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  1. Article: Dinutuximab beta combined with chemotherapy in patients with relapsed or refractory neuroblastoma.

    Wieczorek, Aleksandra / Zaniewska-Tekieli, Anna / Ehlert, Karoline / Pawinska-Wasikowska, Katarzyna / Balwierz, Walentyna / Lode, Holger

    Frontiers in oncology

    2023  Volume 13, Page(s) 1082771

    Abstract: Prognosis in children with refractory and relapsed high-risk neuroblastoma is poor. Only a minority of patients obtain remission when treated with second-line chemotherapy regimens. Chemotherapy combined with anti-GD2 antibodies has previously been shown ...

    Abstract Prognosis in children with refractory and relapsed high-risk neuroblastoma is poor. Only a minority of patients obtain remission when treated with second-line chemotherapy regimens. Chemotherapy combined with anti-GD2 antibodies has previously been shown to increase response and survival rates. We retrospectively analyzed a cohort of 25 patients with relapsed or refractory high-risk neuroblastoma who were treated with irinotecan/temozolomide chemotherapy in combination with the anti-GD2 antibody dinutuximab beta. The therapy resulted in an objective response rate of 64%, with 32% of patients achieving a complete response. Response to treatment was observed in patients with refractory disease (n=5) and those with first (n=12) or consecutive (n=8) relapses, including patients with progressing disease. In four patients, best response was achieved after more than 5 cycles, suggesting that some patients may benefit from prolonged chemotherapy and dinutuximab beta treatment. Fourteen of our 25 patients had previously received dinutuximab beta, four of whom achieved complete response and six partial response (objective response rate 71%). The therapy was well tolerated, even in heavily pre-treated patients and those who had previously received dinutuximab beta treatment. Toxicities were comparable to those previously reported for the individual therapies, and no discontinuations due to toxicities occurred. Combination of chemotherapy with dinutuximab beta is a promising treatment option for patients with relapsed or refractory high-risk neuroblastoma and should be further explored in clinical studies.
    Language English
    Publishing date 2023-02-03
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2023.1082771
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Blinatumomab as a Bridge Therapy for Hematopoietic Stem Cell Transplantation in Pediatric Refractory/Relapsed Acute Lymphoblastic Leukemia.

    Pawinska-Wasikowska, Katarzyna / Wieczorek, Aleksandra / Balwierz, Walentyna / Bukowska-Strakova, Karolina / Surman, Marta / Skoczen, Szymon

    Cancers

    2022  Volume 14, Issue 2

    Abstract: Despite the progress that has been made in recent decades in the treatment of pediatric acute leukemias, e.g., converting acute lymphoblastic leukemia (ALL) from a fatal to a highly curable disease, 15-20% of children still relapse. Blinatumomab, a ... ...

    Abstract Despite the progress that has been made in recent decades in the treatment of pediatric acute leukemias, e.g., converting acute lymphoblastic leukemia (ALL) from a fatal to a highly curable disease, 15-20% of children still relapse. Blinatumomab, a bispecific CD3/CD19 antibody construct, has been successfully used in relapsed/refractory r/r B-cell precursor ALL (BCP-ALL) as a bridge to hematopoietic stem cell transplantation (HSCT). We retrospectively assessed the efficacy and toxicity of blinatumomab in 13 children with r/r BCP-ALL. Between 2017 and 2021, thirteen children, aged 1-18 years, with r/r BCP-ALL were treated with blinatumomab. Two patients were administered blinatumomab for refractory relapse without complete remission (CR), one due to primary refractory disease, and ten patients were in CR with minimal residual disease (MRD) ≥ 10
    Language English
    Publishing date 2022-01-17
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14020458
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Segmental chromosomal aberrations as the poor prognostic factor in children over 18 months with stage 3 neuroblastoma without

    Wieczorek, Aleksandra / Szewczyk, Katarzyna / Klekawka, Tomasz / Stefanowicz, Joanna / Ussowicz, Marek / Drabik, Grazyna / Pawinska-Wasikowska, Katarzyna / Balwierz, Walentyna

    Frontiers in oncology

    2023  Volume 13, Page(s) 1134772

    Abstract: Introduction: Patients with stage 3 neuroblastoma (NBL) according to International Neuroblastoma Staging System (INSS) without MYCN amplification represent a heterogenous group with respect to disease presentation and prognosis.: Methods: ... ...

