Clareo Health | Trial of Pemetrexed or Pemetrexed With Gemcitabine for Patients With Advanced Lung Cancer Who Are Not Eligible for Platinum-Based Chemotherapy and Have Not Previously Been Treated With Chemotherapy
Trial of Pemetrexed or Pemetrexed With Gemcitabine for Patients With Advanced Lung Cancer Who Are Not Eligible for Platinum-Based Chemotherapy and Have Not Previously Been Treated With Chemotherapy
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Eli Lilly and Company
Age
70–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
histologically or cytologically confirmed NSCLC not amenable to surgery or radiotherapy of curative intent
locally advanced or metastatic Stage IIIb (with N3 supraclavicular or T4 for pleural effusion) or IV NSCLC
no prior chemotherapy
measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria (Therasse et al. 2000)
You may not be if
have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry
have symptomatic brain metastases
have a history or presence of other malignancy except in situ carcinoma of the cervix or adequately treated basal cell carcinoma of the skin or prior malignancy treated more than 5 years before without recurrence (excluding melanoma, breast cancer and hypernephroma)
are unable to interrupt therapy with aspirin or other nonsteroidal anti-inflammatory drugs (NSAIDs) such as naproxen, piroxicam, diflunisal, or nabumetone around each dose of pemetrexed (5 days for short-acting or 8 days for long acting preparations)
are unable or unwilling to take steroids
are unable or unwilling to take folic acid or vitamin B12 supplementation
have clinically detectable (by physical examination) third-space fluid collections; for example, ascites or pleural effusions that cannot be controlled by drainage or other procedures prior to study entry
have other serious concomitant illness or medical conditions according to investigator criteria, including but not limited to the following:
* congestive heart failure or angina pectoris, except if it is medically controlled
* previous history of myocardial infarction within 1 year from study entry, uncontrolled hypertension, or arrhythmias
* active infection requiring iv antibiotics
* active ulcer, unstable diabetes mellitus, or other contra-indication to corticotherapy
