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  1. Article

    Open Access

    Proteomic features of soft tissue tumours in adolescents and young adults

    Adolescents and young adult (AYA) patients with soft tissue tumours including sarcomas are an underserved group with disparities in treatment outcomes.

    Yuen Bun Tam, Kaan Low, Hari PS, Madhumeeta Chadha in Communications Medicine (2024)

  2. Article

    Open Access

    Pharmacological EZH2 inhibition combined with retinoic acid treatment promotes differentiation and apoptosis in rhabdomyosarcoma cells

    Rhabdomyosarcomas (RMS) are predominantly paediatric sarcomas thought to originate from muscle precursor cells due to impaired myogenic differentiation. Despite intensive treatment, 5-year survival for patient...

    Eleanor O’Brien, Carmen Tse, Ian Tracy, Ian Reddin, Joanna Selfe in Clinical Epigenetics (2023)

  3. Article

    Open Access

    The proteomic landscape of soft tissue sarcomas

    Soft tissue sarcomas (STS) are rare and diverse mesenchymal cancers with limited treatment options. Here we undertake comprehensive proteomic profiling of tumour specimens from 321 STS patients representing 11...

    Jessica Burns, Christopher P. Wilding, Lukas Krasny, **xuan Zhu in Nature Communications (2023)

  4. No Access

    Article

    Functional genomics of human clear cell sarcoma: genomic, transcriptomic and chemical biology landscape for clear cell sarcoma

    Systemic therapy for metastatic clear cell sarcoma (CCS) bearing EWSR1-CREB1/ATF1 fusions remains an unmet clinical need in children, adolescents, and young adults.

    Samuel V. Rasmussen, Agnieszka Wozniak, Melvin Lathara in British Journal of Cancer (2023)

  5. Article

    Open Access

    Imaging features of primary sites and metastatic patterns of angiosarcoma

    Angiosarcomas are rare, aggressive soft tissue sarcomas originating from endothelial cells of lymphatic or vascular origin and associated with a poor prognosis. The clinical and imaging features of angiosarcom...

    Basrull N. Bhaludin, Khin Thway, Margaret Adejolu, Alexandra Renn in Insights into Imaging (2021)

  6. Article

    Open Access

    NUT Carcinoma Arising from the Parotid Gland: A Case Report and Review of the Literature

    NUT carcinoma is an aggressive carcinoma with an overall poor survival outcome. The mediastinum and head and neck area, especially the sinonasal region, are among the common sites of disease. Histopathological...

    Wei-Ning Saik, Philip Da Forno, Khin Thway, Syed Ali Khurram in Head and Neck Pathology (2021)

  7. Article

    Open Access

    Predictive and prognostic transcriptomic biomarkers in soft tissue sarcomas

    Soft tissue sarcomas (STS) are rare and heterogeneous tumours comprising over 80 different histological subtypes. Treatment options remain limited in advanced STS with high rates of recurrence following resect...

    Eve Merry, Khin Thway, Robin L. Jones, Paul H. Huang in npj Precision Oncology (2021)

  8. Article

    Open Access

    Paraneoplastic dermatomyositis associated with metastatic leiomyosarcoma of unknown primary

    Sarcomas are rare and heterogeneous tumours of mesenchymal origin, with over 100 histological subtypes. Paraneoplastic dermatomyositis has rarely been described in sarcoma. This is the first documented case of...

    Eve Merry, Alannah Smrke, Kapil Halai, Gulam Patel, Khin Thway in Clinical Sarcoma Research (2020)

  9. Article

    Open Access

    Soft Tissue Special Issue: Perivascular and Vascular Tumors of the Head and Neck

    Perivascular and vascular neoplasms of the head and neck are a rare group of tumors comprising a spectrum of clinical/biologic and histological features. They are frequently diagnostically challenging, due to ...

    Uta Flucke, Marie Karanian, Roel W. ten Broek, Khin Thway in Head and Neck Pathology (2020)

  10. Article

    Open Access

    Toxicity management of regorafenib in patients with gastro-intestinal stromal tumour (GIST) in a tertiary cancer centre

    Regorafenib is a multi-kinase inhibitor approved as third line treatment for metastatic GIST. Dose limiting toxicities are frequently seen and many patients require dose reductions. This study aimed to evaluat...

