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An internally and externally validated nomogram for predicting the risk of irinotecan-induced severe neutropenia in advanced colorectal cancer patients.用于预测晚期结直肠癌患者伊立替康诱导的严重中性粒细胞减少风险的内部和外部验证的列线图。
Br J Cancer. 2015 May 12;112(10):1709-16. doi: 10.1038/bjc.2015.122. Epub 2015 Apr 16.
2
Ramucirumab versus placebo in combination with second-line FOLFIRI in patients with metastatic colorectal carcinoma that progressed during or after first-line therapy with bevacizumab, oxaliplatin, and a fluoropyrimidine (RAISE): a randomised, double-blind, multicentre, phase 3 study.雷莫芦单抗联合 FOLFIRI 二线治疗用于贝伐珠单抗、奥沙利铂和氟嘧啶一线治疗后进展的转移性结直肠癌患者:一项随机、双盲、多中心、III 期研究(RAISE)。
Lancet Oncol. 2015 May;16(5):499-508. doi: 10.1016/S1470-2045(15)70127-0. Epub 2015 Apr 12.
3
Host-microbe cross talk in cancer therapy.癌症治疗中的宿主-微生物相互作用
Curr Opin Support Palliat Care. 2015 Jun;9(2):174-81. doi: 10.1097/SPC.0000000000000133.
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A randomized, placebo-controlled phase III trial of masitinib plus gemcitabine in the treatment of advanced pancreatic cancer.一项关于马西替尼联合吉西他滨治疗晚期胰腺癌的随机、安慰剂对照III期试验。
Ann Oncol. 2015 Jun;26(6):1194-1200. doi: 10.1093/annonc/mdv133. Epub 2015 Apr 9.
5
Primary and Acquired Resistance of Colorectal Cancer to Anti-EGFR Monoclonal Antibody Can Be Overcome by Combined Treatment of Regorafenib with Cetuximab.结直肠癌原发和获得性抗 EGFR 单克隆抗体耐药可通过瑞戈非尼联合西妥昔单抗治疗克服。
Clin Cancer Res. 2015 Jul 1;21(13):2975-83. doi: 10.1158/1078-0432.CCR-15-0020. Epub 2015 Apr 2.
6
Prevalence of oral mucositis, dry mouth, and dysphagia in advanced cancer patients.晚期癌症患者口腔黏膜炎、口干和吞咽困难的患病率。
Support Care Cancer. 2015 Nov;23(11):3249-55. doi: 10.1007/s00520-015-2720-y. Epub 2015 Apr 3.
7
Pre-therapy mRNA expression of TNF is associated with regimen-related gastrointestinal toxicity in patients with esophageal cancer: a pilot study.食管癌患者治疗前TNF的mRNA表达与方案相关的胃肠道毒性相关:一项初步研究。
Support Care Cancer. 2015 Nov;23(11):3165-72. doi: 10.1007/s00520-015-2696-7. Epub 2015 Mar 27.
8
Phase II clinical trials on investigational drugs for the treatment of pancreatic cancers.用于治疗胰腺癌的研究性药物的II期临床试验。
Expert Opin Investig Drugs. 2015 Jun;24(6):781-94. doi: 10.1517/13543784.2015.1026963. Epub 2015 Mar 25.
9
Mucositis: pathobiology and management.黏膜炎:病理生物学与管理
Curr Opin Oncol. 2015 May;27(3):159-64. doi: 10.1097/CCO.0000000000000180.
10
Appropriateness of systemic treatments in unresectable metastatic well-differentiated pancreatic neuroendocrine tumors.不可切除转移性高分化胰腺神经内分泌肿瘤全身治疗的适宜性
World J Gastroenterol. 2015 Feb 28;21(8):2450-9. doi: 10.3748/wjg.v21.i8.2450.

治疗相关的胃肠道毒性与晚期结直肠癌或胰腺癌:重要更新

Treatment-related gastrointestinal toxicities and advanced colorectal or pancreatic cancer: A critical update.

作者信息

Aprile Giuseppe, Rihawi Karim, De Carlo Elisa, Sonis Stephen T

机构信息

Giuseppe Aprile, Karim Rihawi, Elisa De Carlo, Department of Medical Oncology, University and General Hospital of Udine, 33100 Udine, Italy.

出版信息

World J Gastroenterol. 2015 Nov 7;21(41):11793-803. doi: 10.3748/wjg.v21.i41.11793.

DOI:10.3748/wjg.v21.i41.11793
PMID:26557003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4631977/
Abstract

Gastrointestinal toxicities (GIT), including oral mucositis, nausea and vomiting, and diarrhea, are common side effects of chemotherapy and targeted agents in patients with advanced colorectal cancer and pancreatic cancer. Being often underreported, it is still difficult to precisely establish their burden in terms of both patient's quality of life and cancer care costs. Moreover, with the use of more intensive upfront combination regimens, the frequency of these toxicities is rapidly growing with a potential negative effect also on patient's outcome, as a result of dose reductions, delays or even discontinuation of active treatments. Thus, identifying patients at higher risk of developing GIT as well as an optimal management are paramount in order to improve patient's compliance and outcome. After the description of the main treatment-induced GIT, we discuss the current knowledge on the pathophysiology of these side effects and comment the scales commonly used to assess and grade them. We then provide a critical update on GIT incidence based on the results of key randomized trials conducted in patients with metastatic colorectal cancer and advanced pancreatic cancer.

摘要

胃肠道毒性(GIT),包括口腔黏膜炎、恶心呕吐和腹泻,是晚期结直肠癌和胰腺癌患者化疗及靶向药物常见的副作用。由于这些副作用常常报告不足,因此在患者生活质量和癌症治疗费用方面,仍难以精确确定其负担。此外,随着更强化的初始联合治疗方案的使用,这些毒性的发生频率迅速增加,由于减少剂量、延迟甚至中断有效治疗,对患者的治疗结果也可能产生负面影响。因此,识别发生胃肠道毒性风险较高的患者以及优化管理对于提高患者的依从性和治疗结果至关重要。在描述了主要的治疗引起的胃肠道毒性之后,我们讨论了关于这些副作用病理生理学的现有知识,并对常用于评估和分级这些毒性的量表进行评论。然后,我们根据在转移性结直肠癌和晚期胰腺癌患者中进行的关键随机试验结果,对胃肠道毒性的发生率进行重要更新。