Investigator

Jinbo Yue

Shandong Cancer Hospital and Institute, Department of Radiation Oncology

Research Interests

JYJinbo Yue
Papers(2)
Concurrent Chemoradio…Differences in cervic…
Collaborators(4)
Jinming YuXiaoling ZhangXiaoyu HuChao Liu
Institutions(3)
Shandong UniversityShandong First Medica…Shandong Tumor Hospit…

Papers

Concurrent Chemoradiotherapy Increases the Levels of Soluble Immune Checkpoint Proteins in Patients with Locally Advanced Cervical Cancer

Purpose. Concurrent chemoradiotherapy (CCRT) has been widely applied to locally advanced cervical cancer (LACC) patients, inducing the massive release of antigen and systematic immunomodulatory effects. However, its effect on the soluble immune checkpoint proteins (sICPs) remains unclear, which might play a key role in the immune response. Therefore, the current study explored changes in the levels of 16 sICPs in LACC patients during CCRT. Methods. We prospectively enrolled fifty-one LACC patients treated with CCRT and collected patients’ blood before, during and after CCRT. The levels of 16 sICPs were measured using the Luminex platform, and the changes were measured using Friedman test with Bonferroni’s posttest. One month after CCRT, the tumor response was evaluated according to the RECIST 1.1 guidelines. Results. The levels of soluble T-cell immunoglobulin and mucin-domain containing-3 (sTIM-3) significantly increased during CCRT ( P = 0.041 ), while those of the soluble B and T lymphocyte attenuator (sBTLA), sCD40, soluble glucocorticoid-induced tumor necrosis factor receptor ligand (sGITRL), sCD80, sCD86, sPD-1, sPD-L1, sCTLA-4, and soluble inducible T-cell costimulator (sICOS) significantly increased after CCRT (all P < 0.05 ). Other sICPs showed no significant changes throughout the CCRT (all P > 0.05 ). 41 (80%), 8 (16%), and 2 (4%) patients showed complete response (CR), partial response (PR), and stable disease (SD) after CCRT, respectively. Interestingly, the level of soluble lymphocyte-activation gene 3 (sLAG-3) was significantly higher among the PR/SD patients as compared to the CR after CCRT ( P = 0.009 ). Conclusions. This study revealed that CCRT might elevate the serum levels of sTIM-3, sBTLA, sCD40, sGITRL, sCD80, sCD86, sPD-1, sPD-L1, sCTLA-4, and sICOS in the patients with LACC. The sLAG-3 level was higher in the patients with poor response to CCRT. These findings revealed the dynamic changes in the sICPs levels during CCRT, which might be helpful in designing optimal treatment strategies for LACC patients.

Differences in cervical cancer stage at diagnosis and survival outcomes among Asian, Native Hawaiian, and other Pacific Islander patients and White patients

To explore disparities in cervical cancer diagnosis and outcomes for Asian patients and Native Hawaiian and other Pacific Islanders (NHPIs). We extracted cervical cancer patient data collected from the Surveillance, Epidemiology, and End Results 17 database. Odds ratios (ORs) for stage and time ratios (TRs) for survival outcomes were estimated using logistic regression and accelerated failure time models, respectively. Of 18770 patients, 15,847 (84.4 %) were White; 2618 (13.9 %) were Asian; and 305 (1.6 %) were NHPI. NHPI patients were less likely than White patients to be diagnosed at an early stage (adjusted OR [aOR]: 0.60; 95 % CI, 0.47-0.77), whereas Asian patients had similar stage-at-diagnosis to White patients (aOR: 0.93; 95 % CI, 0.85-1.02). Asian patients, as a group, had significantly longer overall survival (OS) (adjusted TR [aTR]: 1.46; 95 % CI, 1.33-1.61) and disease-specific survival (DSS) (aTR: 1.35; 95 % CI, 1.21-1.51) than White patients; the opposite was true for NHPIs (OS: aTR, 0.80; 95 % CI, 0.64-1.00; DSS: aTR, 0.75; 95 % CI, 0.59-0.97). We find that NHPI cervical cancer patients tend to be diagnosed later in their disease course than White patients and have shorter survival time post-diagnosis, while Asian patients tend to have longer survival time. These findings support the disaggregation of Asian and NHPI races in cervical cancer investigations.

2Papers
4Collaborators
Uterine Cervical NeoplasmsCarcinoma, HepatocellularHepatitis B virusLiver NeoplasmsPrognosis

Positions

Researcher

Shandong Cancer Hospital and Institute · Department of Radiation Oncology

Country

CN

Links & IDs
0000-0002-5768-8622

Scopus: 35796791200