Cited 21 times in
Comparisons of tumor-infiltrating lymphocyte levels and the 21-gene recurrence score in ER-positive/HER2-negative breast cancer
DC Field | Value | Language |
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dc.contributor.author | 배숭준 | - |
dc.contributor.author | 안성귀 | - |
dc.contributor.author | 윤창익 | - |
dc.contributor.author | 이학우 | - |
dc.contributor.author | 정준 | - |
dc.contributor.author | 차윤진 | - |
dc.date.accessioned | 2018-08-28T17:30:11Z | - |
dc.date.available | 2018-08-28T17:30:11Z | - |
dc.date.issued | 2018 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/162680 | - |
dc.description.abstract | BACKGROUND: Recent studies have shown that tumors with extensive tumor-infiltrating lymphocytes (TILs) have a higher probability of pathologic complete response, even in luminal/human epidermal growth factor 2 (HER2)-negative breast cancer. We compared TIL levels and the 21-gene recurrence score (RS) in estrogen receptor (ER)-positive/HER2-negative breast cancer. METHODS: We evaluated the percentage of stromal TILs in 198 ER-positive/HER2-negative patients in whom RS was obtained by examining slides of surgical specimens by standardized methodology proposed by the international TIL Working Group. TIL levels were categorized as high (>/= 60%), intermediate (11-59%), or low (</= 10%). All tumors were treatment-naive. RESULTS: Ninety-seven (49.0%), 88 (44.4%), and 13 patients (6.6%) had low, intermediate, and high TIL levels, respectively. There was a significant but weak correlation between continuous RS and continuous TIL levels (Pearson's R = 0.201, p = 0.004). The mean RS was significantly highest in high TIL tumors (17.8 +/- 10.7 in low TIL tumors, 19.4 +/- 8.7 in intermediate TIL tumors, and 26.2 +/- 8.2 in high TIL tumors; p = 0.014). However, when we compared categorized RS and TIL levels, we found that tumors with high TIL levels tended to have higher RS (>/= 26) but it was not significant (p = 0.155). Furthermore, multivariate analysis revealed that high RS was not an independent factor associated with high TIL levels. Chemo-endocrine therapy was more frequently performed among patients with high TILs and less frequently among those with low or intermediate TILs (p < 0.001). CONCLUSIONS: Despite of a weak correlation between continuous TIL levels and RS, we found that tumors with high TIL levels tended to have a higher RS in ER-positive/HER2-negative breast cancer. Further study is warranted considering the clinical outcomes. | - |
dc.description.statementOfResponsibility | open | - |
dc.format | application/pdf | - |
dc.language | English | - |
dc.publisher | BioMed Central | - |
dc.relation.isPartOf | BMC CANCER | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.title | Comparisons of tumor-infiltrating lymphocyte levels and the 21-gene recurrence score in ER-positive/HER2-negative breast cancer | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Surgery | - |
dc.contributor.googleauthor | Sung Gwe Ahn | - |
dc.contributor.googleauthor | Yoon Jin Cha | - |
dc.contributor.googleauthor | Soon June Bae | - |
dc.contributor.googleauthor | Chanik Yoon | - |
dc.contributor.googleauthor | Hak Woo Lee | - |
dc.contributor.googleauthor | Joon Jeong | - |
dc.identifier.doi | 10.1186/s12885-018-4228-6 | - |
dc.contributor.localId | A05345 | - |
dc.contributor.localId | A02231 | - |
dc.contributor.localId | A05369 | - |
dc.contributor.localId | A05015 | - |
dc.contributor.localId | A03727 | - |
dc.contributor.localId | A04001 | - |
dc.relation.journalcode | J00351 | - |
dc.identifier.eissn | 1471-2407 | - |
dc.identifier.pmid | 29573739 | - |
dc.subject.keyword | 21-gene recurrence score | - |
dc.subject.keyword | Breast cancer | - |
dc.subject.keyword | Tumor-infiltrating lymphocytes | - |
dc.contributor.alternativeName | Bae, Soong June | - |
dc.contributor.alternativeName | Ahn, Sung Gwe | - |
dc.contributor.alternativeName | Yoon, Changik | - |
dc.contributor.alternativeName | Lee, Hak Woo | - |
dc.contributor.alternativeName | Jeong, Joon | - |
dc.contributor.alternativeName | Cha, Yoon Jin | - |
dc.contributor.affiliatedAuthor | Bae, Soong June | - |
dc.contributor.affiliatedAuthor | Ahn, Sung Gwe | - |
dc.contributor.affiliatedAuthor | Yoon, Changik | - |
dc.contributor.affiliatedAuthor | Lee, Hak Woo | - |
dc.contributor.affiliatedAuthor | Jeong, Joon | - |
dc.contributor.affiliatedAuthor | Cha, Yoon Jin | - |
dc.citation.volume | 18 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 320 | - |
dc.identifier.bibliographicCitation | BMC CANCER, Vol.18(1) : 320, 2018 | - |
dc.identifier.rimsid | 60258 | - |
dc.type.rims | ART | - |
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