Gamal Doaa A, Morsy Aiat, Omar Mervat
Department of Clinical Oncology, Assiut University Hospital, Assiut 71515, Egypt.
Oncotarget. 2025 Feb 12;16:67-78. doi: 10.18632/oncotarget.28687.
Anti-epidermal growth factor receptor therapy showed an overall median survival improvement in metastatic colorectal cancer. Maintenance with anti in metastatic colorectal cancer wild type was studied in many trials with promising results and many of these trials gave combined chemo with the target therapy and this combination had shown benefit in the form of synergistic effect and in delaying the resistance to the anti .
In our study patients received 6 cycles of 5-FU based chemotherapy with Panitumumab and patients who had partial response, complete response or stationary disease received metronomic Capecitabine with Panitumumab every 2 weeks for one year. The primary end point was progression free survival (PFS) and the secondary end points were safety, toxicity and overall survival (OS).
The median PFS for all patients was 18 ± 1.4 months and the median OS was 45 months. Patients with synchronous metastasis and those who received Oxaliplatin based regimen with Panitumumab were found to have longer PFS compared to those with metachronous metastasis or those who received other chemotherapy regimen with accepted toxicity profile to the maintenance therapy.
Using Panitumumab with metronomic Capecitabine is considered an accepted maintenance regimen in wild type metastatic colorectal cancer regardless of the primary site.
抗表皮生长因子受体治疗显示可改善转移性结直肠癌的总体中位生存期。多项试验研究了在野生型转移性结直肠癌中使用抗(药物)进行维持治疗,结果令人鼓舞,其中许多试验将化疗与靶向治疗联合使用,这种联合治疗已显示出协同效应,并能延缓对抗(药物)的耐药性。
在我们的研究中,患者接受了6个周期基于5-氟尿嘧啶的化疗联合帕尼单抗,部分缓解、完全缓解或病情稳定的患者每2周接受节拍性卡培他滨联合帕尼单抗治疗,持续一年。主要终点是无进展生存期(PFS),次要终点是安全性、毒性和总生存期(OS)。
所有患者的中位PFS为18±1.4个月,中位OS为45个月。与异时性转移患者或接受其他化疗方案且维持治疗毒性可接受的患者相比,同时性转移患者以及接受基于奥沙利铂方案联合帕尼单抗治疗的患者的PFS更长。
无论原发部位如何,使用帕尼单抗联合节拍性卡培他滨被认为是野生型转移性结直肠癌可接受的维持治疗方案。