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Nutritional Assessment of Patients With Non-small Cell Lung Cancer Treated With Osimertinib (NUTRI-CPNM)

2026年4月24日 更新者:Fundacin Biomedica Galicia Sur

Nutritional assessment of patients with non-small cell lung cancer treated with osimertinib.

Non-small-cell lung cancer (NSCLC) accounts for approximately 85% of all lung cancer cases and is a leading cause of morbidity and mortality worldwide. Between 35% and 65% of NSCLC patients experience nutritional problems or malnutrition, which significantly affects their prognosis and quality of life. This study aims to describe the nutritional status and body composition of NSCLC patients treated with osimertinib, an oral tyrosine kinase inhibitor, while also assessing the prevalence of sarcopenia, presarcopenia, and dynapenia. Additionally, we explore the relationship between dose-limiting toxicities (DLTs) and nutritional status, as well as the impact of nutritional status on quality of life using the EQ-5D scale.

研究概览

研究类型

观察性的

注册 (实际的)

25

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Pontevedra
      • Vigo、Pontevedra、西班牙、36312
        • University Hospital Complex of Vigo

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

Patients diagnosed with NSCLC undergoing treatment with osimertinib in the Vigo Health Area, who receive pharmaceutical care in the Outpatient Clinics of the Pharmacy Service of the Álvaro Cunqueiro Hospital.

描述

Inclusion Criteria:

  • Patients over 18 years of age.
  • Patients diagnosed with NSCLC.
  • Patients undergoing osimertinib treatment who collect their medication at the Pharmacy Outpatient Clinic of the Álvaro Cunqueiro Hospital.
  • Patients who have consented to participate by signing the informed consent form.

Exclusion Criteria:

  • Patients who have discontinued osimertinib treatment.
  • Patients currently receiving osimertinib treatment for an indication other than those authorized in the product information (compassionate use).
  • Patients who do not sign the informed consent form.

Withdrawal criteria:

- Revocation of consent to participate in the study by the patient.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Unic group
Patients diagnosed with NSCLC undergoing treatment with osimertinib in the Vigo Health Area, who receive pharmaceutical care in the Outpatient Clinics of the Pharmacy Service of the Álvaro Cunqueiro Hospital.

To describe the nutritional status and body composition of patients diagnosed with non-melanoma skin cancer (NMSC) treated with osimertinib in the Vigo health area.

To evaluate the prevalence of sarcopenia in the study patients.

To observe if there is a relationship between low muscle mass or malnutrition and the development of delayed-type hyperplasia (DTH) during osimertinib treatment.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Gender
大体时间:Day 0, During the consultation
Patient gender (Female, Male)
Day 0, During the consultation
Age
大体时间:Day 0, During the consultation
Patient age in years
Day 0, During the consultation
Stage of NSCLC
大体时间:Day 0, During the consultation
Non-Small Cell Lung Cancer (NSCLC) is staged from 0 to IV based on tumor size (T), lymph node involvement (N), and metastasis (M).
Day 0, During the consultation
Start date of Osimertinib treatment
大体时间:Day 0, During the consultation
Date of initiation of osimertinib therapy as recorded in the medical record.
Day 0, During the consultation
Initial and current osimertinib dose
大体时间:Day 0, During the consultation
Dose of osimertinib in milligrams (mg/day) at treatment initiation and at the time of assessment.
Day 0, During the consultation
Total duration of osimertinib treatment
大体时间:Day 0, During the consultation
Total duration of osimertinib therapy calculated from treatment initiation to discontinuation or last follow-up, expressed in days.
Day 0, During the consultation
Dose-limiting toxicities (DLTs)
大体时间:Day 0, During the consultation
Incidence and type of dose-limiting toxicities experienced during osimertinib treatment, graded according to CTCAE criteria. The most common DLTs included diarrhea, mucositis, folliculitis, nausea, thrombocytopenia, paronychia, and elevated transaminases.
Day 0, During the consultation
Body weight
大体时间:Day 0, During the consultation
Body weight measured in kilograms (kg). The tools used for anthropometric data collection included a weighing scale with an integrated stadiometer (Asimed® brand, manufactured by Sibelmed, Barcelona, Spain) and an anthropometric measuring tape.
Day 0, During the consultation
Height
大体时间:Day 0, During the consultation
Height measured in meters (m). The tools used for anthropometric data collection included a weighing scale with an integrated stadiometer (Asimed® brand, manufactured by Sibelmed, Barcelona, Spain) and an anthropometric measuring tape.
Day 0, During the consultation
Calf circumference
大体时间:Day 0, During the consultation
Calf circumference measured in centimeters (cm) at the point of maximum circumference. The tools used for anthropometric data collection included a weighing scale with an integrated stadiometer (Asimed® brand, manufactured by Sibelmed, Barcelona, Spain) and an anthropometric measuring tape.
Day 0, During the consultation
Body mass index (BMI)
大体时间:Day 0, During the consultation
Body mass index calculated as weight in kilograms divided by height in meters squared (kg/m²).
Day 0, During the consultation
Usual body weight
大体时间:Day 0, During the consultation
Self-reported usual body weight prior to disease or treatment, measured in kilograms (kg).
Day 0, During the consultation
Weight loss during treatment
大体时间:Day 0, During the consultation
Percentage and absolute change in body weight from baseline during osimertinib treatment. It was calculated using the following formula: %WL = [(usual weight - current weight)/usual weight] × 100
Day 0, During the consultation
Food intake recall
大体时间:Day 0, During the consultation
Dietary intake assessed 24-hour food recall, including total caloric and macronutrient intake.
Day 0, During the consultation
Fat mass (FM) by bioimpedance
大体时间:Day 0, During the consultation

Fat mass measured in kilograms using bioelectrical impedance analysis (BIA) the InBody S10® body composition analyzer (manufactured by InBody Co., Ltd., Seoul, Republic of Korea), was used, which is a device that measures impedance using 6 frequencies (1, 5, 50, 250, 500, and 1000 kHz) for each of the 5 body segments: right arm, left arm, trunk, right leg, and left leg.

