An update on disease biomarkers for Hodgkin lymphoma

被引:4
作者
Cirillo, Melita [1 ,2 ,3 ,4 ,5 ]
Borchmann, Sven [1 ,2 ,3 ,6 ]
机构
[1] Univ Cologne, Fac Med, Cologne, Germany
[2] Univ Cologne, GHSG, Univ Hosp Cologne, Dept Internal Med 1, Cologne, Germany
[3] Univ Cologne, Ctr Mol Med, Univ Hosp Cologne, Cologne, Germany
[4] Royal Perth Hosp, Dept Hematol, Perth, WA, Australia
[5] Univ Western Australia, Perth, WA, Australia
[6] Univ Cologne, Else Kroner Forsch Kolleg Clonal Evolut Canc, Univ Hosp Cologne, Cologne, Germany
关键词
Hodgkin lymphoma; prognosis; treatment; chemotherapy; TARC; cell free DNA; tumor microenvironment; pet scan; metabolic tumor volume; genotyping; POSITRON-EMISSION-TOMOGRAPHY; RESPONSE-ADAPTED THERAPY; METABOLIC TUMOR VOLUME; INTERNATIONAL PROGNOSTIC SCORE; STEM-CELL TRANSPLANTATION; REED-STERNBERG CELLS; FREE CIRCULATING DNA; SERUM TARC LEVELS; BARR-VIRUS-DNA; INTERGROUP TRIAL;
D O I
10.1080/17474086.2020.1746183
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Hodgkin Lymphoma (HL) carries an overall excellent prognosis for young patients treated with multimodal therapy. Predicting an individual patient's prognosis is currently heavily dependent on imaging modalities such as Positron Emission Tomography (PET). Areas covered: Potential biomarkers from serum, tissue, circulating nucleic acids and non-tumor derived cells have all been reported to be of prognostic relevance in HL. We review a range of these biomarkers and discuss the integration of new biomarkers into individualized patient care. Expert opinion: Better prognostic markers are needed to predict an individuals response to HL therapy. Interim PET-scan improves the ability to predict long-term treatment responders. However, it is our opinion that supplementation of PET results with additional biomarkers (including circulating tumor DNA, protein biomarkers, tissue genotyping and metabolic tumor volume) are likely to improve risk stratification for future patients with HL.
引用
收藏
页码:481 / 488
页数:8
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