Efficacy and safety of sorafenib in a subset of patients with advanced soft tissue sarcoma from a Phase II randomized discontinuation trial
| العنوان: | Efficacy and safety of sorafenib in a subset of patients with advanced soft tissue sarcoma from a Phase II randomized discontinuation trial |
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| المؤلفون: | Ian Judson, Lisa Cupit, Chenghua Xia, Stanley B. Kaye, Keith T. Flaherty, Simon Pacey, Eric K. Rowinsky, Peter J. O'Dwyer, Mark J. Ratain |
| المصدر: | Investigational New Drugs. 29:481-488 |
| بيانات النشر: | Springer Science and Business Media LLC, 2009. |
| سنة النشر: | 2009 |
| مصطلحات موضوعية: | Adult, Male, Niacinamide, Sorafenib, medicine.medical_specialty, Pyridines, Nausea, Antineoplastic Agents, Soft Tissue Neoplasms, Placebo, law.invention, Young Adult, Randomized controlled trial, law, Internal medicine, medicine, Humans, Pharmacology (medical), Aged, Demography, Neoplasm Staging, Pharmacology, business.industry, Phenylurea Compounds, Soft tissue sarcoma, Benzenesulfonates, Sarcoma, Middle Aged, medicine.disease, Rash, Discontinuation, Surgery, Clinical trial, Treatment Outcome, Oncology, Female, medicine.symptom, Tomography, X-Ray Computed, business, medicine.drug |
| الوصف: | Aim Phase II multi-disease randomized discontinuation trial to assess the safety and efficacy of sorafenib including patients with advanced soft tissue sarcoma (STS). Methods Sorafenib (400 mg twice daily) was initially administered for 12 weeks. Patients with: ≥25% tumour shrinkage continued sorafenib; ≥25% tumour growth discontinued; other patients were randomized and received sorafenib or placebo. Results Twenty-six patients (median age 55 years) were enrolled. Common drug-related adverse events, including fatigue, hand–foot skin reaction, rash or gastrointestinal disturbances, were manageable, reversible and generally low grade. Fatigue, skin toxicity, nausea, diarrhoea and hypertension occurred at grade ≥3 in 19% of patients. After 12 weeks eight (31%) patients had not progressed. Three patients who experienced tumour shrinkage and continued on sorafenib, and five (19%) were randomized either to continue sorafenib or to receive placebo. Of the three patients randomized to sorafenib, one achieved a partial response and two had SD. Overall one patient achieved a partial response and three further patients achieved minor responses. Conclusions There was evidence of disease activity in STS as defined by tumor regressions including one objective partial response. Further investigation in STS is warranted. |
| تدمد: | 1573-0646 0167-6997 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dde86b6cff65dc9a0a5cfdf1a0e054b0Test https://doi.org/10.1007/s10637-009-9367-9Test |
| حقوق: | CLOSED |
| رقم الانضمام: | edsair.doi.dedup.....dde86b6cff65dc9a0a5cfdf1a0e054b0 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 15730646 01676997 |
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