Ballo Matthew T, Ross Merrick I, Cormier Janice N, Myers Jeffrey N, Lee Jeffrey E, Gershenwald Jeffrey E, Hwu Patrick, Zagars Gunar K
Department of Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.
Int J Radiat Oncol Biol Phys. 2006 Jan 1;64(1):106-13. doi: 10.1016/j.ijrobp.2005.06.030. Epub 2005 Sep 22.
To evaluate the outcome and patterns of failure for patients with nodal metastases from melanoma treated with combined-modality therapy.
Between 1983 and 2003, 466 patients with nodal metastases from melanoma were managed with lymphadenectomy and radiation, with or without systemic therapy. Surgery was a therapeutic procedure for clinically apparent nodal disease in 434 patients (regionally advanced nodal disease). Adjuvant radiation was generally delivered with a hypofractionated regimen. Adjuvant systemic therapy was delivered to 154 patients.
With a median follow-up of 4.2 years, 252 patients relapsed and 203 patients died of progressive disease. The actuarial 5-year disease-specific, disease-free, and distant metastasis-free survival rates were 49%, 42%, and 44%, respectively. By multivariate analysis, increasing number of involved lymph nodes and primary ulceration were associated with an inferior 5-year actuarial disease-specific and distant metastasis-free survival. Also, the number of involved lymph nodes was associated with the development of brain metastases, whereas thickness was associated with lung metastases, and primary ulceration was associated with liver metastases. The actuarial 5-year regional (in-basin) control rate for all patients was 89%, and on multivariate analysis there were no patient or disease characteristics associated with inferior regional control. The risk of lymphedema was highest for those patients with groin lymph node metastases.
Although regional nodal disease can be satisfactorily controlled with lymphadenectomy and radiation, the risk of distant metastases and melanoma death remains high. A management approach to these patients that accounts for the competing risks of distant metastases, regional failure, and long-term toxicity is needed.
评估接受综合治疗的黑色素瘤淋巴结转移患者的治疗结果和失败模式。
1983年至2003年间,466例黑色素瘤淋巴结转移患者接受了淋巴结清扫术和放疗,部分患者还接受了全身治疗。手术是434例临床可见淋巴结疾病患者(区域晚期淋巴结疾病)的治疗手段。辅助放疗一般采用大分割方案。154例患者接受了辅助全身治疗。
中位随访4.2年,252例患者复发,203例患者死于疾病进展。5年精算疾病特异性生存率、无病生存率和无远处转移生存率分别为49%、42%和44%。多因素分析显示,受累淋巴结数量增加和原发灶溃疡与5年精算疾病特异性生存率和无远处转移生存率较低相关。此外,受累淋巴结数量与脑转移的发生相关,肿瘤厚度与肺转移相关,原发灶溃疡与肝转移相关。所有患者的5年精算区域(区域内)控制率为89%,多因素分析显示,没有患者或疾病特征与区域控制不佳相关。腹股沟淋巴结转移患者发生淋巴水肿的风险最高。
尽管淋巴结清扫术和放疗可令人满意地控制区域淋巴结疾病,但远处转移和黑色素瘤死亡风险仍然很高。需要一种考虑到远处转移、区域治疗失败和长期毒性等相互竞争风险的患者管理方法。