- Research article
- Open Access
- Open Peer Review
Long term follow up and retrospective study on 533 gastric cancer cases
© Zeng et al.; licensee BioMed Central Ltd. 2014
- Received: 2 December 2012
- Accepted: 8 May 2014
- Published: 16 May 2014
Gastric cancer (GC) is the third leading cause of cancer death in China and the outcome of GC patients is poor. The aim of the research is to study the prognostic factors of gastric cancer patients who had curative intent or palliative resection, completed clinical database and follow-up.
This retrospective study analyzed 533 GC patients from three tertiary referral teaching hospitals from January 2004 to December 2010 who had curative intent or palliative resection, complete clinical database and follow-up information. The GC-specific overall survival (OS) status was determined by the Kaplan-Meier method, and univariate analysis was conducted to identify possible factors for survival. Multivariate analysis using the Cox proportional hazard model and a forward regression procedure was conducted to define independent prognostic factors.
By the last follow-up, the median follow-up time of 533 GC patients was 38.6 mo (range 6.9-100.9 mo), and the median GC-specific OS was 25.3 mo (95% CI: 23.1-27.4 mo). The estimated 1-, 2-, 3- and 5-year GC-specific OS rates were 78.4%, 61.4%, 53.3% and 48.4%, respectively. Univariate analysis identified the following prognostic factors: hospital, age, gender, cancer site, surgery type, resection type, other organ resection, HIPEC, LN status, tumor invasion, distant metastases, TNM stage, postoperative SAE, systemic chemotherapy and IP chemotherapy. In multivariate analysis, seven factors were identified as independent prognostic factors for long term survival, including resection type, HIPEC, LN status, tumor invasion, distant metastases, postoperative SAE and systemic chemotherapy.
Resection type, HIPEC, postoperative SAE and systemic chemotherapy are four independent prognostic factors that could be intervened for GC patients for improving survival.
- Gastric cancer
- GC-specific overall survival
- Multivariate analysis
- Clinical pathological factors
Gastric cancer (GC) remains the second leading cause of cancer death worldwide, accounting for 8% of the total cases and 10% of total deaths in 2008. In China, GC is the third leading cause of cancer death and the outcome of GC patients is poor, especially for patients at advanced stage, and the 5-year survival rate is less than 20%-25%.
Early diagnosis and early treatment remain the best strategy for GC. In China, however, a majority of GC patients are not early cancer by the time when they seek medical attention[5, 6]. Therefore, surgery-based multidisciplinary treatment approach is warranted in order to improve both overall survival (OS) and the quality of life.
Despite this common-sense knowledge, there is no commonly accepted multidisciplinary treatment strategy in China, primarily due to the lack of large database information reflecting the clinical reality of the current treatment situation.
In our previous studies on GC patients, we evaluated the common tumor markers for the diagnosis of gastric cancer. In these relatively large cohort studies, stage III and beyond patients accounted for over 65% of the entire patient population[6, 7], a result similar to other reports from China[5, 8]. For these patients, GC is no longer a local disease, but at least a regional or a systemic disease.
Currently, surgery remains the most effective therapy for GC, offering an excellent chance (90%) of a cure for early GC patients. Surgical procedures have a big impact on OS and recurrence. R0 resection with D2 lymphadenectomy is regarded as the standard surgical technique[11, 12], as D2 lymphadenectomy had lower recurrence and GC-related death rates. However, for stage III and beyond patients, the currently adopted surgical procedure only removes local tumor mass but often neglects the micro-metastases. Therefore, additional adjuvant therapies are required to ensure better treatment efficacy.
Over the past years, our database has grown bigger and more detailed information on major clinico-pathological characteristics has been accumulated. Therefore, we conducted this comprehensive analysis of the data collected from three major teaching hospitals in Central China, so as to gain deeper insights to the major features of GC in central China and to identify independent factors for prognosis that could be intervened.
All patients provided written informed consent for their information to be stored in the hospital database; and we obtained separate consent for research. Study approval was obtained from independent ethics committees from Zhongnan Hospital of Wuhan University. The study was undertaken in accordance with the ethical standards of the World Medical Association Declaration of Helsinki.
