Vorobyev V I, Gemdzhian E G, Fedorova L V, Mikhailova N B, Ilyasov R K, Kaleikina L P, Trubyakova O S, Kaplanov K D, Melnichenko E V, Martynova E V, Yakovleva E P, Li O Y, Tarasenko E V, Chumakova E P, Bulieva N B, Nesterova E S, Margolin O V, Zherebtsova V A, Butaev L S, Ptushkin V V
Botkin City Clinical Hospital.
National Research Center for Hematology.
Ter Arkh. 2021 Jul 23;93(7):770-777. doi: 10.26442/00403660.2021.07.200930.
Mantle cell lymphoma (MCL) is a rare and clinically aggressive lymphoma subtype. Current approaches have greatly improved patients outcomes, but relapse is inevitable. In phase IIIII clinical trials, ibrutinib has shown significant activity in patients with relapsed or refractory (R/R) MCL.
To assess efficacy and toxicity of ibrutinib monotherapy in patients with R/R MCL in routine practice outside of clinical trials.
The study enrolled patients with confirmed R/R MCL who had received at least one line of previous chemotherapy. ECOG 24, cytopenia, infectious complications, hemorrhagic syndrome were not exclusion criteria. Patients received daily oral ibrutinib 560 mg until progression or unacceptable toxicity.
From May 2015 to September 2020 ibrutinib therapy was started in 106 patients with R/R MCL in 16 regions of Russia. The median age was 66 years; ECOG2 18%, blastoid variant (or Ki6740% or WBC50109/l) 43%. The median number of previous treatment lines was 2 (111). The ORR was 78.4% (CRR 27.4%). The median PFS was 13.6 months and OS 23.2 months. In the blastoid group the median PFS was 4.4 months vs 36.5 months in the alternative group (p0.001), the median OS 9.0 vs 41.0 (p=0.001). The median OS of patients after progression on ibrutinib was 3.2 months. The common complications are hemorrhages (63%), diarrhea (62%), myalgia and muscle cramps (60%), infections (31%), skin and nail toxicity 15%, arrhythmia 8%. None of recipients had to completely discontinue ibrutinib therapy due to complications.
Ibrutinib is effective and well tolerated in routine practice of R/R MCL treatment and our results are consistent with international clinical trials. The favorable toxicity profile and the high response rate made it possible to prescribe ibrutinib in severe somatic status, cytopenia, and even in the presence of infectious complications.
套细胞淋巴瘤(MCL)是一种罕见且临床侵袭性强的淋巴瘤亚型。目前的治疗方法已显著改善了患者的预后,但复发仍不可避免。在Ⅲ期临床试验中,依鲁替尼在复发或难治性(R/R)MCL患者中显示出显著活性。
评估依鲁替尼单药治疗在临床试验之外的常规实践中对R/R MCL患者的疗效和毒性。
该研究纳入确诊为R/R MCL且既往至少接受过一线化疗的患者。东部肿瘤协作组(ECOG)评分为2、血细胞减少、感染并发症、出血综合征均不是排除标准。患者每日口服依鲁替尼560毫克,直至病情进展或出现不可接受的毒性。
2015年5月至2020年9月,俄罗斯16个地区的106例R/R MCL患者开始接受依鲁替尼治疗。中位年龄为66岁;ECOG评分为2的患者占18%,母细胞样变异型(或Ki67≥40%或白细胞≥50×10⁹/L)患者占43%。既往治疗线数的中位数为2(范围1-11)。客观缓解率(ORR)为78.4%(完全缓解率[CRR]为27.4%)。中位无进展生存期(PFS)为13.6个月,总生存期(OS)为23.2个月。在母细胞样组中,中位PFS为4.4个月,而在非母细胞样组中为36.5个月(p<0.001),中位OS分别为9.0个月和41.0个月(p=0.001)。依鲁替尼治疗病情进展后患者的中位OS为3.2个月。常见并发症包括出血(63%)、腹泻(62%)、肌痛和肌肉痉挛(60%)、感染(31%)、皮肤和指甲毒性(15%)、心律失常(8%)。没有患者因并发症而不得不完全停止依鲁替尼治疗。
依鲁替尼在R/R MCL治疗的常规实践中有效且耐受性良好,我们的结果与国际临床试验一致。良好的毒性特征和高缓解率使得在严重躯体状况、血细胞减少甚至存在感染并发症的情况下也可以使用依鲁替尼。