关键词: AZD2014 DLBCL Vistusertib mTORC1 mTORC2

Mesh : Adult Aged Aged, 80 and over Antineoplastic Agents / adverse effects therapeutic use Antineoplastic Combined Chemotherapy Protocols / adverse effects therapeutic use B-Lymphocyte Subsets / pathology Benzamides / adverse effects therapeutic use Drug Resistance, Neoplasm Female Gastrointestinal Diseases / chemically induced Humans Kaplan-Meier Estimate Lymphoma, Large B-Cell, Diffuse / drug therapy pathology Male Mechanistic Target of Rapamycin Complex 1 / antagonists & inhibitors Mechanistic Target of Rapamycin Complex 2 / antagonists & inhibitors Middle Aged Molecular Targeted Therapy Morpholines / adverse effects therapeutic use Neoplasm Proteins / antagonists & inhibitors Neoplastic Stem Cells / pathology Progression-Free Survival Protein Kinase Inhibitors / adverse effects therapeutic use Pyrimidines / adverse effects therapeutic use Rituximab / administration & dosage adverse effects Salvage Therapy

来  源:   DOI:10.1002/hon.2662   PDF(Sci-hub)

Abstract:
Patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) who are unfit for or relapsed postautologous stem-cell transplantation have poor outcomes. Historically, mTORC1 inhibitors have produced responses in approximately 30% of patients in this setting. mTORC1 inhibitor efficacy may be limited by resistance mechanisms including AKT activation by mTORC2. To date, dual mTORC1/2 inhibitors targeting both the TORC1 and TORC2 complexes have not been investigated in DLBCL. This phase II trial investigated the oral dual mTORC1/2 inhibitor vistusertib in an intermittent dosing schedule of 125 mg b.d. for 2 days per week. Thirty patients received vistusertib and six received vistusertib-rituximab for up to six cycles (28-day cycles). Two partial responses were achieved on monotherapy. Durations of response were 57 and 62 days, respectively, for these patients. 19% had stable disease within six cycles. In the monotherapy arm, the median progression-free survival was1.69 (95% confidence interval [CI] 1.61-2.14) months and median overall survival was 6.58 (95% CI 3.81-not reached) months, respectively. The median duration of response or stable disease across the trial duration was 153 days (95% CI 112-not reached). Tumour responses according to positron emission tomography/computed tomography versus computed tomography were concordant. There were no differences noted in tumour volume response according to cell of origin by either gene expression profiling or immunohistochemistry. Vistusertib ± rituximab was well tolerated; across 36 patients 86% of adverse events were grade (G) 1-2. Common vistusertib-related adverse events were similar to those described with mTORC1 inhibitors: nausea (47% G1-2), diarrhoea (27% G1-2, 6% G3), fatigue (30% G1-2, 3% G3), mucositis (25% G1-2, 6% G3), vomiting (17% G1-2), and dyspepsia (14% G1-2). Dual mTORC1/2 inhibitors do not clearly confer an advantage over mTORC1 inhibitors in relapsed or refractory DLBCL. Potential resistance mechanisms are discussed within.
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