We hypothesize that chemotherapy-induced changes in exhaled metabolites in lung cancer can be detected by changes in VOC profiles (smell-prints) measured by the eNose.
ID
Bron
Verkorte titel
Aandoening
electronic nose
smell-print
exhaled breath
lung cancer
chemotherapy
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary objective is to investigate whether the eNose can discriminate the smellprints obtained before and after 1 cycle of chemotherapy in patients with specific histological types of lung cancer (NSCLC: adenocarcinoma, squamous cell carcinoma and SCLC).
Achtergrond van het onderzoek
Therefore in the present study, we hypothesize that chemotherapy-induced changes in exhaled metabolites in lung cancer can be detected by changes in VOC profiles (smell-prints) measured by the eNose.
Objectives:
1. The primary objective of this study is to investigate whether the eNose can discriminate the smellprints obtained before and after 1 cycle of chemotherapy in patients with specific histological types of lung cancer (NSCLC: adenocarcinoma, squamous cell carcinoma and SCLC);
2. The secondary objectives are:
a. To investigate whether the eNose can discriminate between the baseline smellprints of patients with different histological types of lung cancer (NSCLC: adenocarcinoma, squamous cell carcinoma and SCLC);
b. To investigate whether the baseline smellprint (pre chemotherapy) is related to
i. the stage of the disease according to the stage grouping of the Mountain classification (NSCLC) [21] or division into LD or ED (SCLC) [2].
ii. metabolic activity of the disease as assessed by Standard Uptake Value (SUV) on PET-CT scan.
c. To investigate whether the potential change in smellprint after 1 cycle of chemotherapy is related to tumour response (determined after the second cycle of chemotherapy) as assessed by changes in tumour size and classified according to the RECIST criteria.
Study design:
prospective, observational study.
Scheme:
0 1 15 22 (day)
I___I chemotherapyI_________________I________________I
1 2 3 (visit)
At the Pulmonary Function Department each participant will follow this sequence per visit:
1. questionnaire;
2. exhaled breath collection;
3. spirometry.
1. STUDY POPULATION;
1.1 Population;
Patients with newly diagnosed adenocarcinoma or squamous cell carcinoma stage IIIA, IIIB or IV or small cell lung cancer who are scheduled for their first cycle of chemotherapy at the department of pulmonary diseases.
1.2 Inclusion criteria;
-Informed consent is obtained.
-newly diagnosed adenocarcinoma or squamous cell carcinoma stage IIIA, IIIB or IV or small cell lung cancer).
-Adults 18-80 years.
-scheduled for chemotherapy as first part of the treatment:
Cisplatin/Gemcitabine (NSCLC) and Cisplatin/Etoposide (SCLC).
1.3 Exclusion criteria;
-Previous chemotherapy;
-unable to evaluate response with the RECIST criteria;
-unable to follow the instructions for the eNose measurement.
1.4 Sample size calculation.
This is an observational study with descriptive statistic analysis.
The sample size was calculated for the primary question whether the eNose measurements (smellprints) change during the first chemotherapy cycle. Our intention is to have at least 80% power for the case that the mean difference between the eNose measurements at baseline and after the first chemotherapy cycle is 0.5 SD or more.
This is achieved when we include 25 patients per group or more.
Doel van het onderzoek
We hypothesize that chemotherapy-induced changes in exhaled metabolites in lung cancer can be detected by changes in VOC profiles (smell-prints) measured by the eNose.
Onderzoeksopzet
Day 1(before first cycle of chemotherapy), day 15 (after chemo) and day 22 (just before second chemo).
Onderzoeksproduct en/of interventie
N/A
Publiek
MCL
Leeuwarden
J. Maten, van der
Leeuwarden
The Netherlands
+31 (0)58 286 6190
j.maten@znb.nl
Wetenschappelijk
MCL
Leeuwarden
J. Maten, van der
Leeuwarden
The Netherlands
+31 (0)58 286 6190
j.maten@znb.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Informed consent is obtained;
2. newly diagnosed adenocarcinoma or squamous cell carcinoma stage IIIA, IIIB or IV or small cell lung cancer);
3. adults 18-80 years;
4. scheduled for chemotherapy as first part of the treatment:
Cisplatin/Gemcitabine (NSCLC) and Cisplatin/Etoposide (SCLC).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Previous chemotherapy;
2. unable to evaluate response with the RECIST criteria;
3. unable to follow the instructions for the eNose measurement.
Opzet
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