Effect of atorvastatin versus placebo on efficacy in patients with diffuse large B-cell lymphoma receiving R-CHOP

被引:2
作者
Nemec, Ronald [1 ]
Scherrer-Crosbie, Marielle [2 ]
Abramson, Jeremy S. [1 ]
Redd, Robert [3 ]
Gilman, Hannah K. [4 ]
Ho, Terry [4 ]
Wu, Jessica [4 ]
Heemelaar, Julius [4 ]
Neuberg, Donna [3 ]
Hochberg, Ephraim P. [1 ]
Barnes, Jeffrey A. [1 ]
Armand, Philippe [5 ]
Jacobsen, Eric D. [5 ]
Jacobson, Caron A. [5 ]
Kim, Austin I. [5 ]
Friedman, Robb S. [6 ]
LaCasce, Ann S. [5 ]
Neilan, Tomas G. [4 ]
Soumerai, Jacob D. [1 ,7 ]
机构
[1] Massachusetts Ctr Canc, Massachusetts Gen Hosp, Ctr Lymphoma, Boston, MA 02114 USA
[2] Hosp Univ Penn, Div Cardiol, Philadelphia, PA 19104 USA
[3] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
[4] Massachusetts Gen Hosp, Div Cardiol, Boston, MA 02114 USA
[5] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[6] Newton Wellesley Hosp, Div Med Oncol, Newton, MA USA
[7] Massachusetts Gen Hosp, 55 Fruit St, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
Atorvastatin; R-CHOP; anthracycline; diffuse large B-cell lymphoma; COA REDUCTASE INHIBITORS; STATINS; DRUGS;
D O I
10.1080/10428194.2024.2317343
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
STOP-CA was a multicenter, double-blind, randomized, placebo-controlled trial comparing atorvastatin to placebo in treatment-naive lymphoma patients receiving anthracycline-based chemotherapy. We performed a preplanned subgroup to analyze the impact of atorvastatin on efficacy in patients with diffuse large B-cell lymphoma (DLBCL). Patients received rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) at standard doses for six 21-day cycles and were randomly assigned to receive atorvastatin 40 mg daily (n = 55) or placebo (n = 47) for 12 months. The complete response (CR) rate was numerically higher in the atorvastatin arm (95% [52/55] vs. 85% [40/47], p = .18), but this was not statistically significant. Adverse event rates were similar between the atorvastatin and placebo arms. In summary, atorvastatin did not result in a statistically significant improvement in the CR rate or progression-free survival, but both were numerically improved in the atorvastatin arm. These data warrant further investigation into the potential therapeutic role of atorvastatin added to anthracycline-based chemotherapies.
引用
收藏
页码:783 / 788
页数:6
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