Esophageal Cancer Open Access
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jun 15, 2002; 8(3): 418-422
Published online Jun 15, 2002. doi: 10.3748/wjg.v8.i3.418
Field Population-based blocking treatment of esophageal epithelia dysplasia
Jun Hou, Zhi-Feng Chen, Yu-Tong He, Jian-Ping Duan, Deng-Gui Wen, Hebei Cancer Institute, and The Fourth Affiliated Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei Province, China
Pei-Zhong Lin, Zhen-Wei Ding, Li-Ping Guo, Cancer Institute, China Academy of Medical Science, Beijing 100021
Shao-Sheng Li, Fan-Shu Men, Chui-Yun Qiao, Chui-Lan Guo, Cixian Cancer Institute, Cixian County 056500, Hebei Province, China
Author contributions: All authors contributed equally to the work.
Supported by The National Eighth-Five-Year Scientific Championship Project No. 85-914-01-02
Correspondence to: Dr. Deng-Gui Wen, Hebei Cancer Institute, Jiankanglu 5, Shijiazhuang 050011, China. dengguiwen@hotmail.com
Telephone: +86-311-6033511 Fax:86-311-6077634
Received: December 20, 2001
Revised: January 15, 2002
Accepted: February 7, 2002
Published online: June 15, 2002

Abstract

AIM: To confirm the value of blocking treatment by zenshengping (ZSP), a Chinese herb composite, and Riboflavin for esophageal epithelia dysplasia cases screened out in high risk area in northern china by exfoliative balloon cytology (EBC), so to reduce the incidence rate of esophageal cancer (EC).

METHODS: Esophageal epithelium dysplasia cases including mind esophageal epithelium dysplasia (MEED), stage one severe esophageal epithelium dysplasia (SEED I), and stage two severe esophageal epithelium dysplasia (SEED II) were screened out from people aged 40 years and older in the high risk area of Chixian. These cases were randomly divided into a treatment and control group. Subjects in the treatment and control groups took ZSP, riboflavin, and placebo daily for three years. EC cases registered by cancer registry and identified by EBC re-screening in the treatment and control groups were used to calculate incidence and blocking rates to demonstrate the effects of blocking medication.

RESULTS: It was found that 31.92% and 24.15% of people aged 40 years and older in Cixian could been diagnosed as MEED and SEED cases. The severity of dysplasia increased with age. ZSP had blocked EC occurrence by 47.79% after 3 year medication among the SEED cases.

CONCLUSION: ZSP can block the development from SEED I and SEED II to EC by 47.79%. Efforts should be made to screen and treat dysplasia cases in people aged 40 years and older in high risk areas to reduce the mortality figures.




INTRODUCTION

The prognosis of esophageal and cardia cancer is the worst among digestive carcinomas because more than 90% of all its patients are clinically detected at advanced stages, and most of the patients can undergo only non-curative surgery due to either local tumor invasion 90% or more[4-16]. Because most EC and gastric patients have no apparent symptoms until the disease develops into advanced stages, early diagnosis at hospitals seems unrealistic presently, and early detection is undergone mostly among high risk populations in area with high incidence by means of exfoliative ballon cytology (EBC) and/or endoscopy[17-24].

Besides treatment of early ECs such as carcinoma in situ or intramucosal carcinoma, another promising strategy of secondary prevention is receiving great interest presently. A number of researchers have demonstrated that esophageal epithelium dysplasia (EED) is a precancerous lesion which can either develop further into a more severe stage or cancer, stay unchanged, or reverse back to normal again for a period of several years or even a decade. It is therefore very promising to detect patients with EED and treat the precancerous lesions before they transform into the irreversible malignant stage in high risk populations[25-31]. There are several techniques and chemicals or nutrients that have been reported to be effective in blocking precancerous lesions from transforming into cancer[32-42]. Linpeizhong reported that an herb composite named Zenshengpin (ZSP) had shown an inhibitory rate of 50% after three years of medication for SEED I and SEED II cases[25]. The present report came from "A Comprehensive Field Prevention and Treatment Study of Esophageal Cancer" carried out in the Chixian county of Hebei Province, which is adjacent to the Linxian county of Henan province, and also has the highest incidence rate of ECs in the world. This study was one of The National Eighth-Five-Year Scientific Championship Project. Its aim was to explore the feasibility of massive screening for EED patients among high risk people and to examine the long term effects of blocking treatment by ZSP and micronutrients in large samples of EED cases.

