Napredna pretraga

Pregled bibliografske jedinice broj: 808662

Extracellular Circulating DNA in Lymphoma Patients: Biological Correlates and Prognostic Impact


Dujmovic, Dino; Skaro, Vedrana; Basic-Kinda, Sandra; Markulin, Dora; Samarzija, Ivana; Roncevic, Pavle; Radman, Ivo; Kolenc, Danijela; Dubravcic, Klara; Lauc, Gordan; Aurer, Igor
Extracellular Circulating DNA in Lymphoma Patients: Biological Correlates and Prognostic Impact // Blood
San Francisco, CA, SAD: American Society of Hematology, 2014. str. 5365-5368 (poster, međunarodna recenzija, sažetak, znanstveni)


Naslov
Extracellular Circulating DNA in Lymphoma Patients: Biological Correlates and Prognostic Impact

Autori
Dujmovic, Dino ; Skaro, Vedrana ; Basic-Kinda, Sandra ; Markulin, Dora ; Samarzija, Ivana ; Roncevic, Pavle ; Radman, Ivo ; Kolenc, Danijela ; Dubravcic, Klara ; Lauc, Gordan ; Aurer, Igor

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Blood / - : American Society of Hematology, 2014, 5365-5368

Skup
56th annual meeting of the American Society of Hematology

Mjesto i datum
San Francisco, CA, SAD, 06.-09.2014

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Extracellular circulating DNA; lymphoma; prognostic impact

Sažetak
Extracellular circulating DNA (cfDNA) can be found in small quantities in plasma of healthy persons ; higher concentrations are found in various disorders including malignant and autoimmune diseases, myocardial infarction, trauma, inflammation and complications of pregnancy. In patients with tumors, cfDNA is of tumor origin. Although it has been studied extensively in solid cancers, there is a dearth of information on cfDNA in hematologic neoplasia. The goal of this study was to determine the concentration of cfDNA in patients with lymphoma, its relation to demographic, biologic and clinical patient and tumor characteristics and to investigate its potential role as a marker of disease activity, prognosis or response to treatment. The study was performed in 129 patients with lymphoma treated according to standard guidelines (Table 1). Twenty-nine had Hodgkin's lymphoma (HL) ; 93 B- NHL, 66 aggressive and 27 indolent ; 47 patients had B-large cell lymphoma (B-LCL) and 7 T-NHL. cfDNA concentration was determined using quantitative real-time PCR before and at the end of treatment. In lymphoma patients cfDNA concentration is somewhat higher than in healthy persons (median 20.57 ng/ml vs. 12.1 ng/ml), but is above highest normal values in only 1/3 of cases. We found no correlation between lymphoma type aggressivity and cfDNA concentration. In all patients with NHL and with most NHL types, cfDNA concentration correlated with unfavorable prognostic characteristics: age, LDH, beta-2 microglobulin, disease stage and IPI but not with Ki-67, gender or presence of extranodal disease. Correlation with beta-2 microglobulin was strongest. In univariate analysis, patients with higher cfDNA concentrations had worse treatment outcomes (Fig. 1). In multivariate analysis, cfDNA concentration was not an independent prognostic factor. In patients with HL, cfDNA concentration correlated with LDH, but neither with other tested parameters nor with treatment outcomes. In the vast majority of patients cfDNA concentrations at the end of treatment were lower than at the beginning but neither the absolute nor relative decline correlated with treatment outcomes. In patients with lymphoma, cfDNA concentration prior to treatment start correlates with negative prognostic factors, dominantly with those related to the total tumor mass. However, measuring cfDNA does not add independent clinically meaningful information and seems to be neither of diagnostic nor of prognostic value.

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Temeljne medicinske znanosti



POVEZANOST RADA


Ustanove
Farmaceutsko-biokemijski fakultet, Zagreb,
Medicinski fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Klinički bolnički centar Zagreb,
GENOS d.o.o.

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE