• 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

新辅助吉西他滨化疗后序贯调强放疗同步推量在可切除边缘的胰腺癌患者中实现了高R0切除率

Neoadjuvant Gemcitabine Chemotherapy followed by Concurrent IMRT Simultaneous Boost Achieves High R0 Resection in Borderline Resectable Pancreatic Cancer Patients.

作者信息

Huang Xiaolun, Knoble Jeanna L, Zeng Ming, Aguila Fernando N, Patel Tara, Chambers Lowell W, Hu Honglin, Liu Hao

机构信息

Department of Hepatobiliary-Pancreatic Surgery and Cell Transplant Center, the Affiliated Hospital of University of Electronic Science and Technology, Chengdu, Sichuan, China.

Department of Hematology and Oncology, Zangmeister Cancer Center, Mount Carmel Health System, Columbus, Ohio, United States of America.

出版信息

PLoS One. 2016 Dec 9;11(12):e0166606. doi: 10.1371/journal.pone.0166606. eCollection 2016.

DOI:10.1371/journal.pone.0166606
PMID:27935952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5147831/
Abstract

BACKGROUND

To study the feasibility of down stage the borderline resectable pancreatic cancer (BRPC) to resectable disease, we reported our institutional results using an intensity-modulated radiation therapy (IMRT) simultaneous integrated boost (SIB) dose escalation approach to improve R0 resectability.

METHODS

We reviewed our past 7 years of experience of using neoadjuvant induction chemotherapy with Gemcitabine followed by concurrent chemoradiaiton for BRPC. During the concurrent, chemo was 5-FU and radiation were IMRT with SIB technique to target the key areas with dose escalation to 5600 in 28 fractions. The key areas were defined by PET positive area. This was followed by restaging imaging to rule out distant metastases before resection.

RESULTS

25 finished dose escalation protocol. 2 of the 25 cases developed distant metastases, 23 (92%) patients without distant metastases underwent pancreatectomy. Among the those received pancreatectomy, 22 (95%) achieved negative margin (R0). The gastrointestinal toxicity > grade 2 was 8% and there was no grade 4 toxicity.

CONCLUSION

Neoadjuvant Gemcitabine-based induction chemotherapy followed by 5-FU-based IMRT-SIB is a feasible option in improving the likelihood of R0 resection rate in BRPC without compromising the organs at risk for toxicity.

摘要

背景

为研究将临界可切除胰腺癌(BRPC)降期为可切除疾病的可行性,我们报告了我们机构采用调强放射治疗(IMRT)同步整合加量(SIB)剂量递增方法以提高R0切除率的结果。

方法

我们回顾了过去7年使用吉西他滨进行新辅助诱导化疗,随后对BRPC进行同步放化疗的经验。在同步放化疗期间,化疗药物为5-氟尿嘧啶(5-FU),放疗采用IMRT-SIB技术,针对关键区域进行剂量递增至5600 cGy,分28次照射。关键区域由PET阳性区域定义。在切除术前进行重新分期影像学检查以排除远处转移。

结果

25例完成了剂量递增方案。25例中有2例发生远处转移,23例(92%)无远处转移的患者接受了胰腺切除术。在接受胰腺切除术的患者中,22例(95%)切缘阴性(R0)。胃肠道毒性>2级的发生率为8%,无4级毒性。

结论

以吉西他滨为基础的新辅助诱导化疗后序贯以5-FU为基础的IMRT-SIB是提高BRPC患者R0切除率可能性的可行选择,且不会增加毒性风险器官的损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5787/5147831/fd596649cf7c/pone.0166606.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5787/5147831/da86d2e16c14/pone.0166606.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5787/5147831/fd596649cf7c/pone.0166606.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5787/5147831/da86d2e16c14/pone.0166606.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5787/5147831/fd596649cf7c/pone.0166606.g002.jpg