MATERIALS AND METHODS

Chixian is situated at 36°30" northern latitude, 114°40" eastern longitude, on the east side of the Taihang Mountain, along the Zhanghe River. Across the river to the south is the Anyang City of Henan province. Chixian county occupies an area about 951 square kilometers, and its population is 583611. There is a remarkable variation in the earth stratum of the county, with moutainous, hilly, and level land each constituting about one-third of its total area. The climate is influenced mainly by the warm mainland seasonal wind. The average temperature is 18-25 °C and the waterfall is 600-700 millimeters. The major soil there is brown and light colored weed earth. Farm products include wheat, corn, millet, rice, red potato, and beans. Iron ane coal are the main minerals, and coal is the main local fuel of the county.

The National Eighth-Five-Year Scientific Championship Project chose people aged 40 years and older in nine rural administrative units in the hilly part of Chixian County as the study population. The hilly part of the county has a higher incidence rate of EC than the plain part. The nine rural administrative units were further randomly divided into two districts; a treatment and a control district. The number of the study population was 122497. They resided in 101 villages. There was no significant difference in the sex and age distribution of the study population between the treatment and control districts. In preparation for a massive EBC screen of the study population to detect EC, near esophageal cancer (NEC), MEED, SEED I, and SEED II cases, a county wide conference was convened by the Chixian County government for local leaders and cancer prevention professionals from the three administrative levels including the county, the rural administration unit, and the villages. At the conference, special committees were set up on each of the three administration level to be responsible for the execution of the EBC massive screen in the areas under their authority. After the conference, a forceful propaganda campaign was carried out countywide to advertise the benefits of massive EBC screenings such as early detection, early treatment and satisfactory survival results. One day prior to the screening, personal contacts with potential examinees were made by local physicians to arrange details for the screening. At the beginning of the screening, physical examination was performed by physicians to exclude persons with serious contraindication to EBC examination, then EBC examination was performed by specialists. Four slides were prepared from specimens obtained by the procedure. The slides were afterwards examined by cytologists with no knowledge about the design of the study. Diagnosis was made according to the five grade cytology classification system including gradeInormal, grade II MEED, grade IIIa SEED I, grade IIIb SEED II, grade IV NEC, and grade V EC[28]. A diagnosis of cancer was made only after verification by at least three cytologists. Patients initially diagnosed with grade IIIa, grade IIIb, grade IV, and grade V were reexamined by electronic endoscopy with biopsy.

Finally, 16748 people of the study population in the two districts accepted EBC screening. MEED, SEED I, and SEED II patients screened out from the treatment district were pre-chosen as the treatment group; while those of the MEED, SEED I and SEED II cases detected from the control district were chosen to be the control group. There were 1566 cases of MEED and 1396 cases of SEED (including SEED I and SEED II) in the treatment group; and 3780 MEED and 2649 SEED cases in the control group. The MEED patients in the treatment group took 8 calcium tablets (CT) which were equivalent to 3 grams of caco3 and 5 milligrams of riboflavin. The SEED patients in the treatment group took 8 ZSP tablets daily. The MEED and SEED cases in the control group took 8 placebo tablets which were the same in color and size as ZSP and CT. The medication of ZSP, CT and placebo continued for three years. Half a year after initiation of the medication, EC cases diagnosed in the treatment and control groups were registered by a cancer registry constructed specifically for the study. At the end of the three year medication, EBC screening was re-initiated to identify EC cases in the treatment and control groups. EC cases registered by the registry and identified by the EBC re-screening were summarized to calculate the incidence rates for the treatment and control groups respectively.

RESULTS
Detection rates of MEED, SEED I, SEED II, NEC, and EC

As in Table 1, there were 179 cases of EC, 172 of NEC, 866 of SEED II, 3179 of SEED I, and 5346 of MEED as detected by the initial EBC screening from the 16, 748 high risk participants aged 40 years and older in the treatment and control districts. The detection rates of MEED, SEED I, SEED II, NEC, and EC were 31.92%, 18.98%, 5.17%, 1.03%, and 1.07% respectively. As the age increased by 5 year intervals, the detection rates of MEED, SEED I, SEED II, NEC, and EC all increased from the lowest for the 40-year-old group to the highest for the 60-year-old group, but the amount of increase in the detection rates with increase of age was not equal for MEED, SEED I, SEED II, NEC, and EC. The increase was the sharpest for EC and the lowest for MEED. An odds ratio (OR) defined as the ratio of the detection rates of the 60-year-old group against that of the 40-year-old group was 5.78 for EC, 2.56 for NEC, 1.80 for SEED II, 1.61 for SEED I, and only 1.18 for MEED.

Table 1 Age distribution of detection rates of MEED, SEED I, SEED II, NEC, and EC by EBC screening.
Histology GradeAge
Total
OR
40-
45-
50-
55-
60-
nRate%nRate%nRate%nRate%nRate%nRate%
Normal270350.50157843.83109439.1094535.5974630.09702141.920.60
MEED157429.40110031.7692833.1788233.2286234.77534631.921.18
SEED I82015.3262618.0855019.6657221.5461124.65317919.981.61
SEED II2083.891514.361665.931676.291747.028665.171.80
NEC280.52391.13291.04431.62331.331721.032.56
EC200.37290.84311.11461.73532.141791.075.78
Total5353346327892655247916748
EBC re-screening

EBC re-screening was carried out at the end of the three year medication period to detect EC patients among the MEED, SEED I, and SEED II cases in the treatment and control groups. Among the 4045 SEED cases, 77 EC cases had been diagnosed and registered before EBC re-screening (Table 2). With them excluded, there were 3968 SEED cases who should have been re-screened, and in the end 2976 (75.00%) were re-examined. The re-screening completion rate for the treatment and control groups of SEED was 78.4% and 74.2% respectively. As for the 5346 MEED cases, with the 76 EC cases already diagnosed and registered prior to re-screening excluded, 3775 (71.63%) were re-screened. The re-screening rates for the MEED treatment and control groups were 75.6% and 74% respectively.

Table 2 Effect of blocking treatment of MEED and SEED cases by ZSP, CT, and PLACEBO after three year medication.
GroupNo. subjectsEC Diagnosed
Incidence Rates (%)Block Rates (%)
EBC Re-screeningRegistrationTotal
MEETreatment15661018281.79
Control37802658842.22
Total534636761122.1019.37
SEEDTreatment13961711282.01
Control364936661023.85
Total404553771303.2147.79
Registered EC cases and incidence rates

From half a year after initiation of ZSP and CT medication to the time of re-screening, 77 cases of EC were diagnosed and registered among the 4045 SEED cases (Table 2). The three-year incidence rate by registered EC cases alone for all of the SEED cases was 1.90% (77/4045), and for SEED in the treatment and control groups were 0.78% (11/1396) and 2.49% (66/2649) respectively. A significant difference existed between the incidence rates of the two groups (χ2 = 14.21, P < 0.01). For the 5346 MEED cases, 76 EC patients were registered. The three year incidence rate for all of the MEED cases was 1.42% (76/5346), and was 1.14% (18/1566) and 1.54% (58/3780) for MEED in the treatment and control groups respectively. There was no significant difference between the incidence rates of the two groups (χ2 = 1.17, P > 0.05).

Re-screened EC cases and prevalence rates

By EBC re-screening, 53 EC cases were detected from the 2976 SEED cases. The prevalence rate was 1.78% (53/2976) for all of the SEED cases combined, and was 1.61% (17/1054) and 1.87% (36/1922) for SEED cases in the treatment and control groups respectively. There was no significant difference between the prevalence rates of the two groups (χ2 = 0.26, P > 0.05). Among the 3775 MEED cases, 36 EC cases were diagnosed by EBC re-screening, with a prevalence rate of 0.95% (36/3775) for the MEED combined, 0.89% (10/1114) for the treatment group, and 0.97% (26/2661) for the control group. There was no significant difference in the prevalence rates between the two groups (χ2 = 0.15, P > 0.05).

Combined incidence and blocking rates

During the first three year follow-up, 242 diagnoses of EC were made by registration and re-screening from the 9, 391 SEED and MEED cases, yielding a total incidence rate of 2.58% (242/9391) for SEED and MEED combined, 1.89% (56/2962) for the treatment group, and 2.89% (186/6429) for the control group. A significant difference existed between the two groups (χ2 = 8.12, P < 0.01). A blocking rate of 34.60% calculated as (2.89%-1.89%)/2.89% × 100% was obtained to assess the effects of a three year period of medication by ZSP and CT.

