Esophageal Cancer Open Access
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 1, 2004; 10(5): 626-629
Published online Mar 1, 2004. doi: 10.3748/wjg.v10.i5.626
Long-term effect on carcinoma of esophagus of distal subtotal gastrectomy
Yu-Ping Chen, Jie-Sheng Yang, Di-Tian Liu, Yu-Quan Chen, Wei-Ping Yang, Department of Thoracic Surgery, Tumor Hospital of Shantou University Medical College, Shantou 515031, Guangdong Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Yu-Ping Chen, Department of Thoracic Surgery, Tumor Hospital of Shantou University Medical College, Shantou 515031, Guangdong Province, China. chenyp@pub.shantou.gd.cn
Telephone: +86-754-8630899 Fax: +86-754-8630899
Received: May 13, 2003
Revised: May 25, 2003
Accepted: June 2, 2003
Published online: March 1, 2004

Abstract

AIM: To investigate the surgical treatment and long-term survival for patients with carcinoma of esophagus after distal subtotal gastrectomy.

METHODS: Resections of the tumor through left thoracotomy were performed in 85 patients with esophageal carcinoma following distal subtotal gastrectomy. The procedure involved preserving the left short gastric artery and transporting the residual stomach, the spleen and tail of the pancreas into the left thoracic cavity, and using the residual stomach to reconstruct the alimentary tract.

RESULTS: The resectable rate was 91.8%, complication rate 10.3%, and no death occurred in the postoperative period. The 1-, 3-, 5-, and 10-year survival rates were 85.7%, 50.7%, 30.6% and 18.8%, respectively.

CONCLUSION: Surgical resection is the optimal management method for the patients with esophageal carcinoma after distal subtotal gastrectomy. The reconstruction of digestive tract using anastomosis of the esophagus and the residual stomach is not only simple but also can achieve a better curative effect, promoting the digestive function and improving the quality of life.




INTRODUCTION

The primary management of esophageal carcinoma is surgical resection, and the stomach is the organ most often chosen for substitution following removal of esophagus for carcinoma. However, following the resection of esophageal carcinoma after distal subtotal gastrectomy, the replacement of esophagus mostly selected other organs, such as jejunum or colon[1-11]. Since we first applied this new technique to use the residual stomach in patients all with previous distal subtotal gastrectomy in 1982[12,13], we have treated 85 patients by such approach, and will report it as follows.

MATERIALS AND METHODS
Clinical data

There were 74 men and 11 women with age ranging from 34 to 78 years (mean 60.3 years). The interval between the time of subtotal gastrectomy and the time when the patients were diagnosed having carcinoma of esophagus ranged from 7 to 29 years, averaging 15 years. According to the procedures of subtotal gastrectomy, two cases were classified as Billroth I type, 83 cases Billroth II type, including 27 cases undergoing gastrectomy posterior to colon, and 58 cases anterior to colon. The digestive functions in all of the patients were approximately normal. All the patients presented with the symptoms of dysphagia to some degree with only 42.4% (36/85) being able to take semi-fluiddiet. The average body weight of the patients was 47.7 ± 10.2 kg. With regard to the classification of Performance Status, 30.6% (26/85) patients belonged to class 0-1, and 69.4% (59/85) to class 2-4.

In terms of the location of the tumor, 4 cases were localized in upper thoracic esophagus, 62 cases in mid thoracic, and 19 cases in lower thoracic. With regard to gross type, 60 patients belonged to medullary type, 15 ulcerative type, six constrictive type, three fungating type and one intraluminal type. All of cases received barium meal examination of gastrointestinal tract to measure the maximal diameter of residual stomach that was from the fundus to the gastrojejunal anastomosis, and no lesion was found in the residual stomach. The diameter ranged from 5 cm to 9.2 cm, mean 7.9 cm. Forty-three cases in this group were further examined by fiber-gastroscopy, which revealed nothing pathological in their residual stomachs.

All the patients underwent the resection of involved portion esophagus through left thoracotomy under the intratracheal anesthesia, except for 7 cases being found to have unresectable tumors, in which 5 cases had the local tumors infiltrating the aortic arch or / and bronchus, and two cases were found to be accompanied with metastasis of liver and extensive spread of intra-abdominal cavity.

