Growing Indication for FNA to Study and Analyze Tumor Heterogeneity at Metastatic Sites

被引:10
作者
Beca, Francisco [1 ,2 ,3 ]
Schmitt, Fernando [2 ,4 ,5 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Univ Porto, IPATIMUP Inst Mol Pathol & Immunol, P-4100 Oporto, Portugal
[3] Univ Porto, Fac Med, P-4100 Oporto, Portugal
[4] Univ Toronto, Fac Med, Dept Lab Med & Pathobiol, Toronto, ON M5G 2C4, Canada
[5] Univ Hlth Network, Dept Pathol, Toronto, ON, Canada
关键词
fine-needle aspiration (FNA); metastases; tumoral heterogeneity; FINE-NEEDLE-ASPIRATION; BREAST-CANCER; CELLULAR HETEROGENEITY; CYTOLOGICAL SPECIMENS; ONCOGENIC MUTATIONS; KRAS MUTATION; GROWTH-RATES; BRAF; EVOLUTION; PATHOGENESIS;
D O I
10.1002/cncy.21395
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In routine practice, suspected metastases in patients with cancer are only occasionally biopsied, primarily because of the cost and invasiveness of the procedure. However, biopsies of metastatic lesions can be valuable, not only in confirming the presence of metastatic disease, but also in revealing unsuspected benign disease or secondary malignancies. In addition, such biopsies also allow the assessment of biomarkers that might differ from those on primary tumor cells, and can thereby facilitate selection of the optimal treatment. Because of the increasing recognition of clonal and phenotypic heterogeneity of tumors, we anticipate that in the near future, biopsying of metastatic lesions will constitute a standard-ofcare practice, allowing assessment of molecular differences between the primary tumor and metastatic lesions. In our opinion, fine-needle aspiration is currently the best method for making repeated biopsies to monitor the tumor: it is minimally invasive, safe, and cost effective and can be coupled with modern ancillary techniques. Here we provide an up-todate review of the clinical implications of tumor heterogeneity in metastatic disease and the ancillary molecular techniques used in cytology; we also discuss the role of modern cytology in contemporary diagnosis and management of metastatic cancer. (c) 2014 American Cancer Society.
引用
收藏
页码:504 / 511
页数:8
相关论文
共 57 条
[1]   Cellular Heterogeneity and Molecular Evolution in Cancer [J].
Almendro, Vanessa ;
Marusyk, Andriy ;
Polyak, Kornelia .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 8, 2013, 8 :277-302
[2]   Prospective Study Evaluating the Impact of Tissue Confirmation of Metastatic Disease in Patients With Breast Cancer [J].
Amir, Eitan ;
Miller, Naomi ;
Geddie, William ;
Freedman, Orit ;
Kassam, Farrah ;
Simmons, Christine ;
Oldfield, Maria ;
Dranitsaris, George ;
Tomlinson, George ;
Laupacis, Andreas ;
Tannock, Ian F. ;
Clemons, Mark .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (06) :587-592
[3]   Panitumumab combined with irinotecan for patients with KRAS wild-type metastatic colorectal cancer refractory to standard chemotherapy: a GERCOR efficacy, tolerance, and translational molecular study [J].
Andre, T. ;
Blons, H. ;
Mabro, M. ;
Chibaudel, B. ;
Bachet, J-B. ;
Tournigand, C. ;
Bennamoun, M. ;
Artru, P. ;
Nguyen, S. ;
Ebenezer, C. ;
Aissat, N. ;
Cayre, A. ;
Penault-Llorca, F. ;
Laurent-Puig, P. ;
de Gramont, A. .
ANNALS OF ONCOLOGY, 2013, 24 (02) :412-419
[4]   High-Throughput Molecular Analysis from Leftover of Fine Needle Aspiration Cytology of Mammographically Detected Breast Cancer [J].
Annaratone, Laura ;
Marchio, Caterina ;
Renzulli, Tommaso ;
Castellano, Isabella ;
Cantarella, Daniela ;
Isella, Claudio ;
Macri, Luigia ;
Mariscotti, Giovanna ;
Balmativola, Davide ;
Cantanna, Elisabetta ;
Deambrogio, Cristina ;
Pietribiasi, Francesca ;
Arisio, Riccardo ;
Schmitt, Fernando ;
Medico, Enzo ;
Sapino, Anna .
TRANSLATIONAL ONCOLOGY, 2012, 5 (03) :180-U175
[5]   The Implications of Clonal Genome Evolution for Cancer Medicine [J].
Aparicio, Samuel ;
Caldas, Carlos .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (09) :842-851
[6]   Prevalence and Heterogeneity of KRAS, BRAF, and PIK3CA Mutations in Primary Colorectal Adenocarcinomas and Their Corresponding Metastases [J].
Baldus, Stephan E. ;
Schaefer, Karl-L. ;
Engers, Rainer ;
Hartleb, Dinah ;
Stoecklein, Nikolas H. ;
Gabbert, Helmut E. .
CLINICAL CANCER RESEARCH, 2010, 16 (03) :790-799
[7]   Molecular Diagnostics of Melanoma Fine-Needle Aspirates A Cytology-Histology Correlation Study [J].
Bernacki, Kurt D. ;
Betz, Bryan L. ;
Weigelin, Helmut C. ;
Lao, Christopher D. ;
Redman, Bruce G. ;
Knoepp, Stewart M. ;
Roh, Michael H. .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2012, 138 (05) :670-677
[8]   EGFR and KRAS Mutations in Lung Carcinoma Molecular Testing by Using Cytology Specimens [J].
Billah, Shahreen ;
Stewart, John ;
Staerkel, Gregg ;
Chen, Su ;
Gong, Yun ;
Guo, Ming .
CANCER CYTOPATHOLOGY, 2011, 119 (02) :111-117
[9]   Identification of EGFR mutation, KRAS mutation, and ALK gene rearrangement in cytological specimens of primary and metastatic lung adenocarcinoma [J].
Cai, Guoping ;
Wong, Rebecca ;
Chhieng, David ;
Levy, Gillian H. ;
Gettinger, Scott N. ;
Herbst, Roy S. ;
Puchalski, Jonathan T. ;
Homer, Robert J. ;
Hui, Pei .
CANCER CYTOPATHOLOGY, 2013, 121 (09) :500-507
[10]   Emerging landscape of oncogenic signatures across human cancers [J].
Ciriello, Giovanni ;
Miller, Martin L. ;
Aksoy, Buelent Arman ;
Senbabaoglu, Yasin ;
Schultz, Nikolaus ;
Sander, Chris .
NATURE GENETICS, 2013, 45 (10) :1127-U247