Clinical management of NUT carcinoma (NC) in Germany: Analysis of survival, therapy response, tumor markers and tumor genome sequencing in 35 adult patients

医学 肿瘤科 队列 内科学 融合基因 原发性肿瘤 异环磷酰胺 癌症 化疗 基因 转移 顺铂 生物化学 化学
作者
Linus D. Kloker,Mirjana Sidiras,Tim Flaadt,Ines B. Brecht,Christoph K. W. Deinzer,Thorben Groß,Katrin Benzler,Lars Zender,Ulrich M. Lauer
出处
期刊:Lung Cancer [Elsevier BV]
卷期号:: 107496-107496 被引量:4
标识
DOI:10.1016/j.lungcan.2024.107496
摘要

NUT carcinomas (NC) are very rare and highly aggressive tumors, molecularly defined by an aberrant gene fusion involving the NUTM1 gene. NCs preferentially arise intrathoracically or in the head and neck region, having a highly adverse prognosis with almost no long-term survivors. Here, we report on a cohort of 35 adult NC patients who were evaluated at University Hospital Tuebingen in an eight year time span, i.e. between 2016 and 2023. Primary objectives were overall survival (OS) and influence of primary tumor locations, fusion gene types and staging on OS. Secondary objectives were patient baseline characteristics, risk factors, tumor markers, treatment decisions and responses to therapy comparing thoracic vs non-thoracic origins. Further, data from tumor genome sequencing were analyzed. In this monocentric German cohort, 54 % of patients had thoracic tumors and 65 % harbored a BRD4-NUTM1 fusion gene. Median OS was 7.5 months, being significantly dependent on primary tumor location and nodal status. Initial misdiagnosis was a problem in 31 % of the cases. Surgery was the first treatment in most patients (46 %) and 80 % were treated with polychemotherapies, showing longer progression free survival (PFS) with ifosfamide-based than with platinum-based regimens. Patients treated with an immune checkpoint inhibitor (ICI) in addition to first-line chemotherapy tended to have longer OS. Initial LDH levels could be identified as a prognostic measure for survival prognosis. Sequencing data highlight aberrant NUTM1 fusion genes as unique tumor driver genes. This is the largest adult European cohort of this orphan tumor disease, showing epidemiologic and molecular features as well as relevant clinical data. Awareness to prevent misdiagnosis, fast contact to a specialized nation-wide center and referral to clinical studies are essential as long-term survival is rarely achieved with any of the current therapeutic regimes.
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
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
量子星尘发布了新的文献求助10
1秒前
1秒前
1秒前
1秒前
李健的小迷弟应助pjh采纳,获得10
2秒前
luyjabc完成签到,获得积分10
2秒前
3秒前
jimmyyyyyy发布了新的文献求助10
3秒前
莉莉发布了新的文献求助10
3秒前
传奇3应助君君采纳,获得10
3秒前
yyyyy发布了新的文献求助10
3秒前
孤独的谷南完成签到,获得积分10
4秒前
bai关注了科研通微信公众号
4秒前
Mike完成签到,获得积分10
5秒前
美好的冰蓝关注了科研通微信公众号
6秒前
活泼的冬寒完成签到,获得积分10
6秒前
JW关注了科研通微信公众号
7秒前
热情的天蓝举报终陌求助涉嫌违规
7秒前
accept完成签到,获得积分10
7秒前
风中钥匙完成签到,获得积分10
7秒前
慕青应助FJY采纳,获得10
8秒前
jimmyyyyyy完成签到,获得积分10
8秒前
量子星尘发布了新的文献求助10
8秒前
若灵发布了新的文献求助10
8秒前
莫惜君灬完成签到 ,获得积分10
9秒前
9秒前
FashionBoy应助莉莉采纳,获得10
9秒前
9秒前
顾矜应助xv采纳,获得10
9秒前
9秒前
花生了什么树完成签到,获得积分10
10秒前
10秒前
暴躁的晓啸完成签到 ,获得积分10
10秒前
10秒前
shengdong发布了新的文献求助10
11秒前
12秒前
12秒前
小权拳的权完成签到,获得积分10
12秒前
一切顺利完成签到 ,获得积分10
13秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2700
Neuromuscular and Electrodiagnostic Medicine Board Review 1000
Statistical Methods for the Social Sciences, Global Edition, 6th edition 600
こんなに痛いのにどうして「なんでもない」と医者にいわれてしまうのでしょうか 510
Walter Gilbert: Selected Works 500
An Annotated Checklist of Dinosaur Species by Continent 500
岡本唐貴自伝的回想画集 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3658802
求助须知:如何正确求助?哪些是违规求助? 3220730
关于积分的说明 9737399
捐赠科研通 2929929
什么是DOI,文献DOI怎么找? 1604159
邀请新用户注册赠送积分活动 757044
科研通“疑难数据库(出版商)”最低求助积分说明 734269