Prognostic Factors of Long-Term Outcomes after Primary Chemo-Radiotherapy in Non-Metastatic Anal Squamous Cell Carcinoma: An International Bicentric Cohort.
Soledad IseasDiego ProstSarah BouchereauMariano GolubickiJuan RobbioAna OviedoMariana CoraglioMirta KujarukGuillermo MéndezMarcela CarballidoEnrique RocaLouis GrosVincent de ParadesNabil Baba-HamedJulien AdamMartín Carlos AbbaEric RaymondPublished in: Biomedicines (2023)
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 ( p < 0.0001) and OS ( p < 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 ( p = 0.0002), N0 ( p = 0.035), HIV-positive ( p = 0.047), HIV-HPV coinfection ( p = 0.018), and well-differentiated tumors ( p = 0.037). The three-year OS was 81.6%. Female sex ( p = 0.05), cT1-T2 ( p = 0.02) and well-differentiated tumors ( p = 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, p = 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.
Keyphrases
- prognostic factors
- locally advanced
- hiv positive
- squamous cell carcinoma
- high grade
- antiretroviral therapy
- men who have sex with men
- rectal cancer
- neoadjuvant chemotherapy
- poor prognosis
- south africa
- hiv testing
- free survival
- hiv infected
- radiation therapy
- human immunodeficiency virus
- phase ii study
- cardiac resynchronization therapy
- hiv aids
- long non coding rna
- machine learning
- hepatitis c virus
- image quality
- small cell lung cancer
- cervical cancer screening
- dual energy
- photodynamic therapy
- drug delivery
- left ventricular
- rna seq
- single cell
- end stage renal disease
- magnetic resonance imaging
- radiation induced
- data analysis