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Wyszukujesz frazę "Subocz, Magdalena" wg kryterium: Wszystkie pola


Wyświetlanie 1-7 z 7
Tytuł:
Ocena profilu korzyści i ryzyka leczenia idelalizybem u chorych na przewlekłą białaczkę limfocytową i chłoniaki nie-Hodgkina
Autorzy:
Puła, Bartosz
Giza, Agnieszka
Rej, Magdalena
Piotrowska, Magdalena
Subocz, Edyta
Rybka, Justyna
Waszczuk-Gajda, Anna
Jurczak, Wojciech
Jamroziak, Krzysztof
Długosz-Danecka, Monika
Opis:
Idelalisib is a selective inhibitor of phosphoinositide 3-kinase d, approved in relapsed/refractory (RR) chronic lymphocytic leukemia (CLL), first line CLL with del17p/TP53 mutation in patients unsuitable for immunochemotherapy and RR follicular lymphoma (FL) in whom at least two lines of therapy have failed. Despite good clinical efficacy, the development of this drug has been hampered due to its adverse events (i.e. autoimmune reactions and life-threatening opportunistic infections). In this retrospective study, we summarise the tolerability of idelalisib therapy in a Polish population, analysing 61 patients treated with idelalisib in monotherapy or idelalisib-based combination regimens. Idelalisib treatment was feasible for the majority of patients, with upper respiratory tract infections (N = 13.21%) being the most common adverse event (AE), and pneumonia (N = 11.18%) — the most prevalent grade 3 or higher non-hematological AE. We observed two cases of pneumonitis, one case of gastroenteritis, and no cases of liver transaminases elevation (all regarded as the AEs characteristic of idelalisib). Most of the patients were treated in haematology reference centres where physicians are more accustomed to dealing with opportunistic infections. Cotrimoxazole prophylaxis was given to 20 (32.8%) patients, whereas acyclovir prophylaxis was administered in 33 (54.1%) cases. This could explain the less frequent life-threatening infections and decreased mortality rate compared to the published registration studies. Our study confirms the high clinical efficacy of idelalisib in CLL and RR FL.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
High efficacy of BGD (bendamustine, gemcitabine, and dexamethasone) in relapsed/refractory Hodgkin Lymphoma
Autorzy:
Krzywon, Aleksandra
Szwedyk, Paweł
Czyż, Anna
Mendrek, Włodzimierz
Zaucha, Jan Maciej
Kulikowski, Waldemar
Wilk, Agata
Taszner, Michał
Paszkiewicz-Kozik, Ewa
Spychałowicz, Wojciech
Subocz, Edyta
Czerw, Tomasz
Swoboda, Ryszard
Drozd-Sokołowska, Joanna
Chmielowska, Ewa
Giza, Agnieszka
Knopińska-Posłuszny, Wanda
Giebel, Sebastian
Najda, Jacek
Olszewska-Szopa, Magdalena
Opis:
The optimal salvage therapy in relapsed/refractory Hodgkin lymphoma (R/R HL) has not been defined so far. The goal of this multicenter retrospective study was to evaluate efficacy and safety of BGD (bendamustine, gemcitabine, dexamethasone) as a second or subsequent line of therapy in classical R/R HL. We have evaluated 92 consecutive R/R HL patients treated with BGD. Median age was 34.5 (19–82) years. Fifty-eight patients (63%) had received 2 or more lines of chemotherapy, 32 patients (34.8%) radiotherapy, and 21 patients (22.8%) an autologous hematopoietic stem cell transplantation (autoHCT). Forty-four patients (47.8%) were resistant to first line of chemotherapy. BGD therapy consisted of bendamustine 90 mg/m$^{2}$ on days 1 and 2, gemcitabine 800 mg/$^{2}$ on days 1 and 4, dexamethasone 40 mg on days 1–4. Median number of BGD cycles was 4 (2–7). The following adverse events ≥ 3 grade were noted: neutropenia (22.8%), thrombocytopenia (20.7%), anemia (15.2%), infections (10.9%), AST/ALT increase (2.2%), and skin rush (1.1%). After BGD therapy, 51 (55.4%) patients achieved complete remission, 23 (25%)—partial response, 7 (7.6%)—stable disease, and 11 (12%) patients experienced progression disease. AutoHCT was conducted in 42 (45.7%) patients after BGD therapy, and allogeneic HCT (alloHCT) in 16 (17.4%) patients. Median progression-free survival was 21 months. BGD is a highly effective, well-tolerated salvage regimen for patients with R/R HL, providing an excellent bridge to auto- or alloHCT.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Expression quantitative trait loci of genes predicting outcome are associated with survival of multiple myeloma patients
Autorzy:
Giles, Graham G.
