期刊论文详细信息
BMC Cancer
Incidence, time course and independent risk factors for metachronous peritoneal carcinomatosis of gastric origin – a longitudinal experience from a prospectively collected database of 1108 patients
Alexander G Kerscher3  Jörg OW Pelz2  Christoph-Thomas Germer2  Volker Kunzmann4  Uwe Maeder1  Martin Gasser2  Alexander D Miras5  Burkhard H von Rahden2  Florian Seyfried2 
[1]Cancer Registry Mainfranken, University of Wuerzburg Medical Center, Wuerzburg, Germany
[2]Department of General, Visceral, Vascular- and Pediatric Surgery, University of Wuerzburg Medical Center, Wuerzburg, Germany
[3]Comprehensive Cancer Center Mainfranken, University of Wuerzburg Medical Center, Wuerzburg, Germany
[4]Department of Internal Medicine, University of Wuerzburg Medical Center, Wuerzburg, Germany
[5]Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London, UK
关键词: Survival;    Recurrence;    Perioperative chemotherapy;    Risk factors;    Metachronous;    Peritoneal carcinomatosis;    Gastric cancer;   
Others  :  1131644
DOI  :  10.1186/s12885-015-1081-8
 received in 2014-11-29, accepted in 2015-02-11,  发布年份 2015
PDF
【 摘 要 】

Background

Comprehensive evidence on the incidence, time course and independent risk factors of metachronous peritoneal carcinomatosis (metaPC) in gastric cancer patients treated with curative intent in the context of available systemic combination chemotherapies is lacking.

Methods

Data from a prospectively collected single-institutional Center Cancer Registry with 1108 consecutive patients with gastric adenocarcinoma (GC), clinical, histological and survival data were analyzed for independent risk factors and prognosis with focus on the development of metaPC. Findings were then stratified to the time periods of treatment with surgery alone, 5-Fluorouracil-only and contemporary combined systemic perioperative chemotherapy strategies, respectively.

Results

Despite R0 D2 gastrectomy (n = 560), 49.6% (±5.4%) of the patients were diagnosed with tumour recurrence and 15.5% (±1.8%) developed metaPC after a median time of 17.7 (15.1-20.3) months after surgery resulting in a tumour related mortality of 100% with a median survival of 3.0 months (2.1 – 4.0). Independent risk factors for the development of metaPC were serosa positive T-category, nodal positive-status, signet cell and undifferentiated gradings (G3/G4). Contemporary systemic combination chemotherapy did not improve the incidence and prognosis of metaPC (p = 0.54).

Conclusions

Despite significant improvements in the overall survival for the complete cohort with gastric cancer over time, those patients with metaPC did not experience the same benefits. The lack of change in the incidence, and persistent poor prognosis of metaPC after curative surgery expose the need for further prevention and/or improved treatment options for this devastating condition.

【 授权许可】

   
2015 Seyfried et al.; licensee BioMed Central.

【 预 览 】
附件列表
Files Size Format View
20150303022615387.pdf 1070KB PDF download
Figure 3. 28KB Image download
Figure 2. 70KB Image download
Figure 1. 60KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

