Prognostic impact of interleukin-6 expression in stage I ovarian clear cell carcinoma

被引:15
作者
Kawabata, Ayako [1 ]
Yanaihara, Nozomu [1 ]
Nagata, Chie [1 ,2 ]
Saito, Misato [1 ]
Noguchi, Daito [3 ]
Takenaka, Masataka [1 ]
Iida, Yasushi [1 ]
Takano, Hirokuni [3 ]
Yamada, Kyosuke [1 ]
Iwamoto, Masami [4 ]
Kiyokawa, Takako [4 ]
Okamoto, Aikou [1 ]
机构
[1] Jikei Univ, Sch Med, Dept Obstet & Gynecol, Minato Ku, 3-25-8 Nishi Shinbashi, Tokyo 1058461, Japan
[2] Natl Ctr Child Hlth & Dev, Dept Educ Clin Res, Setagaya Ku, 2-10-1 Okura, Tokyo 1578535, Japan
[3] Jikei Univ, Kashiwa Hosp, Dept Obstet & Gynecol, 163-1 Kashiwashita, Kashiwa, Chiba 2770004, Japan
[4] Jikei Univ, Dept Pathol, Sch Med, Minato Ku, 3-25-8 Nishi Shinbashi, Tokyo 1058461, Japan
基金
日本学术振兴会;
关键词
ARID1A; Interleukin-6; Ovarian clear cell carcinoma; Prognosis; Stage I; Substage; ARID1A EXPRESSION; MUTATIONS; SURVIVAL; ENDOMETRIOSIS; ADENOCARCINOMA; EXPERIENCE; SIGNATURE; OUTCOMES; CANCER; TRIAL;
D O I
10.1016/j.ygyno.2017.06.027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. Ovarian clear cell carcinoma (OCCC) frequently presents at an early stage. In stage I OCCC, the prognosis differs according to substage. In particular, predictive biomarkers and new treatment strategies are needed for stage IC2/IC3 disease. We investigated tumor biology and prognostic factors for stage I OCCC from a clinicopathological perspective, including the expression of ARID1A and IL-6, which are considered critical for OCCC carcinogenesis. Methods. A retrospective cohort study of 192 patients with stage I OCCC treated at a single institution was performed. We calculated overall survival (OS) with respect to 12 clinicopathological parameters that included the unique and diverse histological features of OCCC. Results. The estimated 5-year OS rate in patients with all stage I OCCC was 88.9% during a median of 91 months of follow-up. The multivariate analysis indicated that substage classification and IL-6 expression status were associated with poor OS (p = 0.010 and p = 0.027, respectively). Loss of ARID1A expression had no impact on survival; however, it was associated with substage (p = 0.001), capsule rupture status (p = 0.011), and ascites cytology (p = 0.016). No clear association was found between ARID1A and IL-6 expressions. Histological findings, including the presence of endometriosis, adenofibroma, architectural pattern, and tumor cell type, showed no prognostic effects. Conclusions. Both substage classification and IL-6 expression status may be independent prognostic factors in stage I OCCC. Therefore, IL-6 molecular stratification may be crucial in optimizing therapeutic strategies for early stage OCCC to improve survival. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:609 / 614
页数:6
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