Evidence map›Paper›PMID 42337483›Full record

ArticleBMC cancer2026

Betel nut chewing influences pathologic response in oral squamous cell carcinoma treated by neoadjuvant immunochemotherapy.

Ran Gao, Xu Zhang, Gang Li, Peng Li, Wei Du

Abstract read
In one paragraph

Article in BMC cancer, 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ran GaoDepartment of Head Neck, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, 450008, PR China.
Xu ZhangDepartment of Head Neck, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, 450008, PR China.
Gang LiDepartment of Head Neck, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, 450008, PR China.
Peng LiDepartment of Head Neck, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, 450008, PR China.
Wei DuDepartment of Head Neck, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, 450008, PR China. duweitj@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBetel nut chewing (BNC) is a prevalent risk factor for oral squamous cell carcinoma (SCC) in South and Southeast Asia, yet its influence on response to neoadjuvant immunochemotherapy remains unexplored. This study aimed to evaluate the association between BNC and pathologic response in oral SCC patients receiving neoadjuvant immunochemotherapy.

methodsWe retrospectively reviewed 192 patients with primary oral SCC who received neoadjuvant immunochemotherapy (docetaxel, cisplatin, and PD-1 inhibitors) followed by surgery between January 2020 and October 2024. Pathologic complete response (pCR), major pathologic response (mPR), objective response rate (ORR), clinical to pathological downstaging, adverse pathologic features, and disease-free survival (DFS) were compared between BNC (n = 42) and no-BNC (n = 150) groups.

resultsBNC patients demonstrated significantly lower pCR (16.7% vs. 34.0%; OR = 2.55, p = 0.031) and mPR rates (54.8% vs. 74.7%; OR = 3.17, p = 0.013) compared to no-BNC patients. Multivariable analysis confirmed absence of BNC as an independent predictor of both pCR (adjusted OR = 2.55, 95% CI: 1.20-7.65) and mPR (adjusted OR = 3.17, 95% CI: 1.32-8.53). BNC was also associated with lower ORR (73.8% vs. 86.7%, p = 0.045), reduced downstaging (71.4% vs. 90.0%, p = 0.002), and higher prevalence of adverse pathologic features (19.0% vs. 4.7%, p = 0.005). The poorest outcomes occurred in well/moderately differentiated tumors with BNC history. BNC did not significantly impact DFS (3-year DFS: 71.2% vs. 78.4%, p = 0.194). Number of neoadjuvant cycles did not influence pathologic response.

conclusionsBNC is an independent predictor of suboptimal pathologic response to neoadjuvant immunochemotherapy in oral SCC, although it does not adversely affect DFS. These findings may inform patient selection and treatment stratification.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsArecaCarcinoma, Squamous CellMouth NeoplasmsNeoadjuvant TherapySquamous Cell Carcinoma of Head and NeckAdultAgedCisplatinDocetaxelFemaleHumansMaleMasticationMiddle AgedPathologic Complete ResponseCisplatinDocetaxelBetel nut chewingCycle of neoadjuvant therapyNeoadjuvant immunochemotherapyOral squamous cell carcinomaPathologic response

Identifiers

PMID42337483
PMCPMC13548627

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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.