As in Table 2, 112 EC cases were accumulated by three year registration and EBC-re-screening from the 5346 MEED cases (76 registered and 36 screened out). An incidence rate of 2.10% (112/5346) was calculated for the whole MEED group, 1.79% (28/1566) for MEED in the treatment group, and 2.22% (84/3780) for MEED in the control group. The difference between the incidence rates of the two groups did not reach a significant level (χ2 = 1.02, P > 0.05), and a blocking rate of 19.37% was calculated to demonstrate the effect of CT for MEED cases.

130 EC cases were diagnosed from the 4045 SEED cases by three year registration and EBC re-screening (77 registered and 53 re-screened out). The incidence rate was 3.21% for all of the SEED cases, 2.01% (28/1396) for SEED in the treatment, and 3.85% (102/2649) for SEED in the control group. The difference between the incidence rates of the two groups reached a significant level (χ2 = 10.00, P < 0.01), and the blocking rate by ZSP for SEED was 47.79%.

Incidence and blocking rates of EC for SEED I and SEED II

As in Table 3, 69 EC diagnoses were made during the three year study period among the 3179 SEED I cases. The incidence rate was 2.17% (69/3179) for all of the SEED I cases, 1.66% (20/1206) for SEED I in the treatment group, and 2.48% (49/1973) for SEED I in the control group. There was no significant difference between the incidence rates of the treatment and control group (χ2 = 2.40, P > 0.05), and the corresponding blocking rate was 33.06%.

Table 3 Results of blocking treatment of SEED I and SEED II cases by ZSP and PLACEBO after three years of medication.
GroupNo. subjectsNo. EC DiagnosedIncidence Rates (%)Block Rates (%)
SEED ITreatment1206201.66
Control1973492.48
Total3179692.1733.06
SEED IITreatment27982.87
Control587539.03
Total866617.0468.22

There were 61 EC cases diagnosed from the 866 SEED II cases during the same period, yielding an incidence rate of 7.04% (61/866) for all of the SEED II, 2.87% (8/279) for SEED II in the treatment group, and 9.03% (53/587) for SEED II in the control group. A significant difference was observed between the two incidence rates of the two groups (χ2 = 10.00, P < 0.01), and the blocking rate of ZSP for SEED II was 68.22%.

DISCUSSION

Dysplasia is an atypical state of the epithelium with a basophilic matrix, a high matrix-core ratio, and hyperheterochromatin. It is historically classified into three grades according to the degree of atypical epithelium in comparision with the basal zone as defined by the World Health Organization’s International Histological Classification of Tumors[43]. Atypical cells localized in the basal zone in MEED, while immature cells occupy more than three quadrants of the epithelium in SEED I and SEED II.

In this study, we found that 31.92% and 24.15% of people aged 40 years and older in Chixian could been diagnosed as MEED and SEED cases. Qiu and Yang[44] have reported a similar dysplasia rate of 32.28% in people aged 21 years and older in Linxian, which is a neighboring County to Chixian County situated in the same Taihang Mountain area in northern China where there is the highest incidence of EC. However, the rate of dysplasia in low risk regions was only 4.78%, most of the dysplasia belonged to MEED, and the frequency of dysplasia correlated well with the regional level of ECs.

The severity of dysplasia increased with age. As in Table 1, as patients got older, their chances of being detected as one of the dysplasia states grew higher. This was true with MEED, SEED I, and SEED II. Moreover, the extent of increase in detection rates with age was small for MEED, large for SEED I, and still larger for SEED II. The Odds Ratios of the detection rates of the 60-year-old group versus that of the 40-year-old group for MEED, SEED I and SEED II were 1.18, 1.61, and 1.80 respectively. This increase with age is remarkably similar to the increase of incidence or mortality of EC with age[46-50], but the degree of the latter was much greater. As in Table 1, the Odds Ratio of detection rates of 60-year-olds against that of 40-year-olds grew up to 2.56 and 5.78 for NEC and EC. It may be suggested that the increase of dysplasia rates with age was small and unstable or reversible for the less severe states such as MEED, but became fixed and remarkably large as the dysplasia progressed into more severe stages or transformed into NEC and EC.

While the chances of dysplasia increased with age, the total detection rates for MEED, SEED I and SEED IIdecreased from 31.92%, 18.98% to 5.17% in the direction of dysplasia development. It may suggest that although dysplasia may proceed further, only a limited portion proceeds into more severe or malignant.

