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贝沙罗汀治疗外周 T 细胞淋巴瘤患者的回顾性研究结果。

Bexarotene in Patients With Peripheral T-cell Lymphomas: Results of a Retrospective Study.

机构信息

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.

出版信息

Clin Lymphoma Myeloma Leuk. 2019 Feb;19(2):109-115. doi: 10.1016/j.clml.2018.10.001. Epub 2018 Oct 13.

DOI:10.1016/j.clml.2018.10.001
PMID:30448048
Abstract

BACKGROUND

Peripheral T-cell lymphomas (PTCLs) are generally aggressive non-Hodgkin lymphomas that portend poor prognosis with currently available therapies. Bexarotene, a retinoic acid derivative, has efficacy in cutaneous T-cell lymphomas, but its activity in PTCL is unknown.

PATIENTS AND METHODS

We conducted a retrospective, single-institution, review of off-label bexarotene therapy in patients with PTCL between 2005 and 2016.

RESULTS

Twelve patients were treated with bexarotene as monotherapy: 3 patients with PTCL, not otherwise specified, and 9 patients with angioimmunoblastic T-cell lymphoma. Bexarotene doses of 300 mg/m daily or 150 mg/m were used for all patients. The treatment was well-tolerated. The most common toxicities included hypothyroidism and hyperlipidemia, which were effectively managed. The overall response rate for all patients was 58% with a median duration of response of 11 months (95% confidence interval [CI], 1.3 months to not estimable). Among patients with angioimmunoblastic T-cell lymphoma, there was a 44% overall response rate. The median progression-free survival for all patients was 2.1 months (95% CI, 1.1 months to not estimable), and the median overall survival was 14.9 months (95% CI, 2.1-73.1 months).

CONCLUSION

Bexarotene monotherapy is well-tolerated and has encouraging activity in PTCL that warrants further investigation in prospective clinical trials.

摘要

背景

外周 T 细胞淋巴瘤(PTCL)通常是侵袭性非霍奇金淋巴瘤,目前的治疗方法预后较差。倍他罗汀是一种维甲酸衍生物,在皮肤 T 细胞淋巴瘤中具有疗效,但在 PTCL 中的活性尚不清楚。

患者和方法

我们对 2005 年至 2016 年间接受过标签外倍他罗汀治疗的 PTCL 患者进行了回顾性、单机构研究。

结果

12 名患者接受了倍他罗汀单药治疗:3 名患者患有未特指的 PTCL,9 名患者患有血管免疫母细胞性 T 细胞淋巴瘤。所有患者的倍他罗汀剂量为 300mg/m 每日或 150mg/m。治疗耐受性良好。最常见的毒性包括甲状腺功能减退和高脂血症,这些毒性得到了有效控制。所有患者的总体缓解率为 58%,缓解持续时间中位数为 11 个月(95%置信区间[CI],1.3 个月至不可估计)。血管免疫母细胞性 T 细胞淋巴瘤患者的总体缓解率为 44%。所有患者的无进展生存期中位数为 2.1 个月(95%CI,1.1 个月至不可估计),总生存期中位数为 14.9 个月(95%CI,2.1-73.1 个月)。

结论

倍他罗汀单药治疗耐受性良好,在 PTCL 中具有令人鼓舞的活性,值得在前瞻性临床试验中进一步研究。

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