15 research outputs found
Molecular Monitoring in Acute Myeloid Leukemia Patients Undergoing Matched Unrelated Donor: Hematopoietic Stem Cell Transplantation
Minimal residual disease (MRD) in acute myeloid leukemia (AML) is a complex, multi-modality assessment and much as its clinical implications at different points are extensively studied, it remains even now a challenging area. It is the disease biology that governs the modality of MRD assessment; in patients harboring specific molecular targets, high sensitivity techniques can be applied. In AML patients undergoing allogenic hematopoietic stem cell transplantation (alloHSCT), relapse in considered as leading cause for treatment failure. In post-transplant setting, regular MRD status assessment enables to identify patients at risk of impending relapse when early therapeutic intervention may be beneficent. We analyzed data of AML patients who underwent matched unrelated donor (MUD) HSCT since the introduction of this procedure in the Republic of North Macedonia. Chimeric fusion transcripts were identified in three patients; two of them positive for RUNX-RUNX1T1 transcript and one for CBFB-MYH11. One patient harbored mutation in the transcription factor CCAAT/enhancer binding protein Ξ± (CEBPA). Post-transplant MRD kinetics was measured by quantitative polymerase chain or multiplex fluorescent-PCR every three months after the transplantation during the first two years after the transplant. MRD negativity was achieved in three patients by the sixth month of HSCT, who were pre-transplant MRD positive. They sustained hematological and molecular remission for 19, 9 and 7Β months, respectively. The forth patient died due to transplant-related complication. Our experience suggests, when molecularly-defined AML patients undergo HSCT, regular MRD monitoring helps predict impending relapse and direct future treatment strategies
Clinical Significance of Minimal Residual Disease at the End of Remission Induction Therapy in Childhood Acute Lymphoblastic Leukemia
BACKGROUND: Detection of minimal residual disease (MRD) in the early phase of therapy is the most powerful predictor of relapse risk in children with acute lymphoblastic leukaemia (ALL).
AIM: We aimed to determine the significance of MRD at the end of remission induction therapy in the prediction of treatment outcome in children with ALL.
METHODS: Sixty-four consecutive patients aged 1-14 years with newly diagnosed ALL were enrolled in this study from January 2010 to October 2017. All patients were treated according to the ALL IC BFM 2002 protocol. MRD was detected at the end of remission induction therapy (day 33) by multiparameter 6-colour flow cytometry performed on bone marrow specimens with a sensitivity of 0.01%.
RESULTS: Overall, 42.2% of patients had detectable MRD on day 33 of therapy. MRD measurements were not significantly related to presenting characteristics but were associated with a poorer blast clearance on day 8 and 15 of remission induction therapy. Patients with negative MRD status on day 33 had a 5-year event-free survival of 94.6% compared with 76.1% for those with positive MRD status (P = 0.044).
CONCLUSION: MRD levels at the end of remission induction therapy measured by multiparameter flow cytometry have clinical significance in childhood ALL. High levels of MRD are strongly related to poor treatment outcome
Interplay between lymphocyte subpopulation, inflammatory cytokines and their correlation with oxidative stress parameters in COVID-19
Our objective was to investigate the inflammatory and oxidative stress markers in patients with moderate and severe form of COVID-19. In addition, we show the correlation between changes in lymphocyte subsets and markers of oxidative stress as a tool for patient classification. IL-6 and VEGF were analysed by utilizing a High Sensitivity Evidence Investigatorβ’ Biochip Array technology. The total antioxidant capacity (PAT) and the free radical concentrations (d-ROM) were measured in serum utilizing analytical photometric system FRAS5. Peripheral blood was used to determine CD45 + mononuclear, B, T, and NK cells using a multi-parameter flow cytometric immunophenotypic test.