This study included a total of 533 GC patients from three tertiary referral hospitals, from January 2004 to December 2010. These patients underwent resection with curative intent (D2 lymphadenectomy) or palliative resection. All the detailed clinic-pathological information was available, including demographic variables, underlying co-morbidities, surgical modality, lab and image study information, pathological reports, pre- and post-operative therapies, and follow-up information. Pathological information was mainly focused on tumor type, pathological grading, TNM stages, blood vessel or neural invasions. The pathologic staging was based on the 7th edition of AJCC staging criteria. Postoperative treatments were focused on chemotherapy regimens and cycles, and radiotherapy if applicable. GC patients with T2 or higher, any N tumors should receive systemic chemotherapy except patients who declined the offer. Hyperthermic intraperitoneal chemotherapy (HIPEC) and intraperitoneal chemotherapy (IP chemotherapy) were adjuvant chemotherapy, and only those who had peritoneal carcinomatosis (PC) should receive. In our study, the systemic chemotherapy administered were mainly FOLFOX4 and FOLFOX6, HIPEC were mainly using lobaplatin and paclitaxel, and IP chemotherapy were docetaxel and carboplatin.
These patients were followed-up every 3 months during the first 2 years after operation, every 6 months on the third postoperative year and every year thereafter. All the follow-up information was incorporated into a standardized database.
The above-mentioned information was incorporated into a central database, set up at the Zhongnan Hospital of Wuhan University, which undergoes regular updating every 3 months.
All eligibility cases from the central database were analyzed by SPSS 17.0 statistical package software (SPSS Inc., Chicago, IL, USA). The variables were hospital (Zhongnan Hospital, Heji Hospital or Hubei Tumor Hospital), gender (male or female), age (≤65 yr or > 65 yr), cancer site (upper third [excluding squamous cell carcinoma at gastroesophageal junction], middle third, lower third or whole stomach), pathological type (well or intermediately differentiated adenocarcinoma, poorly differentiated or undifferentiated carcinoma, signet ring cell carcinoma or mucious adenocarcinoma or others), surgery type (proximal gastrectomy, distal gastrectomy or total gastrectomy), resection type (for stomach itself) (palliative resection or curative resection), other organ resection (mainly included liver, spleen, intestines, ovarian, ovarian ducts) (0, 1, 2 or ≥ 3), HIPEC (yes or no), lymph node status (LN status) (N0, N1, N2 or N3), tumor invasion (T1, T2, T3, T4a or T4b), distant metastasis (M0 or M1), pathological stage (I, II, IIIA, IIIB, IIIC or IV), postoperative serious adverse event (postoperative SAE) (defined as life threatening events after operation, including gastrointestinal obstruction, anastomotic leakage, and bleeding leading to grade 3 and above anemia, abdominal abscess) (yes or no), systemic chemotherapy (0, 1 to 6 cycles or > 6 cycles), IP chemotherapy (yes or no), GC-specific overall survival (GC-specific OS, defined as the time interval from first treatment to GC-specific death, with the last follow-up time on May 31, 2012).
The numerical data was analyzed directly. The category data was converted when necessary. The Kaplan-Meier survival curve was used to study the survival status, using log rank test to decipher the statistical significance, which was judged as P < 0.05 throughout this study.
To work out independent factors for survival, a Cox proportional hazard model was used to first obtain the possible factors and then used forward regression procedure to finally identify the independent factors.
Characteristics of the patients
Characteristics of the 533 GC patients enrolled into this study
Total n (%)
Events n (%)
Median GC-specific OS (95% CI) (mo)
Signet ring/mucious Ca
Other organ resection (n)
Systemic chemotherapy (cycles)
1 to 6
Univariate survival analysis
In this study, all variables were analyzed by Kaplan-Meier curve and log-rank test. Among these variables, pathological type had no statistically significant impact on GC-specific OS (P = 0.212), but statistically significant factors were hospital (P = 0.008), age (P < 0.001), gender (P = 0.019), cancer site (P = 0.004), surgery type (P < 0.001), resection type (P < 0.001), other organ resection (P < 0.001), HIPEC (P < 0.001), LN status (P < 0.001), tumor invasion (P < 0.001), distant metastases (P < 0.001), TNM stage (P < 0.001), postoperative SAE (P < 0.001), systemic chemotherapy (P = 0.001), and IP chemotherapy (P = 0.003) (Table 1).
