Search Results - "Świtaj, Tomasz"

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    The clinical prognostic factors and treatment outcomes of adult patients with Ewing sarcoma by Jagodzińska-Mucha, Paulina, Ługowska, Iwona, Świtaj, Tomasz, Koseła-Paterczyk, Hanna, Wągrodzki, Michał, Kozak, Katarzyna, Falkowski, Sławomir, Morysiński, Tadeusz, Goryń, Tomasz, Dawidowska, Anna, Rutkowski, Piotr

    Published in International journal of clinical oncology (01-11-2020)
    “…Background The data about treatment results of Ewing sarcoma in adult patients are limited. The aim of our study was to analyze prognostic factors and outcomes…”
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    Journal Article
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    What is the best front-line approach in patients with desmoid fibromatosis? – A retrospective analysis from a reference center by Sobczuk, Paweł, Agnieszczak, Izabela M., Grycuk, Wiktoria, Czarnecka, Anna M., Świtaj, Tomasz, Koseła-Paterczyk, Hanna, Morysiński, Tadeusz, Zdzienicki, Marcin, Rutkowski, Piotr

    Published in European journal of surgical oncology (01-10-2021)
    “…Desmoid fibromatosis (DF) is a locally aggressive, not metastasizing tumor associated with high local recurrence rates. Surgery was a standard-of-care for DF…”
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    Journal Article
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    Efficacy of immunotherapy beyond RECIST progression in advanced melanoma: a real-world evidence by Czarnecka, Anna Małgorzata, Sobczuk, Paweł, Rogala, Paweł, Świtaj, Tomasz, Placzke, Joanna, Kozak, Katarzyna, Mariuk-Jarema, Anna, Spałek, Mateusz, Dudzisz-Śledź, Monika, Teterycz, Paweł, Borkowska, Aneta, Rutkowski, Piotr

    Published in Cancer Immunology, Immunotherapy (01-08-2022)
    “…Immunotherapy (ITH) holds the possibility of tumor burden decrease after initial RECIST 1.1 defined progression. The clinical concept of treating selected…”
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    Journal Article
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    Genetics of rare mesenchymal tumors: Implications for targeted treatment in DFSP, ASPS, CCS, GCTB and PEComa by Rutkowski, Piotr, Przybył, Joanna, Świtaj, Tomasz

    “…Soft tissue and bone sarcomas comprise a heterogeneous group of mesenchymal tumors that include roughly 130 distinct diagnostic entities. Many of them are…”
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    Management Strategies for Adults with Locally Advanced, Unresectable or Metastatic Malignant Perivascular Epithelioid Cell Tumor (PEComa): Challenges and Solutions by Czarnecka, Anna M, Skoczylas, Jacek, Bartnik, Ewa, Świtaj, Tomasz, Rutkowski, Piotr

    Published in Cancer management and research (01-01-2023)
    “…PEComa (PEC tumor; perivascular epithelioid cell tumors) is a rare group of tumors of mesenchymal origin composed of perivascular epithelioid cells (PEC) with…”
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    Journal Article
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    Efficacy of Sirolimus Treatment in PEComa-10 Years of Practice Perspective by Świtaj, Tomasz, Sobiborowicz, Aleksandra, Teterycz, Paweł, Klimczak, Anna, Makuła, Donata, Wągrodzki, Michał, Szumera-Ciećkiewicz, Anna, Rutkowski, Piotr, Czarnecka, Anna M

    Published in Journal of clinical medicine (20-08-2021)
    “…Perivascular epithelioid cell tumors (PEComa) represent a family of rare mesenchymal tumors resultant from deregulation in mTOR pathway activity. The aim of…”
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    Journal Article
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    Long-term outcomes of sequential chemotherapy in epithelioid sarcoma by Czarnecka, Anna M, Chmiel, Paulina, Błoński, Piotr, Świtaj, Tomasz, Rogala, Paweł, Falkowski, Sławomir, Koseła-Paterczyk, Hanna, Teterycz, Paweł, Kopeć, Sylwia, Morysiński, Tadeusz, Wągrodzki, Michał, Rutkowski, Piotr

    Published in Journal of chemotherapy (Florence) (08-08-2024)
    “…Our study was carried out to define the efficacy of treatment with sequential chemotherapy lines in patients with epithelioid sarcoma (ES) at referral centres…”
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    Journal Article
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    Feasibility and Long-Term Efficacy of PEComa Treatment—20 Years of Experience by Sobiborowicz, Aleksandra, Świtaj, Tomasz, Teterycz, Paweł, Spałek, Mateusz J., Szumera-Ciećkiewicz, Anna, Wągrodzki, Michał, Zdzienicki, Marcin, Czarnecka, Anna M., Rutkowski, Piotr

