Porter G A, Abdalla J, Lu M, Smith S, Montgomery D, Grimm E, Ross M I, Mansfield P F, Gershenwald J E, Lee J E
Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston 77030, USA.
Ann Surg Oncol. 2001 Mar;8(2):116-22. doi: 10.1007/s10434-001-0116-3.
Although sentinel lymph node (SLN) status is the most powerful predictor of prognosis in patients with clinically localized melanoma, a proportion of melanoma patients with histologically negative SLNs will still recur. It is hypothesized that tumor response may be altered or mediated by specific cytokines. We therefore investigated whether levels of IL-4, IL-6, IL-10, TNF-alpha, or IFN-gamma would predict disease recurrence in melanoma patients with histologically negative SLNs.
This prospective cohort study involved 218 patients with clinically localized melanoma who underwent a histologically negative SLN biopsy. Preoperative plasma cytokine levels were determined by enzyme-linked immunosorbent assay on these patients, as well as on 90 healthy controls. Kaplan-Meier life tables were constructed, and Cox proportional hazards analyses were performed to assess predictors of disease-free survival (DFS).
At a median follow-up of 43 months, 33 of 218 patients (15%) had suffered disease recurrence. Melanoma patients had significant elevations of IL-4, IL-6, and IL-10 compared to healthy controls; levels of IFN-gamma were less elevated in melanoma patients compared to controls. Despite this, melanoma patients with detectable IFN-gamma levels were at significantly higher risk for recurrence compared to patients with undetectable levels (5-year DFS 70% vs. 86%, P = .03). On multivariate analysis including standard melanoma prognostic factors, only tumor thickness (P = .004) and the presence of detectable IFN-gamma levels (P = .05) were significant independent prognostic factors for disease-free survival.
Among melanoma patients with clinically localized disease who have undergone a histologically negative SLN biopsy, presence of a detectable plasma level of IFN-gamma is an independent predictor of disease recurrence. Elevated levels of IFN-gamma may identify a group of early-stage melanoma patients who are more likely to have recurrence of disease and who may benefit from adjuvant therapies, including immunotherapies.
尽管前哨淋巴结(SLN)状态是临床局限性黑色素瘤患者预后的最有力预测指标,但一部分组织学检查显示SLN阴性的黑色素瘤患者仍会复发。据推测,肿瘤反应可能会被特定细胞因子改变或介导。因此,我们研究了白细胞介素-4(IL-4)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)、肿瘤坏死因子-α(TNF-α)或干扰素-γ(IFN-γ)水平是否能预测组织学检查显示SLN阴性的黑色素瘤患者的疾病复发情况。
这项前瞻性队列研究纳入了218例临床局限性黑色素瘤患者,他们均接受了组织学检查显示为阴性的SLN活检。通过酶联免疫吸附测定法测定了这些患者以及90名健康对照者术前血浆细胞因子水平。构建了Kaplan-Meier生存表,并进行了Cox比例风险分析,以评估无病生存期(DFS)的预测指标。
在中位随访43个月时,218例患者中有33例(15%)出现疾病复发。与健康对照者相比,黑色素瘤患者的IL-4、IL-6和IL-10水平显著升高;与对照者相比,黑色素瘤患者的IFN-γ水平升高幅度较小。尽管如此,与IFN-γ水平检测不到的患者相比,IFN-γ水平可检测到的黑色素瘤患者复发风险显著更高(5年DFS分别为70%和86%,P = 0.03)。在纳入标准黑色素瘤预后因素的多变量分析中,只有肿瘤厚度(P = 0.004)和可检测到的IFN-γ水平的存在(P = 0.05)是无病生存期的显著独立预后因素。
在接受了组织学检查显示为阴性的SLN活检的临床局限性疾病黑色素瘤患者中,可检测到的血浆IFN-γ水平的存在是疾病复发的独立预测指标。IFN-γ水平升高可能识别出一组更有可能疾病复发且可能从包括免疫疗法在内的辅助治疗中获益的早期黑色素瘤患者。