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.
引用
收藏
页码:412 / 421
页数:10
相关论文
共 31 条
[21]  
2-J
[22]   AN OVERVIEW OF RANDOMIZED CONTROLLED TRIALS OF ADJUVANT CHEMOTHERAPY IN HEAD AND NECK-CANCER [J].
MUNRO, AJ .
BRITISH JOURNAL OF CANCER, 1995, 71 (01) :83-91
[23]  
Myers JN, 2001, CANCER-AM CANCER SOC, V92, P3030, DOI 10.1002/1097-0142(20011215)92:12<3030::AID-CNCR10148>3.0.CO
[24]  
2-P
[25]  
NISHIJIMA W, 1993, ARCH OTOLARYNGOL, V119, P65
[26]   Chemotherapy added to locoregional treatment for head and neck squamous-cell carcinoma:: three meta-analyses of updated individual data [J].
Pignon, JP ;
Bourhis, J ;
Domenge, C ;
Designé, L .
LANCET, 2000, 355 (9208) :949-955
[27]   Distant metastases from laryngeal and hypopharyngeal cancer [J].
Spector, GJ .
ORL-JOURNAL FOR OTO-RHINO-LARYNGOLOGY AND ITS RELATED SPECIALTIES, 2001, 63 (04) :224-228
[28]   FAILURE AT DISTANT SITES FOLLOWING MULTIMODALITY TREATMENT FOR ADVANCED HEAD AND NECK-CANCER [J].
VIKRAM, B ;
STRONG, EW ;
SHAH, JP ;
SPIRO, R .
HEAD & NECK SURGERY, 1984, 6 (03) :730-733
[29]   Simultaneous radiochemotherapy versus radiotherapy alone in advanced head and neck cancer:: A randomized multicenter study [J].
Wendt, TG ;
Grabenbauer, GG ;
Rödel, CM ;
Thiel, HJ ;
Aydin, H ;
Rohloff, R ;
Wustrow, TPU ;
Iro, H ;
Popella, C ;
Schalhorn, A .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) :1318-1324