Seventy-eight cases underwent the resection of the carcinoma of esophagus with a resectability rate of 91.8% (78/85), including 64 cases for radical resection and 14 cases for palliative resection. As for length of the involved segment of esophagus, 21 cases were shorter than 3 cm, 17 cases ranged from 3-5 cm, and 40 cases longer than 5 cm. The maximal diameters of residual stomachs measured from the fundus to the gastrojejunal anastomosis, ranged from 6 cm to 11.3 cm, mean 9.1 cm which was in contrast to X-ray examination. According to the location of anastomosis sites, 5 cases were localized in neck, 51 above aortic arch, and 22 below aortic arch. Sixty-five patients were anastomosed by handwork, 13 by mechanical anastomat, including 10 above aortic arch and 3 below aortic arch. During the operation, a silica-gel catheter with a metal guiding core was inserted into the jejunum through nostril for 30 cases[14]. Those patients were fed with mixed milk or nutritional fluid through the nasal feeding catheter one day after operation. The patients had a meal 5-10 d following operation (mean 7 d). The span of hospitalization ranged from 14 to 52 d (mean 14.6 d).

Procedure of operation

Our approach was through a left thoracotomy incision. The tumor was examined and if it appeared to be resectable, the left diaphragm was opened and the exploration of abdominal cavity was done. After examining the operative condition of previous subtotal gastrectomy, the spleen, splenic hilus and pancreatic tail were dissociated from the back of peritoneum. Meanwhile, two to four short gastric blood vessels should be preserved to provide adequate blood supply for the residual stomach. The residual stomach, afferent and efferent loops of jejunum were mobilized from peripheral cohesion, and the previous gastrojejunal anastomosis was brought into the left thorax, the afferent loop of jejunum close to gastrojejunal anastomosis was transected and the gastric end was closed. If the part of gastrojejunal anastomosis was removed at the same time, the length of the residual stomach may be prolonged (Figure 1: C). The afferent loop is rejoined to the efferent loop 30 cm below the original gastrojejunostomy (Roux-en-Y method, Figure 2: AA’). The cardia was transected and closed (if mechanical approach was used, the cardia was not closed temporarily, Figure 1: D). The residual stomach, gastrojejunal anastomosis, efferent of jejunum, spleen, tail of pancreas were all transposed into the left thoracic cavity. The esophagus was mobilized and the upper end of esophagus resected 5 cm above the tumor as described in Sweet’s esophago-gastrostomy (Figure 2: BB’). If the staple was used, the esophagus was anastomosed to the fundus of the substitution through the cardiac, and the end of cardiac was shut soon after. The splenic ligament was fixed firmly to the thoracic wall to reduce the tension on the esophagogastric anastomosis. If the anastomosis was performed in neck, the fundus of the residual stomach could be brought up into the neck through thoracic cavity or the bed of esophagus. The approach of the operation is represented diagrammatically in Figure 1 and Figure 2. Preoperative and postoperative barium meal examinations, postoperative roentgenogram of chest and field of operation in one of the patients are shown in Figure 3, Figure 4, Figure 5, Figure 6 and Figure 7.

Figure 1
Figure 1 Resection range.
Figure 2
Figure 2 Postoperative situation.
Figure 3
Figure 3 Preoperative barium.
Figure 4
Figure 4 Preoperative barium meal examination, showing meal examination, showing re-mid thoracic esophageal tumor. sidual stomach.
Figure 5
Figure 5 Field of operation, showing the spleen in the left tho-racic cavity.
Figure 6
Figure 6 Postoperative roentgenogram of chest, showing the spleen shadow in the left thoracic cavity.
Figure 7
Figure 7 Postoperative barium meal examination, showing the esophagogastric anastomosis above the aortic arch, the residual stomach with previous gastrointestinal anastomosis, and the Roux-en-Y anastomosis.
Follow-up and statistical analysis

All the patients were followed up after operation. The patients failed to be followedup were deemed as death according to the last time they could be contacted. The survival rate was calculated on the basis of Kaplan-Meier procedure by statistical software SPSS 10.0. The condition of eating, the body weight and the Performance Status for the patients recruited in our study 3 months after the operation. Enumeration data and measurement data were analyzed by χ2 and t test, respectively.

