Your browser doesn't support javascript.
loading
Trop-2 expression and the tumor immune microenvironment in cervical cancer.
Chiba, Yohei; Kojima, Yuki; Yazaki, Shu; Yoshida, Hiroshi; Takamizawa, Shigemasa; Kitadai, Rui; Saito, Ayumi; Okuma, Hitomi Sumiyoshi; Nishikawa, Tadaaki; Shimoi, Tatsunori; Sudo, Kazuki; Noguchi, Emi; Uno, Masaya; Ishikawa, Mitsuya; Kato, Tomoyasu; Fujiwara, Yasuhiro; Yonemori, Kan.
Afiliação
  • Chiba Y; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: ychiba@ncc.go.jp.
  • Kojima Y; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: yuukojim@ncc.go.jp.
  • Yazaki S; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: syazaki@ncc.go.jp.
  • Yoshida H; Department of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: hiroyosh@ncc.go.jp.
  • Takamizawa S; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: htakami@ncc.go.jp.
  • Kitadai R; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: rkitadai@ncc.go.jp.
  • Saito A; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: aysaito@ncc.go.jp.
  • Okuma HS; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: hsumiyos@ncc.go.jp.
  • Nishikawa T; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: tnishika@ncc.go.jp.
  • Shimoi T; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: tshimoi@ncc.go.jp.
  • Sudo K; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: ksudo@ncc.go.jp.
  • Noguchi E; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: enoguchi@ncc.go.jp.
  • Uno M; Department of Gynecology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: mauno@ncc.go.jp.
  • Ishikawa M; Department of Gynecology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: miishika@ncc.go.jp.
  • Kato T; Department of Gynecology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: tokato@ncc.go.jp.
  • Fujiwara Y; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: yfujiwar@ncc.go.jp.
  • Yonemori K; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan. Electronic address: kyonemor@ncc.go.jp.
Gynecol Oncol ; 187: 51-57, 2024 08.
Article em En | MEDLINE | ID: mdl-38723340
ABSTRACT

OBJECTIVE:

Trophoblast Cell Surface Antigen 2 (Trop-2) is a transmembrane glycoprotein that is overexpressed in various cancers, with immunological significance as a target for tumor-reactive T-cells. We aimed to investigate the association between the expression of Trop-2 and the tumor immune microenvironment in cervical cancer.

METHODS:

The study included 123 patients with cervical cancer who underwent primary surgery between 2000 and 2020 in our hospital. Trop-2 expression was evaluated using anti-Trop-2 monoclonal antibody clone MAB650. Immune biomarkers, including PD-L1 (22C3), CD3 (PS1), and CD8 (4B11), were also evaluated. Trop-2 and PD-L1 positivity were defined by an H-score ≥ 10 and a combined positive score (CPS) ≥1, respectively. Tumor-infiltrating lymphocytes (TILs) were assessed in the five selected independent areas. The correlation between Trop-2 expression and immune biomarkers was analyzed.

RESULTS:

The cohort comprised patients with squamous cell carcinoma (SCC) (54.5%) and non-SCC (45.5%). Trop-2 was positive in 84.6% of samples and more commonly expressed in SCC (SCC vs. non-SCC; 97.0% vs. 69.6%, p < 0.001). Intratumoral CD3+ and CD8 + TILs were significantly more common in Trop-2-positive cases (CD3, Mann-Whitney U = 383, p < 0.0001; CD8, U = 442, p < 0.0001). Additionally, significant positive correlations were found between the Trop-2 H-score and immune markers (CD3 + TILs, r = 0.295, p < 0.001; CD8 + TILs, r = 0.267, p = 0.001; PD-L1 CPS, r = 0.178, p = 0.025). No significant associations were detected between TILs and other clinicopathological features, including prognosis.

CONCLUSION:

Expression of Trop-2 in cervical cancer is associated with increased levels of intratumoral TILs, indicating the potential of Trop-2 targeted therapy alone or in combination with immune checkpoint inhibitors.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Moléculas de Adesão Celular / Neoplasias do Colo do Útero / Linfócitos do Interstício Tumoral / Microambiente Tumoral / Antígenos de Neoplasias Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Moléculas de Adesão Celular / Neoplasias do Colo do Útero / Linfócitos do Interstício Tumoral / Microambiente Tumoral / Antígenos de Neoplasias Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article