【 参考文献 】
  • [1]Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM: Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Canc Suppl J Int Canc Suppl 2010, 127(12):2893-917.
  • [2]Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D: Global cancer statistics. CA Cancer J Clin 2011, 61(2):69-90.
  • [3]Siegel R, Naishadham D, Jemal A: Cancer statistics, 2013. CA Cancer J Clin 2013, 63(1):11-30.
  • [4]Thomassen I, van Gestel YR, van Ramshorst B, Luyer MD, Bosscha K, Nienhuijs SW, et al.: Peritoneal carcinomatosis of gastric origin: a population-based study on incidence, survival and risk factors. Int J Canc Suppl J Int Canc Suppl 2014, 134(3):622-8.
  • [5]Cunningham D, Allum WH, Stenning SP, Thompson JN, Van de Velde CJ, Nicolson M, et al.: Perioperative chemotherapy versus surgery alone for resectable gastroesophageal cancer. N Engl J Med 2006, 355(1):11-20.
  • [6]Macdonald JS, Smalley SR, Benedetti J, Hundahl SA, Estes NC, Stemmermann GN, et al.: Chemoradiotherapy after surgery compared with surgery alone for adenocarcinoma of the stomach or gastroesophageal junction. N Engl J Med 2001, 345(10):725-30.
  • [7]Japanese Gastric Cancer Association: Japanese gastric cancer treatment guidelines 2010 (ver. 3) Gastric Cancer 2011, 14(2):113-23.
  • [8]Okines A, Verheij M, Allum W, Cunningham D, Cervantes A: Gastric cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2010, 21(Suppl 5):v50-4.
  • [9]Bang YJ, Kim YW, Yang HK, Chung HC, Park YK, Lee KH, et al.: Adjuvant capecitabine and oxaliplatin for gastric cancer after D2 gastrectomy (CLASSIC): a phase 3 open-label, randomised controlled trial. Lancet 2012, 379(9813):315-21.
  • [10]Xu AM, Huang L, Liu W, Gao S, Han WX, Wei ZJ: Neoadjuvant chemotherapy followed by surgery versus surgery alone for gastric carcinoma: systematic review and meta-analysis of randomized controlled trials. PLoS One 2014, 9(1):e86941.
  • [11]Gallardo-Rincon D, Onate-Ocana LF, Calderillo-Ruiz G: Neoadjuvant chemotherapy with P-ELF (cisplatin, etoposide, leucovorin, 5-fluorouracil) followed by radical resection in patients with initially unresectable gastric adenocarcinoma: a phase II study. Ann Surg Oncol 2000, 7(1):45-50.
  • [12]Guo M, Zheng Q, zhong Di J, Yang Z: Histological complete response to a combined docetaxel/cisplatin/fluorouracil neoadjuvant chemotherapy for T4 stage gastric adenocarcinoma. World J Surg Oncol 2014, 12:150. BioMed Central Full Text
  • [13]Roth AD, Fazio N, Stupp R, Falk S, Bernhard J, Saletti P, et al.: Docetaxel, cisplatin, and fluorouracil; docetaxel and cisplatin; and epirubicin, cisplatin, and fluorouracil as systemic treatment for advanced gastric carcinoma: a randomized phase II trial of the Swiss Group for Clinical Cancer Research. J Clin Oncol 2007, 25(22):3217-23.
  • [14]Glehen O, Schreiber V, Cotte E, Sayag-Beaujard AC, Osinsky D, Freyer G, et al.: Cytoreductive surgery and intraperitoneal chemohyperthermia for peritoneal carcinomatosis arising from gastric cancer. Arch Surg 2004, 139(1):20-6.
  • [15]Rossi CR, Pilati P, Mocellin S, Foletto M, Ori C, Innocente F, et al.: Hyperthermic intraperitoneal intraoperative chemotherapy for peritoneal carcinomatosis arising from gastric adenocarcinoma. Suppl Tumori 2003, 2(5):S54-7.
  • [16]Gill RS, Al-Adra DP, Nagendran J, Campbell S, Shi X, Haase E, et al.: Treatment of gastric cancer with peritoneal carcinomatosis by cytoreductive surgery and HIPEC: a systematic review of survival, mortality, and morbidity. J Surg Oncol 2011, 104(6):692-8.
  • [17]Kuramoto M, Shimada S, Ikeshima S, Matsuo A, Kuhara H, Eto K, et al.: A proposal of a practical and optimal prophylactic strategy for peritoneal recurrence. J Oncol 2012, 2012:340380.
  • [18]Kuramoto M, Shimada S, Ikeshima S, Matsuo A, Yagi Y, Matsuda M, et al.: Extensive intraoperative peritoneal lavage as a standard prophylactic strategy for peritoneal recurrence in patients with gastric carcinoma. Ann Surg 2009, 250(2):242-6.
  • [19]Moehler M, Al-Batran SE, Andus T, Anthuber M, Arends J, Arnold D, et al.: [German S3-guideline “Diagnosis and treatment of esophagogastric cancer”]. Z Gastroenterol 2011, 49(4):461-531.
