Results 11 to 20 of about 121,021 (313)

Advances in the management of gastrointestinal stromal tumors (GISTs)

Nowotwory, 2020
Gastrointestinal stromal tumors are rare neoplasms developing from cells of Cajal in the gastrointestinal tract. The mainstay of such tumors treatment is surgery, whenever possible. The therapeutic management of inoperable and metastatic disease is based
Monika Dudzisz-Śledź, Piotr Rutkowski
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Hypofractionated preoperative radiotherapy for high risk soft tissue sarcomas in a geriatric patient population

Radiology and Oncology, 2021
Standard therapy for localised, resectable high risk soft tissue sarcomas consists of wide excision and radiotherapy over several weeks. This treatment schedule is hardly feasible in geriatric and frail patients.
Potkrajcic Vlatko, Traub Frank, Hermes Barbara, Scharpf Marcus, Kolbenschlag Jonas, Zips Daniel, Paulsen Frank, Eckert Franziska   +7 more
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Current advances in radiotherapy for soft tissue sarcomas

Nowotwory, 2020
Radiotherapy (RT) is a part of the routine treatment of locally advanced or high-grade soft-tissue sarcomas (STS). However, RT has changed significantly over the last 20 years. Modern RT techniques have extended its potential application in STS treatment.
Mateusz J. Spałek, Aneta M. Borkowska
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Wyniki leczenia operacyjnego chorych na chrzęstniakomięsaki miednicy z oszczędzeniem kończyny

Nowotwory, 2021
Analizie poddano 53 kolejnych chorych na chondrosarcoma (ChSa) kości miednicy i kości krzyżowej leczonych operacyjnie w Klinice Nowotworów Tkanek Miękkich, Kości i Czerniaków Narodowego Instytutu Onkologii im.
Andrzej Pieńkowski, Andrzej Komor, Tomasz Goryń, Bartłomiej Szostakowski, Michał Wągrodzki, Donata Makuła, Patrycja Castaneda-Wysocka, Wojciech Michalski, Aneta Borkowska, Piotr Rutkowski   +9 more
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Diagnostic Value of Serum LncRNAs for Bone Metastasis in Lung Cancer

Zhongliu Fangzhi Yanjiu, 2022
Objective To investigate the expression of lncRNA HOTAIR, HOTAIR, CRNDE and AFAP1-AS1 in lung cancer patients with bone metastasis (LCWBM), and to elucidate the diagnostic value of lncRNAs for LCWBM. Methods Serum was collected from 38 LCWBM patients and
ZHANG Peng, GAO Min, FENG Feifei, LI Mengyuan, LIU Jinyan, HUANG Lingling   +5 more
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Phase Ib study of anlotinib combined with TQB2450 in pretreated advanced biliary tract cancer and biomarker analysis

Hepatology, EarlyView., 2022
Phase 1b study of anlotinib combined with TQB2450 in pretreated advanced biliary tract cancer and biomarker analysis. Abstract Background and Aims We evaluated the efficacy and safety of the antiangiogenic tyrosine kinase inhibitor anlotinib plus TQB2450, a programmed death‐ligand 1 inhibitor in pretreated advanced biliary tract cancers (BTCs ...
Jun Zhou, Yongkun Sun, Wen Zhang, Jiajia Yuan, Zhi Peng, Wei Wang, Jifang Gong, Lin Yang, Yanshuo Cao, Hong Zhao, Chao Chen, Weifeng Wang, Lin Shen, Aiping Zhou   +13 more
wiley   +1 more source

Zalecenia Polskiej Grupy Mięsakowej odnośnie postępowania diagnostyczno-terapeutycznego oraz kontroli u chorych na neurofibromatozę typu 1 (NF1) oraz malignant peripheral nerve sheath tumor związany z NF1

Nowotwory, 2022
Neurofibromatoza typu 1 (zespół NF1 in. choroba Recklinghausena, nerwiakowłókniakowatość typu 1), jest dziedziczona autosomalnie dominująco, a odpowiadają za nią mutacje genu NF1 kodującego białko neurofibrominy.
Piotr Rutkowski, Anna Raciborska, Anna Szumera-Ciećkiewicz, Paweł Sobczuk, Mateusz Spałek, Hanna Koseła-Paterczyk, Iwona Ługowska, Katarzyna Bilska, Monika Gos, Janusz Ryś, Ewa Chmielik, Andrzej Tysarowski, Konrad Zaborowski, Małgorzata Oczko-Wojciechowska, Patrycja Castaneda-Wysocka, Donata Makuła, Marcin Zdzienicki, Marcin Ziętek, Piotr Fonrobert, Kamil Dolecki, Marek Dedecjus, Anna M. Czarnecka   +21 more
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Non‐rhabdomyosarcoma soft‐tissue sarcoma [PDF]

Pediatric Blood & Cancer, 2021
AbstractNon‐rhabdomyosarcoma soft‐tissue sarcomas (NRSTS) comprise 4% of childhood cancers and consist of numerous histologic subtypes. Prognostic factors associated with poor outcome include high histologic grade, large tumor size, presence of metastases, and unresectability.
Sarah A. Milgrom, Lynn Million, Henry Mandeville, Akmal Safwat, Ralph P. Ermoian, Stephanie Terezakis   +5 more
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Epithelioid sarcoma

Nowotwory, 2023
Epithelioid sarcoma (ES) is a very rare sarcoma characterized by loss of INI1. Enzinger first described ES in 1970, butthe histopathologic differential diagnosis of ES remains challenging.
Anna M. Czarnecka
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Soft tissue sarcoma

BMJ, 2016
#### What you need to know A 45 year old woman presented to her general practitioner several times over nine months with a gradually enlarging, hard lump in her anterior thigh. An ultrasound scan showed a solid intramuscular mass in the anterior compartment of her thigh, prompting a two week wait referral to the regional sarcoma diagnostic clinic ...
Eastley, Nicholas Charles, Green, P. N., Ashford, R. U.   +2 more
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