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Dive into the research topics where Katarzyna Bilska is active.

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Featured researches published by Katarzyna Bilska.


Pediatric Blood & Cancer | 2013

Vincristine, irinotecan, and temozolomide in patients with relapsed and refractory Ewing sarcoma

Anna Raciborska; Katarzyna Bilska; Katarzyna Drabko; Radosław Chaber; Monika Pogorzała; Elżbieta Wyrobek; Katarzyna Połczyńska; Elżbieta Rogowska; Carlos Rodriguez-Galindo; Wojciech Wozniak

Patients with metastatic, progressive or recurrent Ewing sarcoma (ES) have a dismal outcome. The combination of irinotecan and temozolomide has been proposed as an effective salvage regimen for some pediatric malignancies. Thus, we sought to evaluate this combination with vincristine for patients with relapsed and refractory ES.


Pediatric Blood & Cancer | 2014

Validation of a multi‐modal treatment protocol for Ewing sarcoma—A report from the polish pediatric oncology group

Anna Raciborska; Katarzyna Bilska; Katarzyna Drabko; Radosław Chaber; Grazyna Sobol; Monika Pogorzała; Elżbieta Wyrobek; Katarzyna Połczyńska; Elżbieta Rogowska; Carlos Rodriguez-Galindo; Wojciech Wożniak

Ewing sarcoma (ES) is the second most common paediatric malignant bone tumor. Advances in multi‐disciplinary care have resulted in significant improvement in cure rates over the last decades. However, the generalization of those results in countries traditionally excluded from large cooperative trials has yet to be demonstrated. We report the results of modern multi‐disciplinary care for patients with ES in Poland.


Pediatric Blood & Cancer | 2015

Ovarian function in female survivors after multimodal Ewing sarcoma therapy

Anna Raciborska; Katarzyna Bilska; Ewa Filipp; Katarzyna Drabko; Elżbieta Rogowska; Radosław Chaber; Monika Pogorzała; Katarzyna Połczyńska; Natalia Adrianowska; Carlos Rodriguez-Galindo; Tomasz Maciejewski

With advances in cancer care, more young women with Ewing sarcoma (ES) survive after treatment. Thus, we sought to analyze the ovarian function in prepubertal, pubertal and postpubertal females and young women receiving multimodal therapy for ES, and to identify patients at risk of infertility on whom fertility preservation would be indicated.


Journal of Pediatric Surgery | 2014

Internal hemipelvectomy in the management of pelvic Ewing sarcoma - are outcomes better than with radiation therapy?

Anna Raciborska; Katarzyna Bilska; Magdalena Rychłowska-Pruszyńska; Katarzyna Drabko; Radosław Chaber; Monika Pogorzała; Katarzyna Połczyńska; Jan Godzinski; Carlos Rodriguez-Galindo; Wojciech Wożniak

BACKGROUND Pelvic Ewing sarcoma (ES) is commonly associated with a worse prognosis. Large size and location limit local control options to radiation therapy, and local recurrences are common. We evaluated the impact of hemipelvectomy and radiation on outcomes, including function. MATERIALS AND METHODS Thirty-nine patients (median age 13.5years) with ES of the pelvis and sacral bones were treated during the period 2000-2012. Fifteen were treated with definitive radiotherapy (RT), 9 patients underwent hemipelvectomy alone, and 15 were treated with combined hemipelvectomy and RT. RESULTS Twenty patients (51.2%) are alive with a median follow-up 3.2years from diagnosis. Median time from diagnosis to relapse was 1.3years. Three-year estimates of EFS and OS were 47% and 61%, respectively. Patients treated with surgery or surgery with RT had better outcome than patients treated with RT only (3-year OS 78% or 81% vs. 36%, respectively, p=0.00083). The outcome of patients with pelvic ES treated with hemipelvectomy was not significantly different from the outcome of all patients with Ewing sarcoma treated on the national Polish protocol. CONCLUSIONS Internal hemipelvectomy offers good chances of cure for patients with pelvic ES, with a reasonable rate of complications and good function.


