The current evidence for a biomarker-based approach in cancer of unknown primary

被引:30
作者
El Rassy, Elie [1 ]
Pavlidis, Nicholas [2 ]
机构
[1] St Joseph Univ, Hotel Dieu France Univ Hosp, Fac Med, Dept Med Oncol, Beirut, Lebanon
[2] Univ Ioannina, Niarchos Ave, GR-45110 Ioannina, Greece
关键词
Cancer of unknown primary; Targeted therapy; Monoclonal antibodies; Immune checkpoint inhibitor; PRIMARY SITE; PRIMARY IDENTIFICATION; PROTEIN EXPRESSION; TYROSINE KINASES; DIVERSE CANCERS; PRIMARY ORIGIN; GENE MUTATION; CARCINOMA; TUMOR; DIAGNOSIS;
D O I
10.1016/j.ctrv.2018.04.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer of unknown primary (CUP) accounts for the seventh to eighth most frequently diagnosed cancer yet its prognosis remains poor with conventional chemotherapy. The spectrum of therapeutic management includes both locoregional and systemic therapy and should intend to offer optimal benefit to favorable CUP patients and palliative care to unfavorable cases. The recent molecular advances have revolutionized the armamentarium of cancer treatments though a biomarker-based approach. Unfortunately, solid data in CUP is lacking in the absence of a CUP-specific driver molecular signature. This prompted us to screen the medical literature for clinical data that evaluates the efficacy and safety of the biomarker-based approach in CUP patients. In this review, we will summarize the available evidence for the applicability of targeted therapies in CUP.
引用
收藏
页码:21 / 28
页数:8
相关论文
共 79 条
[1]  
[Anonymous], 2016, SUPER SOLV CANC UNKN
[2]  
[Anonymous], 2016, DRUGS-REAL WOR OUTC
[3]   PDL-1/PD1 inhibitors: antibody or antinobody? [J].
Aoun, Fouad ;
El Rassy, Elie ;
Assi, Tarek ;
Kattan, Joseph .
FUTURE ONCOLOGY, 2017, 13 (19) :1669-1671
[4]   Unknown primary carcinoma, diagnosed as inflammatory breast cancer, and successfully treated with trastuzumab and vinorelbine [J].
Asakura H. ;
Takashima H. ;
Mitani M. ;
Haba R. ;
Seo R. ;
Yokoe K. ;
Toyama Y. ;
Ohkawa M. .
International Journal of Clinical Oncology, 2005, 10 (4) :285-288
[5]  
BARELI M, 1993, ANTICANCER RES, V13, P1619
[6]  
Briasoulis E, 1998, ANTICANCER RES, V18, P1907
[7]   Hyperprogressive Disease Is a New Pattern of Progression in Cancer Patients Treated by Anti-PD-1/PD-L1 [J].
Champiat, Stephane ;
Dercle, Laurent ;
Ammari, Samy ;
Massard, Christophe ;
Hollebecque, Antoine ;
Postel-Vinay, Sophie ;
Chaput, Nathalie ;
Eggermont, Alexander ;
Marabelle, Aurelien ;
Soria, Jean-Charles ;
Ferte, Charles .
CLINICAL CANCER RESEARCH, 2017, 23 (08) :1920-1928
[8]   Pseudoprogression and Immune-Related Response in Solid Tumors [J].
Chiou, Victoria L. ;
Burotto, Mauricio .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (31) :3541-+
[9]   A Poorly Differentiated Malignant Neoplasm Lacking Lung Markers Harbors an EML4-ALK Rearrangement and Responds to Crizotinib [J].
Chung, Jon H. ;
Ali, Siraj M. ;
Davis, Jenni ;
Robstad, Karl ;
McNally, Richard ;
Gay, Laurie M. ;
Erlich, Rachel L. ;
Palma, Norma A. ;
Stephens, Phil J. ;
Miller, Vincent A. ;
Cutugno, Alfonso ;
Ross, Jeffrey S. .
CASE REPORTS IN ONCOLOGY, 2014, 7 (03) :628-632
[10]   Development and validation of a prognostic model to predict the length of survival in patients with carcinomas of an unknown primary site [J].
Culine, S ;
Kramar, A ;
Saghatchian, M ;
Bugat, R ;
Lesimple, T ;
Lortholary, A ;
Merrouche, Y ;
Laplanche, A ;
Fizazi, K .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (24) :4679-4683