Our finding and discussion so far support the notion that dysplasia belongs to a early form of carcinoma. The main difference between dysplasia and EC may be that dysplasia is an unstable or unfixed state of existence. It may develop further, but much of it will stay unchanged, or even return to normal or less severe again. Therefore, if we could detect and treat precancerous dysplasia lesions before they develop into carcinomas, then the long-term survival of ECs should dramatically improve.

The present study has focused primarily on the blocking treatment of dysplasia cases in high risk populations. The result was that ZSP blocked EC incidence rate by 47.79% after 3 years of medication for the SEED cases. In a previous National Seventh Five Research Project carried out in Linxian County, Lin found that ZSP reduced the EC transformation rate of SEED cases by 52.2% after 3 year medication[24]. These consistent findings by a series of population-based prospective cohort studies in the same high risk area enabled us to conclude that EC is preventable on the secondary blocking treatment level, and ZSP is an effective agent to treat precancerous EC lesions in high risk areas[51-53].

Experimental observations indicate that cancer preventive chemical agents take effect by acting on the promotion stage[25]. The anti-carcinogenicity of certain Chinese herbs is considered to share the same mechanism. In this study, the significant blocking rate of 47.79% by ZSP for the SEED cases resulted mainly from the difference in the registered incidence of EC between the treatment and control groups, as there was no significant difference in the re-screened EC incidence rates between the two groups. As we know, registered EC represents clinically diagnosed late-staged EC, while EC screened out by EBC belonged to the early asymptomatic patients. The finding that ZSP reduced only the registered three year incidence rate, but not the EBC re-screened incidence rate of EC suggests that ZSP may have blocked or delayed the appearance of clinically recognizable EC developed from SEED. In other words, ZSP acted mainly on the late stage of EC development. As in Table 3, the more remarkable blocking rate by ZSP for SEED II versus SEED I (68.22% versus 33.06%) also supports the idea that ZSP was effective in blocking or delaying the appearance of EC during the late stages of EC development.

In a previous comprehensive field prevention and treatment study of esophageal cancer carried out in Linxian county, Lin found that Riboflavin had no significant effect on MEED cases at the end of three years of medication, but a blocking rate of 37.0% appeared at the end of 9 year follow up[24,25]. The result at the end of a three year medication period was the same as in the present study. Further findings will be reported by continuous observation.

In conclusion, we regard dysplasia as a precancerous lesion in people aged 40 years and older in high risk areas. Efforts should be made to screen and treat dysplasia cases before the disease transforms into the irreversible malignant state. Effective screening plus blocking treatment in high risk populations may reduce the mortality rate of EC over the long term. ZSP has been made from natural Chinese herbs which are cheap and share rich resources. Repeated demonstration of its ability will make it a promising agent for secondary prevention of EC.