    Abstract Introduction: Patients with stage 3 neuroblastoma (NBL) according to International Neuroblastoma Staging System (INSS) without MYCN amplification represent a heterogenous group with respect to disease presentation and prognosis.
    Methods: Retrospective analysis of 40 stage 3 patients with NBL without MYCN amplification was performed. The prognostic value of age at diagnosis (under 18 vs over 18 months), International Neuroblastoma Pathology Classification (INPC) diagnostic category and presence of segmental or numerical chromosomes aberrations were evaluated, as well as biochemical markers. Array comparative genomic hybridization (aCGH) for analyzing copy number variations and Sanger sequencing for ALK point mutations were done.
    Results: In 12 patients (two patients under 18 months), segmental chromosomal aberrations (SCA) were found and numerical chromosomal aberrations (NCA) were found in 16 patients (14 patients under 18 months). In children over 18 months SCA were more common (p=0.0001). Unfavorable pathology was significantly correlated with SCA genomic profile (p=0.04) and age over 18 months (p=0.008). No therapy failures occurred in children with NCA profile over or under 18 months or in children under 18 months, irrespective of pathology and CGH results. Three treatment failures occurred in the SCA group, in one patient CGH profile was not available. For the whole group at 3, 5 and 10-year OS and DFS were 0.95 (95% CI 0.81-0.99), 0.91 (95% CI 0.77-0.97) and 0.91 (95% CI 0.77-0.97), and 0.95 (95% CI 0.90-0.99), 0.92 (95% CI 0.85-0.98) and 0.86 (95% CI 0.78-0.97), respectively. DFS was significantly lower in the SCA group than in the NCA group (3-years, 5-years, and 10-years DFS 0.92 (95% CI 0.53-0.95), 0.80 (95% CI 0.40-0.95) and 0.60 (95% CI 0.16-0.87) vs 1.0, 1.0 and 1.0, respectively, p=0.005).
    Conclusions: The risk of treatment failure was higher in patients with SCA profile, but only in patients over 18 months. All relapses occurred in children having obtained the complete remission, with no previous radiotherapy. In patients over 18 months, SCA profile should be taken into consideration for therapy stratification as it increases the risk of relapse and this group may require more intensive treatment.
    Language English
    Publishing date 2023-02-14
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2023.1134772
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Dinutuximab Beta Maintenance Therapy in Patients with High-Risk Neuroblastoma in First-Line and Refractory/Relapsed Settings-Real-World Data.

    Wieczorek, Aleksandra / Żebrowska, Urszula / Ussowicz, Marek / Sokół, Agnieszka / Stypińska, Marzena / Dembowska-Bagińska, Bożenna / Pawińska-Wąsikowska, Katarzyna / Balwierz, Walentyna

    Journal of clinical medicine

    2023  Volume 12, Issue 16

    Abstract: Dinutuximab beta is approved for the maintenance treatment of patients with high-risk neuroblastoma (HR-NB), including patients with relapsed/refractory (R/R) disease. However, the data on its use in real-world clinical practice is limited. We ... ...

