基线营养和运动状态对 I 期和 II 期肿瘤临床试验参与者毒性和结局的影响。

Impact of Baseline Nutrition and Exercise Status on Toxicity and Outcomes in Phase I and II Oncology Clinical Trial Participants.

机构信息

Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.

Department of Biostatistics, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.

出版信息

Oncologist. 2020 Feb;25(2):161-169. doi: 10.1634/theoncologist.2019-0289. Epub 2019 Nov 20.

Abstract

BACKGROUND

Malnutrition and physical inactivity are common in patients with advanced cancer and are associated with poor outcomes. There are increasing data that altered body composition is related to the pharmacokinetic properties of cancer therapies. These adverse conditions may impact outcomes in early-phase oncology clinical trials.

MATERIALS AND METHODS

We aimed to understand the relationships between baseline nutrition and exercise status with important trial endpoints including treatment-related toxicity and survival. Baseline assessments of nutrition and exercise status were conducted in patients prior to initiation of phase I and II oncology clinical trials. Patients were followed prospectively for the onset of adverse events. Tumor response and survival data were also obtained. Fisher's exact test and chi-square analysis were used to determine statistical significance. Kaplan-Meier curves were used to compare patient duration on study and survival.

RESULTS

One hundred patients were recruited, of whom 87 were initiating a phase I trial. Sixty percent were initiating trials studying immunotherapeutic agents. Critical malnutrition was found in 39% of patients, and 52% were sedentary. Patients who were malnourished had significantly increased rates of grade ≥ 3 toxicity (p = .001), hospitalizations (p = .001), and inferior disease control rate (p = .019). Six-month overall survival was significantly reduced in malnourished patients versus nonmalnourished patients (47% vs. 84%; p = .0003), as was median duration on study (48 days vs. 105 days; p = .047). Being sedentary at baseline was associated with decreased duration on study (57 days vs. 105 days; p = .019).

CONCLUSION

Malnutrition and sedentary lifestyle are highly prevalent in patients enrolling on early-phase oncology clinical trials and are associated with poor outcomes. The quality of data from these studies may be compromised as a result of these pre-existing conditions.

IMPLICATIONS FOR PRACTICE

Phase I and II trials are critical steps in the development of effective cancer therapeutics, yet only a small percentage of agents are ultimately approved for human cancer care. Despite increasing awareness of the interactions between malnutrition, sarcopenia, and treatment-related outcomes such as toxicity and response, these factors are not commonly incorporated into therapeutic decision making at the time of clinical trial consideration. Nutritional status and physical performance may be key biomarkers of mechanisms mediating treatment-related toxicity, dose modifications, risk of hospitalizations, and success of novel agents. This study advocates that a baseline nutritional assessment and early nutritional support may improve tolerability and response to experimental therapies.

摘要

背景

营养不良和身体活动不足在晚期癌症患者中很常见,并且与不良预后相关。越来越多的数据表明,身体成分的改变与癌症治疗的药代动力学特性有关。这些不良情况可能会影响早期肿瘤临床试验的结果。

材料和方法

我们旨在了解基线营养和运动状况与重要试验终点之间的关系,包括与治疗相关的毒性和生存。在开始进行 I 期和 II 期肿瘤临床试验之前,对患者进行基线营养和运动状况评估。前瞻性地对患者进行不良事件的随访。还获得了肿瘤反应和生存数据。使用 Fisher 确切检验和卡方分析确定统计学意义。使用 Kaplan-Meier 曲线比较患者的研究持续时间和生存。

结果

共招募了 100 名患者,其中 87 名患者开始进行 I 期试验。60%的患者开始研究免疫治疗药物。39%的患者存在严重营养不良,52%的患者久坐不动。营养不良的患者毒性≥3 级的发生率显著增加(p =.001),住院率(p =.001)和疾病控制率较低(p =.019)。与营养良好的患者相比,营养不良的患者 6 个月的总生存率明显降低(47% vs. 84%;p =.0003),中位研究持续时间也缩短(48 天 vs. 105 天;p =.047)。基线时久坐不动与研究持续时间缩短有关(57 天 vs. 105 天;p =.019)。

结论

在参加早期肿瘤临床试验的患者中,营养不良和久坐不动的生活方式非常普遍,并且与不良结局相关。由于这些预先存在的条件,这些研究的数据质量可能会受到影响。

实践意义

I 期和 II 期试验是开发有效癌症治疗方法的关键步骤,但最终只有一小部分药物被批准用于人类癌症治疗。尽管人们越来越意识到营养不良、肌肉减少症和与治疗相关的毒性和反应等之间的相互作用,但在考虑临床试验时,这些因素通常不被纳入治疗决策。营养状况和身体表现可能是介导与治疗相关的毒性、剂量调整、住院风险和新型药物疗效的关键生物标志物。本研究提倡基线营养评估和早期营养支持可能会提高对实验性治疗的耐受性和反应性。

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