Non-small Cell Lung Cancer Metastatic, Quality of Life of Patients
Conditions
Brief summary
A national, multicenter, blind, randomized study of three groups, designed to evaluate the impact on the quality of life of IGEN-0206 (IGEN-0206 is a nutritional product, a food) with nutritional support + standard treatment versus nutritional support + standard treatment versus standard treatment in patients with non-lung cancer metastatic microcytic. The standard treatment can include any line of active treatment (chemotherapy, immunotherapy, biological therapies or targeted therapies), radiotherapy or nonspecific symptomatic treatment. It will include 280 patients older than 18 years, who have a life expectancy of less than 9 months, who will receive or not active treatment. After signing the informed consent and confirmation that the subject meets the eligibility criteria, those will be randomized (2: 2: 1 ratio) to receive treatment: * Group A (112 patients): patients will receive their standard treatment + nutritional support + IGEN-0206 * Group B (112 patients): patients will receive their standard treatment + nutritional support + placebo. * Group C (56 patients): patients will receive standard treatment. The allocation will be random 2: 2: 1 and will be stratified according to ECOG 1 versus 2-3, type of oncological treatment (chemotherapy, immunotherapy and / or radiotherapy versus targeted therapies versus symptomatic treatment) and type of cancer (squamous versus not flaky). The present study seeks to demonstrate that IGEN-0206 improves the quality of life and the nutritional status of patients with non-small cell lung cancer. If an improvement in the quality of life is achieved, this could impact on a reduction in the number of treatment delays / omissions, which could secondarily impact on a response and survival benefit (by improving the relative intensity of the active oncological treatment).
Interventions
DIETARY_SUPPLEMENTIGEN0206
Group A
OTHERPlacebo
Group B
Sponsors
Igen BioLab SLU
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient who has given informed consent in writing, stating that he / she understands the purpose of the study and the procedures it entails, and that he / she agrees to participate. * Patient with metastatic non-small cell lung carcinoma confirmed by Pathology. * Expected life expectancy exceeding 12 weeks. * Age ≥18 years. * Functional status of the ECOG 1-3. * Patients who can consume at least 500 ml per day of the nutritional supplement, added to their diet. * Patients who do not meet criteria for renal failure: the glomerular filtrate, calculated by local formula, must be ≥60 ml / min / 1.73m2. * Patients who are willing to communicate the use of nutritional supplements, including oral supplements, vitamins and mineral supplements and / or any food supplement * Patients who are willing to comply with the protocol procedures after having been thoroughly informed about the treatment, the procedures, reviewing the study methodology and signing the informed consent. * They speak fluent Spanish in order to be able to complete the questionnaires of the study. * Potentially fertile women must be negative in a serum pregnancy test performed within 7 days prior to entry into the study. Potentially fertile patients participating in this study should use effective contraceptive methods (eg, abstinence, intrauterine device, oral or injectable contraceptives, double-barrier method, or surgical sterilization) to prevent pregnancy, which they will begin to use as of signature of the informed consent document and whose use will continue until at least 13 weeks after the last dose of the study medication has been administered.
Exclusion criteria
* Women who are pregnant and / or breast-feeding. * Persistence of the toxicity of a previous treatment (grade\> 1 of the NCI-CTCAE v. 4.03); However, alopecia and sensory neuropathy of grade ≤ 2 are acceptable, as well as other side effects that do not endanger patient safety in the opinion of the researcher. * Evidence of severe or uncontrolled systemic disease or concomitant process that, in the opinion of the investigator, makes the participation of the subject in the study inadvisable or compromises compliance with the protocol. * Dementia or mental state significantly altered that could interfere in the understanding and granting of informed consent. * Parkinson's disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Impact of IGEN-0206 on quality of life in patients with metastatic lung cancer according to the EORTC QLQ-C30. | 52 weeks | The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. Thus a high score for a functional |
| Impact of IGEN-0206 on quality of life in patients with metastatic lung cancer according to the EORTC QLQ-L13 | 52 weeks | The QLQ-LC13 incorporates one multi-item scale to assess dyspnoea, and a series of single items assessing pain, coughing, sore mouth, dysphagia, peripheral neuropathy, alopecia, and haemoptysis. All of the scales and single-item measures range in score from 0 to 100. A high score for the scales and single items represents a high level of symptomatology or problems |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| BMI | 52 weeks | Compare clinical benefits in terms of body mass index (BMI) in the three treatment arms. |
| Changes in the microbiota | 12 weeks | Compare changes in the microbiota profile in terms of microbiota metabolism (faecal samples) in the three treatment arms with proteomics and genomics methods. |
| Interleukin levels | 52 weeks | To evaluate the changes in the inflammatory and immune response and to identify immunological biomarkers in the blood with predictive power and prognosis. |
| Cytokines levels | 52 weeks | To evaluate the changes in the inflammatory and immune response and to identify immunological biomarkers in the blood with predictive power and prognosis. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Number of Adverse events | 52 weeks | To compare adverse events (AEs) in the three treatment groups according to the Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4.1. |
| Progression-free survival | 52 weeks | Time from randomization until the progression of the disease or death from any cause is documented. To compare the efficacy in terms of response and survival among the three arms of the study. |
| Overall survival | 52 weeks | Time elapsed from randomization until death is documented for any reason |
| Objective response rate | 52 weeks | The sum of the complete and partial answers |
| Disease control | 52 weeks | The sum of stable disease and partial / total response. |
| Number of oncological treatment interruptions | 52 weeks | To assess tolerability in terms of interruptions or delays in active oncological treatment by adding IGEN-0206 |
Countries
Spain
Outcome results
None listed