Tsang Matthew, Petkiewicz Stephanie
From the Department of Anatomical Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Arch Pathol Lab Med. 2022 Dec 1;146(12):1535-1539. doi: 10.5858/arpa.2021-0219-OA.
CONTEXT.—: The use of targeted therapy in patients with advanced, BRAF-mutated melanomas has necessitated timely access to BRAF mutational status in order for clinicians to proceed with treatment decisions.
OBJECTIVE.—: To assess the impact of pathologist-initiated reflex BRAF testing in patients with advanced melanoma on laboratory turnaround time and time to systemic treatment.
DESIGN.—: At our tertiary care center and 3 affiliated community hospitals, we implemented a guideline for pathologist-initiated reflex testing for BRAF mutational status in patients diagnosed with melanoma and positive lymph nodes or new diagnosis of a metastatic site. Retrospective review was performed for 65 cases of advanced melanoma for which BRAF testing was ordered, during a period inclusive of 6 months before and after guideline implementation.
RESULTS.—: Implementation of reflex testing guidelines did not significantly affect the overall number of BRAF tests ordered for patients with melanoma. In cases with reflex testing compared to routine testing, total turnaround time was reduced by from 52.5 ± 5.6 to 18.6 ± 1.0 days (P < .001). In patients who received systemic therapy, without intentional delay by interval completion lymph node dissection (CLND), the use of reflex BRAF testing reduced time to systematic treatment from 71.7 ± 11.4 to 37.7 ± 4.6 days (P = .02). Time to systematic treatment was unchanged in those who underwent interval CLND (118.9 ± 10.9 versus 110.5 ± 22.5; P = .75).
CONCLUSIONS.—: These data support a recommendation for pathologist-initiated reflex testing of BRAF mutational status in advanced melanoma as a standard practice in pathology laboratories.
在晚期BRAF突变型黑色素瘤患者中使用靶向治疗,要求及时获取BRAF突变状态,以便临床医生做出治疗决策。
评估病理学家启动的晚期黑色素瘤患者BRAF反射检测对实验室周转时间和全身治疗时间的影响。
在我们的三级医疗中心和3家附属社区医院,我们实施了一项指南,用于对诊断为黑色素瘤且淋巴结阳性或新诊断为转移部位的患者进行病理学家启动的BRAF突变状态反射检测。对65例晚期黑色素瘤患者进行了回顾性研究,这些患者在指南实施前后6个月期间接受了BRAF检测。
反射检测指南的实施对黑色素瘤患者BRAF检测的总体数量没有显著影响。与常规检测相比,反射检测的病例总周转时间从52.5±5.6天缩短至18.6±1.0天(P<.001)。在接受全身治疗的患者中,在没有因间隔完成淋巴结清扫(CLND)而故意延迟的情况下,使用反射BRAF检测将全身治疗时间从71.7±11.4天缩短至37.7±4.6天(P=.02)。接受间隔CLND的患者的全身治疗时间没有变化(118.9±10.9天对110.5±22.5天;P=.75)。
这些数据支持在晚期黑色素瘤中进行病理学家启动的BRAF突变状态反射检测,作为病理实验室的标准做法。