Evidence map›Paper›PMID 42477762›Full record

ArticleWorld journal of surgical oncology2026

Pathological subtype dictates survival and failure pattern in laryngeal neuroendocrine neoplasms: a 15-year single-institution experience.

Feifei Qiao, Na Liu, He Li, Meng Zhang, Shubin Dong

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Article in World journal of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Feifei Qiao *Department of Head and Neck Surgery, Shanxi Hospital Affiliated to Cancer Hospital, Cancer Hospital, Shanxi Provincial Cancer Hospital, Chinese Academy of Medical Sciences, Shanxi Medical University, Taiyuan, 031000, China.
Na Liu *Department of Anesthesiology, Shanxi Hospital Affiliated to Cancer Hospital, Cancer Hospital, Shanxi Provincial Cancer Hospital, Chinese Academy of Medical Sciences, Shanxi Medical University, Taiyuan, 031000, China.
He LiDepartment of Pathology, Shanxi Hospital Affiliated to Cancer Hospital, Cancer Hospital, Shanxi Provincial Cancer Hospital, Chinese Academy of Medical Sciences, Shanxi Medical University, Taiyuan, 031000, China.
Meng ZhangDepartment of Orthopedics, The Second Hospital of Shanxi Medical University, Taiyuan, 031000, China.
Shubin DongDepartment of Head and Neck Surgery, Shanxi Hospital Affiliated to Cancer Hospital, Cancer Hospital, Shanxi Provincial Cancer Hospital, Chinese Academy of Medical Sciences, Shanxi Medical University, Taiyuan, 031000, China. 13313418861@163.com.

Funding

Natural Science Foundation of Shanxi Province 202203021212054
6 · The paper itself

Abstract

backgroundLaryngeal neuroendocrine neoplasms (LNENs) comprise < 1% of laryngeal malignancies, and evidence-based treatment guidelines remain lacking. We sought to delineate clinicopathological features, therapeutic strategies, and survival determinants in a single-institution cohort of consecutive patients with primary LNEN.

methodsWe retrospectively identified 31 consecutive patients with primary LNEN treated between 2010 and 2024. Histology was centrally reviewed by two head-and-neck pathologists and categorized as well-differentiated neuroendocrine tumor (NET, G1-G3) or poorly differentiated neuroendocrine carcinoma (NEC, small-cell/large-cell). All cases underwent immunohistochemistry (Syn, CgA, Ki-67) and multidisciplinary therapy. Survival analyses were performed with Kaplan-Meier and Cox proportional-hazards models.

resultsMedian age was 60 years, 90.3% were male, and 80.6% had a smoking history. NEC accounted for 71% (22/31) and NET for 29% (9/31). NEC exhibited higher Ki-67 index (85% vs. 10%, P < 0.001), more advanced stage (63.6% vs. 33.3%, P = 0.013), and a predilection for distant metastasis (85.7% vs. 25.0%, P = 0.002). Median overall survival (OS) was 27.0 months for NEC vs. not reached for NET (P < 0.001); 5-year OS was 0% vs. 44.4%. Median disease-free survival (DFS) was 19.0 vs. not reached (P < 0.001). Multivariate analysis identified NEC subtype (HR = 4.23, 95% CI 1.39-12.90), T3-4 stage (HR = 2.61, 95% CI 1.02-6.66), and lymph nodal positivity (HR = 3.12, 95% CI 1.20-8.10) as independent predictors of poor OS; NEC subtype (HR = 3.67, 95% CI 1.15-11.70) and N+ (HR = 3.51, 95% CI 1.22-10.10) predicted inferior DFS. Distant metastasis was the first mode of failure in 68.9% of curative-intent cases.

conclusionsPathologic subtype (NEC vs. NET) emerges as the dominant independent predictor of survival in this cohort. NEC demonstrates a systemic biological phenotype characterized by early distant metastasis. These findings support the hypothesis that intensified perioperative systemic therapy, rather than locoregional escalation, warrants prospective investigation. Multi-center, molecularly stratified trials are needed to establish a precision-medicine paradigm for this rare disease.

Indexed as

Carcinoma, NeuroendocrineLaryngeal NeoplasmsNeuroendocrine TumorsAdultAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesSurvival RateLaryngeal neuroendocrine neoplasmsNeuroendocrine carcinomaPrognosisSurgical treatment

Identifiers

PMID42477762
PMCPMC13670497

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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.