Zhang Yaoyi, Li Xiaohui, Li Sheng, Yang Zhijian, Hoffman Robert M, Yu Chen
Department of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University and Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research, Nanjing, P.R. China.
Department of Radiology, Children's Hospital Affiliated to Nanjing Medical University, Nanjing, P.R. China.
Anticancer Res. 2025 Jan;45(1):399-404. doi: 10.21873/anticanres.17428.
BACKGROUND/AIM: Colorectal cancer (CRC) has the third-highest incidence among human cancers. Advancements in chemotherapy and targeted therapy have improved the treatment outcomes for patients with CRC. However, the management of patients with unresectable metastatic CRC (mCRC) continues to be a significant challenge for clinicians worldwide, particularly for those with microsatellite stability (MSS) and the BRAF V600E mutation, as they are associated with the poorest prognosis.
The present study describes two patients with unresectable MSS, BRAF V600E-mutated stage IV metastatic CRC using a biweekly alternating regimen of irinotecan and oxaliplatin combined with capecitabine and bevacizumab. Case 1 stabilized after alternating treatment, whereas Case 2 progressed after alternating treatment, with progression-free survival (PFS) of 20+ and 24.5 months, respectively. Circulating levels of carcinoemryonic antigen (CEA) dropped to near normal in both cases. A partial response (PR) was determined for both cases.
The two cases suggest that an alternating chemotherapy regimen of oxaliplatin and irinotecan, combined with capecitabine and bevacizumab is effective in the treatment of MSS, BRAF V600E-mutated stage IV metastatic CRC. The progression-free survival was significantly prolonged (both exceeding 20 months) compared to the first-line standard chemotherapy regimen for this disease. With a good balance between toxicity and efficacy, this alternating chemotherapy regimen can be considered as a potential first-line option for microsatellite-stable metastatic colon cancer.
背景/目的:结直肠癌(CRC)在人类癌症中的发病率位居第三。化疗和靶向治疗的进展改善了CRC患者的治疗效果。然而,不可切除的转移性CRC(mCRC)患者的管理仍然是全球临床医生面临的重大挑战,特别是对于那些微卫星稳定(MSS)且具有BRAF V600E突变的患者,因为他们的预后最差。
本研究描述了两名不可切除的MSS、BRAF V600E突变的IV期转移性CRC患者,采用伊立替康和奥沙利铂每两周交替方案联合卡培他滨和贝伐单抗治疗。病例1在交替治疗后病情稳定,而病例2在交替治疗后病情进展,无进展生存期(PFS)分别为20多个月和24.5个月。两例患者的癌胚抗原(CEA)循环水平均降至接近正常。两例均确定为部分缓解(PR)。
这两个病例表明,奥沙利铂和伊立替康交替化疗方案联合卡培他滨和贝伐单抗治疗MSS、BRAF V600E突变的IV期转移性CRC有效。与该疾病的一线标准化疗方案相比,无进展生存期显著延长(均超过20个月)。由于毒性和疗效之间取得了良好平衡,这种交替化疗方案可被视为微卫星稳定转移性结肠癌的潜在一线选择。