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

24. dubna 2026 aktualizováno: 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.

Přehled studie

Postavení

Dokončeno

Intervence / Léčba

Typ studie

Pozorovací

Zápis (Aktuální)

25

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní místa

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

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

Ne

Metoda odběru vzorků

Vzorek nepravděpodobnosti

Studijní populace

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.

Popis

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.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

Kohorty a intervence

Skupina / kohorta
Intervence / Léčba
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.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Gender
Časové okno: Day 0, During the consultation
Patient gender (Female, Male)
Day 0, During the consultation
Age
Časové okno: Day 0, During the consultation
Patient age in years
Day 0, During the consultation
Stage of NSCLC
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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)
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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)
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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)
Časové okno: 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
Časové okno: 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

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Diagnosis of malnutrition
Časové okno: 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
Časové okno: 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
Časové okno: 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

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Vyšetřovatelé

  • Vrchní vyšetřovatel: Claudia Barca Díez, Galicia Sur Health Research Institute

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Aktuální)

20. března 2024

Primární dokončení (Aktuální)

24. května 2024

Dokončení studie (Aktuální)

12. července 2024

Termíny zápisu do studia

První předloženo

24. dubna 2026

První předloženo, které splnilo kritéria kontroly kvality

24. dubna 2026

První zveřejněno (Aktuální)

30. dubna 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

30. dubna 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

24. dubna 2026

Naposledy ověřeno

1. dubna 2026

Více informací

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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