than in the thoracotomy group (27.3% vs 47.8%, P < 0.005) [10]. Propensity-matched analysis should be performed to clarify the lower morbidity after VATS more accurately [15].
Recently, Japanese surgeons have been able to perform curative operations for early lung cancer using MIA, especially with the development of advanced instruments and imaging techniques. However, some conservative surgeons still consider thoracotomy better for avoiding vessel injury and thus, have not embraced VATS. Pathological stage II and IIIA disease (up-staging) was observed more frequently in the thoracotomy group than in the MIA group (11.8% vs 7.3%). It is possible that lymph node dissection was more systemic in the thoracotomy group, or that very early lesions tended to be treated by MIA. However, these were only speculations.
Our study was limited by the fact that it focused only on obtaining a representative picture of the surgical treatments for early stage lung cancer in Japan rather than on analyzing comparative effectiveness. However, we acknowledge that the choice of surgical approach is also subject to potential selection bias or operator/center experience. Further analysis of the differences in the frequency of thoracotomy and VATS, as well as in the frequency of lung cancer surgery using MIA among institutions would be important components of our subsequent studies. In the future, we intend to compare changes in surgical outcomes over time and explore the management of a more heterogeneous group, such as patients with stage IIIa disease, that would benefit from a large number of patients in the NCD. We will also consider clarifying primary endpoints and their multivariable analyses. At this stage, the NCD does not include prognostic data; therefore, the relationship between MIA and prognosis cannot yet be analyzed.
In conclusion, our analysis of the surgical treatments for 47,921 clinical stage IA lung cancer patients in Japan indicated that MIA using the VATS technique has become the new standard treatment for early lung cancer. As this study analyzed objective “real world” data from a nationwide database, it presents valuable information for further clinical research on minimally invasive surgery.

Compliance with ethical standards

Conflicts of interest

We have no conflicts of interest to report. The Department of Healthcare Quality Assessment at The University of Tokyo, Japan (Eriko Fukuchi, Hiroyuki Yamamoto, and Hiroaki Miyata) is a social collaboration department supported by grants from the National Clinical Database, Johnson & Johnson K.K. and Nipro Co.
Open AccessThis 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/​.

