Suppr超能文献

硼替佐米联合吉西他滨/卡铂作为晚期非小细胞肺癌的一线治疗:西南肿瘤协作组II期研究(S0339)

Bortezomib plus gemcitabine/carboplatin as first-line treatment of advanced non-small cell lung cancer: a phase II Southwest Oncology Group Study (S0339).

作者信息

Davies Angela M, Chansky Kari, Lara Primo N, Gumerlock Paul H, Crowley John, Albain Kathy S, Vogel Stanley J, Gandara David R

机构信息

Department of Hematology/Oncology, University of California, Davis Cancer Center, Sacramento, California, USA.

出版信息

J Thorac Oncol. 2009 Jan;4(1):87-92. doi: 10.1097/JTO.0b013e3181915052.

Abstract

INTRODUCTION

Bortezomib is a small-molecule proteasome inhibitor with single-agent activity in patients with non-small cell lung carcinoma (NSCLC) and synergy with gemcitabine in preclinical studies. This phase II study of bortezomib in combination with gemcitabine/carboplatin was conducted in chemotherapy-naive advanced NSCLC patients to assess efficacy and safety.

METHODS

Patients with selected stage IIIB/IV NSCLC, performance status 0-1, and no history of brain metastasis received up to six 21-day cycles of gemcitabine 1000 mg/m, days 1 and 8, carboplatin area under curve 5.0, day 1, and bortezomib 1.0 mg/m, days 1, 4, 8, and 11.

RESULTS

One-hundred-fourteen patients (52% adenocarcinoma, 85% stage IV) received a median of 3.6 treatment cycles. Median follow-up was >3 years. Median overall survival was 11 months; 1-year and 2-year survival rates were 47% and 19%, respectively. Median progression-free survival was 5 months; 1-year progression-free survival rate was 7%. Response rate was 23%, and disease control rate (responses + stable disease) was 68%. The most common grade 3/4 toxicities were thrombocytopenia (63%) and neutropenia (52%). One patient experienced febrile neutropenia. Grade 3/4 neuropathy occurred in 4%, and a further 6% experienced grade 2 sensory neuropathy.

CONCLUSIONS

Bortezomib plus gemcitabine/carboplatin resulted in a notable survival benefit in patients with advanced NSCLC, with the anticipated primary toxicity of myelosuppression. Further studies designed to investigate the role of bortezomib in advanced NSCLC are warranted.

摘要

引言

硼替佐米是一种小分子蛋白酶体抑制剂,对非小细胞肺癌(NSCLC)患者具有单药活性,且在临床前研究中与吉西他滨具有协同作用。本II期研究旨在评估硼替佐米联合吉西他滨/卡铂用于未经化疗的晚期NSCLC患者的疗效和安全性。

方法

入选的IIIB/IV期NSCLC患者,体能状态为0 - 1,无脑转移史,接受最多六个21天周期的治疗,具体为第1天和第8天给予吉西他滨1000 mg/m²,第1天给予卡铂曲线下面积5.0,第1、4、8和11天给予硼替佐米1.0 mg/m²。

结果

114例患者(52%为腺癌,85%为IV期)接受了中位3.6个治疗周期。中位随访时间>3年。中位总生存期为11个月;1年和2年生存率分别为47%和19%。中位无进展生存期为5个月;1年无进展生存率为7%。缓解率为23%,疾病控制率(缓解 + 疾病稳定)为68%。最常见的3/4级毒性为血小板减少(63%)和中性粒细胞减少(52%)。1例患者发生发热性中性粒细胞减少。3/4级神经病变发生率为4%,另有6%发生2级感觉神经病变。

结论

硼替佐米联合吉西他滨/卡铂可使晚期NSCLC患者获得显著的生存获益,同时伴有预期的骨髓抑制主要毒性。有必要开展进一步研究以探讨硼替佐米在晚期NSCLC中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f59/3024911/ea2e0189880a/nihms-244778-f0001.jpg

相似文献

引用本文的文献

4
The Influence of Cell Cycle Regulation on Chemotherapy.细胞周期调控对化疗的影响。
Int J Mol Sci. 2021 Jun 28;22(13):6923. doi: 10.3390/ijms22136923.

本文引用的文献

8
Proteasome inhibitors in lung cancer.肺癌中的蛋白酶体抑制剂
Crit Rev Oncol Hematol. 2006 Jun;58(3):177-89. doi: 10.1016/j.critrevonc.2005.12.001. Epub 2006 Jan 19.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验