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顺铂、培美曲塞和贝伐珠单抗治疗后培美曲塞联合贝伐珠单抗与培美曲塞单药治疗晚期非鳞状非小细胞肺癌的随机、II 期研究:TORG(胸部肿瘤研究组)1321。

Randomized, Phase II study of pemetrexed plus bevacizumab versus pemetrexed alone after treatment with cisplatin, pemetrexed, and bevacizumab in advanced non-squamous, non-small cell lung cancer: TORG (thoracic oncology research group) 1321.

机构信息

Division of Thoracic Oncology, Department of Medical Oncology, Tochigi Cancer Center, Utsunomiya, Japan.

Division of Thoracic Oncology, Department of Thoracic Diseases, Utsunomiya Memorial Hospital, Utsunomiya, Japan.

出版信息

Cancer Med. 2023 Jul;12(14):14988-14999. doi: 10.1002/cam4.6135. Epub 2023 May 24.

Abstract

INTRODUCTION

Cisplatin plus pemetrexed followed by pemetrexed is an efficacious platinum combination regimen for advanced non-squamous, non-small cell lung cancer (NSCLC). Data regarding the addition of bevacizumab, especially in maintenance treatment, are insufficient.

METHODS

Eligibility criteria included: no prior chemotherapy; advanced, non-squamous, NSCLC; performance status ≤1; and epidermal growth factor receptor mutation-negative. Patients (N = 108) received induction chemotherapy with cisplatin, pemetrexed, and bevacizumab every 3 weeks for four cycles, and tumor response was needed to confirm four-week response duration. Patients with at least stable disease were randomized to pemetrexed/bevacizumab or pemetrexed alone. The primary endpoint was progression-free survival (PFS) after induction chemotherapy. Myeloid-derived suppressor cell (MDSC) counts of peripheral blood samples were also analyzed.

RESULTS

Thirty-five patients each were randomized to the pemetrexed/bevacizumab group and the pemetrexed alone group. PFS was significantly better in the pemetrexed/bevacizumab group than in the pemetrexed alone group (7.0 vs. 5.4 months, hazard ratio: 0.56 [0.34-0.93], log-rank p = 0.023). In patients with partial response to induction therapy, median overall survival was 23.3 months in the pemetrexed alone group and 29.6 months in the pemetrexed/bevacizumab group (log-rank p = 0.077). Pretreatment monocytic (M)-MDSC counts tended to be greater in the pemetrexed/bevacizumab group with poor PFS than in those with good PFS (p = 0.0724).

CONCLUSIONS

Addition of bevacizumab to pemetrexed as maintenance therapy prolonged PFS in patients with untreated, advanced, non-squamous NSCLC. Furthermore, an early response to induction therapy and pretreatment M-MDSC counts may be related to the survival benefit of the addition of bevacizumab to the combination of cisplatin and pemetrexed.

摘要

简介

顺铂联合培美曲塞序贯培美曲塞是晚期非鳞状非小细胞肺癌(NSCLC)有效的铂类联合方案。贝伐珠单抗的添加数据,特别是维持治疗的数据不足。

方法

入选标准包括:无化疗史;晚期非鳞状 NSCLC;体力状况评分≤1;表皮生长因子受体突变阴性。患者(N=108)接受顺铂、培美曲塞和贝伐珠单抗每 3 周治疗 4 个周期的诱导化疗,且需要肿瘤反应来确认 4 周的缓解持续时间。至少稳定疾病的患者随机分为培美曲塞/贝伐珠单抗或培美曲塞单药组。主要终点是诱导化疗后的无进展生存期(PFS)。还分析了外周血样本中骨髓来源抑制细胞(MDSC)的计数。

结果

35 例患者随机分为培美曲塞/贝伐珠单抗组和培美曲塞单药组。培美曲塞/贝伐珠单抗组的 PFS 明显优于培美曲塞单药组(7.0 与 5.4 个月,风险比:0.56[0.34-0.93],对数秩检验 p=0.023)。在诱导治疗部分缓解的患者中,培美曲塞单药组的中位总生存期为 23.3 个月,培美曲塞/贝伐珠单抗组为 29.6 个月(对数秩检验 p=0.077)。与 PFS 良好的患者相比,培美曲塞/贝伐珠单抗组中无进展生存期较差的患者,其治疗前单核细胞(M)-MDSC 计数倾向更大(p=0.0724)。

结论

在未经治疗的晚期非鳞状 NSCLC 患者中,培美曲塞联合贝伐珠单抗维持治疗可延长 PFS。此外,诱导治疗早期反应和治疗前 M-MDSC 计数可能与培美曲塞联合顺铂中添加贝伐珠单抗的生存获益有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b6/10417045/2a8f76e6e142/CAM4-12-14988-g002.jpg

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