Keisuke Baba, Tomoki Tanie, Yasuo Matsubara, Yoshihiro Hirata, Hiroaki Ikematsu, Chiyo K Imamura, Narikazu Boku
{"title":"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。","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":"{\"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}","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}
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.
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.
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.