External validation of the American Joint Committee on Cancer melanoma staging system eighth edition using the surveillance, epidemiology, and end results program

被引:2
作者
Tjokrowidjaja, Angelina [1 ,2 ,3 ]
Browne, Lois [4 ]
Soudy, Hussein [1 ,2 ,5 ,6 ]
机构
[1] St George Hosp, Dept Med Oncol, Level 1 Canc Care Ctr,1 Short St, Kogarah, NSW 2217, Australia
[2] Sutherland Hosp, Dept Med Oncol, Kogarah, NSW, Australia
[3] Univ Sydney, Natl Hlth & Med Res Council Clin Trials Ctr, Sydney, NSW, Australia
[4] St George Hosp, Dept Radiat Oncol, Kogarah, NSW, Australia
[5] Univ New South Wales, Sch Med, Kensington, NSW, Australia
[6] Cairo Univ, Fac Med, Cairo, Egypt
关键词
AJCC melanoma staging; epidemiology; melanoma; SEER registry; validation; SURVIVAL; IPILIMUMAB; VEMURAFENIB; DABRAFENIB; NIVOLUMAB;
D O I
10.1111/ajco.13689
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim The American Joint Committee on Cancer (AJCC) melanoma staging system eighth edition (AJCC-8) was recently released to provide accurate staging reflecting advances in the treatment of melanoma. Using population registry data, this study independently validates and compares the prognostic performance of AJCC-8 to the seventh edition (AJCC-7). Methods We extracted patient-, tumor-related, and survival data from the SEER-18 registry between 2010 and 2015. To assess overall survival (OS) and cancer-specific survival (CSS) for AJCC-7 and AJCC-8, we performed Kaplan-Meier analysis and computed cumulative hazard functions using Nelson-Aalen function. Results Of 126,408 individuals, 59,989 (47%) and 60,411 (48%) had available data for pathological and clinical-stage OS analysis, respectively. The 3-year OS for AJCC-7 among pathologically staged patients was: stage IA 97%, stage IB 95%, stage IIA 87%, stage IIB 76%, stage IIC 57%, stage IIIA 86%, stage IIIB 69%, stage IIIC 50%, and stage IV 24%. The 3-year OS for AJCC-8 patients was similar but was 56% for stage IIIC and 30% for stage IIID. Stage IV individuals with an elevated LDH had worse OS and CSS at all measured time-points up to 60 months compared to those with a normal LDH. Conclusion The discriminatory ability of AJCC-8 and AJCC-7 appear comparable. Changes in AJCC-8 identified stage IIID as a poor prognostic subgroup among stage III patients and elevated LDH in stage IV. However, patients with advanced T-stage, node-negative tumors experienced worse survival compared to those with earlier T-stage, node-positive tumors, and the results of ongoing trials should inform adjuvant therapy in this subset of patients.
引用
收藏
页码:E280 / E288
页数:9
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