Type of cancer Effects of IDO in experimental models Correlation of IDO expression with clinical outcome
[References] (Methods of evaluation) (Methods of evaluation, n = sample number)
Endometrial cancer [25] N.D. Impaird OS and PFS in stage I-IV patients (IHC, n = 80)
Endometrial cancer [28] N.D. Reduced infitration of CD8 + TIL and CD57 + NK(IHC, n = 65)
Endometrial cancer [29] Induces tumor growth and inhibits NK(in tumor-xenografted mice) N.D.
Ovarian cancer [32] Increases intraperitoneal dissemination(in tumor-xenografted mice) Reduced CD8 + TIL and impaired OS and PFS(IHC, n = 60)
Ovarian cancer [30] Correlates with chemoresistance to paclitaxel (microarray gene profiling and PCR) Impaired OS in stage III-IV serous adenocarcinoma(IHC, n = 24)
Ovarian cancer [31] N.D. Impaired OS in stage III-IV serous adenocarcinoma(IHC, n = 33)
Ovarian cancer [35] Suppresses T-cell proliferation(in vitro) N.D.
Ovarian cancer [33] Increases tumor growth and inhibits NK(in tumor-xenografted mice) N.D.
Cervical cancer [37] N.D. Impaird OS and DFS in stage IB-IIB cervical cancer(IHC, n = 112)
Cervical cancer [38] N.D. Progression from CIN2/3 to microinvasive carcinoma(IHC, n = 46)
Vulvar cancer [39] N.D. Impaird OS in vulvar squamous cell carcinoma(IHC, n = 76)
Vulvar cancer [40] N.D.  No association with the number of CD8 + TIL or Treg(IHC, n = 286)
N.D: Not Done; OS: Overall Survival; PFS: Progression-free Survival; DFS: Disease-free Survival; IHC: Immunohistochemistry; TIL: Tumor-infiltrating Lymphocyte; NK: Natural Killer Cell; Treg: Regulatory T cell; CIN: Cervical Intraepithelial Neoplasia
Table 1: Association of IDO expression with tumor progression and clinical outcome in gynecologic cancers.