Concentrations of Irinotecan and SN-38 in the Ascites and the Fluid Product of Cell-Free and Concentrated Ascites Reinfusion Therapy 9 Days After Administration of Irinotecan in a Patient with Gastric Cancer: A Case Report.

IF 2.7 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
OncoTargets and therapy Pub Date : 2024-11-20 eCollection Date: 2024-01-01 DOI:10.2147/OTT.S486272
Keisuke Baba, Tomoki Tanie, Yasuo Matsubara, Yoshihiro Hirata, Hiroaki Ikematsu, Chiyo K Imamura, Narikazu Boku
{"title":"Concentrations of Irinotecan and SN-38 in the Ascites and the Fluid Product of Cell-Free and Concentrated Ascites Reinfusion Therapy 9 Days After Administration of Irinotecan in a Patient with Gastric Cancer: A Case Report.","authors":"Keisuke Baba, Tomoki Tanie, Yasuo Matsubara, Yoshihiro Hirata, Hiroaki Ikematsu, Chiyo K Imamura, Narikazu Boku","doi":"10.2147/OTT.S486272","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Cell-free and concentrated ascites reinfusion therapy (CART) is frequently used to relieve the symptoms caused by massive ascites due to peritoneal metastasis of gastric cancer, especially in the later stages of its clinical course. Irinotecan (CPT-11) is recommended for third- or later-line chemotherapy according to gastric cancer treatment guidelines. However, the concentrations of anti-cancer drugs in the ascites and the product of CART are not well known, it is considered that some amounts of anti-cancer drugs contained in the product of CART may be readministered and induce severe adverse reactions.</p><p><strong>Case presentation: </strong>A 66-year-old female with gastric cancer and massive ascites received third-line chemotherapy with CPT-11 (150 mg/m<sup>2</sup>) and ramucirumab (8 mg/kg). On day 7, the laboratory test showed a white blood cell count of 1,290/µL and neutrophil count of 480/µL. On day 9, the patient underwent CART, and the concentrations of CPT-11 and its active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38) were 1.18 ng/mL and 0.22 ng/mL in plasma, 0.95 ng/mL and 0.82 ng/mL in ascites, and 0.20 ng/mL and 0.17 ng/mL in the product of CART, respectively.</p><p><strong>Conclusion: </strong>Concentrations of CPT-11 and SN-38 remaining in ascites and the product of CART were low in an advanced gastric cancer patient 9 days after administration of CPT-11.</p>","PeriodicalId":19534,"journal":{"name":"OncoTargets and therapy","volume":"17 ","pages":"1089-1094"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586449/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"OncoTargets and therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/OTT.S486272","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Cell-free and concentrated ascites reinfusion therapy (CART) is frequently used to relieve the symptoms caused by massive ascites due to peritoneal metastasis of gastric cancer, especially in the later stages of its clinical course. Irinotecan (CPT-11) is recommended for third- or later-line chemotherapy according to gastric cancer treatment guidelines. However, the concentrations of anti-cancer drugs in the ascites and the product of CART are not well known, it is considered that some amounts of anti-cancer drugs contained in the product of CART may be readministered and induce severe adverse reactions.

Case presentation: A 66-year-old female with gastric cancer and massive ascites received third-line chemotherapy with CPT-11 (150 mg/m2) and ramucirumab (8 mg/kg). On day 7, the laboratory test showed a white blood cell count of 1,290/µL and neutrophil count of 480/µL. On day 9, the patient underwent CART, and the concentrations of CPT-11 and its active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38) were 1.18 ng/mL and 0.22 ng/mL in plasma, 0.95 ng/mL and 0.82 ng/mL in ascites, and 0.20 ng/mL and 0.17 ng/mL in the product of CART, respectively.

Conclusion: Concentrations of CPT-11 and SN-38 remaining in ascites and the product of CART were low in an advanced gastric cancer patient 9 days after administration of CPT-11.

一名胃癌患者接受伊立替康治疗 9 天后,腹水中伊立替康和 SN-38 的浓度以及无细胞和浓缩腹水再灌注疗法的液体产物:病例报告。
导言:无细胞浓缩腹水再灌注疗法(CART)常用于缓解胃癌腹膜转移引起的大量腹水症状,尤其是在临床病程的后期。根据胃癌治疗指南,伊立替康(CPT-11)被推荐用于三线或晚线化疗。然而,腹水和 CART 产品中抗癌药物的浓度并不十分清楚,有人认为 CART 产品中含有的部分抗癌药物可能会被再次注射,并诱发严重的不良反应:66岁女性胃癌患者,患有大量腹水,接受了CPT-11(150 mg/m2)和ramucirumab(8 mg/kg)的三线化疗。第 7 天,化验结果显示白细胞计数为 1,290 个/微升,中性粒细胞计数为 480 个/微升。第9天,患者接受了CART治疗,血浆中CPT-11及其活性代谢物7-乙基-10-羟基喜树碱(SN-38)的浓度分别为1.18纳克/毫升和0.22纳克/毫升,腹水中分别为0.95纳克/毫升和0.82纳克/毫升,CART产物中分别为0.20纳克/毫升和0.17纳克/毫升:一名晚期胃癌患者在服用 CPT-11 9 天后,腹水和 CART 产物中残留的 CPT-11 和 SN-38 浓度较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信