Clinical nodal stage is an independently significant predictor of distant failure in patients with squamous cell carcinoma of the larynx

被引:47
作者
Matsuo, JMS
Patel, SG
Singh, B
Wong, RJ
Boyle, JO
Kraus, DH
Shaha, AR
Zelefsky, MJ
Pfister, DG
Shah, JP
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Head & Neck Serv, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Lab Epithelial Canc Biol, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, Brachytherapy Serv, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Med, Div Solid Tumor Oncol, New York, NY 10021 USA
关键词
D O I
10.1097/01.sla.0000086660.35809.8a
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: To determine the impact of clinical nodal stage on distant metastasis (DM) in patients with squamous cell carcinoma of the larynx (SCCL). Methods: Six hundred sixty-two previously untreated SCCL patients treated at a tertiary care cancer center from January 1984 to December 1998 were eligible for analysis. The end point of interest was development of DM following treatment. Distant metastasis-free survival (DMFS) was calculated by the Kaplan-Meier method; predictors of outcome were identified by univariate and multivariate analysis. The primary tumor site was glottic in 55%, supraglottic in 40%, and trans/sub glottic in 5%; 40% had locoregionally advanced (stage III/IV) tumors. At initial presentation, 25% of patients (12% N1, 11% N2, and 2% N3) had clinically metastatic nodes. Results: DM were recorded in 67 patients (10%; lung, 45%; soft tissue, 13%; bone, 10%; multiple sites, 28%). The median time to DM was 18 months (range, 1-109). With a median follow-up of 60 months, the 5-year DMFS was 88%. Even after accounting for the type of index treatment, the only significant predictor of worse DMFS on multivariate analysis was a higher clinical N stage (P < 0.0001). The relative risk for DM was 0.5 (95% CI, 0.2-1.4; P = NS) for cN1, 3.2 (95% CI, 1.7-5.9; P < 0.0001) for cN2, and 7.5 (95% CI, 3.1-17.9; P < 0.0001) for cN3 disease compared with clinically NO patients. Conclusion: Regardless of the index treatment modality, primary tumor site, or T stage, a higher clinical N stage at the time of presentation independently and significantly increases the risk of DM in patients with SCCL.
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页码:412 / 421
页数:10
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