Mazurek Agnieszka M, Małusecka Ewa, Jabłońska Iwona, Vydra Natalia, Rutkowski Tomasz W, Giglok Monika, Suwiński Rafał
Center for Translational Research and Molecular Biology of Cancer, Maria Sklodowska-Curie National Research Institute of Oncology Gliwice Branch, Wybrzeze Armii Krajowej 15, 44-102 Gliwice, Poland.
I Radiation and Clinical Oncology Department, Maria Sklodowska-Curie National Research Institute of Oncology Gliwice Branch, Wybrzeze Armii Krajowej 15, 44-102 Gliwice, Poland.
Cancers (Basel). 2023 Jan 30;15(3):867. doi: 10.3390/cancers15030867.
Implementation of anal squamous cell carcinoma (ASCC) treatment modifications requires reliable patient risk stratification. The circulating tumor-related human papillomavirus type 16 (ctHPV16) may play a role in predicting survival or assessing treatment response.
The study included 62 ASCC patients treated with chemoradiotherapy. A threshold of 2.5 was used to determine the maximum standardized uptake value (SUVmax). The ctHPV16 viral load (VL) was quantified by qPCR.
In the multivariate Cox analysis, lower SUVmax ( = 0.047) and ctHPV16-positive ( = 0.054) proved to be independent prognostic factors for favorable overall survival (OS). In the subgroup with the higher SUVmax, ctHPV16 and nodal (N) status were independent prognostic factors with = 0.022 for ctHPV16 and = 0.053 for N. The best survival rate (95%) presented ctHPV16-positive/N-negative patients. High ctHPV16 VL tended to be slightly specific for patients younger than 63 years ( = 0.152). The decrease in ctHPV16 VL to undetectable level after the end of treatment correlated with the overall clinical response.
A prognostic stratification by SUVmax, ctHPV16 and N-positive status allows consideration of more aggressive treatment in high-risk patients (those with high SUVmax, ctHPV16-negative, and N-positive) or de-intensification of therapy in low-risk patients (those with low SUVmax, ctHPV16-positive and N-negative). However, prospective clinical trials on a large group are needed.
实施肛管鳞状细胞癌(ASCC)治疗方案的调整需要可靠的患者风险分层。循环肿瘤相关的人乳头瘤病毒16型(ctHPV16)可能在预测生存或评估治疗反应中发挥作用。
该研究纳入了62例接受放化疗的ASCC患者。采用2.5的阈值来确定最大标准化摄取值(SUVmax)。通过qPCR对ctHPV16病毒载量(VL)进行定量。
在多变量Cox分析中,较低的SUVmax(P = 0.047)和ctHPV16阳性(P = 0.054)被证明是总体生存(OS)良好的独立预后因素。在SUVmax较高的亚组中,ctHPV16和淋巴结(N)状态是独立的预后因素,ctHPV16的P = 0.022,N的P = 0.053。最佳生存率(95%)出现在ctHPV16阳性/N阴性患者中。高ctHPV16 VL往往对63岁以下的患者有一定特异性(P = 0.152)。治疗结束后ctHPV16 VL降至不可检测水平与总体临床反应相关。
通过SUVmax、ctHPV16和N阳性状态进行预后分层,有助于考虑对高危患者(SUVmax高、ctHPV16阴性和N阳性者)采取更积极的治疗,或对低危患者(SUVmax低、ctHPV16阳性和N阴性者)进行治疗降阶梯。然而,需要对大量人群进行前瞻性临床试验。