- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07559526
Nutritional Assessment of Patients With Non-small Cell Lung Cancer Treated With Osimertinib (NUTRI-CPNM)
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.
Panoramica dello studio
Stato
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Contatti e Sedi
Luoghi di studio
-
-
Pontevedra
-
Vigo, Pontevedra, Spagna, 36312
- University Hospital Complex of Vigo
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Metodo di campionamento
Popolazione di studio
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
|---|---|
|
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. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Gender
Lasso di tempo: Day 0, During the consultation
|
Patient gender (Female, Male)
|
Day 0, During the consultation
|
|
Age
Lasso di tempo: Day 0, During the consultation
|
Patient age in years
|
Day 0, During the consultation
|
|
Stage of NSCLC
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Diagnosis of malnutrition
Lasso di tempo: Day 0, During the consultation
|
Following GLIM criteria (Global Leadership Initiative on Malnutrition): Phenotypic Criteria:
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
Lasso di tempo: 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
Lasso di tempo: 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
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Claudia Barca Díez, Galicia Sur Health Research Institute
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Manifestazioni neurologiche
- Malattie del sistema nervoso
- Manifestazioni neuromuscolari
- Disturbi della nutrizione
- Neoplasie per sede
- Neoplasie
- Condizioni patologiche, anatomiche
- Malattie delle vie respiratorie
- Malattie polmonari
- Neoplasie delle vie respiratorie
- Neoplasie toraciche
- Neoplasie polmonari
- Carcinoma, broncogeno
- Neoplasie bronchiali
- Atrofia muscolare
- Atrofia
- Condizioni patologiche, segni e sintomi
- Malattie nutrizionali e metaboliche
- Segni e sintomi
- Malnutrizione
- Carcinoma, polmone non a piccole cellule
- Sarcopenia
Altri numeri di identificazione dello studio
- NUTRI-CPNM
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Qualità della vita
-
Rush University Medical CenterCompletatoAdvanced Cardiac Life Support, rianimazione cardiopolmonare, volume corrente, ventilazione manualeStati Uniti
-
Ewha Womans UniversityCompletatoEquilibrio posturale | Focus of Study is Effects of Neuromuscular Training | PilatesCorea del Sud
-
National Taiwan University HospitalNon ancora reclutamento
-
Research Unit Of General Practice, CopenhagenUniversity of Copenhagen; Region Capital Denmark; The Copenhagen General Practice... e altri collaboratoriCompletato
-
Indiana UniversityReclutamentoEcografia Point of Care (POCUS)Stati Uniti
-
Kirsehir Ahi Evran UniversitesiReclutamentoFocus of AttentionTurchia (Türkiye)
-
University Health Network, TorontoNon ancora reclutamento
-
National Taiwan University HospitalCompletatoEcografia Point-of-careTaiwan
-
Asociacion Española Primera en SaludIntensive Care Unit Pasteur HospitalCompletatoEcografia Point of CareUruguay
-
Aga Khan UniversityThe Hospital for Sick Children; Grand Challenges CanadaSconosciuto
Prove cliniche su Unic group
-
Universidad Central de VenezuelaCompletatoPulpite | Terapia canalare | Pulpite - Irreversibile | PulpotomiaVenezuela
-
Bursa City HospitalReclutamentoBlocco regionale per il controllo del dolore | Chirurgia toracoscopica videoassistita | Funzioni polmonari | Blocchi regionaliTacchino
-
Sandra BucciUniversity of Edinburgh; NHS Lothian; Manchester University NHS Foundation Trust; Greater Manchester Mental Health NHS Foundation Trust e altri collaboratoriCompletatoAbusi sessuali su minori, confermati, sequelRegno Unito
-
Istituto Scientifico Italiano Colonna VertebraleAttivo, non reclutanteScoliosi idiopatica adolescenziale (AIS)Italia
-
M.D. Anderson Cancer CenterCompletatoTumori pediatriciStati Uniti
-
Northwell HealthThe Cleveland Clinic; University of Kansas Medical Center; Cedars-Sinai Medical... e altri collaboratoriReclutamentoProlasso della valvola mitraleStati Uniti
-
University of LisbonAssociacao Protectora dos Diabeticos de PortugalCompletato
-
Rush University Medical CenterCompletato
-
Greater Manchester Mental Health NHS Foundation...Manchester University NHS Foundation Trust; University of Manchester; Anna Freud... e altri collaboratoriCompletatoProblema di salute mentaleRegno Unito
-
Sunnybrook Health Sciences CentreRitiratoIl focus dello studio è sugli atteggiamenti del dentista nei confronti delle misurazioni della pressione arteriosaCanada