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The prognostic role of CD68 and FoxP3 expression in patients with primary central nervous system lymphoma

DC Field Value Language
dc.contributor.author김세훈-
dc.contributor.author장지은-
dc.contributor.author정준원-
dc.contributor.author김수정-
dc.contributor.author김유리-
dc.contributor.author김윤덕-
dc.contributor.author김진석-
dc.contributor.author민유홍-
dc.contributor.author서창옥-
dc.contributor.author양우익-
dc.contributor.author이정연-
dc.contributor.author장종희-
dc.contributor.author조현수-
dc.date.accessioned2017-11-01T08:39:46Z-
dc.date.available2017-11-01T08:39:46Z-
dc.date.issued2017-
dc.identifier.issn0939-5555-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/153493-
dc.description.abstractThe prognostic role of CD68 and FoxP3 in primary central nervous system lymphoma (PCNSL) has not been evaluated. Thus, we examined the prognostic significance of CD68 and FoxP3 expression in tumor samples of 76 newly diagnosed immunocompetent PCNSL patients. All patients were treated initially with high-dose methotrexate (HD-MTX)-based chemotherapy, and 16 (21.1%) patients received upfront autologous stem cell transplantation (ASCT) consolidation. High expression of CD68 (>55 cells/high-power field) or FoxP3 (>15 cells/high-power field) was observed in 10 patients, respectively. High CD68 expression was associated with inferior overall survival (OS) and progression-free survival (PFS) in multivariate analysis (P = 0.023 and P = 0.021, respectively). In addition, we performed subgroup analysis based on upfront ASCT. High CD68 expression was also associated with inferior OS and PFS in multivariate analysis (P = 0.013 and P < 0.001, respectively) among patients who did not receive upfront ASCT (n = 60), but not in patients who received upfront ASCT. The expression of FoxP3 was not significantly associated with survival. Therefore, we identified a prognostic significance of high CD68 expression in PCNSL, which suggests a need for further clinical trials and biological studies on the role of PCNSL tumor microenvironment.-
dc.description.statementOfResponsibilityrestriction-
dc.publisherSpringer International-
dc.relation.isPartOfANNALS OF HEMATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntigens, CD/metabolism*-
dc.subject.MESHAntigens, Differentiation, Myelomonocytic/metabolism*-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/therapeutic use*-
dc.subject.MESHCentral Nervous System Neoplasms/metabolism-
dc.subject.MESHCentral Nervous System Neoplasms/pathology-
dc.subject.MESHCentral Nervous System Neoplasms/therapy*-
dc.subject.MESHCombined Modality Therapy-
dc.subject.MESHFemale-
dc.subject.MESHForkhead Transcription Factors/metabolism*-
dc.subject.MESHHematopoietic Stem Cell Transplantation/methods*-
dc.subject.MESHHumans-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHLymphoma/metabolism-
dc.subject.MESHLymphoma/pathology-
dc.subject.MESHLymphoma/therapy*-
dc.subject.MESHMale-
dc.subject.MESHMethotrexate/administration & dosage-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMultivariate Analysis-
dc.subject.MESHOutcome Assessment (Health Care)/methods-
dc.subject.MESHOutcome Assessment (Health Care)/statistics & numerical data-
dc.subject.MESHPrognosis-
dc.subject.MESHProportional Hazards Models-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHTransplantation, Autologous-
dc.titleThe prognostic role of CD68 and FoxP3 expression in patients with primary central nervous system lymphoma-
dc.typeArticle-
dc.publisher.locationGermany-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Pathology-
dc.contributor.googleauthorHyunsoo Cho-
dc.contributor.googleauthorSe Hoon Kim-
dc.contributor.googleauthorSoo-Jeong Kim-
dc.contributor.googleauthorJong Hee Chang-
dc.contributor.googleauthorWoo Ick Yang-
dc.contributor.googleauthorChang-Ok Suh-
dc.contributor.googleauthorJune-Won Cheong-
dc.contributor.googleauthorYu Ri Kim-
dc.contributor.googleauthorJung Yeon Lee-
dc.contributor.googleauthorJi Eun Jang-
dc.contributor.googleauthorYundeok Kim-
dc.contributor.googleauthorYoo Hong Min-
dc.contributor.googleauthorJin Seok Kim-
dc.identifier.doi10.1007/s00277-017-3014-x-
dc.contributor.localIdA03477-
dc.contributor.localIdA03729-
dc.contributor.localIdA00633-
dc.contributor.localIdA00779-
dc.contributor.localIdA00790-
dc.contributor.localIdA01017-
dc.contributor.localIdA01407-
dc.contributor.localIdA01919-
dc.contributor.localIdA02300-
dc.contributor.localIdA03114-
dc.contributor.localIdA03470-
dc.contributor.localIdA00610-
dc.relation.journalcodeJ00161-
dc.identifier.eissn1432-0584-
dc.identifier.pmid28508176-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs00277-017-3014-x-
dc.subject.keywordAutologous stem cell transplantation-
dc.subject.keywordCD68-
dc.subject.keywordFoxP3-
dc.subject.keywordPrimary central nervous system lymphoma-
dc.subject.keywordTumor microenvironment-
dc.contributor.alternativeNameKim, Se Hoon-
dc.contributor.alternativeNameJang, Ji Eun-
dc.contributor.alternativeNameCheong, June Won-
dc.contributor.alternativeNameKim, Soo Jeong-
dc.contributor.alternativeNameKim, Yu Ri-
dc.contributor.alternativeNameKim, Yun Deok-
dc.contributor.alternativeNameKim, Jin Seok-
dc.contributor.alternativeNameMin, Yoo Hong-
dc.contributor.alternativeNameSuh, Chang Ok-
dc.contributor.alternativeNameYang, Woo Ick-
dc.contributor.alternativeNameLee, Jung Yoen-
dc.contributor.alternativeNameChang, Jong Hee-
dc.contributor.affiliatedAuthorJang, Ji Eun-
dc.contributor.affiliatedAuthorCheong, June-Won-
dc.contributor.affiliatedAuthorKim, Soo Jeong-
dc.contributor.affiliatedAuthorKim, Yu Ri-
dc.contributor.affiliatedAuthorKim, Yun Deok-
dc.contributor.affiliatedAuthorKim, Jin Seok-
dc.contributor.affiliatedAuthorMin, Yoo Hong-
dc.contributor.affiliatedAuthorSuh, Chang Ok-
dc.contributor.affiliatedAuthorYang, Woo Ick-
dc.contributor.affiliatedAuthorLee, Jung Yoen-
dc.contributor.affiliatedAuthorChang, Jong Hee-
dc.contributor.affiliatedAuthorKim, Se Hoon-
dc.citation.titleAnnals of Hematology-
dc.citation.volume96-
dc.citation.number7-
dc.citation.startPage1163-
dc.citation.endPage1173-
dc.identifier.bibliographicCitationANNALS OF HEMATOLOGY, Vol.96(7) : 1163-1173, 2017-
dc.date.modified2017-11-01-
dc.identifier.rimsid42199-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Neurosurgery (신경외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers

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