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ATP-Based Chemotherapy Response Assay in Primary or Recurrent Ovarian and Peritoneal Cancer

DC Field Value Language
dc.contributor.author김상운-
dc.contributor.author김성훈-
dc.contributor.author김영태-
dc.contributor.author김재훈-
dc.contributor.author남은지-
dc.contributor.author조한별-
dc.date.accessioned2015-12-28T11:16:14Z-
dc.date.available2015-12-28T11:16:14Z-
dc.date.issued2014-
dc.identifier.issn0513-5796-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/139076-
dc.description.abstractPURPOSE: To investigate chemosensitivity with an adenosine triphosphate-based chemotherapy response assay in patients with epithelial ovarian or peritoneal cancer according to tumor histology, grade, and disease status. MATERIALS AND METHODS: One hundred specimens were collected during primary or secondary debulking from 67 patients with primary ovarian cancer, 24 patients with recurrent ovarian cancer, 5 patients with primary peritoneal cancer, and 4 patients with recurrent peritoneal cancer; samples were collected between August 2006 and June 2009. Tumor cells were isolated and cultured for 48 hours in media containing chemotherapy. The chemosensitivity index (CI) was calculated as 300 minus the sum of the cell death rate at 0.2×, 1×, and 5× drug concentrations, and the CI values were compared. RESULTS: CI values were obtained from 93 of 100 patients. The most active agents against primary disease were ifosfamide and paclitaxel. For primary serous adenocarcinoma, paclitaxel and irinotecan were the most active, followed by ifosfamide. For clear cell carcinoma, ifosfamide was the most active, followed by paclitaxel and irinotecan. Although not statistically significant, the CIs of cisplatin, carboplatin, paclitaxel, and docetaxel decreased as tumor grade increased. In 14 cases of recurrent disease, paclitaxel was the most active, followed by ifosfamide and cisplatin. CONCLUSION: Ifosfamide and paclitaxel were the most active drugs for primary and recurrent disease. Therefore, we recommend further clinical studies to confirm the efficacy of paclitaxel, ifosfamide, and cisplatin combination chemotherapy for recurrent and primary ovarian cancer.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1664~1671-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdenocarcinoma, Clear Cell/drug therapy*-
dc.subject.MESHAdenocarcinoma, Clear Cell/metabolism-
dc.subject.MESHAdenocarcinoma, Clear Cell/pathology-
dc.subject.MESHAdenosine Triphosphate/metabolism*-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/therapeutic use*-
dc.subject.MESHCamptothecin/administration & dosage-
dc.subject.MESHCamptothecin/analogs & derivatives-
dc.subject.MESHCarboplatin/therapeutic use-
dc.subject.MESHCisplatin/administration & dosage-
dc.subject.MESHDrug Resistance, Neoplasm-
dc.subject.MESHDrug Screening Assays, Antitumor/methods-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIfosfamide/administration & dosage-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Recurrence, Local/drug therapy*-
dc.subject.MESHNeoplasms, Glandular and Epithelial/drug therapy*-
dc.subject.MESHNeoplasms, Glandular and Epithelial/metabolism-
dc.subject.MESHNeoplasms, Glandular and Epithelial/pathology-
dc.subject.MESHOvarian Neoplasms/drug therapy*-
dc.subject.MESHOvarian Neoplasms/metabolism-
dc.subject.MESHOvarian Neoplasms/pathology-
dc.subject.MESHPaclitaxel/therapeutic use-
dc.subject.MESHPeritoneal Neoplasms/drug therapy*-
dc.subject.MESHPeritoneal Neoplasms/metabolism-
dc.subject.MESHPeritoneal Neoplasms/pathology-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHSensitivity and Specificity-
dc.subject.MESHTaxoids/administration & dosage-
dc.titleATP-Based Chemotherapy Response Assay in Primary or Recurrent Ovarian and Peritoneal Cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics & Gynecology (산부인과학)-
dc.contributor.googleauthorMaria Lee-
dc.contributor.googleauthorSang Wun Kim-
dc.contributor.googleauthorEun Ji Nam-
dc.contributor.googleauthorHanbyoul Cho-
dc.contributor.googleauthorJae Hoon Kim-
dc.contributor.googleauthorYoung Tae Kim-
dc.contributor.googleauthorSunghoon Kim-
dc.identifier.doi10.3349/ymj.2014.55.6.1664-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00595-
dc.contributor.localIdA00526-
dc.contributor.localIdA00729-
dc.contributor.localIdA00876-
dc.contributor.localIdA01262-
dc.contributor.localIdA03921-
dc.relation.journalcodeJ02813-
dc.identifier.eissn1976-2437-
dc.identifier.pmid25323906-
dc.subject.keywordAdenosine triphosphate-
dc.subject.keywordcell death-
dc.subject.keywordcombination-
dc.subject.keyworddrug therapy-
dc.subject.keywordovarian cancer-
dc.contributor.alternativeNameKim, Sang Wun-
dc.contributor.alternativeNameKim, Sung Hoon-
dc.contributor.alternativeNameKim, Young Tae-
dc.contributor.alternativeNameKim, Jae Hoon-
dc.contributor.alternativeNameNam, Eun Ji-
dc.contributor.alternativeNameCho, Han Byoul-
dc.contributor.affiliatedAuthorKim, Sung Hoon-
dc.contributor.affiliatedAuthorKim, Sang Wun-
dc.contributor.affiliatedAuthorKim, Young Tae-
dc.contributor.affiliatedAuthorKim, Jae Hoon-
dc.contributor.affiliatedAuthorNam, Eun Ji-
dc.contributor.affiliatedAuthorCho, Han Byoul-
dc.citation.volume55-
dc.citation.number6-
dc.citation.startPage1664-
dc.citation.endPage1671-
dc.identifier.bibliographicCitationYONSEI MEDICAL JOURNAL, Vol.55(6) : 1664-1671, 2014-
dc.identifier.rimsid52470-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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