Non Small Cell Lung Cancer
Conditions
Brief summary
Mistletoe extract is one of the most common complementary treatments used in Europe. Recent basic studies reported tumor response and survival prolongation in number of treatments with Mistletoe preparations. There are evidence based data for using this drug as side effect reducer when use in combination with chemotherapy regimen treatment. Other clinical data, although not well based is that complementary treatment when used in combination with the common oncology treatment has tumor response effect. Combinations with platinum compound and a third generation cytotoxic agent have been accepted as 'standard of care' for patients with advanced NSCLC. The combination of platinum compound and one of the new agents are associated with response rates of 30-40% and a median survival of 8-11 months for advanced NSCLC patients with good performance status. Study objective: Improvement in QOL, Improvement in the toxicity profile of the chemotherapy treatment.
Detailed description
The study design is to include 90 subjects. All subjects are treated with the common chemotherapy treatment. 50 percent will be treated with Iscador as combination with their common chemotherapy regimen. Common chemotherapy regimen used for NSCLC: Carboplatin and Gemcitabine. All study participants will receive this same chemotherapy regimen. This chemotherapy treatment is given every 3 weeks for up to 6 treatment cycles. The first day of the first treatment cycle, the combination of both Carboplatin and Gemcitabine will be administered. After a week (day 8 of treatment cycle) only Gemcitabine will be administered. Drugs would be calculated according to patient's body mass, renal function and general appearance. Once the patient signed Informed Consent he is assigned randomly to be treated with/without the injections of Mistletoe (called Iscador). Patient will receive the study medication (Iscador) as an intravenous injection that can be self injected or injected by any other of the family. Injections would be administered with low dose at the first week of the first treatment cycle and then, dose would be escalated, so as to check high sensitivity to the drug. Dosage would include: 2 injections of 0.1 mg, 2 injections of 0.1 mg and 2 injections of 1 mg. After that, treatment would continue with dosage of 10 g once every 2 days. Patients from both treatment arms would be asked to fill-out QOL questionnaires at every treatment cycle and at follow-up visit after. Study Primary Objectives: 1. Improvement in QOL 2. Improvement in the toxicity profile of the chemotherapy treatment Secondary Objectives: 1. Improvement in time to tumor progression (TTP) and survival. 2. Safety profile of mistletoe extract with combination of chemotherapy treatment This is a single center study, randomized phase II, with patients with advanced NSCLC treated with carboplatin/gemcitabine chemotherapy combination.
Interventions
The drug will be administered 3 times a week at home.
Sponsors
Weleda AG
Rambam Health Care Campus
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Age above 18 years 2. Histology proven of NSCLC 3. Stage IIIB or IV (TNM classification) 4. Performance status \< 2 (ECOG classification 5. Measurable disease with one or more disease sites measured by computed tomography (CT) 6. Life expectancy of more than 12 weeks. 7. Treatment combination of gemcitabine/carboplatin (GC) 8. Sign of written informed consent -
Exclusion criteria
1. Prior chemotherapy 2. Prior radiation- allowed as long as the treatment was not targeted only site of measurable disease and given more than 3 weeks before entry the trial. 3. Central nervous system metastases 4. Hypercalcemia 5. Other life threatening medical conditions 6. Patients not able to comply with s.c. injections
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Quality Of Life | During the trial | To check the effect of the treatment(or lack of it) on the quality of life of the patients enrolled to the trial. |
| Improvement in QOL. Improvement in the toxicity profile of the chemotherapy treatment | During all the trial | To check on the difference in QoL of all patients. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Objective Response | During all the duration of the trial | The patients are asked to answer questions and the doctor will check blood works resolts. |
| Improvement in time to tumor progression (TTP) and survival Safety profile of mistletoe extract with combination of chemotherapy treatment | During duration of all the trial | Looking out for difference in toxicity profile of all patients |
Countries
Israel
Outcome results
None listed