相似文献

1
Neoadjuvant Gemcitabine Chemotherapy followed by Concurrent IMRT Simultaneous Boost Achieves High R0 Resection in Borderline Resectable Pancreatic Cancer Patients.新辅助吉西他滨化疗后序贯调强放疗同步推量在可切除边缘的胰腺癌患者中实现了高R0切除率
PLoS One. 2016 Dec 9;11(12):e0166606. doi: 10.1371/journal.pone.0166606. eCollection 2016.
2
Induction Chemotherapy Followed by Concurrent Full-dose Gemcitabine and Intensity-modulated Radiation Therapy for Borderline Resectable and Locally Advanced Pancreatic Adenocarcinoma.诱导化疗后序贯全剂量吉西他滨与调强放射治疗用于可切除边缘和局部晚期胰腺腺癌
Am J Clin Oncol. 2016 Feb;39(1):1-7. doi: 10.1097/COC.0000000000000003.
3
Phase 2 Trial of Neoadjuvant FOLFIRINOX and Intensity Modulated Radiation Therapy Concurrent With Fixed-Dose Rate-Gemcitabine in Patients With Borderline Resectable Pancreatic Cancer.局部进展期可切除胰腺癌新辅助 FOLFIRINOX 方案联合调强放疗同步固定剂量率吉西他滨治疗的Ⅱ期临床研究。
Int J Radiat Oncol Biol Phys. 2020 Jan 1;106(1):124-133. doi: 10.1016/j.ijrobp.2019.08.057. Epub 2019 Sep 5.
4
A phase II trial of neoadjuvant chemoradiotherapy with intensity-modulated radiotherapy combined with gemcitabine and S-1 for borderline-resectable pancreatic cancer with arterial involvement.一项关于新辅助放化疗的II期试验,采用调强放疗联合吉西他滨和S-1治疗伴有动脉侵犯的可切除边缘性胰腺癌。
Cancer Chemother Pharmacol. 2017 May;79(5):951-957. doi: 10.1007/s00280-017-3288-7. Epub 2017 Apr 4.
5
Phase 2 trial of induction gemcitabine, oxaliplatin, and cetuximab followed by selective capecitabine-based chemoradiation in patients with borderline resectable or unresectable locally advanced pancreatic cancer.局部晚期不可切除或边界可切除的胰腺癌患者诱导吉西他滨、奥沙利铂和西妥昔单抗治疗后行选择性卡培他滨为基础的放化疗的 II 期临床试验。
Int J Radiat Oncol Biol Phys. 2014 Mar 15;88(4):837-44. doi: 10.1016/j.ijrobp.2013.12.030.
6
Phase I Trial Evaluating the Safety of Preoperative Gemcitabine/nab-Paclitaxel With Concurrent Radiation Therapy for Borderline Resectable Pancreatic Cancer.评估术前吉西他滨/纳米白蛋白结合型紫杉醇与同步放疗用于可切除边缘的胰腺癌安全性的I期试验
Pancreas. 2018 Oct;47(9):1135-1141. doi: 10.1097/MPA.0000000000001140.
7
Neoadjuvant Phase II Trial of Chemoradiotherapy in Patients With Resectable and Borderline Resectable Pancreatic Cancer.可切除和边界可切除胰腺癌患者新辅助放化疗的 II 期临床试验。
Am J Clin Oncol. 2020 Jun;43(6):435-441. doi: 10.1097/COC.0000000000000688.
8
Neoadjuvant GTX chemotherapy and IMRT-based chemoradiation for borderline resectable pancreatic cancer.新辅助 GTX 化疗和基于调强放疗的放化疗治疗局部进展期胰腺癌。
J Surg Oncol. 2011 Aug 1;104(2):155-61. doi: 10.1002/jso.21954. Epub 2011 Apr 25.
9
Induction Chemotherapy with Gemcitabine and Cisplatin Followed by Simultaneous Integrated Boost-Intensity Modulated Radiotherapy with Concurrent Gemcitabine for Locally Advanced Unresectable Pancreatic Cancer: Results from a Feasibility Study.吉西他滨和顺铂诱导化疗联合同期调强放疗同步增敏治疗局部进展期不可切除胰腺癌:一项可行性研究结果。
Cancer Res Treat. 2017 Oct;49(4):1022-1032. doi: 10.4143/crt.2016.495. Epub 2017 Jan 19.
10
Concurrent gemcitabine+S-1 neoadjuvant chemotherapy contributes to the improved survival of patients with small borderline-resectable pancreatic cancer tumors.吉西他滨联合S-1新辅助化疗有助于提高小的临界可切除胰腺癌患者的生存率。
Surg Today. 2016 Nov;46(11):1282-9. doi: 10.1007/s00595-016-1310-z. Epub 2016 Feb 9.

引用本文的文献

1
Magnetic nanoparticle hyperthermia for treating locally advanced unresectable and borderline resectable pancreatic cancers: the role of tumor size and eddy-current heating.磁性纳米颗粒热疗治疗局部晚期不可切除和边界可切除胰腺癌:肿瘤大小和涡流加热的作用
Int J Hyperthermia. 2020 Dec;37(3):108-119. doi: 10.1080/02656736.2020.1798514.
2
Neoadjuvant therapy and pancreatic cancer: a national cancer database analysis.新辅助治疗与胰腺癌:一项国家癌症数据库分析
J Gastrointest Oncol. 2019 Aug;10(4):663-673. doi: 10.21037/jgo.2019.02.09.
3
Correlation of tumor size and survival in pancreatic cancer.

