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 Monteiro de Oliveira Novaes,Haiying Cheng
出处
期刊:Lung [Springer Nature]
卷期号:199 (6): 579-587 被引量:31
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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
yearn发布了新的文献求助10
刚刚
划落落完成签到,获得积分10
2秒前
Skymi完成签到,获得积分10
3秒前
HHD完成签到 ,获得积分10
5秒前
AnJaShua完成签到 ,获得积分10
5秒前
yufanhui应助科研通管家采纳,获得20
6秒前
CodeCraft应助科研通管家采纳,获得10
6秒前
小二郎应助科研通管家采纳,获得10
6秒前
上官若男应助科研通管家采纳,获得10
6秒前
bkagyin应助科研通管家采纳,获得10
6秒前
斯文败类应助科研通管家采纳,获得10
6秒前
Ava应助科研通管家采纳,获得10
6秒前
李爱国应助摆渡人采纳,获得10
16秒前
17秒前
yearn完成签到,获得积分20
21秒前
PJ完成签到,获得积分0
22秒前
幸福果汁完成签到,获得积分10
22秒前
肖旻完成签到,获得积分10
22秒前
222123发布了新的文献求助10
23秒前
醉熏的伊发布了新的文献求助20
29秒前
珍惜完成签到,获得积分10
30秒前
Ash完成签到 ,获得积分10
31秒前
earthai完成签到,获得积分10
32秒前
37秒前
38秒前
小二郎应助zhangjianzeng采纳,获得10
38秒前
zxt完成签到,获得积分10
39秒前
摆渡人发布了新的文献求助10
42秒前
默默完成签到 ,获得积分10
42秒前
44秒前
Danish完成签到,获得积分10
46秒前
48秒前
顺顺利利发布了新的文献求助10
48秒前
shuangfeng1853完成签到 ,获得积分10
48秒前
芝麻汤圆完成签到,获得积分10
49秒前
医生小白完成签到 ,获得积分10
50秒前
zokor完成签到 ,获得积分10
51秒前
51秒前
sosodo完成签到,获得积分10
52秒前
zyw完成签到 ,获得积分10
53秒前
高分求助中
Formgebungs- und Stabilisierungsparameter für das Konstruktionsverfahren der FiDU-Freien Innendruckumformung von Blech 1000
The Illustrated History of Gymnastics 800
The Bourse of Babylon : market quotations in the astronomical diaries of Babylonia 680
Division and square root. Digit-recurrence algorithms and implementations 500
The role of a multidrug-resistance gene (lemdrl) in conferring vinblastine resistance in Leishmania enriettii 330
Elgar Encyclopedia of Consumer Behavior 300
機能營養學前瞻(3 Ed.) 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2510290
求助须知:如何正确求助?哪些是违规求助? 2159917
关于积分的说明 5530025
捐赠科研通 1880158
什么是DOI,文献DOI怎么找? 935655
版权声明 564215
科研通“疑难数据库(出版商)”最低求助积分说明 499559