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Literatur
1.
Zurück zum Zitat Sawabata N, Miyaoka E, Asamura H, Nakanishi Y, Eguchi K, Mori M, et al. Japanese lung cancer registry study of 11,663 surgical cases in 2004: demographic and prognosis changes over decade. J Thoracic Oncol. 2011;6:1229–355. Sawabata N, Miyaoka E, Asamura H, Nakanishi Y, Eguchi K, Mori M, et al. Japanese lung cancer registry study of 11,663 surgical cases in 2004: demographic and prognosis changes over decade. J Thoracic Oncol. 2011;6:1229–355.
2.
Zurück zum Zitat Committee for Scientific Affairs, The Japanese Association for Thoracic Surgery, Shimizu H, Endo S, Natsugoe S, Doki Y, Hirata Y, et al. Thoracic and cardiovascular surgery in Japan during 2016. Gen Thorac Cardiovasc Surg. 2019;67:377–411. Committee for Scientific Affairs, The Japanese Association for Thoracic Surgery, Shimizu H, Endo S, Natsugoe S, Doki Y, Hirata Y, et al. Thoracic and cardiovascular surgery in Japan during 2016. Gen Thorac Cardiovasc Surg. 2019;67:377–411.
3.
Zurück zum Zitat Miyata H, Gotoh M, Hashimoto H, Motomura N, Murakami A, Tomotaki A, et al. Challenges and prospects of a clinical database linked to the board certification system. Surg Today. 2014;44:1991–9.PubMed Miyata H, Gotoh M, Hashimoto H, Motomura N, Murakami A, Tomotaki A, et al. Challenges and prospects of a clinical database linked to the board certification system. Surg Today. 2014;44:1991–9.PubMed
4.
Zurück zum Zitat Gotoh M, Miyata H, Hashimoto H, Wakabayashi G, Konno H, Miyakawa S, et al. National Clinical Database feedback implementation for quality improvement of cancer treatment in Japan: from good to great through transparency. Surg Today. 2016;46:38–47.PubMed Gotoh M, Miyata H, Hashimoto H, Wakabayashi G, Konno H, Miyakawa S, et al. National Clinical Database feedback implementation for quality improvement of cancer treatment in Japan: from good to great through transparency. Surg Today. 2016;46:38–47.PubMed
5.
Zurück zum Zitat Endo S, Ikeda N, Kondo T, Nakajima J, Kondo H, Yokoi K, et al. Development of an annually updated Japanese national clinical database for chest surgery in 2014. Gen Thorac Cardiovasc Surg. 2016;64:569–76.PubMedPubMedCentral Endo S, Ikeda N, Kondo T, Nakajima J, Kondo H, Yokoi K, et al. Development of an annually updated Japanese national clinical database for chest surgery in 2014. Gen Thorac Cardiovasc Surg. 2016;64:569–76.PubMedPubMedCentral
6.
Zurück zum Zitat Endo S, Ikeda N, Kondo T, Nakajima J, Kondo H, Yokoi K, et al. Model of lung cancer surgery risk derived from a Japanese nationwide web-based database of 78 594 patients during 2014–2015. Eur J Cardiothorac Surg. 2017;52:1182–9.PubMedPubMedCentral Endo S, Ikeda N, Kondo T, Nakajima J, Kondo H, Yokoi K, et al. Model of lung cancer surgery risk derived from a Japanese nationwide web-based database of 78 594 patients during 2014–2015. Eur J Cardiothorac Surg. 2017;52:1182–9.PubMedPubMedCentral
7.
Zurück zum Zitat Swanson SJ, Herndon JE II, D’ Amico TA, Demmy TL, McKenna RJ Jr, Green MR, et al. Video-assisted thoracic surgery lobectomy: report of CALGB 39802-A prospective multi-institution feasibility study. J Clin Oncol. 2007;25:4993–7.PubMed Swanson SJ, Herndon JE II, D’ Amico TA, Demmy TL, McKenna RJ Jr, Green MR, et al. Video-assisted thoracic surgery lobectomy: report of CALGB 39802-A prospective multi-institution feasibility study. J Clin Oncol. 2007;25:4993–7.PubMed
8.
Zurück zum Zitat Kozower BD, Sheng S, O’Brien SM, Liptay MJ, Lau CL, Jones DR, et al. STS database risk models: predictors of mortality and major morbidity for lung cancer resection. Ann Thorac Surg. 2010;90:875–81.PubMed Kozower BD, Sheng S, O’Brien SM, Liptay MJ, Lau CL, Jones DR, et al. STS database risk models: predictors of mortality and major morbidity for lung cancer resection. Ann Thorac Surg. 2010;90:875–81.PubMed
9.
Zurück zum Zitat Fernandez FG, Kosinski AS, Burfeind W, Park B, DeCamp MM, Seder C, et al. The Society of Thoracic Surgeons lung cancer resection risk model: higher quality data and superior outcomes. Ann Thorac Surg. 2016;102:370–7.PubMedPubMedCentral Fernandez FG, Kosinski AS, Burfeind W, Park B, DeCamp MM, Seder C, et al. The Society of Thoracic Surgeons lung cancer resection risk model: higher quality data and superior outcomes. Ann Thorac Surg. 2016;102:370–7.PubMedPubMedCentral
10.
Zurück zum Zitat Scott WJ, Allen MS, Darling G, Meyers B, Decker PA, Putnum JB, et al. Video-assisted thoracic surgery versus open lobectomy for lung cancer: a secondary analysis of data from the American College of Surgeons Oncology Group Z0030 randomized clinical trial. J Thorac Cardiovasc Surg. 2010;139:976–83.PubMed Scott WJ, Allen MS, Darling G, Meyers B, Decker PA, Putnum JB, et al. Video-assisted thoracic surgery versus open lobectomy for lung cancer: a secondary analysis of data from the American College of Surgeons Oncology Group Z0030 randomized clinical trial. J Thorac Cardiovasc Surg. 2010;139:976–83.PubMed
11.
Zurück zum Zitat Yan TD, Black D, Bannon PG, McCaughan BC. Systematic review and meta-analysis of randomized and nonrandomized trials on safety and efficacy of video-assisted thoracic surgery lobectomy for early-stage non-small-cell-lung cancer. J Clin Oncol. 2009;27:2553–622.PubMed Yan TD, Black D, Bannon PG, McCaughan BC. Systematic review and meta-analysis of randomized and nonrandomized trials on safety and efficacy of video-assisted thoracic surgery lobectomy for early-stage non-small-cell-lung cancer. J Clin Oncol. 2009;27:2553–622.PubMed
12.
Zurück zum Zitat Nwogu CE, D’Cunha J, Pang H, Gu L, Wang X, Richards WG, et al. VATS lobectomy has better perioperative outcomes than open lobectomy: CALGB 31001, an ancillary analysis of CALGB 140202 (Alliance). Ann Thorac Surg. 2015;99:399–405.PubMed Nwogu CE, D’Cunha J, Pang H, Gu L, Wang X, Richards WG, et al. VATS lobectomy has better perioperative outcomes than open lobectomy: CALGB 31001, an ancillary analysis of CALGB 140202 (Alliance). Ann Thorac Surg. 2015;99:399–405.PubMed
13.
Zurück zum Zitat Ikeda N. Updates on minimally invasive surgery in non-small cell lung cancer. Curr Treat Options Oncol. 2019;20:16.PubMed Ikeda N. Updates on minimally invasive surgery in non-small cell lung cancer. Curr Treat Options Oncol. 2019;20:16.PubMed
14.
Zurück zum Zitat Gopaldas RR, Bakaeen FG, Dao TK, Walsh GL, Swisher SG, Chu D. Video-assisted thoracoscopic versus open thoracotomy lobectomy in a cohort of 13619 patients. Ann Thorac Surg. 2010;89:1563–70.PubMed Gopaldas RR, Bakaeen FG, Dao TK, Walsh GL, Swisher SG, Chu D. Video-assisted thoracoscopic versus open thoracotomy lobectomy in a cohort of 13619 patients. Ann Thorac Surg. 2010;89:1563–70.PubMed
15.
Zurück zum Zitat Paul S, Altorki NK, Sheng S, Lee PC, Harpole DH, Onaitis MW, et al. Thoracoscopic lobectomy is associated with lower morbidity than open lobectomy: a propensity-matched analysis from the STS database. J Thorac Cardiovasc Surg. 2010;139:366–78.PubMed Paul S, Altorki NK, Sheng S, Lee PC, Harpole DH, Onaitis MW, et al. Thoracoscopic lobectomy is associated with lower morbidity than open lobectomy: a propensity-matched analysis from the STS database. J Thorac Cardiovasc Surg. 2010;139:366–78.PubMed
Metadaten
Titel
Current status of surgery for clinical stage IA lung cancer in Japan: analysis of the national clinical database
verfasst von
Norihiko Ikeda
Shunsuke Endo
Eriko Fukuchi
Jun Nakajima
Kohei Yokoi
Masayuki Chida
Hiroshi Date
Akinori Iwasaki
Hiroyasu Yokomise
Masami Sato
Meinoshin Okumura
Hiroyuki Yamamoto
Hiroaki Miyata
Takashi Kondo
Publikationsdatum
05.07.2020
Verlag
Springer Singapore
Erschienen in
Surgery Today / Ausgabe 12/2020
Print ISSN: 0941-1291
Elektronische ISSN: 1436-2813
DOI
https://doi.org/10.1007/s00595-020-02063-x

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