Scientific Reports | 2018

Prediction of Ewing Sarcoma treatment outcome using attenuated tissue reflection FTIR tissue spectroscopy

Radosław Chaber; Kornelia Łach; Christopher J. Arthur; Anna Raciborska; Elżbieta Michalak; Krzysztof Ciebiera; Katarzyna Bilska; Katarzyna Drabko; Józef Cebulski

Ewing sarcoma is the second most common type of primary bone cancer and predominantly affects children and young people. Improved outcome prediction is key to delivering risk-adjusted, appropriate and effective care to cancer patients. Advances in the Fourier Transform Infrared (FTIR) spectroscopy of tissues enable it to be a non-invasive method to obtain information about the biochemical content of any biological sample. In this retrospective study, attenuated tissue reflection FTIR spectroscopy of biopsy samples from paediatric patients reveals spectral features that are diagnostic for Ewing Sarcoma. Furthermore, our results suggest that spectral features such as these may be of value for the prediction of treatment outcome independent to well-known, routinely used risk factors.


Clinical & Translational Oncology | 2016

Response to chemotherapy estimates by FDG PET is an important prognostic factor in patients with Ewing sarcoma.

Anna Raciborska; Katarzyna Bilska; Katarzyna Drabko; Elżbieta Michalak; Radosław Chaber; Monika Pogorzała; Katarzyna Połczyńska; Grazyna Sobol; M. Wieczorek; K. Muszyńska-Rosłan; Magdalena Rychłowska-Pruszyńska; Carlos Rodriguez-Galindo; M. Dziuk


Pediatrics and Neonatology | 2016

Solid Cancers in the Premature and the Newborn: Report of Three National Referral Centers

Anna Raciborska; Katarzyna Bilska; Jadwiga Węcławek-Tompol; Marek Ussowicz; Monika Pogorzała; Joanna Janowska; Magdalena Rychłowska-Pruszyńska; Carlos Rodriguez-Galindo; Ewa Helwich


Journal of Pediatric Surgery | 2016

Management and follow-up of Ewing sarcoma patients with isolated lung metastases.

Anna Raciborska; Katarzyna Bilska; Magdalena Rychłowska-Pruszyńska; Marek Duczkowski; Agnieszka Duczkowska; Katarzyna Drabko; Radosław Chaber; Grazyna Sobol; Elżbieta Wyrobek; Elżbieta Michalak; Carlos Rodriguez-Galindo; Wojciech Wożniak


Medical Oncology | 2018

Sorafenib in patients with progressed and refractory bone tumors

Anna Raciborska; Katarzyna Bilska


BioMed Research International | 2017

CNS Metastases from Bone and Soft Tissue Sarcomas in Children, Adolescents, and Young Adults: Are They Really So Rare?

Monika Bekiesińska-Figatowska; Agnieszka Duczkowska; Marek Duczkowski; Hanna Bragoszewska; Anna Romaniuk-Doroszewska; Beata Iwanowska; Sylwia Szkudlińska-Pawlak; Jaroslaw Madzik; Katarzyna Bilska; Anna Raciborska

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Katarzyna Drabko

Medical University of Lublin

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Carlos Rodriguez-Galindo

St. Jude Children's Research Hospital

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Radosław Chaber

Wrocław Medical University

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Monika Pogorzała

Nicolaus Copernicus University in Toruń

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Grazyna Sobol

Medical University of Silesia

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Marek Ussowicz

Wrocław Medical University

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Elżbieta Wyrobek

Boston Children's Hospital

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Agnieszka Zaucha-Prażmo

Nicolaus Copernicus University in Toruń

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Beata Wójcik

Nicolaus Copernicus University in Toruń

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Jerzy Kowalczyk

Medical University of Lublin

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