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

2026년 4월 24일 업데이트: 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.

연구 개요

상태

완전한

개입 / 치료

연구 유형

관찰

등록 (실제)

25

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Pontevedra
      • Vigo, Pontevedra, 스페인, 36312
        • University Hospital Complex of Vigo

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

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.

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
개입 / 치료
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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Gender
기간: Day 0, During the consultation
Patient gender (Female, Male)
Day 0, During the consultation
Age
기간: Day 0, During the consultation
Patient age in years
Day 0, During the consultation
Stage of NSCLC
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Diagnosis of malnutrition
기간: 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
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Claudia Barca Díez, Galicia Sur Health Research Institute

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2024년 3월 20일

기본 완료 (실제)

2024년 5월 24일

연구 완료 (실제)

2024년 7월 12일

연구 등록 날짜

최초 제출

2026년 4월 24일

QC 기준을 충족하는 최초 제출

2026년 4월 24일

처음 게시됨 (실제)

2026년 4월 30일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 4월 30일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 4월 24일

마지막으로 확인됨

2026년 4월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

삶의 질에 대한 임상 시험

Unic group에 대한 임상 시험

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