Update 2021: Management of Small Cell Lung Cancer

医学 拓扑替康 肿瘤科 临床试验 内科学 依托泊苷 杜瓦卢马布 阿替唑单抗 化疗 免疫疗法 养生 疾病 肺癌 放射治疗 癌症 无容量
作者
Sara Tariq,So Yeon Kim,Jose A. Monteiro de Oliveira Novaes,Haiying Cheng
出处
期刊:Lung [Springer Science+Business Media]
卷期号:199 (6): 579-587 被引量:62
标识
DOI:10.1007/s00408-021-00486-y
摘要

Accounting for 14% of lung cancer, small cell lung cancer (SCLC) is a highly aggressive neuroendocrine malignancy with rapid proliferation, early spread, and poor survival. We provide an overview of recent advances regarding SCLC pathogenesis, subtypes, and treatment development through literature review of key trials. There are no validated biomarkers or approved targeted treatments for this overly heterogeneous disease, but recent analyses have identified some promising targets and four major subtypes which may carry unique therapeutic vulnerabilities in SCLC. Treatment wise, only a third of patients present with limited stage SCLC, which can be managed with a combined modality approach with curative intent (usually chemo-radiotherapy, but in some eligible patients, surgery followed by systemic treatment). For advanced or extensive stage SCLC, combined chemotherapy (platinum–etoposide) and immunotherapy (atezolizumab or durvalumab during and after chemotherapy) has become the new standard front-line treatment, with modest improvement in overall survival. In the second-line setting, for disease relapse ≤ 6 months, topotecan, lurbinectedin, and clinical trials are reasonable treatment options; for disease relapse > 6 months, original regimen, topotecan or lurbinectedin can be considered. Moreover, Trilaciclib, a CD4/CD6 inhibitor, was recently FDA-approved to decrease the incidence of chemotherapy-related myelosuppression in SCLC patients. While modest improvements in survival have been made especially in the metastatic setting with chemo-immunotherapy, further research in understanding the biology of SCLC is warranted to develop biomarker-driven therapeutic strategies and combinational approaches for this aggressive disease.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
微小桑应助科研通管家采纳,获得10
1秒前
1秒前
初遇之时最暖应助张旭采纳,获得10
1秒前
Lbc发布了新的文献求助10
2秒前
2秒前
橘颂完成签到,获得积分10
2秒前
东方元语应助科研通管家采纳,获得20
3秒前
aaaaaaaaaaaa应助科研通管家采纳,获得10
3秒前
kevinjy完成签到,获得积分0
3秒前
pengpengyin发布了新的文献求助10
3秒前
3秒前
冰电镜完成签到 ,获得积分10
5秒前
Copyright应助科研通管家采纳,获得10
5秒前
Owen应助科研通管家采纳,获得10
6秒前
6秒前
四月应助科研通管家采纳,获得20
7秒前
ghostR应助科研通管家采纳,获得20
7秒前
无心的小凡完成签到 ,获得积分10
7秒前
7秒前
馍馍完成签到,获得积分10
7秒前
王颖发布了新的文献求助10
7秒前
7秒前
优雅的怀莲完成签到,获得积分10
8秒前
林森森发布了新的文献求助10
8秒前
十二应助科研通管家采纳,获得10
9秒前
毛豆应助科研通管家采纳,获得10
10秒前
10秒前
10秒前
黄利发布了新的文献求助10
11秒前
aaaaaaaaaaaa应助科研通管家采纳,获得10
12秒前
12秒前
瘦瘦的忆梅完成签到,获得积分10
12秒前
Mark完成签到,获得积分10
12秒前
13秒前
13秒前
蓝天应助热情的乐荷采纳,获得10
13秒前
ZENGzeng发布了新的文献求助10
14秒前
Mary发布了新的文献求助10
14秒前
14秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Gründe der Seele:Die Wiener Psychatrie im 20.Jahrhundert 1000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7272194
求助须知:如何正确求助?哪些是违规求助? 8893055
关于积分的说明 18799725
捐赠科研通 6946670
什么是DOI,文献DOI怎么找? 3204639
关于科研通互助平台的介绍 2376870
邀请新用户注册赠送积分活动 2180160