Evidence map›Paper›PMID 41620992›Full record

ArticleInternational journal of clinical oncology2026

CD8/CD4 ratio, CD56, and PD-L1 as prognostic markers in sinonasal mucosal melanoma.

Chiau-Sheng Jang, I-Chieh Chuang

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Article in International journal of clinical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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2 authors.

Chiau-Sheng JangDepartment of Dermatology, Kaohsiung Veterans General Hospital, No. 386, Dazhong 1St Rd., Zuoying District, Kaohsiung City, 813414, Taiwan. macemars@gmail.com.ORCID http://orcid.org/0000-0002-6713-2353
I-Chieh ChuangKaohsiung Cancer Prevention and Screening Center, Kaohsiung, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSinonasal mucosal melanoma (SNMM) is an aggressive malignancy with limited prognostic markers. This study aimed to determine whether immune markers, including the CD8 to CD4 lymphocyte ratio, CD56-positive lymphocytes, and PD-L1 expression, provide prognostic information beyond established clinicopathological factors.

methodsWe retrospectively reviewed 67 patients with surgically treated SNMM at two tertiary medical centers in Taiwan between 2004 and 2023. Standard histopathologic parameters and immunohistochemical assessments of the CD8/CD4 ratio, CD56-positive lymphocytes, and PD-L1 expression in tumor and stromal immune cells were evaluated. Disease-specific survival (DSS) and recurrence-free survival (RFS) were analyzed using Kaplan-Meier estimates and multivariable Cox proportional hazards models.

resultsThe median patient age was 62 years, and 60% were male. During a median follow-up of 42 months, 63% of patients experienced recurrence, and 54% died of the disease. An increased CD8/CD4 ratio and the presence of CD56-positive lymphocytes were associated with better DSS (5-year DSS, 64.3% vs. 32.1% and 70.1% vs. 35.8%, respectively), whereas PD-L1 positivity was associated with shorter RFS (5-year RFS, 28.6% vs. 54.3%). In multivariable analysis, mitotic activity of ≥ 10/mm

conclusionsImmune markers, particularly the CD8/CD4 ratio and CD56-positive lymphocytes, were significantly associated with survival outcomes independent of traditional histopathologic factors. Incorporating immune profiling into risk stratification may improve prognostication and guide the development of immune-targeted strategies in SNMM.

Indexed as

B7-H1 AntigenBiomarkers, TumorCD56 AntigenMelanomaAdultAgedCD4-CD8 RatioFemaleHumansMaleMiddle AgedNasal MucosaPrognosisRetrospective StudiesB7-H1 AntigenBiomarkers, TumorCD274 protein, humanCD56 AntigenNCAM1 protein, humanCD4CD56 antigenCD8 ratioInfiltrating lymphocytesLigand 1MelanomaProgrammed deathTumor

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.