Search Results - "Feuchtgruber, Simone"
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Synovial sarcoma disease characteristics and primary tumor sites differ between patient age groups: a report of the Cooperative Weichteilsarkom Studiengruppe (CWS)
Published in Journal of cancer research and clinical oncology (01-04-2020)“…Background Older age is associated with worse outcome in synovial sarcoma (SS) patients. Differences in disease presentation among distinct age groups,…”
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Fusion transcripts as liquid biopsy markers in alveolar rhabdomyosarcoma and synovial sarcoma: A report of the Cooperative Weichteilsarkom Studiengruppe (CWS)
Published in Pediatric blood & cancer (01-09-2022)“…Background The possible application of gene fusion transcripts as tumor‐specific noninvasive liquid biopsy biomarkers was investigated in blood plasma from…”
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Inflammatory myofibroblastic tumors—A retrospective analysis of the Cooperative Weichteilsarkom Studiengruppe
Published in Pediatric blood & cancer (01-06-2018)“…Background Inflammatory myofibroblastic tumors (IMTs) are a rare subgroup of soft tissue tumors. The outcome of patients with IMT has been reported as…”
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Importance of whole-body imaging with complete coverage of hands and feet in alveolar rhabdomyosarcoma staging
Published in Pediatric radiology (01-05-2018)“…Background Alveolar rhabdomyosarcoma commonly arises in the extremities and is characterized by aggressive biology and high frequency of metastases. Whole-body…”
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Dermatofibrosarcoma protuberans in children and adolescents: Primary and Relapsed disease—Experience of the Cooperative Weichteilsarkomstudiengruppe (CWS)
Published in Journal of surgical oncology (01-08-2020)“…Background Dermatofibrosarcoma protuberans (DFSP) is a rare low‐grade tumor. Little is known about best treatment of primary and relapsed disease (RD). Methods…”
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Localized synovial sarcoma of the foot or ankle: A series of 32 Cooperative Weichteilsarkom Study Group patients
Published in Journal of surgical oncology (01-01-2019)“…Background Synovial sarcoma of the foot/ankle is rare. Mutilating surgery is often discussed. Methods Patients registered from 1981 to 2013 were analyzed…”
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Prognosis of patients with parameningeal rhabdomyosarcoma (PM-RMS): The long term results of five consecutive CWS studies 1981-2009
Published in Journal of clinical oncology (20-05-2016)“…Abstract only…”
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Type, intensity, and duration of chemotherapy (CHT) and their correlation with prognosis of localized soft tissue Ewing tumors (STET): Experience of the Cooperative Weichteilsarkomstudiengruppe (CWS)
Published in Journal of clinical oncology (20-05-2017)“…Abstract only 10527 Background: The optimal type and intensity of CHT in the treatment of STET is still a matter of debate. The CWS group has treated STET…”
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Tumour volume reduction after neoadjuvant chemotherapy impacts outcome in localised embryonal rhabdomyosarcoma
Published in Pediatric blood & cancer (01-01-2015)“…Background Response (tumour volume reduction) to induction chemotherapy has been used to stratify secondary local and systemic treatment of Intergroup…”
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Abstract A47: Self-renewing cellular compartments in embryonal rhabdomyosarcoma are modulated by hedgehog signaling
Published in Cancer research (Chicago, Ill.) (15-10-2014)“…Abstract Rhabdomyosarcoma (RMS) is a heterogeneous group of malignancies with features of impaired skeletal muscle differentiation and represents the majority…”
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Challenges in the Local Treatment of Large Abdominal Embryonal Rhabdomyosarcoma
Published in Annals of surgical oncology (01-10-2014)“…Background Embryonal rhabdomyosarcoma is the most common pediatric soft tissue sarcoma. The best local treatment in large, nonmetastatic primary unresected…”
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Delayed resection can avoid irradiation in localized embryonal rhabdomyosarcoma
Published in Pediatric blood & cancer (2012)Get full text
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