Lung Cancer Clinical Trial
Pemetrexed in Patients With Chemosensitive and Chemoresistant Relapsed Small Cell Lung Cancer
Summary
Patients with relapsed or chemotherapy-refractory SCLC have a dismal prognosis. Unfortunately, available treatments result in few durable responses. Pemetrexed is a well-tolerated agent, which is active in NSCLC. Since chemotherapy agents, which are active in NSCLC, are usually also active in SCLC, this trial will examine the efficacy and activity of pemetrexed in this palliative setting
Full Description
OUTLINE: This is a multi-center study.
Pemetrexed 500 mg/m2 i.v. q 3 wks
All patients will also receive folic acid 350-1000 mcg. po once daily beginning approximately 1 week prior to the first dose of pemetrexed and continuing until completion of pemetrexed, Vitamin B12 1000 mcg. IM every 9 weeks beginning approximately 1 week prior to the first dose of pemetrexed and continuing until completion of pemetrexed, and dexamethasone 4 mg po bid the day before, the day of, and the day following each treatment with pemetrexed
Chest x-ray will be performed prior to each cycle (if other disease assessment by imaging is not performed) in order to ensure patients are not rapidly progressing.
Cycles are repeated every 3 weeks for up to 6 cycles or PD or intolerable side effects.
Performance Status: ECOG 0, 1, or 2
Life Expectancy: Not specified
Hematopoietic:
WBC > 3000/mm3
ANC > 1500/mm3
Platelet count > 100,000/mm3
Hemoglobin > 8 g/dL
Hepatic:
Bilirubin < 1.0 X upper limit of normal
Aspartate aminotransferase (AST, SGOT) < 2.5 x upper limit of normal. AST may be < 5 x upper limit of normal for patients with liver metastasis
Renal:
Creatinine clearance of > 45 ml/ min (by Cockcroft-Gault)
Cardiovascular:
No unstable or uncompensated cardiovascular conditions
Pulmonary:
No unstable or uncompensated respiratory conditions
Eligibility Criteria
Inclusion Criteria:
Histological or cytological proof of neuroendocrine cancers (including small cell cancers of any site [including lung] or poorly differentiated neuroendocrine cancers of the lung with (unidimensionally) measurable disease as per the RECIST criteria
Chemoresistant or chemosensitive disease
Patients must have received treatment with at least one but not more than 2 prior chemotherapy regimens, including one regimen containing a platinum agent
Radiation therapy must have completed their radiation at least 14 days prior to being registered for protocol therapy, and toxicities due to radiation must have recovered to < grade 1 or baseline prior to registration
Negative pregnancy test
Exclusion Criteria:
No clinically significant infections as judged by the treating investigator
No symptomatic CNS metastasis
No radiation to > 25% of the marrow containing spaces
No previous treatment with pemetrexed
No uncontrolled pleural effusions
No current breastfeeding
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There are 16 Locations for this study
Newark Delaware, 19713, United States
Galesburg Illinois, 61401, United States
Elkhart Indiana, 46515, United States
Evansville Indiana, 47714, United States
Fort Wayne Indiana, 46815, United States
Goshen Indiana, 46527, United States
Indianapolis Indiana, 46202, United States
Indianapolis Indiana, 46256, United States
Lafayette Indiana, 47904, United States
Muncie Indiana, 47303, United States
New Albany Indiana, 47150, United States
South Bend Indiana, 46601, United States
South Bend Indiana, 46617, United States
Terre Haute Indiana, 47804, United States
St. Louis Missouri, 63110, United States
Omaha Nebraska, 68114, United States
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