Ziv, Elad
Clay-Gilmou, Alyssa I.
Dudziński, Marek
Ebbesen, Lene Hyldahl
Markiewicz, Mirosław
Mazur, Grzegorz
Martinez-Lopez, Joaquin
Grzasko, Norbert
Jurczyszyn, Artur
Vangsted, Annette Juul
Norman, Aaron D.
Druzd-Sitek, Agnieszka
Brown, Elizabeth E.
Iskierka-Jazdzewska, Elzbieta
Andersen, Niels Frost
Rymko, Marcin
Milne, Roger L.
Garcia-Sanz, Ramon
Kruszewski, Marcin
Jamroziak, Krzysztof
Zawirska, Daria
Pelosini, Matteo
Barington, Torben
Marques, Herlander
Camp, Nicola J.
Vachon, Celine M.
Waller, Rosalie G.
Piredda, Chiara
Campa, Daniele
Prejzner, Witold
Raźny, Małgorzata
Tomczak, Waldemar
Suska, Anna
Dutka, Magdalena
Butrym, Aleksandra
Macauda, Angelica
Berndt, Sonja
Belachew, Alem A.
Gemignani, Federica
Hildebrandt, Michelle A.T.
Buda, Gabriele
Dumontet, Charles
Subocz, Edyta
Varkonyi, Judit
Reis, Rui Manuel
Abildgaard, Niels
Canzian, Federico
Sainz, Juan
Wątek, Marzena
Slager, Susan L.
Spinelli, John
Haastrup, Eva Kannik
Hofmann, Jonathan N.
Opis:
Gene expression profiling can be used for predicting survival in multiple myeloma (MM) and identifying patients who will benefit from particular types of therapy. Some germline single nucleotide polymorphisms (SNPs) act as expression quantitative trait loci (eQTLs) showing strong associations with gene expression levels. We performed an association study to test whether eQTLs of genes reported to be associated with prognosis of MM patients are directly associated with measures of adverse outcome. Using the genotype-tissue expression portal, we identified a total of 16 candidate genes with at least one eQTL SNP associated with their expression with P < $10^{-7}$ either in EBV-transformed B-lymphocytes or whole blood. We genotyped the resulting 22 SNPs in 1327 MM cases from the International Multiple Myeloma rESEarch (IMMEnSE) consortium and examined their association with overall survival (OS) and progression-free survival (PFS), adjusting for age, sex, country of origin and disease stage. Three polymorphisms in two genes (TBRG4-rs1992292, TBRG4- rs2287535 and ENTPD1-rs2153913) showed associations with OS at P < .05, with the former two also associated with PFS. The associations of two polymorphisms in TBRG4 with OS were replicated in 1277 MM cases from the International Lymphoma Epidemiology (InterLymph) Consortium. A meta-analysis of the data from IMMEnSE and InterLymph (2579 cases) showed that TBRG4-rs1992292 is associated with OS (hazard ratio = 1.14, 95% confidence interval 1.04-1.26, P = .007). In conclusion, we found biologically a plausible association between a SNP in TBRG4 and OS of MM patients.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
    Wyświetlanie 1-7 z 7

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