Statistically significant differences in IL-6 and VEGF levels were observed between the two patient groups. Decreased values of the absolute number of lymphocytes and their CD4 + and CD8 + positive T cells, NK cells, and CD8 were obtained. In the moderate group, good correlations were found between IL-6 and VEGF and NK cells (r = 0.6973, p <0.05; for IL6 and r = 0.6498, p <0, for VEGF. 05). Cytokines were correlated with CD45+ (r = 0.5610, p <0.05; for IL-6 and r = 0.5462, p <0.05 for VEGF). The oxidative stress index can be used as a cheaper alternative and as a triage tool between severe and moderate illnesses, after showing good correlation with more expensive patient classification analysis
Use of chronic lymphocytic leukemia-international prognostic index in patient risk stratification-single center experience
Background: Several prognostic factors have been identified to predict the outcome of patients with chronic lymphocytic leukemia (CLL). To predict the time to first treatment (TFT) we integrated the data of clinical and biological markers in CLL-International prognostic index (CLL-IPI). Aim of the study was the determination of the impact of CLL-IPI in prediction of TFS in CLL patents.Methods: The study was set up retrospectively and included 90 patients with CLL diagnosed and treated at the university clinic of hematology for a period of time from January 2012 to January 2020. We incorporated the data of Binet staging system, most adverse cytogenetic marker and mutational status of immunoglobulin heavy chain in CLL-IPI.Results: The statistical data of the 90 patients showed that the median TFS for low CLL-IPI (N=24), intermediate CLL-IPI (N=40), high risk CLL-IPI (N=17) and very high risk group (N=9) according to the CLL-IPI scoring system was 20.1, 17.6, 7.1 and 5.8 months, respectively. Multivariate analysis indicated that del 17p (p<0.008) was independent prognostic factors of TFS.Conclusions: CLL-IPI is a powerful risk stratification tool for CLL patients and this system has also provided treatment recommendations for different patient risk subgroups.