Footnotes

Edited by Pagliarini R

References
1.  Chen KN, Xu GW. Diagnosis and treatment of esophageal cancer. Shijie Huaren Xiaohua Zazhi. 2000;8:196-202.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Liu HF, Liu WW, Fang DC. Study of the relationship between apoptosis and proliferation in gastric carcinoma and its precancerous lesion. Shijie Huaren Xiaohua Zazhi. 1999;7:649-651.  [PubMed]  [DOI]  [Cited in This Article: ]
3.  Sherman JrCD. Digestive carcinomas. Manual of clinical oncology 5. Beijing: The joint publishing house of Beijing Medical University and China Union Medical University 1992; 237-38.  [PubMed]  [DOI]  [Cited in This Article: ]
4.  Urba SG, Orringer MB, Perez-Tamayo C, Bromberg J, Forastiere A. Concurrent preoperative chemotherapy and radiation therapy in localized esophageal adenocarcinoma. Cancer. 1992;69:285-291.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 2]  [Reference Citation Analysis (0)]
5.  China Ministry Of Public Health, ed ; China Ministry Of Public Health. Esophageal cancer. Diagnosis and treatment criteria for common malignances in China 2. Beijing: The joint publishing house of Beijing Medical University and China Saint Medical University 1991; 30-31.  [PubMed]  [DOI]  [Cited in This Article: ]
6.  Wolfe WG, Vaughn AL, Seigler HF, Hathorn JW, Leopold KA, Duhaylongsod FG. Survival of patients with carcinoma of the esophagus treated with combined-modality therapy. J Thorac Cardiovasc Surg. 1993;105:749-55; discussion 755-6.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Wang ZQ, He J, Chen W, Chen Y, Zhou TS, Lin YC. Relationship between different sources of drinking water, water quality improvement and gastric cancer mortality in Changle County-A retrospective-cohort study in high incidence area. World J Gastroenterol. 1998;4:45-47.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Sun JJ, Zhou XD, Zhou G, Liu YK. Expression of intercellular adhesive molecule-1 in liver cancer tissues andliver cancer metastasis. World J Gastroenterol. 1998;4:202-205.  [PubMed]  [DOI]  [Cited in This Article: ]
9.  Yoneda M. Regulation of hepatic function by brain neuropeptides. World J Gastroenterol. 1998;4:192-196.  [PubMed]  [DOI]  [Cited in This Article: ]
10.  Yu JY, Wang LP, Meng YH, Hu M, Wang JL, Bordi C. Classification of gastric neuroendocrine tumors and its clinicopathologic significance. World J Gastroenterol. 1998;4:158-161.  [PubMed]  [DOI]  [Cited in This Article: ]
11.  Deng LY, Zhang YH, Xu P, Yang SM, Yuan XB. Expression of IL 1betaconverting enzyme in 5-FU induced apoptosis in esophageal carcinoma cells. World J Gastroenterol. 1999;5:50-52.  [PubMed]  [DOI]  [Cited in This Article: ]
12.  Xiao B, Jing B, Zhang YL, Zhou DY, Zhang WD. Tumor growth inhibition effect of hIL-6 on colon cancer cells transfected with the target gene by retroviral vector. World J Gastroenterol. 2000;6:89-92.  [PubMed]  [DOI]  [Cited in This Article: ]
13.  Qian SB, Chen SS. Transduction of human hepatocellular carcinoma cells with human alpha-interferon gene via retroviral vector. World J Gastroenterol. 1998;4:210-213.  [PubMed]  [DOI]  [Cited in This Article: ]
14.  Shen ZY, Xu LY, Li EM, Cai WJ, Chen MH, Shen J, Zeng Y. Telomere and telomerase in the initial stage of immortalization of esophageal epithelial cell. World J Gastroenterol. 2002;8:357-362.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Cao WX, Ou JM, Fei XF, Zhu ZG, Yin HR, Yan M, Lin YZ. Methionine-dependence and combination chemotherapy on human gastric cancer cells in vitro. World J Gastroenterol. 2002;8:230-232.  [PubMed]  [DOI]  [Cited in This Article: ]
16.  Wu K, Zhao Y, Liu BH, Li Y, Liu F, Guo J, Yu WP. RRR-alpha-tocopheryl succinate inhibits human gastric cancer SGC-7901 cell growth by inducing apoptosis and DNA synthesis arrest. World J Gastroenterol. 2002;8:26-30.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Ma LS. Intensify improvement of the diagnosis and treatment level of digestive system diseases in China. World J Gastroenterol. 1998;4:287-293.  [PubMed]  [DOI]  [Cited in This Article: ]
