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Atorvastatin in combination with radiotherapy and temozolomide for glioblastoma: a prospective phase II study.
Altwairgi, Abdullah K; Alghareeb, Waleed A; AlNajjar, Fouad H; Alhussain, Hussain; Alsaeed, Eyad; Balbaid, Ali Abdullah O; Aldanan, Sadeq; Orz, Yasser; Alsharm, Abdullah A.
Affiliation
  • Altwairgi AK; Medical Oncology Department, Comprehensive Cancer Center, King Fahad Medical City, Riyadh, Saudi Arabia. aaltwairqi@kfmc.med.sa.
  • Alghareeb WA; Medical Oncology Department, Comprehensive Cancer Center, King Fahad Medical City, Riyadh, Saudi Arabia.
  • AlNajjar FH; Clinical Pharmacy Department, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Alhussain H; Radiation Oncology Department, Comprehensive Cancer Center, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Alsaeed E; Radiation Oncology Department, Comprehensive Cancer Center, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Balbaid AAO; Radiation Oncology Department, Comprehensive Cancer Center, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Aldanan S; Pathology Department, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Orz Y; National Neuroscience Institute, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Alsharm AA; Medical Oncology Department, Comprehensive Cancer Center, King Fahad Medical City, Riyadh, Saudi Arabia.
Invest New Drugs ; 39(1): 226-231, 2021 02.
Article de En | MEDLINE | ID: mdl-32851510
ABSTRACT
Glioblastoma is a fast-growing primary brain tumor observed in adults with the worst prognosis. Preclinical studies have demonstrated the encouraging anticancer activity of statins. This study evaluated the efficacy of atorvastatin in combination with standard therapy in patients with glioblastoma. In this prospective, open-label, single-arm, phase II study, patients were treated with atorvastatin in combination with the standard glioblastoma therapy comprising radiotherapy and temozolomide. The primary endpoint was progression-free survival (PFS) at 6 months (PFS-6). Among 36 patients enrolled from January 2014 to January 2017, the median age was 52 (20-69) years; 22% of the patients were aged ≥60 years, and 62% were male. Patients received atorvastatin for a median duration of 6.2 (0.3-28) months. At a median follow-up of 19 months, the PFS-6 rate was 66%, with a median PFS of 7.6 (5.7-9.4) months. In terms of Grade ≥ 3 hematological adverse events, thrombocytopenia and neutropenia occurred in 7% and 12% of patients, respectively. In multivariate analyses, high baseline low-density lipoprotein levels were associated with worse survival (P = 0.046). Atorvastatin was not shown to improve PFS-6. However, this study identified that high low-density lipoprotein levels are an independent predictor of poor cancer-related outcomes. Future clinical trials testing statins should aim to enroll patients with slow-growing tumors.Clinical trial information NCT0202957 (December 12, 2013).
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du cerveau / Glioblastome / Antinéoplasiques alcoylants / Chimioradiothérapie / Atorvastatine / Témozolomide Type d'étude: Observational_studies / Prognostic_studies Limites: Adult / Aged / Female / Humans / Male / Middle aged Langue: En Journal: Invest New Drugs Année: 2021 Type de document: Article Pays d'affiliation: Arabie saoudite

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du cerveau / Glioblastome / Antinéoplasiques alcoylants / Chimioradiothérapie / Atorvastatine / Témozolomide Type d'étude: Observational_studies / Prognostic_studies Limites: Adult / Aged / Female / Humans / Male / Middle aged Langue: En Journal: Invest New Drugs Année: 2021 Type de document: Article Pays d'affiliation: Arabie saoudite