Dose-dense temozolomide regimen for the treatment of brain metastases from melanoma, breast cancer, or lung cancer not amenable to surgery or radiosurgery: a multicenter phase II study

التفاصيل البيبلوغرافية
العنوان: Dose-dense temozolomide regimen for the treatment of brain metastases from melanoma, breast cancer, or lung cancer not amenable to surgery or radiosurgery: a multicenter phase II study
المؤلفون: M. Vitali, M. Danova, Ilaria Schiavetto, Emilio Bajetta, Stefano Cascinu, S. Del Prete, Stefania Salvagni, Lucio Crinò, Salvatore Siena
المصدر: Annals of Oncology
بيانات النشر: Elsevier BV, 2010.
سنة النشر: 2010
مصطلحات موضوعية: Male, medicine.medical_specialty, Lung Neoplasms, Maximum Tolerated Dose, dose dense, medicine.medical_treatment, Dacarbazine, Breast Neoplasms, temozolomide, NSCLC, breast cancer, Breast cancer, brain metastases, Carcinoma, Non-Small-Cell Lung, melanoma, medicine, Humans, Clinical Trials, Prospective Studies, Progression-free survival, Antineoplastic Agents, Alkylating, Survival rate, Neoplasm Staging, Salvage Therapy, Temozolomide, Brain Neoplasms, business.industry, Palliative Care, Remission Induction, Cancer, Original Articles, Hematology, Middle Aged, medicine.disease, Chemotherapy regimen, Surgery, Survival Rate, Radiation therapy, Treatment Outcome, Oncology, Drug Resistance, Neoplasm, Female, Neoplasm Recurrence, Local, business, medicine.drug
الوصف: Background: Brain metastases reduce survival because therapeutic options are limited. This phase II study evaluated the efficacy of single-agent therapy with alternating weekly, dose-dense temozolomide in pretreated patients with brain metastases prospectively stratified by primary tumor type. Methods: Eligible patients had bidimensionally measurable brain metastases from histologically/cytologically confirmed melanoma, breast cancer (BC), or non-small-cell lung cancer (NSCLC). Prior chemotherapy, radiotherapy, and whole-brain radiotherapy (WBRT) were allowed. Patients received temozolomide 150 mg/m2/day (days 1–7 and 15–21 every 28- or 35-day cycle). Results: In the intent-to-treat population (N = 157; 53 melanoma, 51 BC, and 53 NSCLC), one patient had complete response, nine (6%) had partial responses, and 31 (20%) had stable disease in the brain. Median progression-free survival was 56, 58, and 66 days for melanoma, BC, and NSCLC, respectively. Median overall survival was 100 days for melanoma, 172 days for NSCLC, and not evaluable in the BC group. Thrombocytopenia was the most common adverse event causing dose modification or treatment discontinuation. Grade 4 toxic effects were rare. Conclusions: This alternating weekly, dose-dense temozolomide regimen was well tolerated and clinically active in heavily pretreated patients with brain metastases, particularly in patients with melanoma. Combining temozolomide with WBRT or other agents may improve clinical outcomes.
تدمد: 0923-7534
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9e71eaa1aaed91b9a709322d1350592
https://doi.org/10.1093/annonc/mdp343
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....c9e71eaa1aaed91b9a709322d1350592
قاعدة البيانات: OpenAIRE