Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report

被引:10
作者
Calapre, Leslie [1 ]
Warburton, Lydia [2 ]
Millward, Michael [2 ,3 ]
Gray, Elin S. [4 ]
机构
[1] Edith Cowan Univ, Sch Med Sci, Joondalup, WA, Australia
[2] Sir Charles Gairdner Hosp, Dept Med Oncol, Nedlands, WA, Australia
[3] Univ Western Australia, Sch Med & Pharmacol, Crawley, WA, Australia
[4] Univ Western Australia, Sch Biomed Sci, Crawley, WA, Australia
关键词
BRAF; Melanoma; Circulating tumor DNA; Colon cancer; Survivorship; Case report; CELL-FREE DNA; ACQUIRED-RESISTANCE; MUTATION ANALYSIS; LIQUID BIOPSIES; T790M;
D O I
10.1186/s12885-019-6336-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Circulating tumour DNA (ctDNA) has emerged as a promising blood-based biomarker for monitoring disease status of patients with advanced cancers. The presence of ctDNA in the blood is a result of biological processes, namely tumour cell apoptosis and/or necrosis, and can be used to monitor different cancers by targeting cancer-specific mutation. Case presentation We present the case of a 67 year old Caucasian male that was initially treated with BRAF inhibitors followed by anti-CTLA4 and then anti-PD1 immunotherapy for metastatic melanoma but later developed colorectal cancer. The kinetics of ctDNA derived from each cancer type were monitored targeting BRAF V600R (melanoma) and KRAS G13D (colon cancer), specifically reflected the status of the patient's tumours. In fact, the discordant pattern of BRAF and KRAS ctDNA was significantly correlated with the clinical response of melanoma to pembrolizumab treatment and progression of colorectal cancer noted by PET and/or CT scan. Based on these results, ctDNA can be used to specifically clarify disease status of patients with metachronous cancers. Conclusions Using cancer-specific mutational targets, we report here for the first time the efficacy of ctDNA to accurately provide a comprehensive outlook of the tumour status of two different cancers within one patient. Thus, ctDNA analysis has a potential clinical utility to delineate clinical information in patients with multiple cancer types.
引用
收藏
页数:5
相关论文
共 30 条
[1]  
[Anonymous], MOL ONCOL
[2]  
[Anonymous], ANN ONCOL
[3]  
[Anonymous], SCI TRANSLATIONAL ME
[4]   Detection of Circulating Tumor DNA in Early- and Late-Stage Human Malignancies [J].
Bettegowda, Chetan ;
Sausen, Mark ;
Leary, Rebecca J. ;
Kinde, Isaac ;
Wang, Yuxuan ;
Agrawal, Nishant ;
Bartlett, Bjarne R. ;
Wang, Hao ;
Luber, Brandon ;
Alani, Rhoda M. ;
Antonarakis, Emmanuel S. ;
Azad, Nilofer S. ;
Bardelli, Alberto ;
Brem, Henry ;
Cameron, John L. ;
Lee, Clarence C. ;
Fecher, Leslie A. ;
Gallia, Gary L. ;
Gibbs, Peter ;
Le, Dung ;
Giuntoli, Robert L. ;
Goggins, Michael ;
Hogarty, Michael D. ;
Holdhoff, Matthias ;
Hong, Seung-Mo ;
Jiao, Yuchen ;
Juhl, Hartmut H. ;
Kim, Jenny J. ;
Siravegna, Giulia ;
Laheru, Daniel A. ;
Lauricella, Calogero ;
Lim, Michael ;
Lipson, Evan J. ;
Marie, Suely Kazue Nagahashi ;
Netto, George J. ;
Oliner, Kelly S. ;
Olivi, Alessandro ;
Olsson, Louise ;
Riggins, Gregory J. ;
Sartore-Bianchi, Andrea ;
Schmidt, Kerstin ;
Shih, Ie-Ming ;
Oba-Shinjo, Sueli Mieko ;
Siena, Salvatore ;
Theodorescu, Dan ;
Tie, Jeanne ;
Harkins, Timothy T. ;
Veronese, Silvio ;
Wang, Tian-Li ;
Weingart, Jon D. .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (224)
[5]   Circulating tumour DNA (ctDNA) as a liquid biopsy for melanoma [J].
Calapre, Leslie ;
Warburton, Lydia ;
Millward, Michael ;
Ziman, Mel ;
Gray, Elin S. .
CANCER LETTERS, 2017, 404 :62-69
[6]   Use of cell free DNA in breast oncology [J].
Canzoniero, Jenna VanLiere ;
Park, Ben Ho .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2016, 1865 (02) :266-274
[7]   Analysis of Circulating Tumor DNA to Monitor Metastatic Breast Cancer [J].
Dawson, Sarah-Jane ;
Tsui, Dana W. Y. ;
Murtaza, Muhammed ;
Biggs, Heather ;
Rueda, Oscar M. ;
Chin, Suet-Feung ;
Dunning, Mark J. ;
Gale, Davina ;
Forshew, Tim ;
Mahler-Araujo, Betania ;
Rajan, Sabrina ;
Humphray, Sean ;
Becq, Jennifer ;
Halsall, David ;
Wallis, Matthew ;
Bentley, David ;
Caldas, Carlos ;
Rosenfeld, Nitzan .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (13) :1199-1209
[8]   Capturing intra-tumor genetic heterogeneity by de novo mutation profiling of circulating cell-free tumor DNA: a proof-of-principle [J].
De Mattos-Arruda, L. ;
Weigelt, B. ;
Cortes, J. ;
Won, H. H. ;
Ng, C. K. Y. ;
Nuciforo, P. ;
Bidard, F. -C. ;
Aura, C. ;
Saura, C. ;
Peg, V. ;
Piscuoglio, S. ;
Oliveira, M. ;
Smolders, Y. ;
Patel, P. ;
Norton, L. ;
Tabernero, J. ;
Berger, M. F. ;
Seoane, J. ;
Reis-Filho, J. S. .
ANNALS OF ONCOLOGY, 2014, 25 (09) :1729-1735
[9]   Cerebrospinal fluid-derived circulating tumour DNA better represents the genomic alterations of brain tumours than plasma [J].
De Mattos-Arruda, Leticia ;
Mayor, Regina ;
Ng, Charlotte K. Y. ;
Weigelt, Britta ;
Martinez-Ricarte, Francisco ;
Torrejon, Davis ;
Oliveira, Mafalda ;
Arias, Alexandra ;
Raventos, Carolina ;
Tang, Jiabin ;
Guerini-Rocco, Elena ;
Martinez-Saez, Elena ;
Lois, Sergio ;
Marin, Oscar ;
de la Cruz, Xavier ;
Piscuoglio, Salvatore ;
Towers, Russel ;
Vivancos, Ana ;
Peg, Vicente ;
Ramon y Cajal, Santiago ;
Carles, Joan ;
Rodon, Jordi ;
Gonzalez-Cao, Maria ;
Tabernero, Josep ;
Felip, Enriqueta ;
Sahuquillo, Joan ;
Berger, Michael F. ;
Cortes, Javier ;
Reis-Filho, Jorge S. ;
Seoane, Joan .
NATURE COMMUNICATIONS, 2015, 6
[10]  
Garcia-Murillas I., 2015, Sci Transl Med, V7, p302ra133