RESULTS

Seventy-eight patients received resection of the tumor, including 24 cases having grade I of squamous carcinoma, 47 cases having grade II of squamous carcinoma, 4 cases grade III of squamous carcinoma, 2 cases adenocarcinoma and 1 case carcinosarcoma. There were two cases having positive resection margins. With regard to lymph node status, 34 patients were complicated with metastasis of lymph node, and 43 patients without. According to UICC1997 PTNM stage, 5 patients were classified as stage I, 30 stage II, and 43 stage III. The complication rate following operation was 10.3% (8/78), with two cases suffering from arrhythmia, two cases having pneumonia and four cases having anastomostic leakage. All these patients with complications were cured through conservative management without operation death. The follow-up rate was 91.0% (71/78), six patients lost contact. The 1, 3, 5, and 10yr survival rate were 85.7%, 50.7%, 30.6% and 18.8%, respectively (Figure 8). The patients undergoing resection could take semi-fluid diet, accounting for 92.3% (72/78). Among all the patients, 84.7% (72/85) could have 300 ± 500 mL volume of semi-fluid diet. The mean body mass was 49.8 ± 8.9 kg. Compared with the previous body mass, 41.0% (32/78) patients got a body weight gain after operation. In term of the grade of Performance Status, 72.9% (62/85) patients had grade 0-1, and 27.1% (23/85) grades 2-4. Apart from the body mass, the difference between the index of quality of life before operation and the comparative index after operation was statistically significant (P < 0.05).

Figure 8
Figure 8 Kaplan-Meier survival curve.
DISCUSSION

Cancer of esophagus in Chaoshan region is prevalent with a high incidence, so are the gastroduodenal diseases, especially the peptic ulcer. Therefore, there are some patients with esophageal carcinoma after subtotal gastrectomy in this area. The incidence rate of these patients was 2.3% (85/3632) compared with the patients with esophageal carcinoma treated surgically in our hospital in the same period, which demonstrates the management of these patients should also be emphasized. The average interval between gastrectomy and diagnosis of esophageal carcinoma was 15 years. The mean age of the patients was 60.3 years, with no significant difference compared with other patients suffering from esophageal carcinoma without subtotal gastrectomy. So it may be suggested the development of carcinoma of esophagus is not obviously correlated with the history of surgical operation of stomach. The relationship between esophageal carcinoma and previous gastrectomy for benign ulcer disease are still not clear[9,10,15-19].

As for the influence of previous operation, the colon or jejunum is the most popular choice as a substitution in such patients. This approach is complicated and can greatly affect the postoperative quality of life[13,20,21]. For this reason, some patients were not accessible to resection, but were treated by radiotherapy. When the demand of the resection of esophageal carcinoma was met, the procedure of using the residual stomach to reconstruct the digestive tract, is the best choice, which not only facilitates the recovery of digestive function following operation, but also improves the quality of life in patients with esophageal carcinoma after previous subtotal gastrectomy. In the process of this procedure, the residual stomach must have sufficient length for lifting, and good blood supply. The blood supply of the residual stomach originated from the short artery. Transferring spleen, tail of pancreas to thoracic cavity can provide the residual stomach with good blood supply, and benefit the lifting length of it. Amputating at the jejunual afferent loop near anastomosis, and making the jejunual Roux-Y anastomosis, fully dissociating the previous operative cohesion could also prolong the lifting length and decrease the lifting tension of the residual stomach. After being fully dissociated, the residual stomach can be lifted up by about 20 cm. Four cases were complicated with anastomotic leakage in the group, including 3 cases with thoracic leakage[13] occurring during the early application of this technique. The causes of the thoracic leakage might be related to the local infection and suturing skill. The cause of the other case with anantomotic leakage in neck probably was connected with the tension of the residual stomach. Recently, we replaced manual manipulation with mechanical anastomosis, using staple to close the cardiac and the lesser curvature of stomach. This is better for the extension of the residual stomach, reducing the traction and tension of anastomosis. At the early period after operation, the patients were offered nasal feeding nutrition, which was conducive to the rehabilitation and reduction of complications for patients after resection.

So far, there has been no clear report on the benefit of this procedure, which preserves the residual stomach and anastomoes it to esophagus, in terms of the long-term effect and quality of life for the patients with esophageal carcinoma after subtotal gastrectomy[21-29]. Compared with the management of the other patients with esophageal carcinoma in corresponding period, the difference between the means of operation and the findings of pathology in this group was not significant. The 5- and 10-year survival rates were 30.6% and 18.8% respectively. In comparison of the long-term survival rate of our group and those of the other big groups[10,30-33], no significant difference could be found. All these demonstrate that such an approach can achieve a good efficacy. The patients were satisfied with their quality of life, and the majority of them could have semi-fluid diet. Over 50% of them had a body mass gain. The grade of Performance Status of them also improved greatly. In conclusion, the above evidences further confirm that in the management of the patients with carcinoma of esophagus after previous subtotal gastrectomy, the technique, which used the residual stomach to reconstruct the alimentary tract, not only accomplished a rather good long-term survival rate, but also improved the quality of patients’ life. So it is a simple operative approach with few trauma and good results.

