Negoi Ionut
Department of General Surgery, Faculty of Medicine, Carol Davila University of Medicine and Pharmacy Bucharest, 050474 Bucharest, Romania.
Clinical Emergency Hospital of Bucharest, 014461 Bucharest, Romania.
Medicina (Kaunas). 2025 Jun 24;61(7):1132. doi: 10.3390/medicina61071132.
Rectal cancer management necessitates a rigorous multidisciplinary strategy, emphasizing precise staging and detailed risk stratification to inform optimal therapeutic decision-making. Obtaining an accurate histological diagnosis before initiating treatment is essential. Comprehensive staging integrates clinical evaluation, thorough medical history analysis, assessment of carcinoembryonic antigen (CEA) levels, and computed tomography (CT) imaging of the abdomen and thorax. High-resolution pelvic magnetic resonance imaging (MRI), utilizing dedicated rectal protocols, is critical for identifying recurrence risks and delineating precise anatomical relationships. Endoscopic ultrasound further refines staging accuracy by determining the tumor infiltration depth in early-stage cancers, while preoperative colonoscopy effectively identifies synchronous colorectal lesions. In early-stage rectal cancers (T1-T2, N0, and M0), radical surgical resection remains the standard of care, although transanal local excision can be selectively indicated for certain T1N0 tumors. In contrast, locally advanced rectal cancers (T3, T4, and N+) characterized by microsatellite stability or proficient mismatch repair are optimally managed with total neoadjuvant therapy (TNT), which combines chemoradiotherapy with oxaliplatin-based systemic chemotherapy. Additionally, tumors exhibiting high microsatellite instability or mismatch repair deficiency respond favorably to immune checkpoint inhibitors (ICIs). The evaluation of tumor response following neoadjuvant therapy, utilizing MRI and endoscopic assessments, facilitates individualized treatment planning, including non-operative approaches for patients with confirmed complete clinical responses who comply with rigorous follow-up. Recent advancements in molecular characterization, targeted therapies, and immunotherapy highlight a significant evolution towards personalized medicine. The effective integration of these innovations requires enhanced interdisciplinary collaboration to improve patient prognosis and quality of life.
直肠癌的治疗需要严格的多学科策略,强调精确分期和详细的风险分层,以指导最佳治疗决策。在开始治疗前获得准确的组织学诊断至关重要。全面分期包括临床评估、详细病史分析、癌胚抗原(CEA)水平评估以及腹部和胸部的计算机断层扫描(CT)成像。利用专门的直肠检查方案进行的高分辨率盆腔磁共振成像(MRI)对于识别复发风险和描绘精确的解剖关系至关重要。内镜超声通过确定早期癌症的肿瘤浸润深度进一步提高分期准确性,而术前结肠镜检查可有效识别同步性结直肠病变。在早期直肠癌(T1-T2、N0和M0)中,根治性手术切除仍然是标准治疗方法,尽管对于某些T1N0肿瘤可选择性地采用经肛门局部切除。相比之下,以微卫星稳定性或错配修复功能正常为特征的局部晚期直肠癌(T3、T4和N+)最佳治疗方案是全新辅助治疗(TNT),即将放化疗与基于奥沙利铂的全身化疗相结合。此外,表现出高微卫星不稳定性或错配修复缺陷的肿瘤对免疫检查点抑制剂(ICI)反应良好。利用MRI和内镜评估对新辅助治疗后的肿瘤反应进行评估,有助于制定个体化治疗方案,包括对确诊为完全临床缓解且符合严格随访要求的患者采用非手术方法。分子特征分析、靶向治疗和免疫治疗方面的最新进展凸显了向精准医学的重大转变。有效整合这些创新需要加强跨学科合作,以改善患者预后和生活质量。