ΠΠ΅Π·Π±Π΅Π΄Π½ΠΎΡΡ Π½Π° ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈΡΠ΅ Π²ΠΎ ΠΊΠ»ΠΈΠ½ΠΈΡΠΊΠ° ΠΏΡΠ°ΠΊΡΠ° - ΠΏΡΠΎΠ³ΡΠ°ΠΌΠ° Π·Π° ΠΊΠΎΠ½ΡΡΠΎΠ»ΠΈΡΠ°Π½ ΠΏΡΠΈΡΡΠ°ΠΏ Π΄ΠΎ Π»Π΅ΠΊΠΎΡ Π»Π΅Π½Π°Π»ΠΈΠ΄ΠΎΠΌΠΈΠ΄
ΠΠ΅Π½Π°Π»ΠΈΠ΄ΠΎΠΌΠΈΠ΄ Π΅ Π»Π΅ΠΊ ΠΊΠΎΡ ΠΏΠΎΡΠ΅Π΄ΡΠ²Π° Π°Π½ΡΠΈΠ½Π΅ΠΎΠΏΠ»Π°ΡΡΠΈΡΠ½ΠΎ, Π°Π½ΡΠΈΠ°Π½Π³ΠΈΠΎΠ³Π΅Π½ΠΎ, ΠΏΡΠΎΠ΅ΡΠΈΡΡΠΎΠΏΠΎΠ΅ΡΡΠΊΠΎ ΠΈ
ΠΈΠΌΡΠ½ΠΎΠΌΠΎΠ΄ΡΠ»Π°ΡΠΎΡΠ½ΠΎ Π΄Π΅ΡΡΡΠ²ΠΎ, Π½ΠΎ ΠΏΡΠΈΡΠΎΠ° ΠΏΠΎΡΠ΅Π΄ΡΠ²Π° ΠΈ ΠΈΠ·ΡΠ°Π·Π΅Π½ΠΎ ΡΠ΅ΡΠ°ΡΠΎΠ³Π΅Π½ΠΎ Π΄Π΅ΡΡΡΠ²ΠΎ. ΠΠ»ΠΈΠ½ΠΈΡΠΊΠΈΠΎΡ
ΡΠ°ΡΠΌΠ°ΡΠ΅Π²Ρ ΠΏΡΠΈ ΠΠΠ£ Π£Π½ΠΈΠ²Π΅ΡΠ·ΠΈΡΠ΅ΡΡΠΊΠ° ΠΊΠ»ΠΈΠ½ΠΈΠΊΠ° Π·Π° Ρ
Π΅ΠΌΠ°ΡΠΎΠ»ΠΎΠ³ΠΈΡΠ° - Π‘ΠΊΠΎΠΏΡΠ΅ Π΅ ΠΎΠ΄Π³ΠΎΠ²ΠΎΡΠ΅Π½ Π·Π°
ΡΠΏΡΠΎΠ²Π΅Π΄ΡΠ²Π°ΡΠ΅ Π½Π° ΠΏΡΠΎΡΠ΅ΡΠΎΡ Π½Π° ΡΠ°ΡΠΌΠ°ΠΊΠΎΠ²ΠΈΠ³ΠΈΠ»Π°Π½ΡΠ°. ΠΠ°ΡΠΎΠ°, ΡΠΎ ΡΠ΅Π» ΠΏΠΎΠ΄ΠΎΠ±ΡΡΠ²Π°ΡΠ΅ Π½Π° Π±Π΅Π·Π±Π΅Π΄Π½ΠΎΡΡΠ°
Π½Π° ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈΡΠ΅, Π½Π° ΠΊΠ»ΠΈΠ½ΠΈΠΊΠ°ΡΠ° ΡΠ΅ ΡΠΏΡΠΎΠ²Π΅Π΄Π΅ ΠΊΠΎΠ½ΡΡΠΎΠ»ΠΈΡΠ°Π½Π° Π΄ΠΈΡΡΡΠΈΠ±ΡΡΠΈΡΠ° Π½Π° Π»Π΅ΠΊΠΎΡ ΡΠ°Π±Π»Π΅ΡΠΈ
Π»Π΅Π½Π°Π»ΠΈΠ΄ΠΎΠΌΠΈΠ΄ ΠΎΠ΄ 5 mg. KΠ°ΠΊΠΎ ΠΌΠ΅ΡΠΊΠ° Π·Π° ΠΌΠΈΠ½ΠΈΠΌΠ°Π»ΠΈΠ·Π°ΡΠΈΡΠ° Π½Π° ΡΠΈΠ·ΠΈΠΊΠΎΡ (ΠΠΠ ) Π·Π° ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈΡΠ΅ ΠΊΠΎΠΈ Π³ΠΎ
ΠΏΡΠΈΠΌΠ°Π°Ρ ΠΎΠ²ΠΎΡ Π»Π΅ΠΊ ΡΠ΅ ΡΠΏΡΠΎΠ²Π΅Π΄Π΅ ΠΏΡΠΎΠ³ΡΠ°ΠΌΠ°ΡΠ° Π·Π° ΠΊΠΎΠ½ΡΡΠΎΠ»ΠΈΡΠ°Π½ ΠΏΡΠΈΡΡΠ°ΠΏ (CAP), ΡΠΏΠΎΡΠ΅Π΄ ΠΊΠΎΡΠ°
ΠΏΡΠΎΠΏΠΈΡΡΠ²Π°ΡΠ΅ΡΠΎ Π½Π° Π»Π΅ΠΊΠΎΡ Π³ΠΎ Π²ΡΡΠ°Ρ ΠΈΡΠΊΠ»ΡΡΠΈΠ²ΠΎ Π»Π΅ΠΊΠ°ΡΠΈ ΠΊΠΎΠΈ ΡΠ΅ Π΅Π²ΠΈΠ΄Π΅Π½ΡΠΈΡΠ°Π½ΠΈ Π²ΠΎ Π Π΅Π³ΠΈΡΡΠ°ΡΠΎΡ Π½Π°
Π΅Π΄ΡΡΠΈΡΠ°Π½ΠΈ Π»Π΅ΠΊΠ°ΡΠΈ Π·Π° ΡΠΏΡΠΎΠ²Π΅Π΄ΡΠ²Π°ΡΠ΅ Π½Π° ΠΏΡΠΎΠ³ΡΠ°ΠΌΠ°ΡΠ° Π·Π° ΠΏΡΠ΅Π²Π΅Π½ΡΠΈΡΠ° Π½Π° Π±ΡΠ΅ΠΌΠ΅Π½ΠΎΡΡ (PPP). Π‘ΠΎ ΡΠΎΠ° ΡΠ΅
Π²ΠΎΠ΄Π΅ΡΠ΅ Π³ΡΠΈΠΆΠ° ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΎΡ Π΄Π° Π³ΠΎ ΠΏΡΠΈΠΌΠΈ Π»Π΅ΠΊΠΎΡ ΡΠ°ΠΌΠΎ Π΄ΠΎΠΊΠΎΠ»ΠΊΡ ΡΠ΅ ΠΈΡΠΏΠΎΠ»Π½Π΅ΡΠΈ Π±Π°ΡΠ°ΡΠ°ΡΠ° ΠΎΠ΄ PPP.
