Iseas Soledad, Prost Diego, Bouchereau Sarah, Golubicki Mariano, Robbio Juan, Oviedo Ana, Coraglio Mariana, Kujaruk Mirta, Méndez Guillermo, Carballido Marcela, Roca Enrique, Gros Louis, De Parades Vincent, Baba-Hamed Nabil, Adam Julien, Abba Martín Carlos, Raymond Eric
Oncology Unit, Gastroenterology Hospital "Dr. Carlos Bonorino Udaondo", Av. Caseros 2061, Buenos Aires C1264, Argentina.
Medical Oncology Department, Paris-St Joseph Hospital, 185 Rue Raymond Losserand, 75014 Paris, France.
Biomedicines. 2023 Mar 6;11(3):791. doi: 10.3390/biomedicines11030791.
Anal squamous cell carcinoma (ASCC) is a rare malignancy with a rising incidence associated with human papillomavirus (HPV) infection. The locally advanced disease is associated with a 30% rate of treatment failure after standard chemoradiotherapy (CRT). We aimed to elucidate the prognostic factors for ASCC after curative CRT. A retrospective multicenter study of 176 consecutive patients with ASCC having completed CRT treated between 2010 and 2017 at two centers was performed. Complete response (CR), disease-free survival (DFS), and overall survival (OS) were analyzed by Kaplan-Meier estimates with log-rank tests. The hierarchical clustering on principal components (HCPC) method was employed in an unsupervised and multivariate approach. The CR rate was 70% and was predictive of DFS ( < 0.0001) and OS ( < 0.0001), where non-CR cases were associated with shorter DFS (HR = 16.5, 95% CI 8.19-33.21) and OS (HR = 8.42, 95% CI 3.77-18.81) in a univariate analysis. The median follow-up was 38 months, with a 3-year DFS of 71%. The prognostic factors for DFS were cT1-T2 ( = 0.0002), N0 ( = 0.035), HIV-positive ( = 0.047), HIV-HPV coinfection ( = 0.018), and well-differentiated tumors ( = 0.037). The three-year OS was 81.6%. Female sex ( = 0.05), cT1-T2 ( = 0.02) and well-differentiated tumors ( = 0.003) were associated with better OS. The unsupervised analysis demonstrated a clear segregation of patients in three clusters, identifying that poor prognosis clusters associated with shorter DFS (HR = 1.74 95% CI = 1.25-2.42, = 0.0008) were enriched with the locally advanced disease, anal canal location, HIV-HPV coinfection, and non-CR. In conclusion, our results reinforce the prognostic value of T stage, N stage, sex, differentiation status, tumor location, and HIV-HPV coinfection in ASCC after CRT.
肛管鳞状细胞癌(ASCC)是一种罕见的恶性肿瘤,其发病率随着人乳头瘤病毒(HPV)感染而上升。局部晚期疾病在标准放化疗(CRT)后有30%的治疗失败率。我们旨在阐明根治性CRT后ASCC的预后因素。对2010年至2017年间在两个中心接受CRT治疗的176例连续ASCC患者进行了一项回顾性多中心研究。采用Kaplan-Meier估计法和对数秩检验分析完全缓解(CR)、无病生存期(DFS)和总生存期(OS)。采用主成分分层聚类(HCPC)方法进行无监督多变量分析。CR率为70%,可预测DFS(<0.0001)和OS(<0.0001),单因素分析显示非CR病例的DFS(HR=16.5,95%CI 8.19-33.21)和OS(HR=8.42,95%CI 3.77-18.81)较短。中位随访时间为38个月,3年DFS率为71%。DFS的预后因素为cT1-T2(=0.0002)、N0(=0.035)、HIV阳性(=0.047)、HIV-HPV合并感染(=0.018)和高分化肿瘤(=0.037)。3年OS率为81.6%。女性(=0.05)、cT1-T2(=0.02)和高分化肿瘤(=0.003)与较好的OS相关。无监督分析显示患者明显分为三个簇,表明与较短DFS相关的预后不良簇(HR=1.74,95%CI=1.25-2.42,=0.0008)富含局部晚期疾病、肛管位置、HIV-HPV合并感染和非CR。总之,我们的结果强化了T分期、N分期、性别、分化状态、肿瘤位置和HIV-HPV合并感染在CRT后ASCC中的预后价值。