Browsing Clinical Studies by author "Jones, Robin"
Now showing items 21-40 of 55
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First-in-Human Treatment With a Dendritic Cell-targeting Lentiviral Vector-expressing NY-ESO-1, LV305, Induces Deep, Durable Response in Refractory Metastatic Synovial Sarcoma Patient.
Pollack, SM; Lu, H; Gnjatic, S; Somaiah, N; O'Malley, RB; Jones, RL; Hsu, FJ; Ter Meulen, J (2017-10)Effective induction of antitumor T cells is a pivotal goal of cancer immunotherapy. To this end, lentiviral vectors (LV) are uniquely poised to directly prime CD8 T-cell responses via transduction of dendritic cells in ... -
Isolated limb perfusion for locally advanced angiosarcoma in extremities: A multi-centre study.
Huis In 't Veld, EA; Grünhagen, DJ; Verhoef, C; Smith, HG; van Akkooi, ACJ; Jones, R; van Coevorden, F; Hayes, AJ; van Houdt, WJ (2017-11)<h4>Background</h4>Angiosarcomas are rare and aggressive soft-tissue sarcomas. The only potential curative treatment is complete surgical excision. This study reports the outcome of isolated limb perfusion (ILP) with ... -
Molecular subtypes of gastrointestinal stromal tumors and their prognostic and therapeutic implications.
Szucs, Z; Thway, K; Fisher, C; Bulusu, R; Constantinidou, A; Benson, C; van der Graaf, WT; Jones, RL (2017-01)Gastrointestinal stromal tumors (GISTs) are composed of various molecular subtypes, with differing prognostic and predictive relevance. Previously, tumors lacking mutations in the KIT and PDGFRA genes have been designated ... -
Myoepithelial Carcinoma of the Paracecal Mesentery: Aggressive Behavior of a Rare Neoplasm at an Unusual Anatomic Site.
Thway, K; Noujaim, J; Thomas, DM; Fisher, C; Jones, RL (2017-03-31)Myoepithelial tumors of the soft tissues represent a rare group of neoplasms that vary in their clinical behavior, pathologic features and genetics. They are histopathologically typified by a <i>myoepithelial</i> ... -
Neoadjuvant chemotherapy in localised soft-tissue sarcomas: where do we go from here?
van der Graaf, WTA; Jones, RL (2017-06) -
Novel therapeutic approaches in chondrosarcoma.
Polychronidou, G; Karavasilis, V; Pollack, SM; Huang, PH; Lee, A; Jones, RL (2017-03)Chondrosarcoma is a malignant tumor of bones, characterized by the production of cartilage matrix. Due to lack of effective treatment for advanced disease, the clinical management of chondrosarcomas is exceptionally ... -
Olaratumab for the treatment of soft tissue sarcoma.
Deshpande, HA; Cecchini, M; Ni Choileain, S; Jones, R (2017-04)Soft tissue sarcoma represents about 1% of all solid malignancies. The standard chemotherapy regimens have included doxorubicin alone or in combination with other agents. Despite recent advances in treatment beyond first ... -
Olaratumab for the treatment of soft-tissue sarcoma.
Pender, A; Jones, RL (2017-10)The outcome for patients with unresectable/metastatic soft tissue sarcoma remains poor with few treatment options. In the first line setting, a number of randomized trials have shown no difference in overall survival between ... -
Olaratumab in soft tissue sarcoma - Current status and future perspectives.
Antoniou, G; Lee, ATJ; Huang, PH; Jones, RL (2018-03)Recent randomised phase II trial data have indicated that the addition of olaratumab, a novel monoclonal antibody against platelet-derived growth factor receptor alpha (PDGFRα), to doxorubicin confers an unprecedented ... -
Olaratumab: a platelet-derived growth factor receptor-α-blocking antibody for the treatment of soft tissue sarcoma.
Pender, A; Jones, RL (2017-01)The outcome of patients with unresectable or metastatic soft tissue sarcoma (STS) remains poor with few treatment options. A number of randomized trials in the first-line setting have shown no difference in overall survival ... -
Outcomes of Elderly Patients with Advanced Soft Tissue Sarcoma Treated with First-Line Chemotherapy: A Pooled Analysis of 12 EORTC Soft Tissue and Bone Sarcoma Group Trials.
