Search Results - "Martín‐Broto, J."
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1
Hidradenitis suppurativa secondary to treatment with a gamma secretase inhibitor
Published in Journal of the European Academy of Dermatology and Venereology (01-03-2024)Get full text
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Giant cell tumour of bone: new treatments in development
Published in Clinical & translational oncology (01-06-2015)“…Giant cell tumour of bone (GCTB) is a benign osteolytic tumour with three main cellular components: multinucleated osteoclast-like giant cells, mononuclear…”
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SEOM Clinical Guideline of management of soft-tissue sarcoma (2020)
Published in Clinical & translational oncology (01-05-2021)“…Soft-tissue sarcomas constitute an uncommon and heterogeneous group of tumors of mesenchymal origin. Diagnosis, treatment, and management should be performed…”
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The paediatric cancer clinical research landscape in Spain: a 13-year multicentre experience of the new agents group of the Spanish Society of Paediatric Haematology and Oncology (SEHOP)
Published in Clinical & translational oncology (01-12-2021)“…Purpose Early phase trials are crucial in developing innovative effective agents for childhood malignancies. We report the activity in early phase paediatric…”
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Phase I trial of sorafenib in combination with ifosfamide in patients with advanced sarcoma: a Spanish group for research on sarcomas (GEIS) study
Published in Investigational new drugs (01-04-2014)“…Summary Background This phase I trial assessed safety, pharmacokinetics (PK), dose limiting toxicity (DLT), maximum tolerated dose and recommended dose (RD) of…”
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Short, full-dose adjuvant chemotherapy (CT) in high-risk adult soft tissue sarcomas (STS): long-term follow-up of a randomized clinical trial from the Italian Sarcoma Group and the Spanish Sarcoma Group
Published in Annals of oncology (01-12-2016)“…The equivalence of a short full-dose regimen of neoadjuvant CT with anthracycline-ifosfamide compared with standard dosing in localized high-risk soft tissue…”
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Best practices for the management of local-regional recurrent chordoma: a position paper by the Chordoma Global Consensus Group
Published in Annals of oncology (01-06-2017)“…Chordomas are rare, malignant bone tumors of the skull-base and axial skeleton. Until recently, there was no consensus among experts regarding appropriate…”
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Final analysis of the randomized trial on imatinib as an adjuvant in localized gastrointestinal stromal tumors (GIST) from the EORTC Soft Tissue and Bone Sarcoma Group (STBSG), the Australasian Gastro-Intestinal Trials Group (AGITG), UNICANCER, French Sarcoma Group (FSG), Italian Sarcoma Group (ISG), and Spanish Group for Research on Sarcomas (GEIS)
Published in Annals of oncology (01-04-2021)“…In 2004, we started an intergroup randomized trial of adjuvant imatinib versus no further therapy after R0-R1 surgery in localized, high/intermediate-risk…”
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Gemcitabine plus sirolimus for relapsed and progressing osteosarcoma patients after standard chemotherapy: a multicenter, single-arm phase II trial of Spanish Group for Research on Sarcoma (GEIS)
Published in Annals of oncology (01-12-2017)“…Patients with relapsed unresectable osteosarcoma represents an unmet need, so active and safe systemic treatments are required. Fas cell surface death receptor…”
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SEOM Clinical Guideline of management of soft-tissue sarcoma (2016)
Published in Clinical & translational oncology (01-12-2016)“…Soft-tissue sarcomas are uncommon and heterogeneous tumors of mesenchymal origin. A soft-tissue mass that is increasing in size, greater than 5 cm, or located…”
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Prognostic time dependence of deletions affecting codons 557 and/or 558 of KIT gene for relapse-free survival (RFS) in localized GIST: a Spanish Group for Sarcoma Research (GEIS) Study
Published in Annals of oncology (01-07-2010)“…To assess whether deletions involving codons 557 and/or 558 (critical deletions) of exon 11 of KIT are relevant in the prognosis of relapse-free survival (RFS)…”
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An update on the management of sporadic desmoid-type fibromatosis: a European Consensus Initiative between Sarcoma PAtients EuroNet (SPAEN) and European Organization for Research and Treatment of Cancer (EORTC)/Soft Tissue and Bone Sarcoma Group (STBSG)
Published in Annals of oncology (01-10-2017)“…Desmoid-type fibromatosis is a rare and locally aggressive monoclonal, fibroblastic proliferation characterized by a variable and often unpredictable clinical…”
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Follow-up strategies for patients with gastrointestinal stromal tumour treated with or without adjuvant imatinib after surgery
Published in European journal of cancer (1990) (01-08-2015)“…Abstract Background Patients with gastrointestinal stromal tumour (GIST) are often followed up after surgery with longitudinally repeated imaging examinations…”
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Systemic treatment in advanced phyllodes tumor of the breast: a multi-institutional European retrospective case-series analyses
Published in Breast cancer research and treatment (01-04-2022)“…Background We aimed at investigating outcome of systemic treatments in advanced breast PT. Methods All cases of advanced breast PT treated with systemic…”
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Indirect comparisons in cost-effectiveness analysis: are we being naïve?
Published in Clinical & translational oncology (01-01-2015)Get full text
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Is There a Role for Neo-Adjuvant Systemic Treatment in Sts?
Published in Annals of oncology (01-09-2014)Get full text
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84INIS THERE A ROLE FOR NEO-ADJUVANT SYSTEMIC TREATMENT IN STS?
Published in Annals of oncology (01-09-2014)“…Abstract I will try to answer this question after first replying this one: Is there any room for complementary systemic treatment in STS and if so, then are…”
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GEIS-21: a multicentric phase II study of intensive chemotherapy including gemcitabine and docetaxel for the treatment of Ewing sarcoma of children and adults: a report from the Spanish sarcoma group (GEIS)
Published in British journal of cancer (05-09-2017)“…Background: First Spanish trial of Ewing sarcoma (ES) including adults and children with the aim to test the efficacy of Gemcitabine and Docetaxel (G/D) in…”
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Synovial sarcoma: characteristics, challenges and evolving therapeutic strategies
Published in ESMO open (01-10-2023)“…Synovial sarcoma (SS) is a rare and aggressive disease that accounts for 5%-10% of all soft tissue sarcomas. Although it can occur at any age, it typically…”
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