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

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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

View Eligibility Criteria

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

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

43

Study ID:

NCT00216216

Recruitment Status:

Terminated

Sponsor:

Hoosier Cancer Research Network

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There are 16 Locations for this study

See Locations Near You

Helen F. Graham Cancer Center
Newark Delaware, 19713, United States
Medical & Surgical Specialists, LLC
Galesburg Illinois, 61401, United States
Elkhart Clinic
Elkhart Indiana, 46515, United States
Oncology Hematology Associates of SW Indiana
Evansville Indiana, 47714, United States
Fort Wayne Oncology & Hematology, Inc
Fort Wayne Indiana, 46815, United States
Center for Cancer Care at Goshen Health System
Goshen Indiana, 46527, United States
Indiana University Cancer Center
Indianapolis Indiana, 46202, United States
Community Regional Cancer Center
Indianapolis Indiana, 46256, United States
Arnett Cancer Care
Lafayette Indiana, 47904, United States
Medical Consultants, P.C.
Muncie Indiana, 47303, United States
Center for Cancer Care, Inc., P.C.
New Albany Indiana, 47150, United States
Northern Indiana Cancer Research Consortium
South Bend Indiana, 46601, United States
Northern Indiana Oncology Associates
South Bend Indiana, 46617, United States
AP&S Clinic
Terre Haute Indiana, 47804, United States
Siteman Cancer Center
St. Louis Missouri, 63110, United States
Methodist Cancer Center
Omaha Nebraska, 68114, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

43

Study ID:

NCT00216216

Recruitment Status:

Terminated

Sponsor:


Hoosier Cancer Research Network

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