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BACKGROUND: In this study, we evaluated the prognostic value of Immunoscore in patients with stage I−III colon cancer (CC) in the Asian population. These patients were originally included in an international study led by the Society for Immunotherapy of Cancer (SITC) on 2681 patients with AJCC/UICC-TNM stages I−III CC. METHODS: CD3+ and cytotoxic CD8+ T-lymphocyte densities were quantified in the tumor and invasive margin by digital pathology. The association of Immunoscore with prognosis was evaluated for time to recurrence (TTR), disease-free survival (DFS), and overall survival (OS). RESULTS: Immunoscore stratified Asian patients (n = 423) into different risk categories and was not impacted by age. Recurrence-free rates at 3 years were 78.5%, 85.2%, and 98.3% for a Low, Intermediate, and High Immunoscore, respectively (HR[Low-vs-High] = 7.26 (95% CI 1.75−30.19); p = 0.0064). A High Immunoscore showed a significant association with prolonged TTR, OS, and DFS (p < 0.05). In Cox multivariable analysis stratified by center, Immunoscore association with TTR was independent (HR[Low-vs-Int+High] = 2.22 (95% CI 1.10−4.55) p = 0.0269) of the patient’s gender, T-stage, N-stage, sidedness, and MSI status. A significant association of a High Immunoscore with prolonged TTR was also found among MSS (HR[Low-vs-Int+High] = 4.58 (95% CI 2.27−9.23); p ≤ 0.0001), stage II (HR[Low-vs-Int+High] = 2.72 (95% CI 1.35−5.51); p = 0.0052), low-risk stage-II (HR[Low-vs-Int+High] = 2.62 (95% CI 1.21−5.68); p = 0.0146), and high-risk stage II patients (HR[Low-vs-Int+High] = 3.11 (95% CI 1.39−6.91); p = 0.0055). CONCLUSION: A High Immunoscore is significantly associated with the prolonged survival of CC patients within the Asian population.
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http://dx.doi.org/10.3390/cancers14184346 | DOI Listing |
Am J Med Genet B Neuropsychiatr Genet
August 2025
Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Genomic instability is a prominent hallmark of cancer, and Long non-coding RNAs (LncRNAs) have been implicated in cancer biology. This study aimed to develop a prognostic model for glioma by focusing on genomic instability-associated lncRNAs (GILnc). A computational framework was implemented to identify GILnc, followed by immuno-scoring and immune cell infiltration analyses using the ESTIMATE and CIBERSORT algorithms.
View Article and Find Full Text PDFCancers (Basel)
August 2025
Joint Cancer Research Unit, IVO-CIPF, 46009 Valencia, Spain.
: Angiosarcomas (ASs) represent a heterogeneous and highly aggressive subset of tumors that respond poorly to systemic treatments and are associated with short progression-free survival (PFS) and overall survival (OS). The aim of this study was to develop and validate an immune-related prognostic model-termed the AS score-using data from two independent sarcoma cohorts. : A prognostic model was developed using a previously characterized cohort of 25 angiosarcoma samples.
View Article and Find Full Text PDFFront Immunol
August 2025
Department of Pathology, General Hospital of Southern Theater Command, People's Liberation Army of China, Guangzhou, China.
Introduction: Circulating tumor DNA (ctDNA) methylation markers show potential for early detection of cancer metastasis. This study aimed to identify ctDNA methylation markers predictive of recurrence and prognosis in colorectal cancer (CRC) patients, and to explore the influence of the tumor immune microenvironment on outcomes.
Methods: We analyzed 603 overlapping methylation markers from both plasma and tissue samples and developed a risk model to predict CRC recurrence and prognosis.
Ther Adv Med Oncol
July 2025
Department of Gynecological Radiotherapy, Zhejiang Cancer Hospital, 1 Banshan East Road, Hangzhou 310022, Zhejiang, China.
Background: Gastric-type endocervical adenocarcinoma (GAS), the predominant non-human papillomavirus cervical cancer, is highly aggressive with poor prognosis. No drugs are effective against advanced or recurrent GAS.
Objective: This study aimed to analyze the clinical and pathological characteristics of GAS, evaluate the expression of targets for targeted drug therapy, and assess the predictive value of Immunoscore for prognosis.
Purpose: Tumor immune cell infiltration patterns in the tumor microenvironment serve as prognostic biomarkers in metastatic colorectal cancer (mCRC). This study analyzed the spatially resolved tumor immune microenvironment for prognostic and predictive impact in patients with RAS wildtype mCRC receiving FU/FA ± Pmab maintenance after Pmab + FOLFOX induction (PanaMa AIO KRK0212; NCT01991873).
Patients And Methods: Twelve immune parameters (lymphocyte markers: CD3, CD8, CD45RO, FOXP3, CD20, Granzyme B, Perforin; immune checkpoints: PD-1, PD-L1, IDO1, LAG3; monocyte marker CD163) were quantified in spatially resolved tumor and stroma regions (invasive-margin [Inv], center [Cen]) on tissue microarrays from available surgical resections using digital pathology.