Prognostic significance of prospectively detected bone marrow micrometastases in esophagogastric cancer: 10-year follow-up confirms prognostic significance

被引:6
作者
Ryan, Paul [1 ,2 ]
Furlong, Heidi [3 ]
Murphy, Conleth G. [4 ]
O'Sullivan, Finbarr [5 ]
Walsh, Thomas N. [3 ]
Shanahan, Fergus [6 ]
O'Sullivan, Gerald C. [2 ,7 ]
机构
[1] Bon Secours Hosp, Dept Pathol, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Cork Canc Res Ctr, Cork, Ireland
[3] Connolly Hosp, Royal Coll Surg Ireland, Dept Surg, Dublin, Ireland
[4] Bon Secours Hosp, Dept Oncol, Cork, Ireland
[5] Natl Univ Ireland Univ Coll Cork, Sch Math Sci Stat, Cork, Ireland
[6] Natl Univ Ireland Univ Coll Cork, Dept Med, Cork, Ireland
[7] Natl Univ Ireland Univ Coll Cork, Dept Surg, Cork, Ireland
关键词
10-year follow-up; bone marrow micrometastases; esophagogastric cancer; ESOPHAGEAL CANCER; TUMOR-CELLS; CARCINOMA; SURGERY; ADENOCARCINOMA; SURVIVAL;
D O I
10.1002/cam4.470
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have previously reported that most patients with esophagogastric cancer (EGC) undergoing potentially curative resections have bone marrow micrometastases (BMM). We present 10-year outcome data of patients with EGC whose rib marrow was examined for micrometastases and correlate the findings with treatment and conventional pathologic tumor staging. A total of 88 patients with localized esophagogastric tumors had radical en-bloc esophagectomy, with 47 patients receiving neoadjuvant (5-fluorouracil/cisplatin based) chemoradiotherapy (CRT) and the remainder being treated with surgery alone. Rib marrow was examined for cytokeratin-18-positive cells. Standard demographic and pathologic features were recorded and patients were followed for a mean 10.04 years. Disease recurrences and all deaths in the follow-up period were recorded. No patients were lost to follow-up. 46 EGC-related and 10 non-EGC-related deaths occurred. Multivariate Cox analysis of interaction of neoadjuvant chemotherapy, nodal status, and BMM positivity showed that the contribution of BMM to disease-specific and overall survival is significant (P = 0.014). There is significant interaction with neoadjvant CRT (P < 0.005), and lymph node positivity (P < 0.001) but BMM positivity contributes to increase in risk of cancer-related death in patients treated with either CRT or surgery alone. Bone marrow micrometastases detected at the time of surgery for EGC is a long-term prognostic marker. Detection is a readily available, technically noncomplex test which offers a window on the metastatic process and a refinement of pathologic staging and is worthy of routine consideration.
引用
收藏
页码:1281 / 1288
页数:8
相关论文
共 40 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   Recent advances in the detection of bone marrow micrometastases: A promising area for research or just another false hope? A review of the literature [J].
Athanassiadou, Pauline ;
Grapsa, Dimitra .
CANCER AND METASTASIS REVIEWS, 2006, 25 (04) :507-519
[3]   Bone marrow-disseminated tumor cells in patients with carcinoma of the esophagus or cardia [J].
Bonavina, L ;
Soligo, D ;
Quirici, N ;
Bossolasco, P ;
Cesana, B ;
Deliliers, GL ;
Peracchia, A .
SURGERY, 2001, 129 (01) :15-22
[4]   Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell [J].
Bonnet, D ;
Dick, JE .
NATURE MEDICINE, 1997, 3 (07) :730-737
[5]   Cytokeratin-positive cells in the bone marrow and survival of patients with stage I, II, or III breast cancer. [J].
Braun, S ;
Pantel, K ;
Muller, P ;
Janni, W ;
Hepp, F ;
Kentenich, CRM ;
Gastroph, S ;
Wischnik, A ;
Dimpfl, T ;
Kindermann, G ;
Riethmuller, G ;
Schlimok, G .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (08) :525-533
[6]   A pooled analysis of bone marrow micrometastasis in breast cancer [J].
Braun, S ;
Vogl, FD ;
Naume, B ;
Janni, W ;
Osborne, MP ;
Coombes, RC ;
Schlimok, G ;
Diel, IJ ;
Gerber, B ;
Gebauer, G ;
Pierga, JY ;
Marth, C ;
Oruzio, D ;
Wiedswang, G ;
Solomayer, EF ;
Kundt, G ;
Strobl, B ;
Fehm, T ;
Wong, GYC ;
Bliss, J ;
Vincent-Salomon, A ;
Pantel, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (08) :793-802
[7]  
Collett D., 1994, Modeling Survival Data in Medical Research
[8]   Oesophageal cancer incidence in the United States by race, sex, and histologic type, 1977-2005 [J].
Cook, M. B. ;
Chow, W-H ;
Devesa, S. S. .
BRITISH JOURNAL OF CANCER, 2009, 101 (05) :855-859
[9]  
COTE RJ, 1995, ANN SURG, V222, P415
[10]   Circulating tumor cells, disease progression, and survival in metastatic breast cancer [J].
Cristofanilli, M ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Matera, J ;
Miller, MC ;
Reuben, JM ;
Doyle, GV ;
Allard, WJ ;
Terstappen, LWMM ;
Hayes, DF .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) :781-791