    Abstract Dinutuximab beta is approved for the maintenance treatment of patients with high-risk neuroblastoma (HR-NB), including patients with relapsed/refractory (R/R) disease. However, the data on its use in real-world clinical practice is limited. We retrospectively reviewed the clinical records of 54 patients with HR-NB who received maintenance therapy with dinutuximab beta in first-line (37 patients) or R/R settings (17 patients) at three centers in Poland. Of the 37 patients who received first-line treatment, twenty-eight had a complete response, two had a partial response, three had progressive disease, and four relapsed at the end of treatment. The median overall survival (OS) was 24.37 months, and the three-year progression-free survival (PFS) and OS were 0.63 and 0.80, respectively. Of the 17 patients in the R/R group, 11 had a complete response, two had a partial response, one had stable disease, and three had progressive disease or relapsed at the end of treatment. The median OS was 33.1 months and the three-year PFS and OS were 0.75 and 0.86, respectively. Treatment was generally well tolerated, including in patients with co-morbidities and those who had experienced toxicities with previous therapies. These findings demonstrate that the use of dinutuximab beta is feasible and beneficial as a first-line or R/R treatment in routine clinical practice in Poland.
    Language English
    Publishing date 2023-08-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm12165252
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  5. Article: Case Report: Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy Application in Intraperitoneally Disseminated Inflammatory Myofibroblastic Tumor and in the Youngest Patient in the World: New Indication and Modification of Technique.

    Garnier, Hanna / Murawski, Maciej / Jastrzebski, Tomasz / Pawinska-Wasikowska, Katarzyna / Balwierz, Walentyna / Sinacka, Katarzyna / Gorecki, Wojciech / Izycka-Swieszewska, Ewa / Czauderna, Piotr

    Frontiers in surgery

    2021  Volume 8, Page(s) 746700

    Abstract: Introduction: ...

    Abstract Introduction:
    Language English
    Publishing date 2021-10-12
    Publishing country Switzerland
    Document type Case Reports
    ZDB-ID 2773823-1
    ISSN 2296-875X
    ISSN 2296-875X
    DOI 10.3389/fsurg.2021.746700
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Anti-PD-1 Therapy in Advanced Pediatric Malignancies in Nationwide Study: Good Outcome in Skin Melanoma and Hodgkin Lymphoma.

    Marjańska, Agata / Pawińska-Wąsikowska, Katarzyna / Wieczorek, Aleksandra / Drogosiewicz, Monika / Dembowska-Bagińska, Bożenna / Bobeff, Katarzyna / Młynarski, Wojciech / Adamczewska-Wawrzynowicz, Katarzyna / Wachowiak, Jacek / Krawczyk, Małgorzata A / Irga-Jaworska, Ninela / Węcławek-Tompol, Jadwiga / Kałwak, Krzysztof / Sawicka-Żukowska, Małgorzata / Krawczuk-Rybak, Maryna / Raciborska, Anna / Mizia-Malarz, Agnieszka / Sobocińska-Mirska, Agata / Łaguna, Paweł /
    Balwierz, Walentyna / Styczyński, Jan

    Cancers

    2024  Volume 16, Issue 5

    Abstract: Background/aim: The role of immune checkpoint inhibitors (ICIs; anti-PD1) in the treatment of childhood cancers is still evolving. The aim of this nationwide retrospective study was to assess the safety and effectiveness of ICIs used in a group of 42 ... ...

    Abstract Background/aim: The role of immune checkpoint inhibitors (ICIs; anti-PD1) in the treatment of childhood cancers is still evolving. The aim of this nationwide retrospective study was to assess the safety and effectiveness of ICIs used in a group of 42 patients, with a median age of 13.6 years, with various types of advanced malignancies treated in pediatric oncology centers in Poland between 2015 and 2023.
    Results: The indications for treatment with anti-PD1 were as follows: Hodgkin lymphoma (11); malignant skin melanoma (9); neuroblastoma (8); and other malignancies (14). At the end of follow-up, complete remission (CR) was observed in 37.7% (15/42) of children and disease stabilization in 9.5% (4/42), with a mean survival 3.6 (95% CI = 2.6-4.6) years. The best survival (OS = 1.0) was observed in the group of patients with Hodgkin lymphoma. For malignant melanoma of the skin, neuroblastoma, and other rare malignancies, the estimated 3-year OS values were, respectively, 0.78, 0.33, and 0.25 (
    Language English
    Publishing date 2024-02-28
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers16050968
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Pre-Exposure Prophylaxis and Treatment with Tixagevimab/Cilgavimab for COVID-19 among Immunocompromised Pediatric Patients.

