-
Je něco špatně v tomto záznamu ?
Evaluation of serum levels of selected cytokine receptors in adult B-cell precursor acute lymphoblastic leukemia and their association with prognostic factors and survival
JM. Horacek, T. Kupsa, J. Vanek, M. Jakl, M. Stajer, L. Jebavy, P. Zak
Jazyk angličtina Země Ukrajina
Typ dokumentu časopisecké články
- MeSH
- dospělí MeSH
- indukční chemoterapie mortalita MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- mladý dospělý MeSH
- nádorové biomarkery krev MeSH
- následné studie MeSH
- pre-B-buněčná leukemie krev farmakoterapie mortalita patologie MeSH
- prognóza MeSH
- protokoly antitumorózní kombinované chemoterapie terapeutické užití MeSH
- receptory cytokinové krev MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
AIM: To evaluate serum levels of selected cytokine receptors in B-cell precursor acute lymphoblastic leukemia (B-ALL) and their association with acknowledged prognostic factors, relapse-free survival (RFS) and overall survival (OS). MATERIALS AND METHODS: A total of 42 de novo adult B-ALL patients, 19 BCR/ABL positive, were included in this study. Soluble receptor α for IL-2 (sIL-2Rα), soluble receptor for IL-6 (sIL-6R), soluble receptor for TNF-α type I and II (sTNFR-1, sTNFR-2) and matrix metalloproteinase-9 (MMP-9) were measured by biochip array technology at diagnosis and in complete remission (CR). RESULTS: At diagnosis of B-ALL, we found significantly higher levels of sIL-2Rα, sIL-6R, sTNFR-1, sTNFR-2 and significantly lower levels MMP-9 in comparison with CR (p < 0.001 in all cases). BCR/ABL positive patients had higher levels of sIL-2Rα at diagnosis (r = 0.484; p = 0.014). Serum levels of evaluated cytokines were not associated with achievement of CR after one cycle of induction therapy, RFS or OS. CONCLUSION: Serum levels of all evaluated cytokines are significantly altered in newly diagnosed B-ALL reflecting activity of the disease. No significant correlations with response to first induction therapy, RFS or OS were found. Further studies with a longer follow-up will be needed.
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22012240
- 003
- CZ-PrNML
- 005
- 20240206151827.0
- 007
- ta
- 008
- 220425s2021 un f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.32471/exp-oncology.2312-8852.vol-43-no-3.16548 $2 doi
- 035 __
- $a (PubMed)34591424
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a un
- 100 1_
- $a Horacek, J M $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences, 500 01 Hradec Kralove, Czech Republic
- 245 10
- $a Evaluation of serum levels of selected cytokine receptors in adult B-cell precursor acute lymphoblastic leukemia and their association with prognostic factors and survival / $c JM. Horacek, T. Kupsa, J. Vanek, M. Jakl, M. Stajer, L. Jebavy, P. Zak
- 520 9_
- $a AIM: To evaluate serum levels of selected cytokine receptors in B-cell precursor acute lymphoblastic leukemia (B-ALL) and their association with acknowledged prognostic factors, relapse-free survival (RFS) and overall survival (OS). MATERIALS AND METHODS: A total of 42 de novo adult B-ALL patients, 19 BCR/ABL positive, were included in this study. Soluble receptor α for IL-2 (sIL-2Rα), soluble receptor for IL-6 (sIL-6R), soluble receptor for TNF-α type I and II (sTNFR-1, sTNFR-2) and matrix metalloproteinase-9 (MMP-9) were measured by biochip array technology at diagnosis and in complete remission (CR). RESULTS: At diagnosis of B-ALL, we found significantly higher levels of sIL-2Rα, sIL-6R, sTNFR-1, sTNFR-2 and significantly lower levels MMP-9 in comparison with CR (p < 0.001 in all cases). BCR/ABL positive patients had higher levels of sIL-2Rα at diagnosis (r = 0.484; p = 0.014). Serum levels of evaluated cytokines were not associated with achievement of CR after one cycle of induction therapy, RFS or OS. CONCLUSION: Serum levels of all evaluated cytokines are significantly altered in newly diagnosed B-ALL reflecting activity of the disease. No significant correlations with response to first induction therapy, RFS or OS were found. Further studies with a longer follow-up will be needed.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a protokoly antitumorózní kombinované chemoterapie $x terapeutické užití $7 D000971
- 650 _2
- $a nádorové biomarkery $x krev $7 D014408
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a následné studie $7 D005500
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a indukční chemoterapie $x mortalita $7 D060828
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a pre-B-buněčná leukemie $x krev $x farmakoterapie $x mortalita $x patologie $7 D015452
- 650 _2
- $a prognóza $7 D011379
- 650 _2
- $a receptory cytokinové $x krev $7 D018121
- 650 _2
- $a míra přežití $7 D015996
- 650 _2
- $a mladý dospělý $7 D055815
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kupsa, T $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences, 500 01 Hradec Kralove, Czech Republic
- 700 1_
- $a Vanek, J $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences, 500 01 Hradec Kralove, Czech Republic
- 700 1_
- $a Jakl, Martin $7 xx0135493
- 700 1_
- $a Stajer, M $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences, 500 01 Hradec Kralove, Czech Republic
- 700 1_
- $a Jebavy, L $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences, 500 01 Hradec Kralove, Czech Republic
- 700 1_
- $a Zak, P $u Department of Internal Medicine IV - Hematology, University Hospital and Charles University, Faculty of Medicine, 500 05 Hradec Kralove, Czech Republic
- 773 0_
- $w MED00174402 $t Experimental oncology $x 1812-9269 $g Roč. 43, č. 3 (2021), s. 234-236
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34591424 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220425 $b ABA008
- 991 __
- $a 20240206151824 $b ABA008
- 999 __
- $a ok $b bmc $g 1789710 $s 1163441
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 43 $c 3 $d 234-236 $e - $i 1812-9269 $m Experimental oncology $n Exp Oncol $x MED00174402
- LZP __
- $a Pubmed-20220425