    Florence Chamberlain, Sheima Farag, Constance Williams-Sharkey in Clinical Sarcoma Research (2020)

  11. Article

    Contemporary approaches to soft tissue and bone pathology

    Khin Thway, Andrew L. Folpe in Virchows Archiv (2020)

  12. No Access

    Article

    Update on selected advances in the immunohistochemical and molecular genetic analysis of soft tissue tumors

    Although traditional morphological evaluation remains the cornerstone for the diagnosis of soft tissue tumors, ancillary diagnostic modalities such as immunohistochemistry and molecular genetic analysis are of...

    Khin Thway, Andrew L Folpe in Virchows Archiv (2020)

  13. Article

    Open Access

    Adult soft tissue myoepithelial carcinoma: treatment outcomes and efficacy of chemotherapy

    Soft tissue myoepithelial carcinomas are a rare, malignant subgroup of myoepithelial tumours mostly arising in the extremities with equal predilection for women and men. The mainstay of management of localised...

    Florence Chamberlain, Elena Cojocaru, Mariana Scaranti in Medical Oncology (2019)

  14. Article

    Open Access

    Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma

    Cancer patients with advanced disease routinely exhaust available clinical regimens and lack actionable genomic medicine results, leaving a large patient population without effective treatments options when th...

    Noah E. Berlow, Rishi Rikhi, Mathew Geltzeiler, **u Abraham in BMC Cancer (2019)

  15. Article

    Open Access

    Clinical Characteristics and efficacy of chemotherapy in sclerosing epithelioid fibrosarcoma

    Sclerosing epithelioid fibrosarcoma (SEF) is a very rare soft tissue sarcoma subtype. Clinically it is an aggressive tumour; however, to our knowledge there are no published reports regarding the efficacy of c...

    Winston Chew, Charlotte Benson, Khin Thway, Andrew Hayes, Aisha Miah in Medical Oncology (2018)

  16. Article

    Open Access

    Poor treatment outcomes with palliative gemcitabine and docetaxel chemotherapy in advanced and metastatic synovial sarcoma

    The outcome for patients with unresectable or metastatic soft tissue sarcoma remains poor with few treatment options. Synovial sarcoma is a rare type of sarcoma, predominantly affecting adolescents and young a...

    Alexandra Pender, Elizabeth J. Davis, Dharmisha Chauhan in Medical Oncology (2018)

  17. No Access

    Article

    Desmoplastic small round cell tumor: evaluation of reverse transcription-polymerase chain reaction and fluorescence in situ hybridization as ancillary molecular diagnostic techniques

    Desmoplastic small round cell tumor (DSRCT) is a rare, biologically aggressive soft tissue neoplasm of uncertain differentiation, most often arising in the abdominal and pelvic cavities of adolescents and youn...

    Mustafa Mohamed, David Gonzalez, Karen J. Fritchie, John Swansbury in Virchows Archiv (2017)

  18. No Access

    Article

    Does histotype-tailored neoadjuvant therapy improve outcomes?

    Patients with metastatic soft-tissue sarcoma can benefit from systemic therapy, but the best drug combinations for the different disease subtypes remain to be established. Recently, great emphasis has been pla...

    Robin L. Jones, Khin Thway in Nature Reviews Clinical Oncology (2017)

  19. Article

    Open Access

    The spectrum of EWSR1-rearranged neoplasms at a tertiary sarcoma centre; assessing 772 tumour specimens and the value of current ancillary molecular diagnostic modalities

    EWSR1 rearrangements were first identified in Ewing sarcoma, but the spectrum of EWSR1-rearranged neoplasms now includes many soft tissue tumour subtypes including desmoplastic small round cell tumour (DSRCT), my...

    Jonathan Noujaim, Robin L Jones, John Swansbury in British Journal of Cancer (2017)

  20. Article

    Open Access

    Endosialin expression in soft tissue sarcoma as a potential marker of undifferentiated mesenchymal cells

    Soft tissue sarcomas are a group of neoplasms with differentiation towards mesenchymal tissue, many of which are aggressive and chemotherapy resistant. Histology and immunoprofiles often overlap with neoplasms...

    Khin Thway, David Robertson, Robin L Jones, Joanna Selfe in British Journal of Cancer (2016)

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