多种癌症类型围手术期免疫疗法试验中的后续疗法概况

Karl Semaan, Rashad Nawfal, Elizabeth Nally, Yelena Y Janjigian, Caroline Robert, Solange Peters, Thomas Powles, Toni K Choueiri
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引用次数: 0

摘要

接受后续治疗的患者最初,我们评估了对照组中在无病生存事件后接受任何后续治疗(包括手术、放疗或系统治疗)的患者人数。在所考察的 15 项 ICI 围手术期试验中,只有 8 项试验提供了接受任何后续治疗的患者人数数据。在黑色素瘤临床试验中,69例患者中有62例(89-8%)(CheckMate 76K)和323例患者中有282例(87-3%)(EORTC 18071)发生了无病生存事件。在15项ICI围手术期试验中,有13项提供了接受后续系统治疗的患者人数数据。在黑色素瘤试验中,115例患者中有44例(38-2%)(KEYNOTE-716)、69例患者中有49例(71-0%)(CheckMate 76K)、302例患者中有218例(72-2%)(KEYNOTE-054)发生无病生存事件后接受了系统治疗。在 NSCLC 试验中,131 例(61-8%)患者接受了后续免疫疗法我们随后回顾了对照组或非试验组中出现无病生存事件的患者中接受后续全身免疫疗法的比例。在黑色素瘤试验KEYNOTE-716和KEYNOTE-054(这两项试验是唯一有内置交叉试验的试验)中,115例(KEYNOTE-716)和302例(KEYNOTE-054)无病生存事件患者中分别有35例(30-4%)和195例(64-6%)接受了ICI作为后续治疗。在 NSCLC 试验中,212 名患者中有 102 人(48-1%)接受了非免疫性后续系统治疗。5 化疗一直被认为是治疗转移性尿路上皮癌患者的全球标准疗法,在全球范围内均可使用。为了进一步了解肿瘤复发后的各种情况,我们创建了围手术期试验中报告后续疗法的真实情况的可视化图表,特别关注 KEYNOTE-564 中的肾细胞癌(附录 p.3),这是实体瘤中唯一一项具有总体生存获益的纯辅助免疫疗法试验。我们想说明的是,对后续疗法的分析具有时间依赖性和复杂性。例如,在围手术期试验中,似乎只有一部分患者接受了后续治疗,这表明在实践中,从教育和医疗系统组织到标准和创新治疗的可及性,还有一些需求没有得到满足。临床试验数据收集方面的潜在差距也是可能的,这可归因于对长期临床试验患者的跟踪,甚至是适当输入数据方面的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Landscape of subsequent therapies in perioperative immunotherapy trials across multiple cancer types

Section snippets

Patients receiving subsequent therapy

Initially, we assessed the number of patients in the control groups who underwent any subsequent treatment (including surgery, radiotherapy, or systemic therapy) after a disease-free survival event. Among the 15 perioperative ICI trials examined, only eight trials provided data on the number of patients receiving any subsequent therapy. In the melanoma clinical trials, 62 (89·8%) of 69 patients (CheckMate 76K) and 282 (87·3%) of 323 patients (EORTC 18071) who had a disease-free survival event

Patients receiving subsequent systemic therapy

We examined the number of patients who underwent systemic therapy following disease-free survival events in the control group. Among the 15 perioperative ICI trials examined, 13 provided data on the number of patients receiving subsequent systemic therapy. In the melanoma trials, 44 (38·2%) of 115 patients (KEYNOTE-716), 49 (71·0%) of 69 (CheckMate 76K), and 218 (72·2%) of 302 (KEYNOTE-054) who experienced a disease-free survival event received systemic therapy. In the NSCLC trials, 131 (61·8%)

Patients receiving subsequent immunotherapy

We then reviewed the proportion of patients receiving subsequent systemic immunotherapy among the patients who experienced a disease-free survival event in the control or non-experimental group. In the melanoma trials KEYNOTE-716 and KEYNOTE-054, which were the only trials with a built-in cross-over, 35 (30·4%) of 115 patients (KEYNOTE-716) and 195 (64·6%) of 302 (KEYNOTE-054) with a disease-free survival event received ICI as subsequent therapy. In the NSCLC trials, 102 (48·1%) of 212 patients

Non-immune subsequent systemic therapy

Relapses after surgery in some types of cancers are typically aggressive and surveillance or local therapies are not recommended. An example is urothelial carcinoma, for which regular radiology monitoring within adjuvant trials should enable early detection, necessitating timely intervention.5 Chemotherapy has been considered the global standard of care for the management of patients with metastatic urothelial carcinoma and is globally available. Therefore, upon relapse, most patients should

Real-world scenarios after recurrence

To further understand the vast range of scenarios following tumour relapses, we created a visualisation of real-world instances of reporting subsequent therapies in perioperative trials, specifically focusing on renal cell carcinoma from KEYNOTE-564 (appendix p 3), the only pure adjuvant immunotherapy trial in solid cancers with an overall survival benefit. Our point was to illustrate that analyses of subsequent therapies are time-dependent and complex. For instance, by capturing subsequent

Discussion

Only a subset of patients seem to receive subsequent therapies in perioperative trials, suggesting some unmet needs in practice, from education and health-system organisation to accessibility to standard and innovative treatments. Potential gaps in clinical trials data collection are also possible and could be attributed to challenges in keeping track of patients in long-term clinical trials, or even entering data appropriately.11, 12 A review by Fitzpatrick and colleagues13 showed that longer
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