Footnotes

Edited by Ma JY Proofread by Zhu LH

References
1.  Xie ZL, Zhu KS, Liu SY, Zhang LD. Surgical Treatment of esoph-ageal carcinoma in gastrectomized patients. Zhongguo Zhongliu Linchuang. 1998;25:570-572.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Zhang YM, Chi QM, Li ZM, Zhang BJ, Yang RS, Chen JC, Zhang LM, Li DT, Gao HJ. Surgical Treatment of esophageal carcinoma and cardiac carcinoma after gastrectomy: a report of 24 cases. Zhongliu Fangzhi Zazhi. 1999;6:188-189.  [PubMed]  [DOI]  [Cited in This Article: ]
3.  Wei JY, Chen BJ, Sun M. Surgical mode of esophageal and cardiac carcinoma after gastrectomy. Jiangshu Yiyao. 1999;25:742-744.  [PubMed]  [DOI]  [Cited in This Article: ]
4.  Fu CG, Gao HC, Cai YJ, Kang JR. Surgical Treatment of esoph-ageal and cardiac cancer after gastrectomy: report of 22 cases. Fujian Yiyao Zazhi. 2000;22:10-11.  [PubMed]  [DOI]  [Cited in This Article: ]
5.  Jia P, Lin HX. Reconstruction of esophagus with colon by ante-rior sterna for esophageal cancer after gastrectomy: report of 12 cases. Xiandai Zhenduan Yu Zhiliao. 1998;9:295.  [PubMed]  [DOI]  [Cited in This Article: ]
6.  Xu ZF, Sun YC, Da ZW, Zhao XW, Chen HQ. Surgical Treat-ment of primary cardiac and esophageal carcinoma of remnant stomach. Jiefangjun Yixue Zazhi. 1997;22:167-168.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Ping YM, Yan JS, Du XQ. [Clinical application and technical problems of colonic interposition for esophageal substitution]. Zhonghua Waike Zazhi. 1994;32:755-756.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Takemura M, Higashino M, Osugi H, Tokuhara T, Kaseno S, Kinoshita H. [Surgical treatment of esophageal cancer in four patients after gastrectomy for gastric cancer]. Nihon Kyobu Geka Gakkai Zasshi. 1996;44:89-94.  [PubMed]  [DOI]  [Cited in This Article: ]
9.  Mafune K, Tanaka Y, Ma YY, Takubo K. Synchronous cancers of the esophagus and the ampulla of Vater after distal gastrectomy: successful removal of the esophagus, gastric remnant, duodenum, and pancreatic head. J Surg Oncol. 1995;60:277-281.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 14]  [Cited by in F6Publishing: 13]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
10.  Tachibana M, Abe S, Yoshimura H, Suzuki K, Matsuura H, Nagasue N, Nakamura T. Squamous cell carcinoma of the esophagus after partial gastrectomy. Dysphagia. 1995;10:49-52.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 10]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
11.  Kato H, Tachimori Y, Watanabe H. Surgical treatment for tho-racic esophageal carcinoma in patients after gastrectomy. J Surg Oncol. 1992;51:94-99.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 16]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
12.  Lu SJ, Chen JQ, Chen YQ, Yang JS. Surgical operation of esoph-ageal carcinoma after subtotal gastrectomy: esophagogastrostomy. Aizheng. 1986;5:41-44.  [PubMed]  [DOI]  [Cited in This Article: ]
13.  Lu SJ, Chen BX. Operative technique for carcinoma of the oe-sophagus after distal subtotal gastrectomy: a new method using the residual stomach to reconstruct the alimentary tract. Aust N Z J Surg. 1990;60:719-722.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 4]  [Article Influence: 0.1]  [Reference Citation Analysis (0)]
14.  Yang JS, Yang WP, Chen YP, Chen YQ, Yang XH. Clinical appli-cation of silica-gel catheter with a metal guiding core in 43 severe patients. Zhongguo Weizhongbing Jijiu Yixue. 1995;7:242-243.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Hsu NY, Chen CY, Chen JT, Hsu CP. Oesophageal squamous cell carcinoma after gastrectomy for benign ulcer disease. Scand J Thorac Cardiovasc Surg. 1996;30:29-33.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 6]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
