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2
Who benefit from adjuvant chemotherapy in stage I lung adenocarcinoma? A multi-dimensional model for candidate selection.Ⅰ期肺腺癌患者中哪些人能从辅助化疗中获益?候选患者选择的多维模型。
Neoplasia. 2024 Apr;50:100979. doi: 10.1016/j.neo.2024.100979. Epub 2024 Feb 21.
3
The International Association for the Study of Lung Cancer Lung Cancer Staging Project: Proposals for the Revisions of the T-Descriptors in the Forthcoming Ninth Edition of the TNM Classification for Lung Cancer.国际肺癌研究协会肺癌分期项目:对即将出版的第九版肺癌 TNM 分类中 T 描述符修订的建议。
J Thorac Oncol. 2024 May;19(5):749-765. doi: 10.1016/j.jtho.2023.12.006. Epub 2023 Dec 7.
4
Overall Survival with Osimertinib in Resected -Mutated NSCLC.奥希替尼治疗可切除突变型 NSCLC 的总生存期。
N Engl J Med. 2023 Jul 13;389(2):137-147. doi: 10.1056/NEJMoa2304594. Epub 2023 Jun 4.
5
Association of Prenatal Care Services, Maternal Morbidity, and Perinatal Mortality With the Advanced Maternal Age Cutoff of 35 Years.产前保健服务、产妇发病率和围产儿死亡率与 35 岁高龄产妇截止线的关联。
JAMA Health Forum. 2021 Dec 3;2(12):e214044. doi: 10.1001/jamahealthforum.2021.4044. eCollection 2021 Dec.
6
A Real-World Systematic Analysis of Driver Mutations' Prevalence in Early- and Advanced-Stage NSCLC: Implications for Targeted Therapies in the Adjuvant Setting.早期和晚期非小细胞肺癌驱动基因突变发生率的真实世界系统分析:对辅助治疗中靶向治疗的意义
Cancers (Basel). 2022 Jun 16;14(12):2971. doi: 10.3390/cancers14122971.
7
Neoadjuvant Immunotherapy for Resectable Non-small Cell Lung Cancer: Exciting New Horizon in Early-Stage Lung Cancer Care.可切除非小细胞肺癌的新辅助免疫治疗:早期肺癌治疗中令人兴奋的新视野。
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Preoperative and Postoperative Systemic Therapy for Operable Non-Small-Cell Lung Cancer.可切除非小细胞肺癌的术前和术后全身治疗。
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边缘生存:T分期临界值2毫米内原发性肺癌切除术后辅助治疗的作用

Living on the edge: Role of adjuvant therapy after resection of primary lung cancer within 2 millimeters of a T-stage cutoff.

作者信息

Udelsman Brooks V, Bedrosian Christina K, Kawaguchi Eric S, Ding Li, Wallace Williams D, Rosenberg Graeme, Harano Takashi, Wightman Sean, Atay Scott, Kim Anthony W, Woodard Gavitt

机构信息

Surgery, Keck School of Medicine of USC, Los Angeles, Calif; Keck School of Medicine of USC, Los Angeles, Calif.

Keck School of Medicine of USC, Los Angeles, Calif.

出版信息

J Thorac Cardiovasc Surg. 2025 May;169(5):1338-1345.e15. doi: 10.1016/j.jtcvs.2024.10.053. Epub 2024 Nov 7.

DOI:10.1016/j.jtcvs.2024.10.053
PMID:39521371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12034478/
Abstract

OBJECTIVES

To evaluate the use of systemic therapy and overall survival in patients with resected non-small cell lung cancer whose pathologic tumor size was within 2 mm of a T-stage cutoff.

METHODS

This was retrospective cohort study using the National Cancer Database of patients who underwent resection of tumors within 2 mm of the T1c/T2a, T2a/T2b, and T2b/T3 T-stage cutoffs. Patients with nodal involvement or whose T stage was determined on the basis of pathologic features other than tumor size were excluded. A multistate model compared the primary outcomes of systemic therapy and overall survival.

RESULTS

From the National Cancer Database, 18,490 patients were identified: 9966 at the T1c/T2a cutoff, 5593 at the T2a/T2b cutoff, and 2931 at the T2b/T3 cutoff. Peaks in tumor size distribution occurred at 5-mm intervals. On the basis of an expected normalized curve, 2050 patients (11.1%) may have been understaged. Use of systemic therapy was greater among patients with larger tumors at the T1c/T2a cutoff (7.1% vs 8.9%; P < .001), the T2a/T2b cutoff (20.0% vs 25.5%; P < .001), and the T2b/T3 cutoff (31.2% vs 41.8%; P < .001). In a multistate model, mortality was greater above the T1c/T2a cutoff (hazard ratio [HR], 1.10; P = .01), T2a/T2b cutoff (HR, 1.17; P < .01), and T2b/T3 cutoff (HR, 1.13; P = .03). In patients who received systemic therapy, this trend was eliminated (HR, 1.24; P = .14, HR, 0.79; P = .07, and HR, 1.23; P = .09, respectively).

CONCLUSIONS

Rounding of tumor size for pathologic staging is common. Although seemingly trivial, rounding may downstage patients and is associated with decreased rates of adjuvant therapy use and potentially worse overall survival.

摘要

目的

评估病理肿瘤大小在T分期临界值±2mm范围内的可切除非小细胞肺癌患者的全身治疗使用情况和总生存期。

方法

这是一项回顾性队列研究,使用国家癌症数据库中肿瘤切除在T1c/T2a、T2a/T2b和T2b/T3 T分期临界值±2mm范围内的患者。排除有淋巴结受累或T分期基于肿瘤大小以外的病理特征确定的患者。多状态模型比较全身治疗和总生存期的主要结局。

结果

从国家癌症数据库中识别出18490例患者:T1c/T2a临界值处9966例,T2a/T2b临界值处5593例,T2b/T3临界值处2931例。肿瘤大小分布峰值以5mm间隔出现。根据预期的标准化曲线,2050例患者(11.1%)可能分期过低。在T1c/T2a临界值(7.1%对8.9%;P<0.001)、T2a/T2b临界值(20.0%对25.5%;P<0.001)和T2b/T3临界值(31.2%对41.8%;P<0.001)时,肿瘤较大的患者全身治疗使用率更高。在多状态模型中,T1c/T2a临界值以上(风险比[HR],1.10;P=0.01)、T2a/T2b临界值以上(HR,1.17;P<0.01)和T2b/T3临界值以上(HR,1.13;P=0.03)死亡率更高。在接受全身治疗的患者中,这种趋势被消除(HR分别为1.24;P=0.14、HR为0.79;P=0.07和HR为1.23;P=0.09)。

结论

病理分期时肿瘤大小四舍五入很常见。虽然看似微不足道,但四舍五入可能使患者分期过低,并与辅助治疗使用率降低以及潜在更差的总生存期相关。