Multivariate survival analysis
Independent prognostic factors of 533 GC patients identified by multivariate analysis
Several important points should be considered from this study. First, a majority of GC patients are at advanced clinical stage. In our series of 533 patients, 354 cases (66.4%) were clinically stage III and beyond. For these patients, GC is no longer a local disease, but at least a regional or a systemic disease. Although surgery could remove the bulky tumor mass itself, it may leave some unseen cancer cells in the operating field. Therefore, more intensive adjuvant chemotherapy should be followed in order to eradicate these left-over cancer cells. Two large scale randomized clinical trials have already demonstrated the superiority of this approach over conventional surgery alone[17, 18]. Another reasonable approach is to start perioperative chemotherapy, to down-stage the tumor, followed by curative resection. It has been proven that such a treat modality indeed could improve the clinical outcomes of GC patients.
Secondly, our analysis found that over 40% of GC death occurred in the first year after operation, and another 30% plus of GC death occurred during the second year after operation[20–22]. Therefore, it is clinically important to design rational strategies to address these problems. One key consideration is that high risk factors should be investigated and identified, so as to reduce them and reduce the death risk. Another strategy is to design a close follow-up plan and strictly implement it, so as to identify those patients with early signs of recurrence and apply appropriate therapies. Among the currently used methods, serum tumor markers study and medical imaging studies are most widely used approaches. Regular monitoring blood tumor markers carcinoembryonic antigen (CEA) and carboxyl antigen 19–9 (CA19-9) could help provide warning information on cancer recurrence.
Various clinicopathological factors have been reported to impact on GC-specific OS, such as age, gender, cancer site, surgery type, resection type, other organ resection, HIPEC, LN status, tumor invasion, distant metastases, TNM stage, postoperative SAE, systemic chemotherapy and IP chemotherapy[5, 7, 8, 20, 24–28]. These results are in accordance with our study. In our study, pathological type had no impact on GC-specific OS, which is not in conformity with several previous studies that concluded that pathological type was an important factor for prognosis and survival of GC[5, 24], but is in agreement with some other studies that reported that pathological type had no influence on GC-specific OS[7, 27]. This could be due to the different typing method used. It has been documented that Lauren histological classification is a simple and practical typing method to have significant correlation with survival of GC. Clinicalpathological information of this study was obtained from hospital department of pathology, and they did not adopt Lauren classification. In future studies, we should adopt this classification.
For cancer patients, the clinical outcomes depend on several important factors, which could be divided into those that cannot be intervened such as TNM stage, and those can be intervened such as treatment models. After the Cox proportional hazard model analysis, we worked out seven independent factors that had significant impact on survival, six of these seven factors have already been well recognized as the most important determinants of patients’ survival[5, 7, 8, 29]. What deserves special attention is the finding that HIPEC is also an independent factor for improved survival. Several phases I to III studies have already demonstrated the treatment advantage of HIPEC. Glehen et al. consecutively treated 49 advanced GC patients with HIPEC, which resulted in 10.3 months of GC-specific OS, against 6.1 months of GC-specific OS treated with only standard curative resection. In another study by Yonemura et al., 107 GC patients also treated with HIPEC, and the GC-specific OS was 11.5 months. More importantly, a recent phase III prospective randomized clinical trial also confirmed the survival advantage of 11.0 months in the HIPEC group against 6.5 months in the CRS group. In addition, a systematic review and meta-analysis of 13 acceptable qualities randomized controlled trials also have established that HIPEC has significant survival advantage over the currently standard treatment for advanced GC. Taken together, all these facts confirm the value of HIPEC for the treatment of stage III and beyond GC patients. In this study, the median survival of patients with HIPEC was 13.4 mo (95% CI: 9.6-17.2), which was shorter than others without HIPEC (39.7 mo [95% CI: 32.4-47.0]). It was due to patients with HIPEC were gastric cancer with metastasis and prognosis was not optimistic. However, the median survival of patients with HIPEC was longer than patients with metastasis (13.4 mo vs 10.6 mo, P < 0.05). It supports HIPEC has significant survival advantage even though there could be selection bias in this regard, due to the limited number of patients treated by HIPEC.
