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A phase II study of everolimus (RAD001), an mTOR inhibitor plus CHOP for newly diagnosed peripheral T-cell lymphomas

DC FieldValueLanguage
dc.contributor.author김진석-
dc.date.accessioned2017-10-26T07:58:57Z-
dc.date.available2017-10-26T07:58:57Z-
dc.date.issued2016-
dc.identifier.issn0923-7534-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/152779-
dc.description.abstractBACKGROUND: Everolimus, an oral mTOR inhibitor, has single-agent activity against relapsed lymphomas. Thus, we carried out a phase II study of everolimus in combination with CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) as a first-line treatment for patients with peripheral T-cell lymphoma (PTCL) based on our phase I study results. PATIENTS AND METHODS: Participants (n = 30) received CHOP with 5 mg everolimus per day from day 1 to 14 every 21 days for a total of six cycles. The primary end point was the overall response rate (ORR), which included complete response (CR) and partial response (PR) to this regimen. Immunohistochemistry was used to evaluate the expression of phosphatase and tensin homology (PTEN) and phosphorylated S6 kinase (pS6K) as a response. RESULTS: The objective response rate was 90% with CR (n = 17) and PR (n = 10). The CR rate was different among subtypes; angioimmunoblastic T-cell lymphoma (AITL, n = 3) had a CR whereas PTCL-not-otherwise specified and ALK-negative anaplastic large-cell lymphoma (ALCL) patients showed 63% (12/19) and 29% (2/7) of CR rate, respectively. This difference in CR rate among subtypes was associated with PTEN loss because PTEN loss was not seen in AITL but 33% of ALCL patients. The most common toxicity was hematological, with 80% of patients experiencing at least one event of grade 3/4 neutropenia, and 60% of patients had grade 3/4 thrombocytopenia. CONCLUSION: The everolimus plus CHOP was effective for PTCL patients, and its efficacy might be related with the preservation of PTEN.-
dc.description.statementOfResponsibilityrestriction-
dc.publisherOxford University Press-
dc.relation.isPartOfANNALS OF ONCOLOGY-
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.MESHAntineoplastic Combined Chemotherapy Protocols/administration & dosage*-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/adverse effects-
dc.subject.MESHCyclophosphamide/administration & dosage-
dc.subject.MESHCyclophosphamide/adverse effects-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHDoxorubicin/administration & dosage-
dc.subject.MESHDoxorubicin/adverse effects-
dc.subject.MESHDrug Administration Schedule-
dc.subject.MESHEverolimus/administration & dosage*-
dc.subject.MESHEverolimus/adverse effects-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLymphoma, T-Cell, Peripheral/drug therapy*-
dc.subject.MESHLymphoma, T-Cell, Peripheral/pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHPTEN Phosphohydrolase/biosynthesis-
dc.subject.MESHPTEN Phosphohydrolase/genetics*-
dc.subject.MESHPrednisone/administration & dosage-
dc.subject.MESHPrednisone/adverse effects-
dc.subject.MESHTOR Serine-Threonine Kinases/antagonists & inhibitors-
dc.subject.MESHTOR Serine-Threonine Kinases/genetics-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHVincristine/administration & dosage-
dc.subject.MESHVincristine/adverse effects-
dc.titleA phase II study of everolimus (RAD001), an mTOR inhibitor plus CHOP for newly diagnosed peripheral T-cell lymphomas-
dc.typeArticle-
dc.publisher.locationEngland-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorS. J. Kim-
dc.contributor.googleauthorD.-Y. Shin-
dc.contributor.googleauthorJ. S. Kim-
dc.contributor.googleauthorD. H. Yoon-
dc.contributor.googleauthorW. S. Lee-
dc.contributor.googleauthorH. Lee-
dc.contributor.googleauthorY. R. Do-
dc.contributor.googleauthorH. J. Kang-
dc.contributor.googleauthorH. S. Eom-
dc.contributor.googleauthorY. H. Ko-
dc.contributor.googleauthorS. H. Lee-
dc.contributor.googleauthorH. Y. Yoo-
dc.contributor.googleauthorM. Hong-
dc.contributor.googleauthorC. Suh-
dc.contributor.googleauthorW. S. Kim-
dc.identifier.doi10.1093/annonc/mdv624-
dc.contributor.localIdA01017-
dc.relation.journalcodeJ00171-
dc.identifier.eissn1569-8041-
dc.identifier.pmid26861608-
dc.identifier.urlhttps://academic.oup.com/annonc/article-lookup/doi/10.1093/annonc/mdv624-
dc.subject.keywordCHOP-
dc.subject.keywordT-cell lymphoma-
dc.subject.keywordeverolimus-
dc.contributor.alternativeNameKim, Jin Seok-
dc.contributor.affiliatedAuthorKim, Jin Seok-
dc.citation.volume27-
dc.citation.number4-
dc.citation.startPage712-
dc.citation.endPage718-
dc.identifier.bibliographicCitationANNALS OF ONCOLOGY, Vol.27(4) : 712-718, 2016-
dc.date.modified2017-10-24-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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