ΠΠΈΠ΄Π΅ΡΡΠΈ Π»Π΅ΠΊΠΎΡ ΡΠ΅ ΠΈΠ·Π»Π°ΡΡΠ²Π° ΠΈ Π²ΠΎ ΡΠΏΠ΅ΡΠΌΠ°ΡΠ°, Π²ΠΎ ΠΏΡΠΎΠ³ΡΠ°ΠΌΠ°ΡΠ° ΠΏΠΎΠΊΡΠ°Ρ ΠΆΠ΅Π½ΠΈ ΠΌΠΎΡΠ°ΡΠ΅ Π΄Π° Π±ΠΈΠ΄Π°Ρ Π²ΠΊΠ»ΡΡΠ΅Π½ΠΈ
ΠΈ ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈ ΠΎΠ΄ ΠΌΠ°ΡΠΊΠ° ΠΏΠΎΠΏΡΠ»Π°ΡΠΈΡΠ°. ΠΠ° Π»Π΅ΠΊΠΎΡ ΡΠ°Π±Π»Π΅ΡΠΈ Π»Π΅Π½Π°Π»ΠΈΠ΄ΠΎΠΌΠΈΠ΄ 5 mg, PPP Π΅ ΡΠΏΡΠΎΠ²Π΅Π΄Π΅Π½Π° ΠΊΠ°Ρ 36
ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈ (23 ΠΌΠ°ΠΆΠΈ ΠΈ 13 ΠΆΠ΅Π½ΠΈ), Π²ΠΎ ΡΠ΅ΠΊ Π½Π° 18 ΠΌΠ΅ΡΠ΅ΡΠΈ, Π·Π°ΠΏΠΎΡΠ½ΡΠ²Π°ΡΡΠΈ ΠΎΠ΄ ΠΎΠΊΡΠΎΠΌΠ²ΡΠΈ 2021 Π³ΠΎΠ΄ΠΈΠ½Π°. Πo
ΠΎΠ²ΠΎΡ ΠΏΠ΅ΡΠΈΠΎΠ΄ Π»Π΅ΠΊΠΎΡ Π΅ ΠΈΠ·Π΄Π°Π΄Π΅Π½ Π½Π° 14 ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈ ΡΠΎ ΠΌΡΠ»ΡΠΈΠΏΠ΅Π½ ΠΌΠΈΠ΅Π»ΠΎΠΌ ΠΊΠΎΠΈ ΠΏΡΠ΅ΡΡ
ΠΎΠ΄Π½ΠΎ ΠΏΡΠΈΠΌΠΈΠ»Π΅ Π±Π°ΡΠ΅ΠΌ
Π΅Π΄Π½Π° Π»ΠΈΠ½ΠΈΡΠ° Π½Π° ΡΠ΅ΡΠ°ΠΏΠΈΡΠ° (Π²ΠΎ ΠΊΠΎΠΌΠ±ΠΈΠ½Π°ΡΠΈΡΠ° ΡΠΎ Π΄Π΅ΠΊΡΠ°ΠΌΠ΅ΡΠ°Π·ΠΎΠ½), 22 ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈ ΡΠΎ ΡΠ΅ΡΠ°ΠΏΠΈΡΠ° Π½Π°
ΠΎΠ΄ΡΠΆΡΠ²Π°ΡΠ΅ Π½Π° Π½ΠΎΠ²ΠΎΠ΄ΠΈΡΠ°Π³Π½ΠΎΡΡΠΈΡΠΈΡΠ°Π½ ΠΌΡΠ»ΡΠΈΠΏΠ΅Π½ ΠΌΠΈΠ΅Π»ΠΎΠΌ ΠΊΠ°Ρ ΠΊΠΎΠΈ Π΅ ΡΠΏΡΠΎΠ²Π΅Π΄Π΅Π½Π° ΡΡΠ°Π½ΡΠΏΠ»Π°Π½ΡΠ°ΡΠΈΡΠ° Π½Π°
Π°Π²ΡΠΎΠ»ΠΎΠ³Π½ΠΈ ΠΌΠ°ΡΠΈΡΠ½ΠΈ ΠΊΠ»Π΅ΡΠΊΠΈ ΠΈ 1 ΠΏΠ°ΡΠΈΠ΅Π½Ρ ΡΠΎ Π΄ΠΈΡΠ°Π³Π½ΠΎΠ·Π° ΠΠ΅-Π₯ΠΎΡΠΊΠΈΠ½ΠΎΠ² ΡΠΎΠ»ΠΈΠΊΡΠ»Π°ΡΠ΅Π½ Π»ΠΈΠΌΡΠΎΠΌ. Π‘ΠΎ
Π΅Π΄ΡΡΠΈΡΠ°ΡΠ΅ Π½Π° ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΈΡΠ΅ ΠΈ ΠΏΡΠ΅Π·Π΅ΠΌΠ°ΡΠ΅ Π½Π° ΡΠΈΡΠ΅ ΠΏΡΠΎΠΏΠΈΡΠ°Π½ΠΈ ΠΌΠ΅ΡΠΊΠΈ ΠΎΠ΄ PPP, ΠΏΠΎΡΠ΅Π½ΡΠΈΡΠ°Π»Π½ΠΈΠΎΡ ΡΠΈΠ·ΠΈΠΊ
ΠΎΠ΄ ΡΠ΅ΡΠ°ΡΠΎΠ³Π΅Π½ΠΎΡΠΎ Π΄Π΅ΡΡΡΠ²ΠΎ Π½Π° Π»Π΅ΠΊΠΎΡ Π±Π΅ΡΠ΅ ΡΠ²Π΅Π΄Π΅Π½ Π½Π° ΠΌΠΈΠ½ΠΈΠΌΡΠΌ
Determination of non-adherence in patients receiving Eltrombopag
Eltrombopag, an orally administered thrombopoietin receptor agonist, selectively binds to the transmembrane domain of the thrombopoietin receptor on the surface of platelets, megakaryocytes and megakaryocyte precursor cells (1). The aim of our research is to determine patient non-adherence and its impact on the effectiveness and safety of prescribed therapy, as well as the possibility of treatment failure. The observational, longitudinal, and retrospective study was conducted in the PHO University Clinic of Hematology in Skopje, R.N.Macedonia. 17 patients (9 men and 8 women) were followed from January to August 2023. Five of them were with diagnose aplastic anemia and 12 with immune thrombocytopenia. All of them treated with Eltrombopag. We have systematically reviewed medical records from the Department of Hospital pharmacy, collected anamnestic data and determine non-adherence to therapy, followed by dose frequency, double taking therapy, omitted doses, drug-drug interactions and food/supplement-drug interactions. Thirteen types of non-adherence were identified, of which 3(23,08%) were related to dose frequency, 1(7,69 %) was related to double taking therapy, 5(38,46%) were related to the possibility of drug-drug interactions, 2(15,38%) with possibility for