Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

Preoperative Pemetrexed and Carboplatin for Select Stage IB, II, and III Non-Squamous Non-Small-Cell Lung Cancer

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Eli Lilly and Company
Information provided by (Responsible Party):
SCRI Development Innovations, LLC
ClinicalTrials.gov Identifier:
NCT00906282
First received: May 19, 2009
Last updated: December 27, 2013
Last verified: December 2013

May 19, 2009
December 27, 2013
June 2009
July 2015   (final data collection date for primary outcome measure)
To determine the overall survival rate at 3 years. [ Time Frame: 54 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00906282 on ClinicalTrials.gov Archive Site
  • To determine the objective tumor response. [ Time Frame: 54 months ] [ Designated as safety issue: No ]
  • To determine the pathologic tumor response rate (complete/partial) in patients with potentially resectable stage IB, II, and III non-squamous non-small-cell lung cancer receiving preoperative (neoadjuvant) therapy. [ Time Frame: 54 months ] [ Designated as safety issue: No ]
  • To determine the complete resection rate. [ Time Frame: 54 months ] [ Designated as safety issue: No ]
  • To assess post-surgical morbidity/mortality. [ Time Frame: 54 months ] [ Designated as safety issue: No ]
  • To assess progression-free survival (PFS). [ Time Frame: 54 months ] [ Designated as safety issue: No ]
  • To assess overall survival. [ Time Frame: 54 months ] [ Designated as safety issue: No ]
  • To identify predictive factors of overall survival and PFS. [ Time Frame: 54 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Preoperative Pemetrexed and Carboplatin for Select Stage IB, II, and III Non-Squamous Non-Small-Cell Lung Cancer
Phase II Trial of Preoperative Pemetrexed and Carboplatin in Patients With Select Stage IB, II, and III Non-Squamous Non-Small-Cell Lung Cancer

The purpose of this multi-center Phase II trial is to examine the impact of pemetrexed/carboplatin in the preoperative treatment of patients with select stage IB, II,and III non-squamous NSCLC. Because patients with non-squamous type NSCLC have been shown to have better survival rates than patients with squamous tumors when given pemetrexed with a platinum agent, only patients with non-squamous NSCLC (adenocarcinoma, large cell, and undifferentiated), not including squamous histology, will be allowed to participate in this study. If this novel regimen proves to be safe and active in this setting, it will provide rationale for further investigation in a larger, prospective, randomized trial.

Not Provided
Interventional
Phase 2
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Non Small Cell Lung Cancer
  • Drug: Pemetrexed
    500 mg/m2 IV over 10 minutes on Day 1 of every 3-week (21-day) treatment cycle for a total of 4 cycles (12 weeks).
    Other Name: Alimta
  • Drug: Carboplatin
    AUC=6 IV on Day 1 of every 3-week (21-day) treatment cycle for a total of 4 cycles (12 weeks).
    Other Name: 41575-94-4
Experimental: Pemetrexed/Carboplatin

4 cycles of preoperative treatment as follows:

Pemetrexed: 500 mg/m2 given intravenously (IV) over 10 minutes on Day 1 of every 21-day treatment cycle

Carboplatin: AUC=6 given IV on Day 1 of every 21-day treatment cycle

Interventions:
  • Drug: Pemetrexed
  • Drug: Carboplatin
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
46
December 2015
July 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Age >=18 years.
  2. Histologically-confirmed NSCLC (adenocarcinoma, large cell, and undifferentiated). Patients with squamous histology are not eligible.
  3. Life expectancy of at least 12 weeks.
  4. Patients with the following stages of NSCLC:

    • T2 N0 tumors: Limited to tumors >=4 cm.
    • T1-2 N1 tumors.
    • T3 N0-1 tumors (excluding superior sulcus tumors): Including tumors involving the chest wall, proximal airway, or mediastinal pleura where preoperative radiotherapy is not planned.
    • T1-2 N2 tumors: For patients with N2 disease involving one zone (Upper zone (R), AP zone (L), subcarinal zone, or lower zone) and nodes <=2cm in diameter.
    • T4 N0-1 tumors (excluding superior sulcus tumors): T4 lesions other than malignant effusions where radiotherapy is not planned.
  5. Patients with clinical N2 involvement must have histologic confirmation by mediastinoscopy (or alternate biopsy procedure).
  6. Tumors should be considered potentially resectable.
  7. No evidence of extrathoracic metastatic disease.
  8. Patients must have measurable disease by RECIST criteria.
  9. Patients must be candidates (medically) for chemotherapy followed by surgical resection.
  10. Adequate recovery from recent surgery. At least 1 week must have elapsed from the time of a minor surgery; at least 3 weeks must have elapsed from the time of a major surgery.
  11. Laboratory values as follows:

    • Absolute neutrophil count (ANC) >=1500/μL
    • Hemoglobin (Hgb) >=10 g/dL
    • Platelets >=100,000/uL
    • AST/SGOT and ALT/SGPT within normal limits (WNL)
    • Total bilirubin within normal limits (WNL)
    • Calculated creatinine clearance >=45 mL/min
  12. ECOG Performance Status grade 0 or 1.
  13. The ability to interrupt NSAIDS 2 days before (5 days for long-acting NSAIDs), the day of, and 2 days following administration of Alimta.
  14. The ability to take folic acid, Vitamin B12, and dexamethasone according to protocol.
  15. Women of childbearing potential must have a negative serum or urine pregnancy test performed within 7 days prior to start of treatment. Women of childbearing potential or men with partners of childbearing potential must use effective birth control measures during treatment. If a woman becomes pregnant or suspects she is pregnant while participating in this study, she must agree to inform her treating physician immediately.
  16. Patient must be accessible for treatment and follow-up.
  17. Patients must be able to understand the investigational nature of this study and give written informed consent prior to study entry.

Exclusion Criteria:

  1. Patients with the following stages are excluded:

    • T1 N0;
    • T2 N0, with primary tumor <4 cm;
    • T1-2 N2, with multiple zones of N2 involvement;
    • T3-4 N2;
    • Any N3;
    • Any TxNxM1 disease; or
    • Any stage where surgery and/or chemoradiotherapy is the preferred initial approach in management, as deemed by the treating physician.
  2. Squamous or predominant squamous mixed histologies.
  3. Mixed small-cell and non-small cell histologies.
  4. Pulmonary carcinoid tumors.
  5. Presence of third space fluid which cannot be controlled by drainage.
  6. Use of erythropoietin as a hematopoietic growth factor is not allowed.
  7. Cardiac disease, including: congestive heart failure (CHF) > Class II per New York Heart Association (NYHA) classification; unstable angina (anginal symptoms at rest) or new-onset angina (i.e., began within the last 3 months), or myocardial infarction within the past 6 months; symptomatic CHF, unstable angina pectoris, cardiac arrhythmia, or cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.
  8. Women who are pregnant (positive pregnancy test) or lactating.
  9. Use of any non-approved or investigational agent within 30 days of administration of the first dose of study drug.
  10. Patients may not receive any other investigational or anti-cancer treatments while participating in this study.
  11. Concurrent severe, intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements.
  12. Mental condition that would prevent patient comprehension of the nature of, and risk associated with, the study.
  13. History of hypersensitivity to active or inactive excipients of any component of treatment.
  14. Inability to comply with study and/or follow-up procedures.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00906282
SCRI LUN 186
No
SCRI Development Innovations, LLC
SCRI Development Innovations, LLC
Eli Lilly and Company
Study Chair: David R Spigel, M.D. SCRI Development Innovations, LLC
SCRI Development Innovations, LLC
December 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP