Literature DB >> 22729699

Gastric cancer treated in 2002 in Japan: 2009 annual report of the JGCA nationwide registry.

Atsushi Nashimoto1, Kohei Akazawa, Yoh Isobe, Isao Miyashiro, Hitoshi Katai, Yasuhiro Kodera, Shunichi Tsujitani, Yasuyuki Seto, Hiroshi Furukawa, Ichiro Oda, Hiroyuki Ono, Satoshi Tanabe, Michio Kaminishi.   

Abstract

BACKGROUND: The Japanese Gastric Cancer Association (JGCA) started a new nationwide gastric cancer registration in 2008.
METHODS: From 208 participating hospitals, 53 items including surgical procedures, pathological diagnosis, and survival outcomes of 13,626 patients with primary gastric cancer treated in 2002 were collected retrospectively. Data were entered into the JGCA database according to the JGCA classification (13th edition) and UICC TNM classification (5th edition) using an electronic data collecting system. Finally, data of 13,002 patients who underwent laparotomy were analyzed.
RESULTS: The 5-year follow-up rate was 83.3 %. The direct death rate was 0.48 %. UICC 5-year survival rates (5YEARSs)/JGCA 5YEARSs were 92.2 %/92.3 % for stage IA, 85.3 %/84.7 % for stage IB, 72.1 %/70.0 % for stage II, 52.8 %/46.8 % for stage IIIA, 31.0 %/28.8 % for stage IIIB, and 14.9 %/15.3 % for stage IV, respectively. The proportion of patients more than 80 years old was 7.8 %, and their 5YEARS was 51.6 %. Postoperative outcome of the patients with primary gastric carcinoma in Japan have apparently improved in advanced cases and among the aged population when compared with the archival data. Further efforts to improve the follow-up rate are needed.
CONCLUSIONS: Postoperative outcome of the patients with primary gastric carcinoma in Japan have apparently improved in advanced cases and among the aged population when compared with the archival data. Further efforts to improve the follow-up rate are needed.

Entities:  

Mesh:

Year:  2012        PMID: 22729699      PMCID: PMC3549249          DOI: 10.1007/s10120-012-0163-4

Source DB:  PubMed          Journal:  Gastric Cancer        ISSN: 1436-3291            Impact factor:   7.370


Introduction

The registration committee of the Japanese Gastric Cancer Association (JGCA) started a new registration program in 2008 after a 10-year blank period, and we reported the 5-year follow-up data of the patients treated in 2001 [1]. The registration has been continuing, and here we report the results of those treated in 2002.

Materials and methods

Leading hospitals in Japan voluntarily downloaded and fulfilled the database provided by the JGCA and sent the anonymized data to the JGCA data center. The collected data were analyzed according to the previously reported methods [1].

Results

Data of 14,394 patients were collected from 208 hospitals; 126 (60.6 %) hospitals participated in both years, but 82 hospitals were new, which was a 10 % increase as compared to the previous year (13,067 patients from 187 hospitals). The geographic distribution of the registered patients among the 47 prefectures is illustrated in Fig. 1. In Tokyo, 2,332 patients per year were registered, followed by 1,464 in Osaka. Four other prefectures registered more than 500 patients. On the other hand, the number of registered patients was fewer than 100 in 10 prefectures, and there were no registered patients in 2 prefectures.
Fig. 1

Geographic distribution of registered patients by prefecture

Geographic distribution of registered patients by prefecture Patients with remnant stomach cancer, non-epithelial malignant tumor, and gastric cancer combined with malignant tumor of other organs were excluded. Patients who were treated by endoscopic mucosal resection were also excluded. Data of 768 patients lacked essential items. Consequently, data of the remaining 13,002 patients were used for the final analysis. The results are shown in Tables 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, and 28. Data given for each category of patients are: total number of patients, survival rates by year, standard error of 5YEARS, the number of direct death within 30 postoperative days, the number of patients lost to follow-up within 5 years, the number of 5-year survivors, and main cause of death, such as local and/or lymph node metastasis, peritoneal metastasis, liver metastasis, distant metastasis, recurrence at unknown site, other cancer, and other disease. Figures 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, and 17 provide cumulative survival curves of patients stratified by essential categories.
Table 1

Primary cancer

CategoriesNo. of patientsDirect deathLost f.u.1 years (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Primary cancer1362689223388.179.674.571.268.90.474364541483388243322167567333

lost f.u. lost to follow-up, years(%) years of cumulative survival rate, SE standard error, rec recurrence, peritoneal peritoneal recurrence, R recurrence of unknown site

Table 2

Resected cases and unresected cases and other surgeries

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Resected cases1300263217389.881.676.573.170.70.472864101283357215278158539303
Unresected cases355212525.77.32.91.91.50.743718324243221212
Table 3

Sex (resected cases)

CategoriesNo. ofpatientsDirect deathLost f.u.1 years (%)2 years(%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Male888743146489.781.476.172.570.00.54939292805280136203133425210
Female41152070990.182.277.474.372.30.723471184787779752511493
Table 4

Age (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
<3929705093.083.282.180.279.42.4190536144016
40–5936221058193.486.783.280.378.80.7231678327676164284258
60–79807540127989.180.574.871.468.90.54450282798255142180110387192
>8010081326381.671.663.957.051.41.833045122348302010947
Table 5

Tumor location (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
U26811843487.377.571.167.164.31.013561042679976683915088
M5182888193.688.484.481.779.70.63322102339101627248153102
L42492876690.381.876.873.270.80.7233815938012446905920087
Whole58486263.737.928.722.919.31.7883725620244552225

U upper third, M middle third, L lower third

Table 6

Macroscopic type (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Type0686913129498.196.194.092.190.20.44959406931222410524481
Type136306289.178.671.168.265.52.61871222249952013
Type217172129187.075.868.163.060.41.27988614711849612010542
Type325751736479.663.354.349.146.01.09141815321587910222115108
Type492398663.737.928.221.517.71.31275545012397223644
Type533924383.974.567.063.760.62.81711651912831313
Table 7

Histological type (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 years (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Papillary adenocarcinoma (pap)46468688.278.870.766.764.32.4227153036713102614
tub 12846954296.292.488.385.983.60.7187732714714295114637
tub 234581858591.082.877.073.370.80.8193612025913164634816983
por 117461030185.075.170.166.364.41.286781192724163136947
por 224491530983.070.264.259.657.01.01148120530436380168159
Signet-ring cell carcinoma (sig)1581527994.289.085.883.681.51.010301812741718163042
Mucinous adenocarcinoma (muc)25903483.768.661.959.355.23.2116145345621114
Adenosquamous carcinoma170052.929.423.523.523.510.3421410113
Squamous cell carcinoma600100.066.750.050.050.020.4300201000
Miscellaneous carcinoma7501877.969.064.262.458.86.129461111023

tub 1 tubular adenocarcinoma, well-differentiated type; tub 2 tubular adenocarcinoma, moderately differentiated type; por 1 poorly differentiated adenocarcinoma, solid type, por 2, poorly differentiated adenocarcinoma, non-solid type

Table 8

Histological findings (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Differentiated type676833121393.086.681.378.175.70.5404016736021485105109341134
Undifferentiated type60353092386.576.571.567.865.50.6316123390212312616747191162
Other type9801874.961.555.754.451.85.336671722136
Table 9

Lymphatic invasion(ly) (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
ly0574410108997.895.393.391.389.60.44108221082121238020270
ly131561652492.684.979.775.472.70.81833672788842583814880
ly222081432183.269.159.854.951.31.189113537014274872510360
ly317692321767.146.136.431.228.61.138718351610577103127891
Table 10

Venous invasion(v) (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 years (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
v0802722145695.891.688.385.883.40.45344105384685769107308129
v128002140585.172.965.160.357.61.0128414644611081843212191
v213471118375.557.848.342.940.81.4425100291974475136851
v3676910466.145.538.233.331.51.91515414580314433430
Table 11

Depth of invasion (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
pT1(M)3293968998.897.896.494.993.50.52410373244010926
pT1(SM)3110655098.095.893.591.789.70.622681712171395112944
pT2(MP)1341425295.891.587.284.882.11.18692531271613176229
pT2(SS)21151430687.876.067.962.559.11.199611023612873692910464
pT3(SE)25672630172.551.040.333.630.31.06141928391539413814109113
pT4(SI)45845257.734.626.321.920.62.0684715428174242125
Table 12

pT classification (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
pT1640315123998.496.995.093.391.70.4467820192015139123870
pT234561855890.982.075.371.167.90.8186513526715589824616693
pT325672630172.551.040.333.630.31.06141928391539413814109113
pT445845257.734.626.321.920.62.0684715428174242125
Table 13

Lymph node metastasis (resected cases)

categoriesNo. of patientsDirect deathLost f.u.1 yearr (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
pN0760320148297.695.392.990.988.90.453502913252213410730393
pN126191737486.373.966.661.458.91.0124011540212459812812472
pN220321524676.456.044.538.134.61.154717254213288114157997
pN352294154.930.120.316.514.31.6618615836434132231
Table 14

Peritoneal cytology (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver recDistant meta. R Other cancerOther diseaseUnknown
CY050751676189.980.073.268.665.60.7267522957620011711260199146
CY1761167152.226.118.315.012.31.3724538628365223336
Table 15

Peritoneal metastasis (P) (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year(%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
fP01200447208292.385.280.377.074.50.47087349862308184218154503257
fP1762156248.923.313.99.98.31.1494840244285643138
Table 16

Liver metastasis (H) (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
fH01244157211491.083.178.074.672.20.471143861197229200247156517281
fH132663439.822.315.512.711.41.9231063122122801717
Table 17

Distant metastasis including peritoneal and liver metastasis (M) (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver recDistant meta. R Other cancerOther diseaseUnknown
fM01253056212890.482.577.574.171.70.471043761186322185262155518294
fM121661553.229.518.113.512.42.42221732826151114
Table 18

Japanese stage (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
StageIA564014111398.597.195.493.892.20.441261111104118621553
StageIB1822536497.294.490.888.185.30.912161441251512277929
StageII1424322095.086.580.275.572.11.283450100433030156933
StageIIIA1178615988.674.063.156.152.81.550181199553040145643
StageIIIB67848582.158.043.834.931.01.91616120538313153229
StageIV19023018055.631.021.717.414.90.921818070818010114988098
Table 19

Japanese stage (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
StageI746219147798.296.494.392.490.50.45342255235192311329482
StageII1424322095.086.580.275.572.11.283450100433030156933
StageIII18561024486.268.256.148.444.91.2662142404936171198872
StageIV19023018055.631.021.717.414.90.921818070818010114988098
Table 20

TNM stage (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Stage IA556415111198.297.195.593.992.30.4406210994118421054
Stage IB1950538597.093.889.987.584.70.912941749251520288433
Stage II1614526194.085.478.473.370.01.290362125643534148036
Stage IIIA1048913386.168.458.250.646.81.639975204443337155553
Stage IIIB47715879.655.641.932.228.82.21074516619182841715
Stage IV19242718457.332.822.417.915.20.92231807041891071421283100
Table 21

TNM stage (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
StageI751420149698.196.294.192.290.30.45356275834193111229487
StageII1614526194.085.478.473.370.01.290362125643534148036
StageIII15251019184.164.453.244.941.21.3506120370635165197268
StageIV19242718457.332.822.417.915.20.92231807041891071421283100
Table 22

Surgical approach (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Laparotomy1216659202189.681.276.072.469.90.467453911238346204273147514287
Thoracolaparotomy15221370.752.041.438.535.44.045143561053129
Laparoscopic658213697.796.495.094.493.31.0481464008136
Others60280.060.060.060.060.021.9210000001
Table 23

Surgical procedures (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Distal gastrectomy774332140593.186.982.679.977.70.547421975151797212483283143
Total gastrectomy39662554881.267.560.154.951.90.8163520775216413814545194138
Proximal gastrectomy523211194.891.388.386.585.11.634151292472210
Pylorus-preserving gastrectomy39713799.598.295.994.892.61.3332123113143
Segmental or local gastrectomy35136795.091.286.282.981.22.22240222417249
Surgical mucosal resection2205100.089.578.978.973.310.21200000320
Table 24

Lymph node dissection (D) (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 ysr (%)2 ysr (%)3 ysr (%)4 ysr (%)5 ysr (%)SE at 5 ysrAliveLocal rec.Peri-tonealLiver rec.Distant meta. R Other cancerOther diseaseUn-known
D08021212580.573.769.167.065.61.74201795341017184917
D125531545786.479.174.671.268.81.01356582766529564814563
D1 + α1684734992.086.183.280.978.61.110083994271331217725
D1 + β882216593.588.385.683.581.41.45631845198993313
D260562090791.682.276.072.169.60.6342424065418312612453201144
D334323582.866.658.451.147.72.813828672117173611
Table 25

Resection margins (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
PM− and DM−1221756208991.083.178.174.772.30.469843551102332192240155500268
PM+ and/or DM+39774350.932.223.418.416.22.0503414418153422730
Table 26

Combined resection of neighboring organs (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
No combined resection795533149492.085.681.478.676.50.547291935881618013298326154
Combined resection43092961585.173.266.361.558.70.8203219165118312313555192132

PM proximal margin, DM distal margin

Table 27

Combined resected organs (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
Caudal pancreas31313574.254.545.539.737.52.996287715172231010
Spleen14441018984.768.859.653.749.71.457380288617049156851
Transverse colon10111971.652.343.038.036.75.225527429073
Transverse mesocolon531782.961.453.240.338.17.015315214051
Diaphragma90150.825.40.00.00.00.0000420011
Liver9621163.649.240.234.533.25.0247111748266
Gallbladder21211233989.181.977.373.571.21.0121559213732240288052
Adrenal gland100090.080.080.080.080.012.6810000001
Kidney70285.785.785.768.668.618.6300000110
Small intestine100190.070.060.060.060.015.5501000021
Abdominal wall1000.00.00.00.00.00.0000100000
Ovary220367.452.141.741.741.711.07011010000
Pancreas head (PD)202285.069.158.441.835.911.3620102151
Others660486.475.667.967.967.95.84115321423

PD pancreatoduodenectomy

Table 28

Curative potential (resected cases)

CategoriesNo. of patientsDirect deathLost f.u.1 year (%)2 years (%)3 years (%)4 years (%)5 years (%)SE at 5 yearsAliveLocal rec.PeritonealLiver rec.Distant meta. R Other cancerOther diseaseUnknown
A810220158597.895.492.990.688.60.4567458119663939113300109
B30781439888.372.562.156.152.50.913182065081379411539155108
C15052814949.024.716.412.19.90.81091266241507812037175
Fig. 2

Kaplan–Meier survival for all patients with primary gastric cancer. 5YEARS 5-year survival rate

Fig. 3

Kaplan–Meier survival for resected cases and unresected cases

Fig. 4

Kaplan–Meier survival of resected cases stratified by sex

Fig. 5

Kaplan–Meier survival of resected cases stratified by age

Fig. 6

Kaplan–Meier survival of resected cases stratified by tumor location. W whole stomach

Fig. 7

Kaplan–Meier survival of resected cases stratified by macroscopic type

Fig. 8

Kaplan–Meier survival of resected cases stratified by histological findings

Fig. 9

Kaplan–Meier survival of resected cases stratified by lymphatic invasion

Fig. 10

Kaplan–Meier survival of resected cases stratified by depth of tumor invasion

Fig. 11

Kaplan–Meier survival of resected cases stratified by pT classification

Fig. 12

Kaplan–Meier survival of resected cases stratified by lymph node metastasis

Fig. 13

Kaplan–Meier survival of resected cases stratified by peritoneal cytology

Fig. 14

Kaplan–Meier survival of resected cases stratified by peritoneal metastasis

Fig. 15

Kaplan–Meier survival of resected cases stratified by Japanese Gastric Cancer Association (JGCA) stage

Fig. 16

Kaplan–Meier survival of resected cases stratified by TNM stage

Fig. 18

Chronological change of gastric cancer patients older than 80 years. The nationwide registry was suspended for a decade from 1992

Primary cancer lost f.u. lost to follow-up, years(%) years of cumulative survival rate, SE standard error, rec recurrence, peritoneal peritoneal recurrence, R recurrence of unknown site Resected cases and unresected cases and other surgeries Sex (resected cases) Age (resected cases) Tumor location (resected cases) U upper third, M middle third, L lower third Macroscopic type (resected cases) Histological type (resected cases) tub 1 tubular adenocarcinoma, well-differentiated type; tub 2 tubular adenocarcinoma, moderately differentiated type; por 1 poorly differentiated adenocarcinoma, solid type, por 2, poorly differentiated adenocarcinoma, non-solid type Histological findings (resected cases) Lymphatic invasion(ly) (resected cases) Venous invasion(v) (resected cases) Depth of invasion (resected cases) pT classification (resected cases) Lymph node metastasis (resected cases) Peritoneal cytology (resected cases) Peritoneal metastasis (P) (resected cases) Liver metastasis (H) (resected cases) Distant metastasis including peritoneal and liver metastasis (M) (resected cases) Japanese stage (resected cases) Japanese stage (resected cases) TNM stage (resected cases) TNM stage (resected cases) Surgical approach (resected cases) Surgical procedures (resected cases) Lymph node dissection (D) (resected cases) Resection margins (resected cases) Combined resection of neighboring organs (resected cases) PM proximal margin, DM distal margin Combined resected organs (resected cases) PD pancreatoduodenectomy Curative potential (resected cases) Kaplan–Meier survival for all patients with primary gastric cancer. 5YEARS 5-year survival rate Kaplan–Meier survival for resected cases and unresected cases Kaplan–Meier survival of resected cases stratified by sex Kaplan–Meier survival of resected cases stratified by age Kaplan–Meier survival of resected cases stratified by tumor location. W whole stomach Kaplan–Meier survival of resected cases stratified by macroscopic type Kaplan–Meier survival of resected cases stratified by histological findings Kaplan–Meier survival of resected cases stratified by lymphatic invasion Kaplan–Meier survival of resected cases stratified by depth of tumor invasion Kaplan–Meier survival of resected cases stratified by pT classification Kaplan–Meier survival of resected cases stratified by lymph node metastasis Kaplan–Meier survival of resected cases stratified by peritoneal cytology Kaplan–Meier survival of resected cases stratified by peritoneal metastasis Kaplan–Meier survival of resected cases stratified by Japanese Gastric Cancer Association (JGCA) stage Kaplan–Meier survival of resected cases stratified by TNM stage The 5YEARS in 13,626 patients with primary gastric cancer was 68.9 % (Table 1; Fig. 2). During the 5-year follow-up, 2,233 patients were lost; the follow-up rate was 83.6 %. Of the 13,626 patients, 13,002 underwent gastric resection. Accordingly, the resection rate was 95.4 %, and the 5YEARS of the resected patients was 70.7 % (Table 2; Fig. 3). Sixty-three of 13,002 resected cases died within 30 days postoperatively. The direct death rate was 0.48 %. The frequent causes of death in patients who had undergone gastrectomy were peritoneal metastasis (n = 1,283), followed by other diseases (n = 539), local recurrence including node metastasis (n = 410), liver metastasis (n = 357), recurrence at unknown site (n = 278), and other cancer (n = 158). The proportion of male patients was 68.4 % with 5YEARS of 70.0 %; for female patients 5YEARS was 72.3 %, which was better statistically (Table 3; Fig. 4). Patients more than 80 years old were 7.8 % of all patients, and their 5YEARS was 51.4 % (Table 4; Fig. 5). On the other hand, 5YEARS of the patients under 39 years old was 79.4 % (P < 0.001). Cancer was located in the upper-third of the stomach in 21.1 % of the cases, and its 5YEARS was relatively low at 64.3 % (Table 5; Fig. 6). Patients with type 4 cancer amounted to 7.2 %, and their 5YEARS was markedly low at 17.7 % (Table 6; Fig. 7). The 5YEARS of type 3 was 46.0 % and that of type 2 was 60.4 %. For histological type, frequency of the undifferentiated type including poorly differentiated adenocarcinoma, signet-ring cell carcinoma, and mucinous adenocarcinoma was 46.8 % and its 5YEARS was 65.5 %, which was inferior to that of the differentiated type (75.7 %, P < 0.001; Tables 7, 8; Fig. 8). The grade of lymphatic invasion (ly0–ly3) and venous invasion (v0–v3) showed significant correlations with the prognosis (Tables 9, 10; Fig. 9). A high incidence of early-stage cancer remained characteristic in 2002, as shown in Tables 11 and 12. The proportion of pathological M and SM (pT1) cancer was 49.7 %, and its primary cause of death was not cancer recurrence (17.9 %, n = 87) or other cancer (18.7 %), but other diseases (49.0 %, n = 238). The proportion of pathological MP and SS (pT2) was 26.8 %, SE (pT3) 19.9 %, and SI (pT4) 3.6 %. The 5YEARS of these subsets were 67.9 %, 30.3 %, and 20.6 %, respectively (Figs. 10, 11). The primary cause of death in advanced cancer was cancer recurrence, and the peritoneal recurrence rate was remarkably high in the pT3 and pT4 subsets. For the lymph node metastasis, the proportion of pN0 was 59.5 %, pN1 20.4 %, pN2 15.9 %, and pN3 4.1 %, and the 5YEARS of each subset was 88.9 %, 58.9 %, 34.6 %, and 14.3 %, respectively (Table 13; Fig. 12). Peritoneal washing cytology was carried out in 5,836 patients with advanced gastric cancer; the positive rate was 13.0 %. The 5YEARS of cytology-positive (CY1) patients was 12.3 %, which was almost as dismal as the 5YEARS of the P1 patients (8.3 %; Tables 14, 15; Figs. 13, 14). The 5YEARS of patients with liver metastasis (H1) was 11.4 %, and of those with other types of distant metastasis was 12.4 % (Tables 16, 17). The 5YEARS of the patients stratified by JGCA staging system was 92.2 % for stage IA, 85.3 % for stage IB, 72.1 % for stage II, 52.8 % for stage IIIA, 31.0 % for stage IIIB, and 14.9 % for stage IV. These JGCA 5YEARSs seemed to correlate well with TNM 5YEARSs, which were 92.3 % for stage IA, 84.7 % for stage IB, 70.0 % for stage II, 46.8 % for stage IIIA, 28.8 % for stage IIIB, and 15.2 % for stage IV (Table 18, 19, 20, 21; Figs. 15, 16). For operative procedures, the proportion of patients who underwent laparoscopic gastrectomy was only 5.1 % in 2002, and their 5YEARS was 93.3 % (Table 22). Eligibility for laparoscopic surgery was strictly limited at that time, and the laparoscopic approach was selected almost exclusively in patients with the preoperative diagnosis of early gastric cancer. Only 1.2 % of the patients were treated by thoracolaparotomy, and their 5YEARS was 35.4 %. Thoracolaparotomy was usually carried out in patients with advanced gastric cancer with esophageal invasion more than 3 cm in length. Total gastrectomy was performed for 30.5 % of the patients, and their 5YEARS was 51.9 % (Table 23). D2 lymph node dissection, a standard procedure for resectable advanced gastric cancer according to the JGCA treatment guidelines, was performed in 49.2 % of the patients (Table 24) [2, 3]. The risk of direct death among those who underwent D2 gastrectomy was only 0.3 %. The proportion of patients treated with less invasive surgery such as proximal gastrectomy, pylorus-preserving gastrectomy, segmental gastrectomy, and local resection of the stomach was 9.8 %. D0, D1, D1 + α, and D1 + β dissection were carried out in 6.5 %, 20.7 %, 13.7 %, and 7.2 % of the patients, respectively. D0 and D1 dissection were carried out mainly in patients with noncurative factors or poor surgical risks. The incidence of positive resection margin (PM+ and/or DM+) was 3.1 % (Table 25). Combined resection of other organs was performed in 35.1 % (Table 26). The frequent combined resected organs in patients who underwent gastrectomy were gallbladder (n = 2121), spleen (n = 1444), caudal pancreas (n = 313), transverse colon (n = 101), liver (n = 96), and so on in descending order (Table 27). The curative potential of gastric resection was an important prognostic factor. The proportion of patients with no residual tumors with high probability of cure (resection A) was 63.9 %, and their 5YEARS was 88.6 %. On the other hand, patients with definite residual tumors (resection C) amounted to 11.9 % of all patients who underwent laparotomy, and their 5YEARS was 9.9 % (Table 28; Fig. 17).
Fig. 17

Kaplan–Meier survival of resected cases stratified by curative potential of gastric resection

Kaplan–Meier survival of resected cases stratified by curative potential of gastric resection

Discussion

Estimates of the worldwide incidence, mortality, and prevalence of 26 cancers in the year 2002 were available in the GLOBOCAN series of the International Agency for Research on Cancer [4]. With an estimated 934,000 new cases per year in 2002 (8.6 % of new cancer cases), the incidence of stomach cancer is in fourth place, after cancers of the lung, breast, and colon and rectum. It is the second most common cause of death from cancer (700,000 deaths annually). The data presented in this report were collected from 208 hospitals in Japan. Cancer incidence rate (annual number of newly diagnosed cases per 100,000 population) in Japan in 2002 was approximately 520 for males and 370 for females. The incidences of various cancers in Japan are estimated from data collected by the cancer registry system in a dozen prefectures. According to these statistics, the number of cancer incidences in 2002 was approximately 589,000. The stomach was the leading site (21 %) for males and the second highest site (14 %) for females. The number of new patients who were diagnosed as gastric cancer in 2002 was estimated to be 106,760 [5]. Accordingly, 13,626 patients registered by this program corresponded to approximately 13 % of the whole population affected by gastric cancer in Japan. Even though these patients may not represent the average features of gastric cancer found in this country, this report is considered to have analyzed the largest number of patients for the past 10 years, clarifying the trends of gastric cancer in Japan. Just for reference, the proportion of patients registered in the nationwide registry of other organs of all patients diagnosed were 6 % in colon cancer, 24 % in esophageal cancer, 25 % in liver cancer, and 26 % in lung cancer, respectively [6]. The reliability of the results in this report depends on the quality of data accumulated in the JGCA database. Because of the complexity of the JGCA staging system, the error checking system on the data entry screen did not function completely. In several categories such as lymph node metastasis (N), the JGCA system could not be converted to the TNM system automatically. Therefore, the registration committee had to make great efforts to confirm raw data sent to the data center from the participating hospitals. As compared with our archived data of 12,004 patients treated in 2001 [1], the proportion of early cancer declined from 51.2 % to 49.7 % [pT1 (M) cancer, 27.4 % to 25.6 %, and pT1 (SM) cancer, 23.8 % to 24.1 %], suggesting that an increasing number of patients with mucosal cancer were sent for endoscopic treatment. These data suggest that we should start to register gastric patients treated with endoscopic mucosal resection (EMR) and/or endoscopic submucosal dissection (ESD) as soon as possible. The surgical mortality within 30 days significantly improved, from 0.6 % to 0.48 % (P < 0.001). Just for reference, it was 4.0 % in 1963 and 1.0 % in 1991 [7], Moreover, the nationwide database of gastrointestinal surgery in 2008 showed that was 0.2 % in gastrectomy and 0.4 % in total gastrectomy [8]. Accordingly with the rapidly aging society in Japan, the proportion of patients more than 80 years old continued increasing (Fig. 18): it was 0.7 % in 1963, 4.9 % in 1990, 7.0 % in 2001, and 7.8 % in 2002, respectively. Although the risk for surgery increases in elderly patients who have comorbidities, evaluations of risk can allow interventions that may decrease morbidity and mortality. Appropriate treatments should be offered to the elderly. However, these data have the intrinsic weakness of being retrospectively collected 7 years after surgery. Unfortunately, we in Japan continue to have a legal difficulty in registering personal information, which is essential for long-term and prospective follow-up. The overall follow-up rate in our program was 83.5 %. In other words, the outcome of 17.5 % of the patients is unknown. The proportion of patients who were lost to follow-up in the Japanese nationwide registry of colon cancer, liver cancer, and thyroid cancer was 19.6 %, 25.8 %, and 20.6 %, respectively [6]. Rules and regulations regarding handling of these data will have to change radically to overcome the issue of accuracy and reliability of the nationwide registry in Japan, and this could be out of the hands of the surgeons who have contributed to the best of their abilities to gather these data. On the other hand, the Japanese Association of Clinical Cancer Centers, consisting of 25 cancer center hospitals, reported that their follow-up rate was 98.5 %, and 5YEARS of 9,980 patients who underwent surgery from 1997 to 2000 were 90.4 % for TNM stage I, 67.8 % for stage II, 43.3 % for stage III, and 9.3 % for stage IV, respectively [9]. When the patients with gastric cancer had a medical examination in clinical cancer centers, they registered the place where their family records were registered, and office workers of the clinical cancer centers confirmed regularly their safety from the family registration; this was the reason for the extremely high follow-up rate. In the current analyses, 5YEARS in stage IV patients was 15.2 %. We might have overestimated our 5YEARS in stage IV patients, but we found that our follow-up rate increased as the stage advanced; the follow-up rate of stage IV patients was 90.4 %. These data suggest that the lower follow-up rate may not have had serious effects on 5YEARSs in our program. Although, the correlation between follow-up rate and survival rate is complicated, our follow-up system needs to be improved if we are to evaluate the survival rates more accurately. Chronological change of gastric cancer patients older than 80 years. The nationwide registry was suspended for a decade from 1992 Cytological examination was conducted in 3,481 (59.4 %) of 5,857 patients with T2, T3, or T4 cancer. The 5YEARS of CY1 patients was 12.3 % and their 5YEARS was as poor as that of patients with peritoneal metastasis. Although this examination was not carried out commonly in the days of 2002, it could still be regarded as a significant and independent prognostic factor from the data that were available. These findings further support the need for staging laparoscopy for accurate preoperative staging in patients with advanced gastric cancer. JGCA restarted a nationwide registration from 2008. The object of the new nationwide registry was primarily to calculate the stage-specific 5YEARSs among patients who underwent gastrectomy. Therefore, the structure of the database was required to be simple, and the number of registration items was kept to a minimum. Undoubtedly, the next objective would be to collect and analyze data of patients with inoperable disease, remnant gastric cancer, gastrointestinal stromal tumor, malignant lymphoma of the stomach, and other entities that were excluded in the current project. We also began to register patients who were treated by EMR/ESD by adding additional items and updating data entry software from 2011. We hope that this report will be useful when surveying trends and changes in the clinical practice and treatment results of gastric cancer in Japan. Details of the individual data presented in this report will soon become available for scientific and clinical research with the permission of the registration committee. In addition, most of the surgical and pathological data could easily be transferred to the international database in the near future for various analyses. The registration committee will continue the efforts to improve the registration system, ultimately to collect meaningful annual data.
  2 in total

1.  Cancer incidence and incidence rates in Japan in 2002: based on data from 11 population-based cancer registries.

Authors:  Tomohiro Matsuda; Tomomi Marugame; Ken-ichi Kamo; Kota Katanoda; Wakiko Ajiki; Tomotaka Sobue
Journal:  Jpn J Clin Oncol       Date:  2008-08-16       Impact factor: 3.019

2.  Gastric cancer treatment in Japan: 2008 annual report of the JGCA nationwide registry.

Authors:  Yoh Isobe; Atsushi Nashimoto; Kohei Akazawa; Ichiro Oda; Kenichi Hayashi; Isao Miyashiro; Hitoshi Katai; Shunichi Tsujitani; Yasuhiro Kodera; Yasuyuki Seto; Michio Kaminishi
Journal:  Gastric Cancer       Date:  2011-09-07       Impact factor: 7.370

  2 in total
  190 in total

1.  Technical aspects and short- and long-term outcomes of totally laparoscopic total gastrectomy for advanced gastric cancer: a single-institution retrospective study.

Authors:  Masaya Nakauchi; Koichi Suda; Shinichi Kadoya; Kazuki Inaba; Yoshinori Ishida; Ichiro Uyama
Journal:  Surg Endosc       Date:  2015-12-24       Impact factor: 4.584

2.  Prognostic impact of venous invasion in stage IB node-negative gastric cancer.

Authors:  Ippeita Araki; Kei Hosoda; Keishi Yamashita; Natsuya Katada; Shinichi Sakuramoto; Hiromitsu Moriya; Hiroaki Mieno; Akira Ema; Shiro Kikuchi; Tetuo Mikami; Masahiko Watanabe
Journal:  Gastric Cancer       Date:  2014-04-01       Impact factor: 7.370

3.  Validity of response assessment criteria in neoadjuvant chemotherapy for gastric cancer (JCOG0507-A).

Authors:  Yukinori Kurokawa; Taro Shibata; Mitsuru Sasako; Takeshi Sano; Akira Tsuburaya; Yoshiaki Iwasaki; Haruhiko Fukuda
Journal:  Gastric Cancer       Date:  2013-09-03       Impact factor: 7.370

4.  Chemoprevention of gastric cancer development after Helicobacter pylori eradication therapy in an East Asian population: Meta-analysis.

Authors:  Mitsushige Sugimoto; Masaki Murata; Yoshio Yamaoka
Journal:  World J Gastroenterol       Date:  2020-04-21       Impact factor: 5.742

5.  Long-term oncological outcomes of submucosal manipulation during non-curative endoscopic submucosal dissection for submucosal invasive gastric cancer: a multicenter retrospective study in Japan.

Authors:  Hirotaka Ito; Takuji Gotoda; Tsuneo Oyama; Noboru Kawata; Akiko Takahashi; Yoshikazu Yoshifuku; Shu Hoteya; Masahiro Nakagawa; Waku Hatta; Masaaki Hirano; Mitsuru Esaki; Mitsuru Matsuda; Ken Ohnita; Ryo Shimoda; Motoyuki Yoshida; Osamu Dohi; Jun Takada; Keiko Tanaka; Shinya Yamada; Tsuyotoshi Tsuji; Yoshiaki Hayashi; Naoki Nakaya; Tomohiro Nakamura; Tooru Shimosegawa
Journal:  Surg Endosc       Date:  2017-06-21       Impact factor: 4.584

Review 6.  How to stomach an epigenetic insult: the gastric cancer epigenome.

Authors:  Nisha Padmanabhan; Toshikazu Ushijima; Patrick Tan
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2017-05-17       Impact factor: 46.802

Review 7.  Treatment of gastric cancer.

Authors:  Michele Orditura; Gennaro Galizia; Vincenzo Sforza; Valentina Gambardella; Alessio Fabozzi; Maria Maddalena Laterza; Francesca Andreozzi; Jole Ventriglia; Beatrice Savastano; Andrea Mabilia; Eva Lieto; Fortunato Ciardiello; Ferdinando De Vita
Journal:  World J Gastroenterol       Date:  2014-02-21       Impact factor: 5.742

8.  Clinicopathological characteristics and prognosis of gastric cancer with malignant ascites.

Authors:  Nian Fang; Hui-Qing Zhang; Bo He; Mei Xie; Shan Lu; Yi-Ye Wan; Nong-Rong Wang
Journal:  Tumour Biol       Date:  2013-11-27

9.  Treatment of patients with stage IV gastric cancer.

Authors:  Masahide Ikeguchi; Abdul Kader; Seigo Takaya; Youji Fukumoto; Tomohiro Osaki; Hiroaki Saito; Shigeru Tatebe; Toshiro Wakatsuki
Journal:  J Gastrointest Cancer       Date:  2013-06

Review 10.  Evaluation and treatment of malignant ascites secondary to gastric cancer.

Authors:  Hiromichi Maeda; Michiya Kobayashi; Junichi Sakamoto
Journal:  World J Gastroenterol       Date:  2015-10-21       Impact factor: 5.742

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