food/supplement-drug interactions and 2(15,38 %) were related with omitted doses. Failure to adherence is a serious problem which not only affects the patient but also the health care system. The clinical pharmacist intervention can improve patient adherencΠ΅, because the most important determinants effectiveness and safety are adherence to the prescribed therapy, multiple drug and food/supplement interactions which can vary on dose-response relationship, and risk of insufficient effectiveness of therapy (2)
A Rare Case of Soft Tissue Erdheim Chester Disease: Diagnostic Dilemma and Management
BACKGROUND: Erdheim Chester disease (ECD) is a rare form of non-Langerhans histiocytosis that still presents a diagnostic and clinical dilemma.
CASE PRESENTATION: We present a rare case of ECD, young 31 male with atypical localisation and soft tissue presentation and no bone involvement. He started clinical investigations due to subcutaneous tumour mass in the lumbar spine that caused severe back pain. Skin biopsy revealed ECD with Immunohistochemistry CD68+, CD10+, CD11c+, vimentin+, S100A4+. Activating BRAFV600E mutation was positive from the tumour tissue. The patient was referred to the haematology department. PET CT was performed for initial disease staging. Treatment was started with corticosteroids (methylprednisolone 0.5 mg/kg per day), and after 7 days, a significant clinical improvement was noticed in terms of pain disappearance with no need for pain killers. After two weeks, treatment with interferon Alfa (IFN-ΓΒ±) was started in a dose of 3 million units 3 times per week. After 4 months of interim treatment PET, CT revealed a significant reduction of the tumour mass. Therapy with IFN-ΓΒ± was continued, and the patient is still clinically in good condition.
CONCLUSION: It can be concluded that shortening the time of diagnosis of ECD is essential in treatment outcome of this disease. Still, large studies have to confirm the best treatment of this rare condition
Essential Thrombocythemia Associated With Germline JAK2 G571S Variant and Somatic CALR Type 1 Mutation
International audienceIn this study, we report on a family with a germline JAK2 G571S mutation with only one individual presenting with thrombocytosis, who also had a somatic CALR mutation (insertion p.K385fs*47). Our results highlight the complexity of the diagnosis of chronic thrombocytosis, and confirm that genetic alterations in the JAK2 and CALR genes are not always mutually exclusive, nor always responsible for disease phenotype. Our findings suggest that, in routine clinical practice, the diagnostic workup of patients with thrombocytosis should include the simultaneous investigation of JAK2, CALR, and MPL mutations (ie, should not stop once a mutation is identified in the JAK2 gene)