Perrier Marine, Scoazec Jean-Yves, Walter Thomas
Université Reims Champagne-Ardenne, Department of Gastroenterology and Digestive Oncology, Reims University Hospital, Reims, France.
Department of Surgical and Molecular Pathology, Gustave Roussy, Villejuif, France.
Ther Adv Med Oncol. 2023 Apr 29;15:17588359231171041. doi: 10.1177/17588359231171041. eCollection 2023.
According to the neuroendocrine tumour (NET) characteristics, 3 to 7 different treatment options are available, corresponding to 6 to 5,040 theoretical different sequences. Even though each patient is unique and despite a large heterogeneity in NET characteristics, the present review aims to discuss the main sequences and addresses how one can propose the best sequence to treat metastatic NET (mNET) on a case-by-case basis. Each treatment must be discussed during dedicated multi-disciplinary meetings, and inclusions in clinical trials should be favoured. After a thorough characterization of patients and their mNET, and taking into account the availability of drugs, the first-line treatment should be chosen according to the treatment aim. The latter is determined based on three main topics (efficacy, safety, and patient preferences) that do not necessarily converge and must be defined . At baseline, physicians should design an full therapeutic sequence, which may evolve at each step depending on the response to previous treatment, the occurrence of chronic toxicities, and the patients' perception of the prior treatment. To improve knowledge in terms of effectiveness and risk of cumulative toxicities regarding the different sequences, real-world data using long follow-up durations are necessary; such issues will not be resolved by randomized clinical trials.
根据神经内分泌肿瘤(NET)的特征,有3至7种不同的治疗选择,对应6至5040种理论上不同的治疗顺序。尽管每个患者都是独特的,且NET特征存在很大异质性,但本综述旨在讨论主要的治疗顺序,并探讨如何根据具体病例为转移性NET(mNET)提出最佳治疗顺序。每次治疗都必须在专门的多学科会议上进行讨论,并且应优先考虑纳入临床试验。在对患者及其mNET进行全面特征分析并考虑药物可用性后,应根据治疗目标选择一线治疗方案。治疗目标基于三个主要方面(疗效、安全性和患者偏好)来确定,这三个方面不一定一致,必须明确界定。在基线时,医生应设计一个完整的治疗方案,该方案可能会根据对先前治疗的反应、慢性毒性的发生以及患者对先前治疗的感受在每个步骤中发生变化。为了提高对不同治疗顺序的有效性和累积毒性风险的认识,需要使用长期随访的真实世界数据;此类问题无法通过随机临床试验解决。