18.  Gu QL, Li NL, Zhu ZG, Yin HR, Lin YZ. A study on arsenic trioxide inducing in vitro apoptosis of gastric cancer cell lines. World J Gastroenterol. 2000;6:435-437.  [PubMed]  [DOI]  [Cited in This Article: ]
19.  Zou SC, Qiu HS, Zhang CW, Tao HQ. A clinical and long-term follow-up study of peri-operative sequential triple therapy for gastric cancer. World J Gastroenterol. 2000;6:284-286.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Chen GR, Jiang XL, Wang YP. Endoscopic treatment skill on sub-mucosal benign tumors. Dia Treat Dig Dis. 2001;1:43-45.  [PubMed]  [DOI]  [Cited in This Article: ]
21.  Zhang XY. Some recent works on diagnosis and treatment of gastric cancer. World J Gastroenterol. 1999;5:1-3.  [PubMed]  [DOI]  [Cited in This Article: ]
22.  Qiao GB, Han CL, Jiang RC, Sun CS, Wang Y, Wang YJ. Overexpression of P53 and its risk factors in esophageal cancer in urban areas of Xi'an. World J Gastroenterol. 1998;4:57-60.  [PubMed]  [DOI]  [Cited in This Article: ]
23.  Chai L, Yu SZ. Gastric cancer molecular epidemiology in Fujian Changle. Shijie Huaren Xiaohua Zazhi. 1999;7:652-655.  [PubMed]  [DOI]  [Cited in This Article: ]
24.  Lin PZ, Chen ZF, Hou J, Liu TG, Wang JX, Ding ZW, Guo LP, Li SS, Men FS, Du CL. Chemical prevention of esophageal cancer. Zhongguo Yixue Keixue Yuan Xuebao. 1998;20:413-417.  [PubMed]  [DOI]  [Cited in This Article: ]
25.  Lin P. [Medicamentous inhibitory therapy of precancerous lesions of the esophagus--3 and 5 year inhibitory effect of antitumor B, retinamide and riboflavin]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1990;12:235-245.  [PubMed]  [DOI]  [Cited in This Article: ]
26.  Shen Q, Wang DL, Xiang YY, Wang C, Ren ZC, Yan AH, Ren XH, Chang FJ, Zhang JM, Ye XJ. A preliminary report of nutritional intervention in dysplasia of the esophagus. Zhongguo Zhongliu Lichuang. 1991;18:31-35.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Hou J, Yuan FR, Li SS, Li ZY, Chen ZF. A clinical study on the treatment results of esophageal dysplasia by composite Dangsheng pill. Zhongguo Yixue Xuebao. 1992;7:11-13.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  Kitamura K, Kuwano H, Yasuda M, Sonoda K, Sumiyoshi K, Tsutsui S, Kitamura M, Sugimachi K. What is the earliest malignant lesion in the esophagus? Cancer. 1996;77:1614-1619.  [PubMed]  [DOI]  [Cited in This Article: ]
29.  Harry XH. Association between Helicobacter pylori and gastric cancer: current knowledge and future research. World J Gastroenterol. 1998;4:93-96.  [PubMed]  [DOI]  [Cited in This Article: ]
30.  Xue JT, Wu J, Meng L, Dong ZW, Shou CC. Expression of VEGF(121) in gastric carcinoma MGC803 cell line. World J Gastroenterol. 2000;6:281-283.  [PubMed]  [DOI]  [Cited in This Article: ]
31.  Assy N, Paizi M, Gaitini D, Baruch Y, Spira G. Clinical implication of VEGF serum levels in cirrhotic patients with or without portal hypertension. World J Gastroenterol. 1999;5:296-300.  [PubMed]  [DOI]  [Cited in This Article: ]
32.  Xiao ZF, Yang ZY, Zhou ZM, Yin WB, Gu XZ. Radiotherapy of double primary esophageal carcinoma. World J Gastroenterol. 2000;6:145-146.  [PubMed]  [DOI]  [Cited in This Article: ]
33.  Xiao B, Shi YQ, Zhao YQ, You H, Wang ZY, Liu XL, Yin F, Qiao TD, Fan DM. Transduction of Fas gene or Bcl-2 antisense RNA sensitizes cultured drug resistant gastric cancer cells to chemotherapeutic drugs. World J Gastroenterol. 1998;4:421-425.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Zhang QX, Dou YL, Shi XY, Ding Y. Expression of somatostatin mRNA in various differentiated types of gastric carcinoma. World J Gastroenterol. 1998;4:48-51.  [PubMed]  [DOI]  [Cited in This Article: ]
35.  Hou J, Chen ZF, Li SS, Li ZY, Yan HR. Clinical study on treatment of esophageal precancerous lesion with CangdouwanPill. Zhongguo Zonglun Lingchuang. 1996;23:117-119.  [PubMed]  [DOI]  [Cited in This Article: ]
36.  Wu QM, Li SB, Wang Q, Wang DH, Li XB, Liu CZ. The expression of COX-2 in esophageal carcinoma and its relation toclinicopathologic characteristic. Shijie Huaren Xiaohua Zazhi. 2001;9:11-14.  [PubMed]  [DOI]  [Cited in This Article: ]