16.  Caygill CP, Hill MJ, Kirkham JS, Northfield TC. Oesophageal cancer in gastric surgery patients. Ital J Gastroenterol. 1993;25:168-170.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Caygill CP, Hill MJ. Malignancy following surgery for benign peptic disease: a review. Ital J Gastroenterol. 1992;24:218-224.  [PubMed]  [DOI]  [Cited in This Article: ]
18.  Maeta M, Koga S, Shimizu T, Matsui K. Possible association between gastrectomy and subsequent development of esophageal cancer. J Surg Oncol. 1990;44:20-24.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 10]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
19.  Lundegårdh G, Adami HO, Helmick C, Zack M. Risk of cancer following partial gastrectomy for benign ulcer disease. Br J Surg. 1994;81:1164-1167.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 20]  [Cited by in F6Publishing: 18]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
20.  Deshmane VH, Sharma S, Shinde SR, Vyas JJ. Functional results following esophagogastrectomy for carcinoma of the esophagus. J Surg Oncol. 1992;50:153-155.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
21.  Guo QX, Xu JH, Lin JQ, Zheng JF. Surgical Treatment of esoph-ageal carcinoma in patients who had had partial gastrectomy: a report of 30 cases. Zhongguo Zhongliu Linchuang. 1998;25:573-575.  [PubMed]  [DOI]  [Cited in This Article: ]
22.  Shu ZD, Guo XY, Tu YR, Li X, Lin M, Wang Y. Surgical Treatment of the esophageal carcinoma after subtotal gastrectomy: (report of 18 cases). Zhongguo Shiyong Waike Zazhi. 2000;20:159-160.  [PubMed]  [DOI]  [Cited in This Article: ]
23.  Xu M, Zhang SL, Zhou Y. Improving surgical mode for the carci-noma of mid-lower thoracic esophagus after gastrectomy. Zhonghua Xiongxinxueguan Waike Zazhi. 1998;14:265.  [PubMed]  [DOI]  [Cited in This Article: ]
24.  Wu XY, Zhang XH, Yin FZ, Lu HS, Guan GX. Clinical study of surgical treatment of esophageal cancer after gastrectomy. Zhongliu. 1998;18:158-160.  [PubMed]  [DOI]  [Cited in This Article: ]
25.  Chen J, Cheng KL, He YG. Treatment of esophageal cancer in post-subtotal gastrectomy with esophagogastrostomy. Linchuang Waike Zazhi. 1998;6:25-26.  [PubMed]  [DOI]  [Cited in This Article: ]
26.  Zhang YJ, Zhang L. Again Operation of esophageal and cardiac cancer after gastrectomy. Zhonghua Xiongxinxueguan Waike Zazhi. 1997;13:234-235.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Wang JS, Feng LG, Wang WD, Yang L. Again Operation for car-diac and esophageal carcinoma after gastrectomy. Tongji Yike Daxue Xuebao. 1994;23:420-422.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  Song QQ, Zeng L, Ge D, Chou DH. Surgical Treatment of esoph-ageal and cardiac cancer after gastrectomy. Shiyong Zhongliu Zazhi. 2001;16:132-133.  [PubMed]  [DOI]  [Cited in This Article: ]
29.  Huang HR, Huang Y. Surgical treatment for patients with esoph-ageal cancer after gastrectomy. Xinyixue. 2003;34:498-499.  [PubMed]  [DOI]  [Cited in This Article: ]
30.  Zhang DW, Cheng GY, Huang GJ, Zhang RG, Liu XY, Mao YS, Wang YG, Chen SJ, Zhang LZ, Wang LJ. Operable squamous esophageal cancer: current results from the East. World J Surg. 1994;18:347-354.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 51]  [Cited by in F6Publishing: 53]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
31.  Shao LF. [Long-term results of surgical resection of early esophageal and cardiac carcinomas]. Zhonghua Waike Zazhi. 1993;31:131-133.  [PubMed]  [DOI]  [Cited in This Article: ]
32.  Shao LF, Chen YH, Gao ZR, Wei GQ, Xu JL, Chen MY, Cheng JH. Surgical treatment of carcinoma of esophagus and gastric cardia: a 34-year Investigation. Chine Germ J Clinical Oncol. 2002;1:61-63.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 4]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
33.  Huang YT, Luo YG. Management of esophageal cancer: what progress has been made. Zhonghua Weichang Waike Zazhi. 2001;4:133-141.  [PubMed]  [DOI]  [Cited in This Article: ]