The measurements were performed with patients standing barefoot, with their legs apart and arms not touching the torso. The 8-point tactile electrodes were placed on the thumb and middle finger of each hand and on both ankles. The data obtained were analyzed using the LookinBody 120® software.

Day 0, During the consultation
Lean body mass (LBM) by bioimpedance
大体时间:Day 0, During the consultation

Lean body mass measured in kilograms using bioelectrical impedance analysis (BIA) the InBody S10® body composition analyzer (manufactured by InBody Co., Ltd., Seoul, Republic of Korea), was used, which is a device that measures impedance using 6 frequencies (1, 5, 50, 250, 500, and 1000 kHz) for each of the 5 body segments: right arm, left arm, trunk, right leg, and left leg.

The measurements were performed with patients standing barefoot, with their legs apart and arms not touching the torso. The 8-point tactile electrodes were placed on the thumb and middle finger of each hand and on both ankles. The data obtained were analyzed using the LookinBody 120® software.

Day 0, During the consultation
Lean body mass index (LBMI)
大体时间:Day 0, During the consultation

Lean body mass index calculated as lean body mass divided by height squared (kg/m²). A reduced muscle mass was considered for LBMI < 17 kg/m2 in men and <15 kg/m2 in women. Using bioelectrical impedance analysis (BIA) the InBody S10® body composition analyzer (manufactured by InBody Co., Ltd., Seoul, Republic of Korea), was used, which is a device that measures impedance using 6 frequencies (1, 5, 50, 250, 500, and 1000 kHz) for each of the 5 body segments: right arm, left arm, trunk, right leg, and left leg.

The measurements were performed with patients standing barefoot, with their legs apart and arms not touching the torso. The 8-point tactile electrodes were placed on the thumb and middle finger of each hand and on both ankles. The data obtained were analyzed using the LookinBody 120® software.

Day 0, During the consultation
Muscle functionality
大体时间:Day 0, During the consultation
Muscle functionality was assessed through hand grip strength using a hydraulic dynamometer (Jamar®, manufactured by Performance Health, Warrenville, IL, USA), providing the strength of the dominant arm (kg). Three measurements were taken with the subject seated and without arm support, with a 60 s rest between each measurement to prevent muscle fatigue. Dynapenia or reduced strength was considered if the value was <27 kg in men and <16 kg in women.
Day 0, During the consultation

次要结果测量

结果测量
措施说明
大体时间
Diagnosis of malnutrition
大体时间:Day 0, During the consultation

Following GLIM criteria (Global Leadership Initiative on Malnutrition):

Phenotypic Criteria:

  • Involuntary weight loss: >5% in the last 6 months or >10% in more than 6 months.
  • Low BMI: <20 kg/m2 if <70 years or <22 kg/m2 if ≥70 years.
  • Muscle mass evaluation: assessed by LBMI (BIA) or by CC if BIA was not performed.
  • Etiological Criteria:
  • Reduced food intake or absorption: ≤50% of energy requirements for more than

    1 week, any reduction for more than 2 weeks, or any chronic gastrointestinal condition negatively affecting food absorption or assimilation.

  • Inflammation or acute/chronic disease: the presence of inflammatory conditions or chronic diseases affecting nutritional status.

The combination of at least one phenotypic criterion and one etiological criterion enabled the diagnosis of malnutrition. The etiological criterion of inflammation, required for the diagnosis of malnutrition, was met in all study patients as they were diagnosed with NSCLC.

Day 0, During the consultation
Sarcopenia detection and diagnosis
大体时间:Day 0, During the consultation

Applying the EWGSOP2 algorithm proposed by the European Working Group on Sarcopenia in Older People (EWGSOP).

The screening was performed using the Strength, Assistance walking, Rise from a chair, Climb stairs, and Falls (SARC-F) questionnaire, and a score of 4 or higher was considered to indicate a risk of sarcopenia. Muscle strength was determined by dynamometry, and BIA or CC assessed muscle mass. Patients with low muscle strength were classified as dynapenic; presarcopenia was diagnosed in patients showing reduced muscle mass and no significant decrease in muscle strength; finally, sarcopenia was diagnosed in patients who, in addition to low hand grip strength, also exhibited a reduction in muscle mass.

Day 0, During the consultation
Quality of Life of the patients
大体时间:Day 0, During the consultation
It was assessed using the EQ-5D scale, a standardized tool that measures five dimensions of health: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Additionally, patients completed a visual Analog scale (VAS) ranging from 0 to 100, reflecting their general health status.
Day 0, During the consultation

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Claudia Barca Díez、Galicia Sur Health Research Institute

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2024年3月20日

初级完成 (实际的)

2024年5月24日

研究完成 (实际的)

2024年7月12日

研究注册日期

首次提交

2026年4月24日

首先提交符合 QC 标准的

2026年4月24日

首次发布 (实际的)

2026年4月30日

研究记录更新

最后更新发布 (实际的)

2026年4月30日

上次提交的符合 QC 标准的更新

2026年4月24日

最后验证

2026年4月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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