Postoperative SAE included gastrointestinal obstruction, anastomotic leakage, and bleeding leading to grade 3 and above anemia, abdominal abscess. All these have been confirmed to have a significant negative impact on GC-specific OS. In the study of Sierzega et al., the median OS of patients with anastomotic leakage was significantly lower than patients with non-anastomotic leakage (4.1 mo vs. 23 mo, P < 0.001), and the progression-free survival of patients with anastomotic leakage was also significantly shorter than patients with non-anastomotic leakage (11 mo vs. 19 mo, P = 0.021). In another study by Yoo et al., the mean OS of patients with anastomotic leakage was significantly lower than patients with non-anastomotic leakage (30.5 mo vs. 96.2 mo, P < 0.001). Anastomotic leakage could promote gastric cancer progression by prolonging inflammation[34–36]. According to Tokunaga et al., GC patients with intra-abdominal infection had a poorer 5-year OS rate and 5-relapse-free survival rate than patients without intra-abdominal infectins (66.4% vs. 86.8%, P < 0.001 and 64.9% vs. 84.5%, P < 0.001). In another study by Li et al., postoperative complications including gastrointestinal obstruction, anastomotic leakage, and bleeding leading and abdominal abscess all were independent and negative prognostic factors for GC. Therefore, all efforts should be made to reduce the risk for postoperative SAE, including careful patient selection for surgery and optimized perioperative patient care.
In summary, this study identified four independent prognostic factors that could be intervened for GC patients, including curative resection, HIPEC, postoperative SAE and systemic chemotherapy, and three independent prognostic factors that cannot be intervened: tumor invasion, LN status and distant metastasis. Therefore, increasing attention should be directed at better understanding tumor biology involved in cancer invasion and metastasis, and refining multi-disciplinary comprehensive treatment strategies to enhance efficacy and reduce SAE.
This work is supported by Award for Excellent PhD. Candidates Funded by Ministry of Education of China (No. 5052011303014), Science Fund of the National Natural Science Foundation of China (No. 81171396), Science Fund for Creative Research Groups of the National Natural Science Foundation of China (No. 20621502, 20921062), and the Fundamental Research Funds for the Central Universities of Ministry of Education of China (No. 4103005).
- Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM: Estimates of worldwide burden of cancer in, GLOBOCAN 2008. Int J Cancer. 2008, 2010 (127): 2893-2917.Google Scholar
- Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D: Global cancer statistics. CA Cancer J Clin. 2011, 61: 69-90. 10.3322/caac.20107.View ArticlePubMedGoogle Scholar
- Yang L: Incidence and mortality of gastric cancer in China. World J Gastroenterol. 2006, 12: 17-20.View ArticlePubMedPubMed CentralGoogle Scholar
- Hartgrink HH, Jansen EP, van Grieken NC, van de Velde CJ: Gastric cancer. Lancet. 2009, 374: 477-490. 10.1016/S0140-6736(09)60617-6.View ArticlePubMedPubMed CentralGoogle Scholar
- Wang W, Sun XW, Li CF, Lv L, Li YF, Chen YB, Xu DZ, Kesari R, Huang CY, Li W, Zhan YQ, Zhou ZW: Comparison of the 6th and 7th editions of the UICC TNM staging system for gastric cancer: results of a Chinese single-institution study of 1,503 patients. Ann Surg Oncol. 2011, 18: 1060-1067. 10.1245/s10434-010-1424-2.View ArticlePubMedGoogle Scholar
- Chen C, Chen LQ, Chen LD, Yang GL, Li Y: Evaluation of tumor markers biochip C12 system in the diagnosis of gastric cancer and the strategies for improvement: analysis of 100 cases. Hepatogastroenterology. 2008, 55: 991-997.PubMedGoogle Scholar
- Wu HL, Tian Q, Peng CW, Liu SP, Li Y: Multivariate survival and outcome analysis of 154 patients with gastric cancer at a single Chinese institution. Asian Pac J Cancer Prev. 2011, 12: 3341-3345.PubMedGoogle Scholar
- Zhang XF, Huang CM, Lu HS, Wu XY, Wang C, Guang GX, Zhang JZ, Zheng CH: Surgical treatment and prognosis of gastric cancer in 2,613 patients. World J Gastroenterol. 2004, 10: 3405-3408.View ArticlePubMedPubMed CentralGoogle Scholar
- Li BS, Zhao YL, Guo G, Li W, Zhu ED, Luo X, Mao XH, Zou QM, Yu PW, Zuo QF, Li N, Tang B, Liu KY, Xiao B: Plasma microRNAs, miR-223, miR-21 and miR-218, as novel potential biomarkers for gastric cancer detection. PLoS One. 2012, 7: e41629-10.1371/journal.pone.0041629.View ArticlePubMedPubMed CentralGoogle Scholar
- Yokota T, Ishiyama S, Saito T, Teshima S, Shimotsuma M, Yamauchi H: Treatment strategy of limited surgery in the treatment guidelines for gastric cancer in Japan. Lancet Oncol. 2003, 4: 423-428. 10.1016/S1470-2045(03)01140-9.View ArticlePubMedGoogle Scholar
- Diaz DLA, Yarnoz C, Aguilar R, Artieda C, Ortiz H: Rationale for gastrectomy with D2 lymphadenectomy in the treatment of gastric cancer. Gastric Cancer. 2008, 11: 96-102. 10.1007/s10120-008-0460-0.View ArticleGoogle Scholar
- D'Annibale A, Pende V, Pernazza G, Monsellato I, Mazzocchi P, Lucandri G, Morpurgo E, Contardo T, Sovernigo G: Full robotic gastrectomy with extended (D2) lymphadenectomy for gastric cancer: surgical technique and preliminary results. J Surg Res. 2011, 166: e113-e120. 10.1016/j.jss.2010.11.881.View ArticlePubMedGoogle Scholar
- Songun I, Putter H, Kranenbarg EM, Sasako M, van de Velde CJ: Surgical treatment of gastric cancer: 15-year follow-up results of the randomised nationwide Dutch D1D2 trial. Lancet Oncol. 2010, 11: 439-449. 10.1016/S1470-2045(10)70070-X.View ArticlePubMedGoogle Scholar
- Washington K: 7th edition of the AJCC cancer staging manual: stomach. Ann Surg Oncol. 2010, 17: 3077-3079. 10.1245/s10434-010-1362-z.View ArticlePubMedGoogle Scholar
- Ajani JA, Bentrem DJ, Besh S, D'Amico TA, Das P, Denlinger C, Fakih MG, Fuchs CS, Gerdes H, Glasgow RE, Hayman JA, Hofstetter WL, Ilson DH, Keswani RN, Kleinberg LR, Korn WM, Lockhart AC, Meredith K, Mulcahy MF, Orringer MB, Posey JA, Sasson AR, Scott WJ, Strong VE, Varghese TJ, Warren G, Washington MK, Willett C, Wright CD, McMillian NR: Gastric cancer, version 2.2013: featured updates to the NCCN Guidelines. J Natl Compr Canc Netw. 2013, 11: 531-546.PubMedGoogle Scholar
- Yonemura Y, Endou Y, Sasaki T, Hirano M, Mizumoto A, Matsuda T, Takao N, Ichinose M, Miura M, Li Y: Surgical treatment for peritoneal carcinomatosis from gastric cancer. Eur J Surg Oncol. 2010, 36: 1131-1138. 10.1016/j.ejso.2010.09.006.View ArticlePubMedGoogle Scholar
- Sakuramoto S, Sasako M, Yamaguchi T, Kinoshita T, Fujii M, Nashimoto A, Furukawa H, Nakajima T, Ohashi Y, Imamura H, Higashino M, Yamamura Y, Kurita A, Arai K: Adjuvant chemotherapy for gastric cancer with S-1, an oral fluoropyrimidine. N Engl J Med. 2007, 357: 1810-1820. 10.1056/NEJMoa072252.View ArticlePubMedGoogle Scholar
- Macdonald JS, Smalley SR, Benedetti J, Hundahl SA, Estes NC, Stemmermann GN, Haller DG, Ajani JA, Gunderson LL, Jessup JM, Martenson JA: Chemoradiotherapy after surgery compared with surgery alone for adenocarcinoma of the stomach or gastroesophageal junction. N Engl J Med. 2001, 345: 725-730. 10.1056/NEJMoa010187.View ArticlePubMedGoogle Scholar
- Cunningham D, Allum WH, Stenning SP, Thompson JN, Van de Velde CJ, Nicolson M, Scarffe JH, Lofts FJ, Falk SJ, Iveson TJ, Smith DB, Langley RE, Verma M, Weeden S, Chua YJ, MAGIC TP: Perioperative chemotherapy versus surgery alone for resectable gastroesophageal cancer. N Engl J Med. 2006, 355: 11-20. 10.1056/NEJMoa055531.View ArticlePubMedGoogle Scholar
- Shiraishi N, Inomata M, Osawa N, Yasuda K, Adachi Y, Kitano S: Early and late recurrence after gastrectomy for gastric carcinoma: Univariate and multivariate analyses. Cancer. 2000, 89: 255-261. 10.1002/1097-0142(20000715)89:2<255::AID-CNCR8>3.0.CO;2-N.View ArticlePubMedGoogle Scholar
- Kodera Y, Ito S, Yamamura Y, Mochizuki Y, Fujiwara M, Hibi K, Ito K, Akiyama S, Nakao A: Follow-up surveillance for recurrence after curative gastric cancer surgery lacks survival benefit. Ann Surg Oncol. 2003, 10: 898-902. 10.1245/ASO.2003.12.009.View ArticlePubMedGoogle Scholar
- Yoo CH, Noh SH, Shin DW, Choi SH, Min JS: Recurrence following curative resection for gastric carcinoma. Br J Surg. 2000, 87: 236-242. 10.1046/j.1365-2168.2000.01360.x.View ArticlePubMedGoogle Scholar
- Yang XQ, Yan L, Chen C, Hou JX, Li Y: Application of C12 multi-tumor marker protein chip in the diagnosis of gastrointestinal cancer: results of 329 surgical patients and suggestions for improvement. Hepatogastroenterology. 2009, 56: 1388-1394.PubMedGoogle Scholar
- Yang D, Hendifar A, Lenz C, Togawa K, Lenz F, Lurje G, Pohl A, Winder T, Ning Y, Groshen S, Lenz HJ: Survival of metastatic gastric cancer: Significance of age, sex and race/ethnicity. J Gastrointest Oncol. 2011, 2: 77-84.PubMedPubMed CentralGoogle Scholar
- Nanthakumaran S, Fernandes E, Thompson AM, Rapson T, Gilbert FJ, Park KG: Morbidity and mortality rates following gastric cancer surgery and contiguous organ removal, a population based study. Eur J Surg Oncol. 2005, 31: 1141-1144. 10.1016/j.ejso.2005.03.013.View ArticlePubMedGoogle Scholar
- Li C, Yan M, Chen J, Xiang M, Zhu ZG, Yin HR, Lin YZ: Surgical resection with hyperthermic intraperitoneal chemotherapy for gastric cancer patients with peritoneal dissemination. J Surg Oncol. 2010, 102: 361-365. 10.1002/jso.21628.View ArticlePubMedGoogle Scholar
- Landry CS, Brock G, Scoggins CR, McMasters KM, Martin RN: A proposed staging system for gastric carcinoid tumors based on an analysis of 1,543 patients. Ann Surg Oncol. 2009, 16: 51-60. 10.1245/s10434-008-0192-8.View ArticlePubMedGoogle Scholar
