Mielgo-Rubio Xabier, Rojo Federico, Mezquita-Pérez Laura, Casas Francesc, Wals Amadeo, Juan Manel, Aguado Carlos, Garde-Noguera Javier, Vicente David, Couñago Felipe
Department of Medical Oncology, Hospital Universitario Fundación Alcorcón, Madrid 28922, Spain.
Department of Pathology, IIS-Jiménez Díaz-CIBERONC Foundation, Madrid 28040, Spain.
World J Clin Oncol. 2020 Nov 24;11(11):898-917. doi: 10.5306/wjco.v11.i11.898.
After publication of the PACIFIC trial results, immune checkpoint inhibitor-based immunotherapy was included in the treatment algorithm of locally advanced non-small cell lung cancer (NSCLC). The PACIFIC trial demonstrated that 12 mo of durvalumab consolidation therapy after radical-intent platinum doublet chemotherapy with concomitant radiotherapy improved both progression-free survival and overall survival in patients with unresectable stage III NSCLC. This is the first treatment in decades to successfully improve survival in this clinical setting, with manageable toxicity and without deterioration in quality of life. The integration of durvalumab in the management of locally advanced NSCLC accentuates the need for multidisciplinary, coordinated decision-making among lung cancer specialists, bringing new challenges and controversies as well as important changes in clinical work routines. The aim of the present article is to review-from a practical, multidisciplinary perspective-the findings and implications of the PACIFIC trial. We evaluate the immunobiological basis of durvalumab as well as practical aspects related to programmed cell death ligand 1 determination. In addition, we comprehensively assess the efficacy and toxicity data from the PACIFIC trial and discuss the controversies and practical aspects of incorporating durvalumab into routine clinical practice. Finally, we discuss unresolved questions and future challenges. In short, the present document aims to provide clinicians with a practical guide for the application of the PACIFIC regimen in routine clinical practice.
在PACIFIC试验结果公布后,基于免疫检查点抑制剂的免疫疗法被纳入局部晚期非小细胞肺癌(NSCLC)的治疗方案中。PACIFIC试验表明,对于不可切除的III期NSCLC患者,在进行根治性铂类双药化疗并同步放疗后,使用度伐利尤单抗巩固治疗12个月可改善无进展生存期和总生存期。这是数十年来首次在这种临床情况下成功提高生存率的治疗方法,毒性可控且生活质量没有下降。度伐利尤单抗纳入局部晚期NSCLC的治疗凸显了肺癌专家之间进行多学科、协调决策的必要性,带来了新的挑战和争议以及临床工作流程的重要变化。本文的目的是从实用的多学科角度回顾PACIFIC试验的结果及其意义。我们评估了度伐利尤单抗的免疫生物学基础以及与程序性细胞死亡配体1检测相关的实际问题。此外,我们全面评估了PACIFIC试验的疗效和毒性数据,并讨论了将度伐利尤单抗纳入常规临床实践的争议和实际问题。最后,我们讨论了未解决的问题和未来的挑战。简而言之,本文旨在为临床医生在常规临床实践中应用PACIFIC方案提供实用指南。