    Published in Journal of clinical medicine (19-05-2021)
    “…Perivascular epithelioid cell tumors (PEComas) represent a family of rare mesenchymal neoplasms, some of which are malignant. There are no specific management…”
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    Journal Article
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    Real-world outcomes of metastatic clear cell sarcoma sequential chemotherapy by Czarnecka, Anna M, Chmiel, Paulina, Błoński, Piotr J, Świtaj, Tomasz, Rogala, Paweł, Falkowski, Sławomir, Koseła-Paterczyk, Hanna, Teterycz, Paweł, Morysiński, Tadeusz, Spałek, Mateusz, Wągrodzki, Michał, Rutkowski, Piotr

    Published in Journal of chemotherapy (Florence) (08-07-2024)
    “…Clear cell sarcoma is an ultra-rare chemoresistant subtype of soft tissue sarcoma. This retrospective analysis aimed to clarify the efficacy of palliative…”
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    Journal Article
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    Inflammatory myofibroblastic tumor from molecular diagnostics to current treatment by Chmiel, Paulina, SłOWIKOWSKA, Aleksandra, Banaszek, Łukasz, Szumera-CIEćKIEWICZ, Anna, Szostakowski, BARTłOMIEJ, SPAłEK, Mateusz J, Świtaj, Tomasz, Rutkowski, Piotr, Czarnecka, Anna M

    Published in Oncology research (01-01-2024)
    “…Inflammatory myofibroblastic tumor (IMT) is a rare neoplasm with intermediate malignancy characterized by a propensity for recurrence but a low metastatic…”
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    The Use of ctDNA for BRAF Mutation Testing in Routine Clinical Practice in Patients with Advanced Melanoma by Sobczuk, Paweł, Kozak, Katarzyna, Kopeć, Sylwia, Rogala, Paweł, Świtaj, Tomasz, Koseła-Paterczyk, Hanna, Gos, Aleksandra, Tysarowski, Andrzej, Rutkowski, Piotr

    Published in Cancers (02-02-2022)
    “…Assessment of mutation status is mandatory in advanced, treatment-naïve melanoma patients. Liquid biopsy can be an alternative in cases with inadequate or…”
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    Journal Article
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    Diagnostics and Treatment of Extrameningeal Solitary Fibrous Tumors by Janik, Anna Maria, Terlecka, Anna, Spałek, Mateusz J, Boye, Kjetil, Szostakowski, Bartłomiej, Chmiel, Paulina, Szumera-Ciećkiewicz, Anna, Bobak, Klaudia, Świtaj, Tomasz, Rutkowski, Piotr, Czarnecka, Anna M

    Published in Cancers (01-12-2023)
    “…Solitary fibrous tumors (SFT) are rare mesenchymal neoplasms that account for less than 2% of all soft tissue masses. In the latest WHO 2020 Classification of…”
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    Long-term Results of Therapy with Sunitinib in Metastatic Alveolar Soft Part Sarcoma by Jagodzińska-Mucha, Paulina, Świtaj, Tomasz, Kozak, Katarzyna, Koseła-Paterczyk, Hanna, Klimczak, Anna, Ługowska, Iwona, Rogala, Pawel, Wągrodzki, Michał, Falkowski, Sławomir, Rutkowski, Piotr

    Published in Tumori (01-05-2017)
    “…Background Alveolar soft part sarcoma (ASPS) is a rare, highly vascularized soft tissue sarcoma characterized by a high frequency of metastatic disease and…”
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    Malignant peripheral nerve sheath tumors – Outcomes and prognostic factors based on the reference center experience by Sobczuk, Paweł, Teterycz, Paweł, Czarnecka, Anna M., Świtaj, Tomasz, Koseła-Paterczyk, Hanna, Kozak, Katarzyna, Falkowski, Sławomir, Goryń, Tomasz, Zdzienicki, Marcin, Morysiński, Tadeusz, Rutkowski, Piotr

    Published in Surgical oncology (01-12-2020)
    “…Malignant peripheral nerve sheath tumor (MPNST) accounts for about 5% of soft tissue sarcomas. It can occur as sporadic diseases or can be associated with type…”
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