- Cheong JH, Shen JY, Song CS, Hyung WJ, Shen JG, Choi SH, Noh SH: Early postoperative intraperitoneal chemotherapy following cytoreductive surgery in patients with very advanced gastric cancer. Ann Surg Oncol. 2007, 14: 61-68.View ArticlePubMedGoogle Scholar
- Heise K, Bertran E, Andia ME, Ferreccio C: Incidence and survival of stomach cancer in a high-risk population of Chile. World J Gastroenterol. 2009, 15: 1854-1862. 10.3748/wjg.15.1854.View ArticlePubMedPubMed CentralGoogle Scholar
- Glehen O, Schreiber V, Cotte E, Sayag-Beaujard AC, Osinsky D, Freyer G, Francois Y, Vignal J, Gilly FN: Cytoreductive surgery and intraperitoneal chemohyperthermia for peritoneal carcinomatosis arising from gastric cancer. Arch Surg. 2004, 139: 20-26. 10.1001/archsurg.139.1.20.View ArticlePubMedGoogle Scholar
- Yonemura Y, Kawamura T, Bandou E, Takahashi S, Sawa T, Matsuki N: Treatment of peritoneal dissemination from gastric cancer by peritonectomy and chemohyperthermic peritoneal perfusion. Br J Surg. 2005, 92: 370-375. 10.1002/bjs.4695.View ArticlePubMedGoogle Scholar
- Yang XJ, Huang CQ, Suo T, Mei LJ, Yang GL, Cheng FL, Zhou YF, Xiong B, Yonemura Y, Li Y: Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy improves survival of patients with peritoneal carcinomatosis from gastric cancer: final results of a phase III randomized clinical trial. Ann Surg Oncol. 2011, 18: 1575-1581. 10.1245/s10434-011-1631-5.View ArticlePubMedPubMed CentralGoogle Scholar
- Yan TD, Black D, Sugarbaker PH, Zhu J, Yonemura Y, Petrou G, Morris DL: A systematic review and meta-analysis of the randomized controlled trials on adjuvant intraperitoneal chemotherapy for resectable gastric cancer. Ann Surg Oncol. 2007, 14: 2702-2713. 10.1245/s10434-007-9487-4.View ArticlePubMedGoogle Scholar
- Sierzega M, Kolodziejczyk P, Kulig J: Impact of anastomotic leakage on long-term survival after total gastrectomy for carcinoma of the stomach. Br J Surg. 2010, 97: 1035-1042. 10.1002/bjs.7038.View ArticlePubMedGoogle Scholar
- Yoo HM, Lee HH, Shim JH, Jeon HM, Park CH, Song KY: Negative impact of leakage on survival of patients undergoing curative resection for advanced gastric cancer. J Surg Oncol. 2011, 104: 734-740. 10.1002/jso.22045.View ArticlePubMedGoogle Scholar
- Kubota T, Hiki N, Sano T, Nomura S, Nunobe S, Kumagai K, Aikou S, Watanabe R, Kosuga T, Yamaguchi T: Prognostic significance of complications after curative surgery for gastric cancer. Ann Surg Oncol. 2014, 21: 891-898. 10.1245/s10434-013-3384-9.View ArticlePubMedGoogle Scholar
- Tokunaga M, Tanizawa Y, Bando E, Kawamura T, Terashima M: Poor survival rate in patients with postoperative intra-abdominal infectious complications following curative gastrectomy for gastric cancer. Ann Surg Oncol. 2013, 20: 1575-1583. 10.1245/s10434-012-2720-9.View ArticlePubMedGoogle Scholar
- Li QG, Li P, Tang D, Chen J, Wang DR: Impact of postoperative complications on long-term survival after radical resection for gastric cancer. World J Gastroenterol. 2013, 19: 4060-4065. 10.3748/wjg.v19.i25.4060.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2482/14/29/prepub
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