Younger, E; Litière, S; Le Cesne, A; Mir, O; Gelderblom, H; Italiano, A; Marreaud, S; Jones, RL; Gronchi, A; van der Graaf, WTA (2018-10)BACKGROUND:Almost half of patients diagnosed with soft tissue sarcoma (STS) are older than 65 years; however, the outcomes of elderly patients with metastatic disease are not well described. PATIENTS AND METHODS:An elderly ... -
p.(L576P) -KIT mutation in GIST: Favorable prognosis and sensitive to imatinib?
Noujaim, J; Gonzalez, D; Thway, K; Jones, RL; Judson, I (2016-05)Exon 11 KIT mutations are found in a majority of gastrointestinal stromal tumors (GIST) and are usually predictive of response to imatinib, a KIT, PDGFRA and ABL inhibitor. Exon 11 mutations with poor sensitivity to imatinib ... -
Pazopanib in advanced soft tissue sarcomas.
Lee, ATJ; Jones, RL; Huang, PH (2019-01)Pazopanib is the first and only tyrosine kinase inhibitor currently approved for the treatment of multiple histological subtypes of soft tissue sarcoma (STS). Initially developed as a small molecule inhibitor of vascular ... -
Pazopanib in advanced vascular sarcomas: an EORTC Soft Tissue and Bone Sarcoma Group (STBSG) retrospective analysis.
Kollár, A; Jones, RL; Stacchiotti, S; Gelderblom, H; Guida, M; Grignani, G; Steeghs, N; Safwat, A; Katz, D; Duffaud, F; Sleijfer, S; van der Graaf, WT; Touati, N; Litière, S; Marreaud, S; Gronchi, A; Kasper, B (2017-01)<h4>Background</h4>Pazopanib is a multitargeted tyrosine kinase inhibitor approved for the treatment of patients with selective subtypes of advanced soft tissue sarcoma (STS) who have previously received standard chemotherapy ... -
Pazopanib in patients with advanced intermediate-grade or high-grade liposarcoma.
Chamberlain, FE; Wilding, C; Jones, RL; Huang, P (2019-06)<b>Introduction</b>: Liposarcomas (LPS) are a heterogeneous group of adipocytic soft tissue sarcomas with limited treatment options in the advanced/metastatic setting. Pazopanib is a multi-target tyrosine kinase inhibitor ... -
Pazopanib, a promising option for the treatment of aggressive fibromatosis.
Szucs, Z; Messiou, C; Wong, HH; Hatcher, H; Miah, A; Zaidi, S; van der Graaf, WTA; Judson, I; Jones, RL; Benson, C (2017-04)Desmoid tumour/aggressive fibromatosis (DT/AF) is a rare soft-tissue neoplasm that is locally aggressive but does not metastasize. There is no standard systemic treatment for symptomatic patients, although a number of ... -
Phase III Soft Tissue Sarcoma Trials: Success or Failure?
Lee, ATJ; Pollack, SM; Huang, P; Jones, RL (2017-03)<h4>Opinion statement</h4>Two recently reported phase III randomised control trials (RCTs) have resulted in the registration of two new systemic therapies for advanced soft tissue sarcoma. Both of these trials' designs ... -
Poor treatment outcomes with palliative gemcitabine and docetaxel chemotherapy in advanced and metastatic synovial sarcoma.
Pender, A; Davis, EJ; Chauhan, D; Messiou, C; Al-Muderis, O; Thway, K; Fisher, C; Zaidi, S; Miah, A; Judson, I; van der Graaf, W; Keedy, VL; Benson, C; Jones, RL (2018-08-20)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 adults. Following ... -
Preserving quality of life as a key treatment goal in advanced soft tissue sarcomas.
Jones, RL; Le Cesne, A; Ibrahim, T; Garcia Del Muro, X; Menge, F (2018-12)<h4>Introduction</h4>Health-related quality of life (HRQoL) is a patient-reported outcome that addresses patients' perceptions of symptoms across physical, emotional, cognitive and social domains. As HRQoL is currently ... -
Promising novel therapeutic approaches in the management of gastrointestinal stromal tumors.
Szucs, Z; Thway, K; Fisher, C; Bulusu, R; Constantinidou, A; Benson, C; van der Graaf, WT; Jones, RL (2017-01)Primary and secondary resistance to currently available licensed tyrosine kinase inhibitors poses a real clinical challenge in the management of advanced gastrointestinal stromal tumors. Within the frame of early phase ...