    Frączkiewicz, Jowita / Pawińska-Wąsikowska, Katarzyna / Szymbor, Katarzyna / Balwierz, Walentyna / Skoczeń, Szymon / Czyżewski, Krzysztof / Kołtan, Sylwia / Styczyński, Jan / Małecka, Anna / Irga-Jaworska, Ninela / Trelińska, Joanna / Młynarski, Wojciech / Zając-Spychała, Olga / Sobkowiak-Sobierajska, Agnieszka / Derwich, Katarzyna / Bal, Wioletta / Chaber, Radosław / Książek, Agnieszka / Szczepański, Tomasz /
    Zawitkowska, Joanna / Drabko, Katarzyna / Chodała-Grzywacz, Agnieszka / Karolczyk, Grażyna / Kobierzycki, Christopher / Kałwak, Krzysztof

    Journal of clinical medicine

    2024  Volume 13, Issue 7

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2024-03-31
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm13072029
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  8. Article: Go with the Flow-Early Assessment of Measurable Residual Disease in Children with Acute Lymphoblastic Leukemia Treated According to ALL IC-BFM2009.

    Pawinska-Wasikowska, Katarzyna / Bukowska-Strakova, Karolina / Surman, Marta / Rygielska, Monika / Sadowska, Beata / Ksiazek, Teofila / Klekawka, Tomasz / Wieczorek, Aleksandra / Skoczen, Szymon / Balwierz, Walentyna

    Cancers

    2022  Volume 14, Issue 21

    Abstract: Measurable residual disease (MRD) is a well-known tool for the evaluation of the early response to treatment in patients with acute lymphoblastic leukemia (ALL). In respect to predicting the relapse the most informative cut-off and time point of MRD ... ...

    Abstract Measurable residual disease (MRD) is a well-known tool for the evaluation of the early response to treatment in patients with acute lymphoblastic leukemia (ALL). In respect to predicting the relapse the most informative cut-off and time point of MRD measurement during therapy were evaluated in our study. Between 1 January 2013 and 31 December 2019, multiparametric flow cytometry (MFC) MRD was measured in the bone marrow of 140 children with ALL treated according to the ALL IC-BFM2009 protocol. The MRD cut-off of 0.1% and day 33, end of induction, were the most discriminatory for all patients. Patients with negative MRD on day 15 and 33 had a higher 5-year overall survival-OS (100%) and a higher relapse-free survival-RFS rate (97.6%) than those with positive levels of MRD (≥0.01%) at both time points (77.8% and 55.6%,
    Language English
    Publishing date 2022-10-30
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14215359
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  9. Article: Monitoring of treatment with L-asparaginase in children with acute lymphoblastic leukaemia, with a focus on silent inactivation and its influence on the treatment outcome.

    Czogala, Malgorzata / Rogatko, Iwona / Pawińska-Wąsikowska, Katarzyna / Czogała, Wojciech / Bal, Wioletta / Ciebiera, Małgorzata / Chaber, Radosław / Chodała-Grzywacz, Agnieszka / Karolczyk, Grażyna / Sztefko, Krystyna / Balwierz, Walentyna / Skoczeń, Szymon

    Contemporary oncology (Poznan, Poland)

    2022  Volume 26, Issue 4, Page(s) 282–288

    Abstract: Introduction: The aim of the study was to analyse the frequency of silent inactivation and allergic reaction to asparaginase (ASP) and its impact on treatment results in patients with lymphoblastic leukaemia.: Material and methods: Seventy patients ... ...

