Cited 51 times in
Tumor-related leukocytosis is associated with poor radiation response and clinical outcome in uterine cervical cancer patients
DC Field | Value | Language |
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dc.contributor.author | 김용배 | - |
dc.contributor.author | 윤홍인 | - |
dc.contributor.author | 조연아 | - |
dc.date.accessioned | 2017-10-26T07:50:45Z | - |
dc.date.available | 2017-10-26T07:50:45Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 0923-7534 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/152585 | - |
dc.description.abstract | BACKGROUND: To evaluate response to radiation and clinical outcome of uterine cervical cancer patients with tumor-related leukocytosis (TRL) at initial diagnosis and during definitive radiotherapy. PATIENTS AND METHODS: We retrospectively analyzed 2456 patients with stage IA-IVA uterine cervical cancer who received definitive radiotherapy with (37.4%) or without (62.6%) platinum-based chemotherapy between 1986 and 2012. TRL was defined as two or more occurrences of leukocytosis over 9000/μl at the time of diagnosis and during the course of treatment. Locoregional failure-free survival (LFFS) and overall survival (OS) were compared between patients with or without TRL. RESULTS: The median age of all patients was 55 years, and the median follow-up time was 65.1 months. TRL was observed in 398 patients (16%) at initial diagnosis; TRL (+) patients were younger and had larger tumors, advanced stage, and more frequent lymph node metastases (all P < 0.05). TRL (+) patients showed a significantly lower rate of complete remission than TRL (-) patients (89.9% versus 96.3%, respectively, P = 0.042). Ten-year LFFS and OS for all patients were 84% and 78%, respectively. LFFS and OS were significantly lower in TRL (+) patients than TRL (-) patients (10-year LFFS: 69% versus 87% respectively, P < 0.001; 10-year OS: 63% versus 81% respectively P < 0.001). After propensity score matching, LFFS and OS rates in TRL (+) patients remained significantly lower than for TRL (-) patients; this significant difference was also observed on multivariate analysis. Twenty-six percent of patients with locoregional failure (n = 345) were TRL (+) and had significantly poorer median OS (6 versus 12 months, P = 0.001). CONCLUSION: This study reveals the aggressive nature of cervical cancer with TRL and its poor response to radiation therapy. Given the unfavorable prognosis and higher probability of treatment failure, optimal diagnostic and therapeutic approaches and careful monitoring for early detection of recurrence should be considered for these patients. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.publisher | Oxford University Press | - |
dc.relation.isPartOf | ANNALS OF ONCOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Cell Hypoxia | - |
dc.subject.MESH | Cell Line | - |
dc.subject.MESH | Erythropoietin/genetics | - |
dc.subject.MESH | Gene Expression Regulation | - |
dc.subject.MESH | Gene Transfer Techniques | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Neural Stem Cells/metabolism | - |
dc.subject.MESH | Neural Stem Cells/transplantation* | - |
dc.subject.MESH | Neuralgia/genetics | - |
dc.subject.MESH | Neuralgia/pathology | - |
dc.subject.MESH | Neuralgia/physiopathology | - |
dc.subject.MESH | Neuralgia/therapy* | - |
dc.subject.MESH | Plasmids/genetics | - |
dc.subject.MESH | Promoter Regions, Genetic | - |
dc.subject.MESH | Rats | - |
dc.subject.MESH | Rats, Sprague-Dawley | - |
dc.subject.MESH | Sciatic Nerve/injuries* | - |
dc.subject.MESH | Sciatic Nerve/metabolism | - |
dc.subject.MESH | Sciatic Nerve/pathology | - |
dc.subject.MESH | Sciatic Nerve/physiopathology | - |
dc.subject.MESH | Up-Regulation* | - |
dc.subject.MESH | Vascular Endothelial Growth Factor A/genetics* | - |
dc.title | Tumor-related leukocytosis is associated with poor radiation response and clinical outcome in uterine cervical cancer patients | - |
dc.type | Article | - |
dc.publisher.location | England | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Radiation Oncology | - |
dc.contributor.googleauthor | Y. Cho | - |
dc.contributor.googleauthor | K. H. Kim | - |
dc.contributor.googleauthor | H. I. Yoon | - |
dc.contributor.googleauthor | G. E. Kim | - |
dc.contributor.googleauthor | Y. B. Kim | - |
dc.identifier.doi | 10.1093/annonc/mdw308 | - |
dc.contributor.localId | A04777 | - |
dc.contributor.localId | A04680 | - |
dc.contributor.localId | A00744 | - |
dc.relation.journalcode | J00171 | - |
dc.identifier.eissn | 1569-8041 | - |
dc.identifier.pmid | 27502717 | - |
dc.identifier.url | https://academic.oup.com/annonc/article-lookup/doi/10.1093/annonc/mdw308 | - |
dc.subject.keyword | cervical cancer | - |
dc.subject.keyword | leukocytosis | - |
dc.subject.keyword | neutrophil/lymphocyte ratio | - |
dc.subject.keyword | radiation response | - |
dc.contributor.alternativeName | Kim, Yong Bae | - |
dc.contributor.alternativeName | Yoon, Hong In | - |
dc.contributor.alternativeName | Cho, Yeona | - |
dc.contributor.affiliatedAuthor | Yoon, Hong In | - |
dc.contributor.affiliatedAuthor | Cho, Yeona | - |
dc.contributor.affiliatedAuthor | Kim, Yong Bae | - |
dc.citation.volume | 27 | - |
dc.citation.number | 11 | - |
dc.citation.startPage | 2067 | - |
dc.citation.endPage | 2074 | - |
dc.identifier.bibliographicCitation | ANNALS OF ONCOLOGY, Vol.27(11) : 2067-2074, 2016 | - |
dc.date.modified | 2017-10-24 | - |
dc.identifier.rimsid | 48786 | - |
dc.type.rims | ART | - |
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