  • [20]Waddell T, Verheij M, Allum W, Cunningham D, Cervantes A, Arnold D: Gastric cancer: ESMO-ESSO-ESTRO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2013, 24 Suppl 6:vi57-63.
  • [21]Eom BW, Ryu KW, Lee JH, Choi IJ, Kook MC, Cho SJ, et al.: Oncologic effectiveness of regular follow-up to detect recurrence after curative resection of gastric cancer. Ann Surg Oncol 2011, 18(2):358-64.
  • [22]Hur H, Song KY, Park CH, Jeon HM: Follow-up strategy after curative resection of gastric cancer: a nationwide survey in Korea. Ann Surg Oncol 2010, 17(1):54-64.
  • [23]Chae S, Lee A, Lee JH: The effectiveness of the new (7th) UICC N classification in the prognosis evaluation of gastric cancer patients: a comparative study between the 5th/6th and 7th UICC N classification. Gastric Cancer 2011, 14(2):166-71.
  • [24]Geary J, Sasieni P, Houlston R, Izatt L, Eeles R, Payne SJ, et al.: Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC). Fam Cancer 2008, 7(2):163-72.
  • [25]Vasen HF, Moslein G, Alonso A, Bernstein I, Bertario L, Blanco I, et al.: Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer). J Med Genet 2007, 44(6):353-62.
  • [26]Kuipers EJ, Rosch T, Bretthauer M: Colorectal cancer screening–optimizing current strategies and new directions. Nat Rev Clin Oncol 2013, 10(3):130-42.
  • [27]Sun Z, Li DM, Wang ZN, Huang BJ, Xu Y, Li K, et al.: Prognostic significance of microscopic positive margins for gastric cancer patients with potentially curative resection. Ann Surg Oncol 2009, 16(11):3028-37.
  • [28]Wang SY, Yeh CN, Lee HL, Liu YY, Chao TC, Hwang TL, et al.: Clinical impact of positive surgical margin status on gastric cancer patients undergoing gastrectomy. Ann Surg Oncol 2009, 16(10):2738-43.
  • [29]Abbasi SY, Taani HE, Saad A, Badheeb A, Addasi A: Advanced gastric cancer in jordan from 2004 to 2008: a study of epidemiology and outcomes. Gastrointest Cancer Res 2011, 4(4):122-7.
  • [30]Gretschel S, Siegel R, Estevez-Schwarz L, Hunerbein M, Schneider U, Schlag PM: Surgical strategies for gastric cancer with synchronous peritoneal carcinomatosis. Br J Surg 2006, 93(12):1530-5.
  • [31]Hioki M, Gotohda N, Konishi M, Nakagohri T, Takahashi S, Kinoshita T: Predictive factors improving survival after gastrectomy in gastric cancer patients with peritoneal carcinomatosis. World J Surg 2010, 34(3):555-62.
  • [32]Sugarbaker PH, Yonemura Y: Clinical pathway for the management of resectable gastric cancer with peritoneal seeding: best palliation with a ray of hope for cure. Oncology 2000, 58(2):96-107.
  • [33]Yang D, Hendifar A, Lenz C, Togawa K, Lenz F, Lurje G, et al.: Survival of metastatic gastric cancer: significance of age, sex and race/ethnicity. J Gastrointest Oncol 2011, 2(2):77-84.
  • [34]Paoletti X, Oba K, Burzykowski T, Michiels S, Ohashi Y, Pignon JP, et al.: Benefit of adjuvant chemotherapy for resectable gastric cancer: a meta-analysis. JAMA 2010, 303(17):1729-37.
  • [35]Duhr CD, Kenn W, Kickuth R, Kerscher AG, Germer CT, Hahn D, et al.: Optimizing of preoperative computed tomography for diagnosis in patients with peritoneal carcinomatosis. World J Surg Oncol 2011, 9:171. BioMed Central Full Text
  • [36]Huang KH, Chen JH, Wu CW, Lo SS, Hsieh MC, Li AF, et al.: Factors affecting recurrence in node-negative advanced gastric cancer. J Gastroenterol Hepatol 2009, 24(9):1522-6.
  • [37]Roviello F, Marrelli D, de Manzoni G, Morgagni P, Di Leo A, Saragoni L, et al.: Prospective study of peritoneal recurrence after curative surgery for gastric cancer. Br J Surg 2003, 90(9):1113-9.
  • [38]Yoo CH, Noh SH, Shin DW, Choi SH, Min JS: Recurrence following curative resection for gastric carcinoma. Br J Surg 2000, 87(2):236-42.
  • [39]Maehara Y, Hasuda S, Koga T, Tokunaga E, Kakeji Y, Sugimachi K: Postoperative outcome and sites of recurrence in patients following curative resection of gastric cancer. Br J Surg 2000, 87(3):353-7.
  • [40]Elias D, Honore C, Dumont F, Ducreux M, Boige V, Malka D, et al.: Results of systematic second-look surgery plus HIPEC in asymptomatic patients presenting a high risk of developing colorectal peritoneal carcinomatosis. Ann Surg 2011, 254(2):289-93.
  文献评价指标  
  下载次数:34次 浏览次数:20次