    Abstract Introduction: The aim of the study was to analyse the frequency of silent inactivation and allergic reaction to asparaginase (ASP) and its impact on treatment results in patients with lymphoblastic leukaemia.
    Material and methods: Seventy patients with acute lymphoblastic leukaemia treated with ASP were enrolled in the study. Asparaginase activity was monitored. The patients were switched to another ASP formulation after allergy or inactivation. The treatment results were analysed.
    Results: Silent inactivation of native
    Conclusions: Monitoring of ASP activity is crucial to recognize silent inactivation and to guarantee treatment effectiveness by switching to other ASP preparations.
    Language English
    Publishing date 2022-12-30
    Publishing country Poland
    Document type Journal Article
    ISSN 1428-2526
    ISSN 1428-2526
    DOI 10.5114/wo.2023.124972
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  10. Article: Zmiany ekspresji determinant komórkowych w trakcie leczenia indukcyjnego dzieci z ostra białaczka limfoblastyczna.

    Pawińska-Wasikowska, Katarzyna / Balwierz, Walentyna

    Przeglad lekarski

    2010  Volume 67, Issue 6, Page(s) 361–365

    Abstract: Leukemias are the most common malignancy in children, and acute lymphoblastic leukemia (ALL) accounts for 85% of all childhood leukemias. Sequential monitoring of MRD (minimal residual disease) in a set time points during the induction therapy in ALL ... ...

    Title translation Cells antigens' expression modulation during induction treatment of childhood acute lymphoblastic leukemia.
    Abstract Leukemias are the most common malignancy in children, and acute lymphoblastic leukemia (ALL) accounts for 85% of all childhood leukemias. Sequential monitoring of MRD (minimal residual disease) in a set time points during the induction therapy in ALL proves to be a powerful and independent predictor of treatment outcome. Crucial limitation of MRD monitoring by flow cytometry is immunophenotypic changes seen at relapse. Up to now there are single publications about immunophenotypic changes during treatment of ALL in children. Objective was to assess changes in expression of cell antigens during induction treatment of ALL. From May 2005 to January 2008, from among 78 patients with ALL treated in Oncology and Hematology Department, Children's University Hospital in Krakow according to international treatment protocol ALL IC-BFM-2002, 42 were enrolled in assessment of antigens' cells modulation expression during induction. Finally, 24 boys and 18 girls were eligible for evaluation. For MRD detection 4-colour flow cytometry with FACS Diva Software v.5.1 (BD Immunocytometry Systems) was used. The panel of monoclonal antibodies used for MRD detection was based on ALL IC-BFM-2002 standard, modified by additional antibodies combinations from ALL-BFM-2000 protocol. Identification of leukemia associated phenotype (LAP), used for cell analysis in sequential time points, with a set monoclonal antibodies panel, was possible in all analyzed patients. Superficial and cytoplasmic antigens modulation was observed in most of the patients during MRD monitoring. Changes of antigens were seen mostly in PB on day 8 and on day 15 both in PB and BM. The most common antigen modulation found in children with cALL was: downmodulation of CD10, CD34, CD19, and upmodulation of CD45, CD11a, CD20. Unequivocal character of modulation of CD66c, CD58, CD38 was difficult to define (up and downmodulation). Introduction of treatment monitoring based on flow cytometry MRD measurement could lead to further individualization of therapy and improovement of cure rates in ALL, as well as to reducing side effects of ALL treatment and decrease total cost of patient therapy.
    MeSH term(s) Adolescent ; Antibodies, Monoclonal/analysis ; Antigenic Modulation/immunology ; Antigens, CD/analysis ; Child ; Child, Preschool ; Drug Monitoring ; Female ; Flow Cytometry ; Humans ; Infant ; Male ; Neoplasm, Residual/diagnosis ; Neoplasm, Residual/immunology ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/immunology ; Remission Induction/methods
    Chemical Substances Antibodies, Monoclonal ; Antigens, CD
    Language Polish
    Publishing date 2010
    Publishing country Poland
    Document type English Abstract ; Journal Article
    ZDB-ID 414053-9
    ISSN 0033-2240 ; 0860-0422
    ISSN 0033-2240 ; 0860-0422
    Database MEDical Literature Analysis and Retrieval System OnLINE

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