Biomarkers of systemic inflammation provide additional prognostic stratification in cancers of unknown primary

被引:2
作者
Harvey, Svenja [1 ]
Stares, Mark [1 ,2 ,8 ]
Scott, Julie-Anne [3 ]
Thottiyil, Tharun Joseph Vattam [4 ]
Conway, Alicia-Marie [5 ,6 ]
Haigh, Rachel [2 ]
Brown, Jackie [2 ]
Knowles, Gillian [2 ]
Dasgupta, Sonali [7 ]
Shiu, Kai-Keen [4 ]
Mitchell, Claire [6 ]
Barrie, Colin [2 ]
Cook, Natalie [3 ]
Clive, Sally [2 ]
机构
[1] Univ Edinburgh, Western Gen Hosp, Inst Genet & Canc, Canc Res UK Edinburgh Ctr, Edinburgh, Scotland
[2] Western Gen Hosp, Edinburgh Canc Ctr, NHS Lothian, Edinburgh, Scotland
[3] Christie NHS Fdn Trust, Expt Canc Med Team ECMT, Manchester, England
[4] Univ Coll London Hosp NHS Fdn Trust, London, England
[5] Univ Manchester, Canc Res UK Manchester Inst, Manchester, England
[6] Christie NHS Fdn Trust, Manchester, England
[7] Velindre Univ NHS Trust, Cardiff, Wales
[8] Univ Edinburgh, Inst Genet & Canc, Canc Res UK Edinburgh Ctr, Edinburgh, Scotland
关键词
cancer of unknown primary; c-reactive protein; prognosis; Scottish inflammatory prognostic score; systemic anticancer therapy; PRIMARY SITE; CARCINOMAS; DIAGNOSIS; SURVIVAL; PREDICT; TRIAL;
D O I
10.1002/cam4.6988
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Biomarkers of systemic inflammation have been shown to predict outcomes in patients with cancer of unknown primary (CUP). We sought to validate these findings in patients with confirmed CUP (cCUP) and explore their role alongside existing clinicopathological prognostic categories. Patients and Methods CUP oncologist from across the United Kingdom were invited to include patients with cCUP referred to their local CUP multidisciplinary team. Patient demographics, clinical, pathological and outcome data were recorded and analysed. Results Data were available for 548 patients from four CUP services. 23% (n = 124) of patients met clinicopathological criteria for favourable-risk cCUP. On multivariate analysis c-reactive protein (CRP) (p < 0.001) and the Scottish Inflammatory Prognostic Score (SIPS: combining albumin and neutrophil count) (p < 0.001) were independently predictive of survival. CRP and SIPS effectively stratified survival in patients with both favourable-risk and poor-risk cCUP based on clinicopathological features. Conclusions Biomarkers of systemic inflammation are reliable prognostic factors in patients with cCUP, regardless of clinicopathological subgroup. We recommend that CRP or SIPS are incorporated into routine clinical assessments of patients with cCUP as a tool to aid investigation and/or treatment decision-making across all groups. Established clinicopathological factors can then be used to inform management pathways and specific systemic anticancer therapy selection.
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共 40 条
[1]   Prognostic value of performance status assessed by patients themselves, nurses, and oncologists in advanced non-small cell lung cancer [J].
Ando, M ;
Ando, Y ;
Hasegawa, Y ;
Shimokata, K ;
Minami, H ;
Wakai, K ;
Ohno, Y ;
Sakai, S .
BRITISH JOURNAL OF CANCER, 2001, 85 (11) :1634-1639
[2]   Intrahepatic cholangiocarcinoma hidden within cancer of unknown primary [J].
Conway, Alicia-Marie ;
Morris, Georgina C. ;
Smith, Sarah ;
Vekeria, Monique ;
Manoharan, Prakash ;
Mitchell, Claire ;
Backen, Alison ;
Oliveira, Pedro ;
Hubner, Richard A. ;
Lamarca, Angela ;
McNamara, Mairead G. ;
Valle, Juan W. ;
Cook, Natalie .
BRITISH JOURNAL OF CANCER, 2022, 127 (03) :531-540
[3]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[4]  
CRUK, 2020, Cancer Research UK Cancer of Unknown Primary Statistics [Internet]
[5]   Cisplatin in combination with either gemcitabine or irinotecan in carcinomas of unknown primary site:: Results of a randomized phase II study-trial for the French Study Group on Carcinomas of Unknown Primary (GEFCAPI 01) [J].
Culine, S ;
Lortholary, A ;
Voigt, JJ ;
Bugat, R ;
Théodore, C ;
Priou, F ;
Kaminsky, MC ;
Lesimple, T ;
Pivot, X ;
Coudert, B ;
Douillar, JY ;
Merrouche, Y ;
Allouache, J ;
Goupil, A ;
Négrier, S ;
Viala, J ;
Petrow, P ;
Bouzy, J ;
Laplanche, A ;
Fizazi, K .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (18) :3479-3482
[6]   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
[7]   Cancers of unknown primary site: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-upaEuro [J].
Fizazi, K. ;
Greco, F. A. ;
Pavlidis, N. ;
Daugaard, G. ;
Oien, K. ;
Pentheroudakis, G. .
ANNALS OF ONCOLOGY, 2015, 26 :V133-V138
[8]   Effect of specialist palliative care services on quality of life in adults with advanced incurable illness in hospital, hospice, or community settings: systematic review and meta-analysis [J].
Gaertner, Jan ;
Siemens, Waldemar ;
Meerpohl, Joerg J. ;
Antes, Gerd ;
Meffert, Cornelia ;
Xander, Carola ;
Stock, Stephanie ;
Mueller, Dirk ;
Schwarzer, Guido ;
Becker, Gerhild .
BMJ-BRITISH MEDICAL JOURNAL, 2017, 358
[9]   Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases [J].
Gatalica, Zoran ;
Millis, Sherri Z. ;
Vranic, Semir ;
Bender, Ryan ;
Basu, Gargi D. ;
Voss, Andreas ;
Von Hoff, Daniel D. .
ONCOTARGET, 2014, 5 (23) :12440-12447
[10]   Cancer of unknown primary: progress in the search for improved and rapid diagnosis leading toward superior patient outcomes [J].
Greco, F. A. ;
Oien, K. ;
Erlander, M. ;
Osborne, R. ;
Varadhachary, G. ;
Bridgewater, J. ;
Cohen, D. ;
Wasan, H. .
ANNALS OF ONCOLOGY, 2012, 23 (02) :298-304