STAT3 Polymorphism Can Predict the Response to Interferon-α Therapy in Patients with Metastatic Renal Cell Carcinoma

被引:26
作者
Eto, Masatoshi [1 ,2 ]
Kamba, Tomomi [3 ]
Miyake, Hideaki [4 ]
Fujisawa, Masato [4 ]
Kamai, Takao [5 ]
Uemura, Hirotsugu [6 ]
Tsukamoto, Taiji [7 ]
Azuma, Haruhito [8 ]
Matsubara, Akio [9 ]
Nishimura, Kazuo [10 ]
Nakamura, Tsuyoshi [11 ]
Ogawa, Osamu [3 ]
Naito, Seiji [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Urol, Fukuoka 812, Japan
[2] Kumamoto Univ, Dept Urol, Fac Life Sci, Kumamoto, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Urol, Kyoto, Japan
[4] Kobe Univ, Grad Sch Med, Dept Surg Related, Div Urol, Kobe, Hyogo 657, Japan
[5] Dokkyo Med Univ, Dept Urol, Mibu, Tochigi, Japan
[6] Kinki Univ, Sch Med, Dept Urol, Osaka 589, Japan
[7] Sapporo Med Univ, Dept Urol Surg & Androl, Sch Med, Sapporo, Hokkaido, Japan
[8] Osaka Med Coll, Dept Urol, Takatsuki, Osaka 569, Japan
[9] Hiroshima Univ, Dept Urol, Grad Sch Biomed Sci, Hiroshima, Japan
[10] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Urol, Osaka, Japan
[11] Nagasaki Univ, Fac Environm Studies, Nagasaki 852, Japan
关键词
Interferon-alpha; Renal cell carcinoma; Single nucleotide polymorphisms; STAT3; IMMUNE-RESPONSES; CANCER; SUNITINIB; PATHWAY;
D O I
10.1016/j.eururo.2012.09.052
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: In our 2007 retrospective study, we reported that single nucleotide polymorphisms (SNPs) in the signal transducer and activator of transcription 3 (acute-phase response factor) (STAT3) gene were significantly associated with better response to interferon (IFN)-alpha in patients with metastatic renal cell carcinoma (mRCC). Objective: To prospectively confirm those results, the Japan Immunotherapy SNPs-Study Group for Kidney Cancer conducted this trial. Design, setting, and participants: In this multicenter, prospective study, 203 eligible patients were enrolled. We evaluated the correlation between the antitumor effects of IFN-alpha and 11 SNPs (STAT3-2, STAT3-0, SOCS3-1, IL4R-34, PTGS1-3, PTGS1-4, PTGS1-5, PTGS2-12, IRF2-67, ICSBP-38, and TAP2-5) in eight genes in 180 patients who received IFN-alpha for >12 wk. Interventions: Patients were treated with three doses per week of IFN-alpha 5 million IU. Outcome measurements and statistical analysis: We analyzed the association of response to IFN-alpha and overall survival (OS) with genetic polymorphisms using a chi-square test and a logistic regression model. Results and limitations: The response rate of IFN-alpha was 13.8% (28 of 203 patients; 9 complete responses [CRs], 19 partial responses [PRs]). The CR rate of 4.4% was higher than we expected. Response to IFN-alpha was not associated with any of the 11 SNPs examined. However, when we assessed patients with CR, PR, and stable disease >24 wk as a group representing those with clinical response, a significant association was observed between STAT3-2 (rs1905341) and the clinical response of IFN-alpha (p = 0.039). Namely, C/C genotype of STAT3-2 was significantly associated with the clinical response of IFN-alpha and OS. These results were generated in Japanese patients and should be studied in other ethnic groups. Conclusions: This is the first prospective study demonstrating that a STAT3 polymorphism can be a predictive marker for treatment with IFN-alpha for patients with mRCC. (c) 2012 European Association of Urology. Published by Elsevier B.V. All rights reserved.
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页码:745 / 752
页数:8
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