37.  Hou J, Yan FR. [Treatment of esophageal precancerous lesion with cang dou pill]. Zhongguo Zhong Xi Yi Jie He Za Zhi. 1992;12:604-66, 604-66.  [PubMed]  [DOI]  [Cited in This Article: ]
38.  Abe M, Takahashi M. Intraoperative radiotherapy: the Japanese experience. Int J Radiat Oncol Biol Phys. 1981;7:863-868.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 215]  [Cited by in F6Publishing: 221]  [Article Influence: 5.1]  [Reference Citation Analysis (0)]
39.  Swisher SG, Hunt KK, Holmes EC, Zinner MJ, McFadden DW. Changes in the surgical management of esophageal cancer from 1970 to 1993. Am J Surg. 1995;169:609-614.  [PubMed]  [DOI]  [Cited in This Article: ]
40.  Tao DM, Xu YZ, Wang XH, Gu YK, Wang DY, Wang TX. Follow up of 417 cases of severe esophageal dysplasia. Henan Zhongliuxue Zhazi. 1997;10:38-43.  [PubMed]  [DOI]  [Cited in This Article: ]
41.  Li JY, Blot , LI B, Tailor , Guo WD, Wang W, Liu PQ, Zhen SF, Yang ZS, Liu FS. Preliminary reports of population-based nutritional preventive experiment of cancer and other common diseases. Zhonghua Zhongliu Zhazi. 1993;15:165-181.  [PubMed]  [DOI]  [Cited in This Article: ]
42.  Semba S, Yokozaki H, Yamamoto S, Yasui W, Tahara E. Microsatellite instability in precancerous lesions and adenocarcinomas of the stomach. Cancer. 1996;77:1620-1627.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 11]  [Reference Citation Analysis (0)]
43.  Correa P. Precursors of gastric and esophageal cancer. Cancer. 1982;50:2554-2565.  [PubMed]  [DOI]  [Cited in This Article: ]
44.  Qiu SL, Yang GR. Precursor lesions of esophageal cancer in high-risk populations in Henan Province, China. Cancer. 1988;62:551-557.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 6]  [Reference Citation Analysis (0)]
45.  Mimori K, Mori M, Tanaka S, Akiyoshi T, Sugimachi K. The overexpression of elongation factor 1 gamma mRNA in gastric carcinoma. Cancer. 1995;75:1446-1449.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 6]  [Reference Citation Analysis (0)]
46.  Forastiere AA, Orringer MB, Perez-Tamayo C, Urba SG, Husted S, Takasugi BJ, Zahurak M. Concurrent chemotherapy and radiation therapy followed by transhiatal esophagectomy for local-regional cancer of the esophagus. J Clin Oncol. 1990;8:119-127.  [PubMed]  [DOI]  [Cited in This Article: ]
47.  Cao GH, Yan SM, Yuan ZK, Wu L, Liu YF. A study of the relationship between trace element Mo and gastric cancer. World J Gastroenterol. 1998;4:55-56.  [PubMed]  [DOI]  [Cited in This Article: ]
48.  Jiang YF, Yang ZH, Hu JQ. Recurrence or metastasis of HCC: predictors, early detection and experimental antiangiogenic therapy. World J Gastroenterol. 2000;6:61-65.  [PubMed]  [DOI]  [Cited in This Article: ]
49.  Qiao YL, Hou J, Yang L, He YT, Liu YY, Li LD, Li SS, Lian SY, Dong ZW. [The trends and preventive strategies of esophageal cancer in high-risk areas of Taihang Mountains, China]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2001;23:10-14.  [PubMed]  [DOI]  [Cited in This Article: ]
50.  Inoue H, Takeshita K, Hori H, Muraoka Y, Yoneshima H, Endo M. Endoscopic mucosal resection with a cap-fitted panendoscope for esophagus, stomach, and colon mucosal lesions. Gastrointest Endosc. 1993;39:58-62.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 412]  [Cited by in F6Publishing: 355]  [Article Influence: 11.5]  [Reference Citation Analysis (0)]
51.  Dong ZW, Tang PZ, Li LD. Control strategy in high risk area of esophageal cancer in China. Zhongguo Zhongliu. 2000;9:71-73.  [PubMed]  [DOI]  [Cited in This Article: ]
52.  Shen Q, Zhen HZ, Cai XS, Chen HM, Zhang JQ, Wang DL, Xiang YY, Chang YF, Luo DS, Wang C. Compound riboflavin used in nutritional intervention of esophageal dysplasia-A long-term study. Henan Zhongliuxue Zhazi. 1991;4:1-5.  [PubMed]  [DOI]  [Cited in This Article: ]
53.  Ding ZW, Gao F, Lin PZ, Wang JX, Guo LP. Long term effect of block treatment for esophageal dysplasia cases. Zhonghua Zhongliu Zhazi. 1999;21:275-277.  [PubMed]  [DOI]  [Cited in This Article: ]