本文引用的文献

1
Long-term outcomes of induction chemotherapy and neoadjuvant stereotactic body radiotherapy for borderline resectable and locally advanced pancreatic adenocarcinoma.诱导化疗联合新辅助立体定向体部放疗治疗可切除边缘和局部晚期胰腺腺癌的长期疗效
Acta Oncol. 2015 Jul;54(7):979-85. doi: 10.3109/0284186X.2015.1004367. Epub 2015 Mar 3.
2
Upper abdominal normal organ contouring guidelines and atlas: a Radiation Therapy Oncology Group consensus.上腹部正常器官轮廓勾画指南与图谱:放射治疗肿瘤学组共识
Pract Radiat Oncol. 2014 Mar-Apr;4(2):82-89. doi: 10.1016/j.prro.2013.06.004. Epub 2013 Aug 7.
3
Phase 2 trial of induction gemcitabine, oxaliplatin, and cetuximab followed by selective capecitabine-based chemoradiation in patients with borderline resectable or unresectable locally advanced pancreatic cancer.
胰腺癌中肿瘤大小与生存情况的相关性。
J Gastrointest Oncol. 2018 Oct;9(5):910-921. doi: 10.21037/jgo.2018.08.06.
局部晚期不可切除或边界可切除的胰腺癌患者诱导吉西他滨、奥沙利铂和西妥昔单抗治疗后行选择性卡培他滨为基础的放化疗的 II 期临床试验。
Int J Radiat Oncol Biol Phys. 2014 Mar 15;88(4):837-44. doi: 10.1016/j.ijrobp.2013.12.030.
4
Preoperative gemcitabine-based chemoradiation therapy for resectable and borderline resectable pancreatic cancer.术前吉西他滨为基础的放化疗治疗可切除和交界可切除胰腺癌。
Ann Surg. 2013 Dec;258(6):1040-50. doi: 10.1097/SLA.0b013e31829b3ce4.
5
A multi-institutional phase 2 study of neoadjuvant gemcitabine and oxaliplatin with radiation therapy in patients with pancreatic cancer.一项多机构的 II 期研究,评估新辅助吉西他滨和奥沙利铂联合放化疗治疗胰腺癌患者的疗效。
Cancer. 2013 Aug 1;119(15):2692-700. doi: 10.1002/cncr.28117. Epub 2013 May 29.
6
Response of borderline resectable pancreatic cancer to neoadjuvant therapy is not reflected by radiographic indicators.边缘可切除胰腺癌对新辅助治疗的反应不能通过影像学指标反映。
Cancer. 2012 Dec 1;118(23):5749-56. doi: 10.1002/cncr.27636. Epub 2012 May 17.
7
A phase I/II trial of intensity modulated radiation (IMRT) dose escalation with concurrent fixed-dose rate gemcitabine (FDR-G) in patients with unresectable pancreatic cancer.一项强度调制放射治疗(IMRT)剂量递增联合不可切除胰腺癌患者固定剂量率吉西他滨(FDR-G)同步治疗的 I/II 期临床试验。
Int J Radiat Oncol Biol Phys. 2012 Dec 1;84(5):1166-71. doi: 10.1016/j.ijrobp.2012.02.051. Epub 2012 Apr 27.
8
Neoadjuvant therapy in pancreatic adenocarcinoma: a meta-analysis of phase II trials.新辅助治疗在胰腺导管腺癌中的应用:II 期临床试验的荟萃分析。
Surgery. 2011 Sep;150(3):466-73. doi: 10.1016/j.surg.2011.07.006.
9
Neoadjuvant GTX chemotherapy and IMRT-based chemoradiation for borderline resectable pancreatic cancer.新辅助 GTX 化疗和基于调强放疗的放化疗治疗局部进展期胰腺癌。
J Surg Oncol. 2011 Aug 1;104(2):155-61. doi: 10.1002/jso.21954. Epub 2011 Apr 25.
10
Borderline resectable pancreatic cancer: what have we learned and where do we go from here?可切除边缘的胰腺癌:我们学到了什么,未来何去何从?
Ann Surg Oncol. 2011 Mar;18(3):608-10. doi: 10.1245/s10434-010-1460-y.