# Clinical Characteristics and Prognosis Analysis of Thoracic SMARCA4-deficient Undifferentiated Tumor versus SMARCA4-deficient Non-small Cell Lung Cancer

**Authors:** Yingxue GUO, Jinlan YANG, Xiang LV, Xijun LIU, Fengxiang LI, Jinzhi WANG, Peng ZHANG, Jianbin LI, Wei WANG

PMC · DOI: 10.3779/j.issn.1009-3419.2025.102.45 · Chinese Journal of Lung Cancer · 2025-12-20

## TL;DR

This study compares the clinical features and outcomes of two rare lung tumors, SMARCA4-UT and SMARCA4-dNSCLC, finding similar survival but differences in tumor location and spread.

## Contribution

The study provides the first detailed comparison of clinical characteristics and prognosis between SMARCA4-UT and SMARCA4-dNSCLC, identifying NLR as a potential prognostic marker.

## Key findings

- SMARCA4-UT and SMARCA4-dNSCLC show similar survival outcomes but differ in tumor location and lymph node spread.
- Both tumor types respond well to radiotherapy, but neither shows improved survival from it.
- Elevated NLR (≥3.57) is a poor prognostic factor for both tumor types.

## Abstract

胸部SMARCA4缺失性未分化肿瘤（thoracic SMARCA4-deficient undifferentiated tumor, SMARCA4-UT）是2021年世界卫生组织（World Health Organization, WHO）第5版胸部肿瘤分类中新定义的一种上皮性肿瘤类型，发病率低，目前对其治疗及预后尚不明确。病理上可通过组织学形态、免疫组化与SMARCA4缺失性非小细胞肺癌（SMARCA4-deficient non-small cell lung cancer, SMARCA4-dNSCLC）相鉴别，但其临床特征、对放疗的敏感性以及预后是否有差异仍未可知。本研究通过分析SMARCA4-UT及SMARCA4-dNSCLC患者的临床特征，明确预后相关影响因素。

回顾性分析2022年6月至2025年2月山东第一医科大学附属肿瘤医院收治的SMARCA4-UT及SMARCA4-dNSCLC患者，患者均经病理确诊，且随访资料完整。统计分析两组患者临床病理特征及影像学表现的差异，并评估手术、放疗、免疫治疗及临床病理因素对两组患者预后的影响。

共27例SMARCA4-UT及40例SMARCA4-dNSCLC患者入组，两组患者在性别、吸烟史、年龄、肿瘤最大径、症状、分期、是否有胸膜转移及中性粒细胞/淋巴细胞计数比值（neutrophil to lymphocyte ratio, NLR）、系统免疫炎症指数（systemic immune-inflammation index, SII）方面均表现出相似的生物学特性。但两者好发部位有所差异，SMARCA4-UT更易发生在纵隔胸膜（22.22%）、右肺下叶（25.93%），而SMARCA4-dNSCLC更易发生在右肺上叶（25.00%）及左肺上叶（22.50%）（P<0.05）；SMARCA4-UT更常表现为局部浸润侵犯邻近结构且淋巴结转移更广泛（淋巴结转移≥5站者55.56% vs 27.50%）。两者对放疗的敏感性均高，放疗后6个月局部控制率（local control rate, LCR）分别为84.62% vs 83.33%，免疫治疗的客观缓解率（objective response rate, ORR）分别为91.67% vs 68.18%，均无统计学差异（P>0.05）。生存方面，两组患者在无进展生存期（progression-free survival, PFS）与总生存期（overall survival, OS）方面均未表现出显著差异。Cox多因素回归分析显示，手术可以改善这两类患者的预后，而NLR≥3.57为其预后不良预测因子。

SMARCA4-UT与SMARCA4-dNSCLC具有相似的临床特征，生存预后相似，在局部浸润侵犯邻近结构、纵隔淋巴结转移及肿瘤原发部位上略有不同。手术可以改善两组患者的生存，且两者对放疗均表现出高的敏感性，但放疗未表现出患者的生存获益。治疗前NLR值可作为预后预测指标。

Comparison of clinical characteristics of patients in the SMARCA4-UT group and the SMARCA4-dNSCLC group

Regression models of prognostic factors of SMARCA4-UT and SMARCA4-dNSCLC

## Linked entities

- **Genes:** SMARCA4 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4) [NCBI Gene 6597]
- **Diseases:** non-small cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, SMARCA2 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2) [NCBI Gene 6595] {aka BAF190, BIS, BRM, NCBRS, SAMRCA2, SNF2}, ECH1 (enoyl-CoA hydratase 1) [NCBI Gene 1891] {aka HPXEL}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, SMARCA4 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4) [NCBI Gene 6597] {aka BAF190, BAF190A, BRG1, CSS4, MRD16, OTSC12}, Kras (KRAS proto-oncogene, GTPase) [NCBI Gene 24525] {aka K-ras, Kras2, c-Ki-ras, p21}, GRP (gastrin releasing peptide) [NCBI Gene 2922] {aka BN, GRP-10, preproGRP, proGRP}, Egfr (epidermal growth factor receptor) [NCBI Gene 24329] {aka ERBB1, ErbB-1, Errp}, ENO2 (enolase 2) [NCBI Gene 2026] {aka HEL-S-279, NSE}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, Pik3ca (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha) [NCBI Gene 170911], RAD21 (RAD21 cohesin complex component) [NCBI Gene 5885] {aka CDLS4, HR21, HRAD21, MCD1, MGS, NXP1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657] {aka ANOP3, MCOPS3}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}, STK11 (serine/threonine kinase 11) [NCBI Gene 6794] {aka LKB1, PJS, hLKB1}, Tp53 (tumor protein p53) [NCBI Gene 24842] {aka Trp53, p53}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, SALL4 (spalt like transcription factor 4) [NCBI Gene 57167] {aka DRRS, HSAL4, IVIC, ZNF797}
- **Diseases:** thoracic sarcoma (MESH:D012509), Non-small Cell Lung Cancer (MESH:D002289), thoracic tumors (MESH:D013899), lymph node metastasis (MESH:D008207), hypercalcemic type (MESH:D006969), immune (MESH:D007154), Tumor (MESH:D009369), malignant rhabdoid tumor (MESH:D018335), Poorly differentiated adenocarcinoma (MESH:D000230), Undifferentiated Tumor (MESH:D002277), inflammation (MESH:D007249), small-cell carcinoma of the ovary (MESH:D018288), pleural metastasis (MESH:D009362), Ki-67 (MESH:C564352)
- **Chemicals:** eosin (MESH:D004801), HE (MESH:D006371), hematoxylin (MESH:D006416)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** L858R, serine/threonine

## Full text

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## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12972582/full.md

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Source: https://tomesphere.com/paper/PMC12972582