• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

相似文献

1
Chronological improvement in precision oncology implementation in Japan.日本精准肿瘤学实施的时间性改善。
Cancer Sci. 2022 Nov;113(11):3995-4000. doi: 10.1111/cas.15517. Epub 2022 Sep 2.
2
The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan.日本癌症基因组医学核心医院专家组表现的初步评估。
Int J Clin Oncol. 2021 Mar;26(3):443-449. doi: 10.1007/s10147-020-01844-1. Epub 2021 Jan 1.
3
Effect of a Collaboration Between a Health Plan, Oncology Practice, and Comprehensive Genomic Profiling Company from the Payer Perspective.从支付方角度看,一项健康计划、肿瘤学实践和综合基因组分析公司之间合作的效果。
J Manag Care Spec Pharm. 2019 May;25(5):601-611. doi: 10.18553/jmcp.2019.18309. Epub 2019 Jan 11.
4
[Current Status and Prospects of the Comprehensive Cancer Genome Profiling].[癌症综合基因组分析的现状与展望]
Gan To Kagaku Ryoho. 2021 Jan;48(1):7-11.
5
Identification of barriers to implementation of precision oncology in patients with rare cancers.罕见癌症患者精准肿瘤学实施障碍的识别。
Cancer Sci. 2024 Jun;115(6):2023-2035. doi: 10.1111/cas.16165. Epub 2024 Mar 27.
6
Current Clinical Practice of Precision Medicine Using Comprehensive Genomic Profiling Tests in Biliary Tract Cancer in Japan.日本胆管癌中综合基因组分析检测精准医学的现行临床实践。
Curr Oncol. 2022 Sep 30;29(10):7272-7284. doi: 10.3390/curroncol29100573.
7
The impact of rare cancer and early-line treatments on the benefit of comprehensive genome profiling-based precision oncology.罕见癌症和一线治疗对基于全面基因组分析的精准肿瘤学获益的影响。
ESMO Open. 2024 Apr;9(4):102981. doi: 10.1016/j.esmoop.2024.102981. Epub 2024 Apr 12.
8
First-Line Genomic Profiling in Previously Untreated Advanced Solid Tumors for Identification of Targeted Therapy Opportunities.一线治疗前未治疗的晚期实体瘤的基因组分析,以确定靶向治疗机会。
JAMA Netw Open. 2023 Jul 3;6(7):e2323336. doi: 10.1001/jamanetworkopen.2023.23336.
9
Clinical utility of Todai OncoPanel in the setting of approved comprehensive cancer genomic profiling tests in Japan.日本在批准的全面癌症基因组分析检测背景下,评估 Todai OncoPanel 的临床实用性。
Cancer Sci. 2023 Apr;114(4):1710-1717. doi: 10.1111/cas.15717. Epub 2023 Jan 17.
10
[From the Standpoint of a Core Center Hospital for Cancer Genome Medicine-Establishment of a Provision System for Wide-Area Precision Oncology].[从癌症基因组医学核心中心医院的角度——建立广域精准肿瘤学供应体系]
Gan To Kagaku Ryoho. 2021 Jul;48(7):866-872.

引用本文的文献

1
Potential Resistance to Oxaliplatin-Based Regimens in Gastric Cancer Patients with ERBB2 R678Q Mutation: Evidence from a National Genomic Database.携带ERBB2基因R678Q突变的胃癌患者对基于奥沙利铂方案的潜在耐药性:来自国家基因组数据库的证据
Curr Issues Mol Biol. 2025 Jun 6;47(6):430. doi: 10.3390/cimb47060430.
2
Clinical utility and characteristics of comprehensive genomic profiling tests in patients with gynecologic cancer: a multi-institutional survey in Kinki District, Japan.妇科癌症患者综合基因组分析检测的临床效用及特征:日本近畿地区的多机构调查
Int J Clin Oncol. 2025 Jul 22. doi: 10.1007/s10147-025-02835-w.
3
Risk factors for early mortality among patients with gastrointestinal malignancy in the C-CAT database.C-CAT数据库中胃肠道恶性肿瘤患者早期死亡的危险因素。
Int J Clin Oncol. 2025 Jun 19. doi: 10.1007/s10147-025-02802-5.
4
First-Line Genomic Profiling in Previously Untreated Advanced Solid Tumors: 1-Year Follow-Up of the FIRST-Dx Study.既往未治疗的晚期实体瘤一线基因组分析:FIRST-Dx研究的1年随访
Cancer Sci. 2025 Jul;116(7):1908-1919. doi: 10.1111/cas.70077. Epub 2025 Apr 11.
5
The 2024 revised clinical guidelines on the management of thyroid tumors by the Japan Association of Endocrine Surgery.日本内分泌外科学会2024年修订的甲状腺肿瘤管理临床指南。
Endocr J. 2025 May 7;72(5):545-635. doi: 10.1507/endocrj.EJ24-0644. Epub 2025 Mar 8.
6
Profiling in advanced hepatocellular carcinoma: opening new doors for precision medicine.晚期肝细胞癌的分析:为精准医学打开新大门。
Hepatol Int. 2025 Feb;19(1):87-89. doi: 10.1007/s12072-024-10770-7. Epub 2024 Dec 20.
7
A 5-year review of genomic medicine in breast cancer: insights from C-CAT data on 3776 Japanese patients.乳腺癌基因组医学的5年回顾:来自3776名日本患者C-CAT数据的见解
Breast Cancer. 2025 Mar;32(2):314-328. doi: 10.1007/s12282-024-01656-5. Epub 2024 Dec 4.
8
Association between homologous recombination deficiency and time to treatment failure to platinum-based chemotherapy for pancreatic cancer by using the C-CAT database.利用C-CAT数据库分析同源重组缺陷与胰腺癌铂类化疗治疗失败时间之间的关联。
J Gastroenterol. 2025 Feb;60(2):247-256. doi: 10.1007/s00535-024-02173-0. Epub 2024 Nov 21.
9
Nationwide survey of the secondary findings in cancer genomic profiling: survey including liquid biopsy.癌症基因组分析中次要发现的全国性调查:包括液体活检的调查
J Hum Genet. 2025 Jan;70(1):33-40. doi: 10.1038/s10038-024-01294-x. Epub 2024 Sep 17.
10
Familial and hereditary pancreatic cancer in Japan.日本的家族性和遗传性胰腺癌。
Fam Cancer. 2024 Aug;23(3):365-372. doi: 10.1007/s10689-024-00395-y. Epub 2024 May 11.

本文引用的文献

1
The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan.日本癌症基因组医学核心医院专家组表现的初步评估。
Int J Clin Oncol. 2021 Mar;26(3):443-449. doi: 10.1007/s10147-020-01844-1. Epub 2021 Jan 1.
2
Precision Oncology and the Universal Health Coverage System in Japan.精准肿瘤学与日本的全民健康覆盖体系
JCO Precis Oncol. 2019 Dec 11;3. doi: 10.1200/PO.19.00291. eCollection 2019.

日本精准肿瘤学实施的时间性改善。

Chronological improvement in precision oncology implementation in Japan.

机构信息

Department of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.

Department of Breast and Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

出版信息

Cancer Sci. 2022 Nov;113(11):3995-4000. doi: 10.1111/cas.15517. Epub 2022 Sep 2.

DOI:10.1111/cas.15517
PMID:35976133
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9633287/
Abstract

In Japan, comprehensive genomic profiling (CGP) tests for refractory cancer patients have been approved since June 2019, under the requirement that all cases undergoing CGP tests are annotated by the molecular tumor board (MTB) at each government-designated hospital. To investigate improvement in precision oncology, we evaluated and compared the proportion of cases receiving matched treatments according to CGP results and those recommended to receive genetic counseling at all core hospitals between the first period (11 hospitals, June 2019 to January 2020) and second period (12 hospitals, February 2020 to January 2021). A total of 754 and 2294 cases underwent CGP tests at core hospitals in the first and second periods, respectively; 28 (3.7%) and 176 (7.7%) patients received matched treatments (p < 0.001). Additionally, 25 (3.3%) and 237 (10.3%) cases were recommended to receive genetic counseling in the first and second periods, respectively (p < 0.001). The proportion was associated with the type of CGP test: tumor-only (N = 2391) vs. tumor-normal paired (N = 657) analysis (10.0% vs. 3.5%). These results suggest that recommendations regarding available clinical trials in networked MTBs might contribute to increasing the numbers of matched treatments, and that tumor-normal paired rather than tumor-only tests can increase the efficiency of patient referrals for genetic counseling.

摘要

在日本,自 2019 年 6 月以来,针对难治性癌症患者的综合基因组分析(CGP)测试已获得批准,要求所有接受 CGP 测试的病例均由各政府指定医院的分子肿瘤委员会(MTB)进行注释。为了研究精准肿瘤学的改进,我们评估并比较了根据 CGP 结果接受匹配治疗的病例比例,以及建议在所有核心医院接受遗传咨询的病例比例,这些核心医院在第一阶段(11 家医院,2019 年 6 月至 2020 年 1 月)和第二阶段(12 家医院,2020 年 2 月至 2021 年 1 月)各有 754 例和 2294 例病例接受了 CGP 测试。在第一阶段和第二阶段,分别有 28(3.7%)和 176(7.7%)例患者接受了匹配治疗(p<0.001)。此外,在第一阶段和第二阶段,分别有 25(3.3%)和 237(10.3%)例患者被建议接受遗传咨询(p<0.001)。这种比例与 CGP 测试的类型有关:肿瘤分析(N=2391)与肿瘤-正常配对分析(N=657)(10.0% vs. 3.5%)。这些结果表明,网络 MTB 中关于现有临床试验的建议可能有助于增加匹配治疗的数量,并且肿瘤-正常配对分析而非肿瘤分析可以提高患者遗传咨询的效率。