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Trial of Carboplatin/Paclitaxel/Cetuximab in Stage IIIB/IV Non-Small Cell Lung Cancer (NSCLC)

8 avril 2010 mis à jour par: Eli Lilly and Company

A Randomized Phase II Trial of Two Dose Schedules of Carboplatin/Paclitaxel/Cetuximab in Stage IIIB/IV Non-small Cell Lung Cancer

The purpose of the study is to determine if the combination of cetuximab, carboplatin and paclitaxel will shrink a specific type of lung cancer known as non-small cell lung cancer (NSCLC). The safety of this combination will also be evaluated.

Aperçu de l'étude

Statut

Complété

Les conditions

Intervention / Traitement

Description détaillée

Lung cancer is the second most common cancer diagnosed for both genders in the United States. Approximately 173,770 new cases are estimated for 2004. It is the leading cause of cancer deaths in both men and women, with approximately 160,440 deaths estimated for 2004. Prognosis for many is poor if not diagnosed at an early stage, and therapy for advanced disease is limited. The study will test two chemotherapy agents, carboplatin and paclitaxel, in combination with a newly approved drug called cetuximab, which is continuing to be tested in colorectal cancer and other cancers. Cetuximab is a monoclonal antibody, which is believed to work by attaching to an epidermal growth factor receptor (EGFR) on tumor cells and thereby blocking tumor cells from reproducing. It is an antibody to the EGFR. Fifty percent of lung cancers overexpress EGFR.

Rationale:

The present study is built upon the data from previous studies, incorporating cetuximab into each of two regimens of paclitaxel plus carboplatin. The results of prior studies using paclitaxel and carboplatin demonstrate that these drugs in combination, using a variety of schedules, are both safe and effective as therapy for advanced or metastatic NSCLC. The addition of biologic therapy with the anti-EGFR agent cetuximab to the combination will presumably maximize the therapeutic index while keeping toxicity to a minimum in patients with Stage IIIB/IV NSCLC.

Research Hypothesis:

Subjects with previously-untreated stage IIIB/IV NSCLC who receive a combination of paclitaxel, carboplatin, and cetuximab will have a progression-free survival rate greater than that previously reported for subjects receiving the combination of paclitaxel and carboplatin.

Type d'étude

Interventionnel

Inscription (Réel)

165

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

  • États-Unis
    • California
      • Los Angeles, California, États-Unis, 90089
        • ImClone Investigational Site
      • Santa Monica, California, États-Unis, 90404
        • ImClone Investigational Site
    • Delaware
      • Newark, Delaware, États-Unis, 19713
        • ImClone Investigational Site
    • Florida
      • Orlando, Florida, États-Unis, 32804
        • ImClone Investigational Site
      • St. Petersburg, Florida, États-Unis, 33705
        • ImClone Investigational Site
    • Georgia
      • Tucker, Georgia, États-Unis, 30084
        • ImClone Investigational Site
    • Indiana
      • Terra Haute, Indiana, États-Unis, 47804
        • ImClone Investigational Site
    • Kentucky
      • Louisville, Kentucky, États-Unis, 40202
        • ImClone Investigational Site
    • Maryland
      • Baltimore, Maryland, États-Unis, 21204
        • ImClone Investigational Site
    • Michigan
      • Ypsilanti, Michigan, États-Unis, 48197
        • ImClone Investigational Site
    • New Jersey
      • Newark, New Jersey, États-Unis, 07112
        • ImClone Investigational Site
    • North Carolina
      • Chapel Hill, North Carolina, États-Unis, 27599
        • ImClone Investigational Site
    • Pennsylvania
      • Philadelphia, Pennsylvania, États-Unis, 19141
        • ImClone Investigational Site
    • South Carolina
      • Columbia, South Carolina, États-Unis, 29209
        • ImClone Investigational Site
    • Tennessee
      • Knoxville, Tennessee, États-Unis, 37920
        • ImClone Investigational Site
    • Texas
      • Houston, Texas, États-Unis, 77024
        • ImClone Investigational Site
      • Temple, Texas, États-Unis, 76508
        • ImClone Investigational Site
    • Virginia
      • Richmond, Virginia, États-Unis, 23230
        • ImClone Investigational Site
    • Washington
      • Tacoma, Washington, États-Unis, 98405
        • ImClone Investigational Site
    • West Virginia
      • Morgantown, West Virginia, États-Unis, 26506
        • ImClone Investigational Site

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

To be eligible for the study, subjects must fulfill all of the following criteria and have a complete signed informed consent form.

  • Subjects must have signed an approved informed consent.
  • Subjects with histologically or cytologically documented stage IIIB (supraclavicular lymph node, high neck node, or pleural effusion involvement) or IV NSCLC. Disease must be newly diagnosed or recurrent at least 1 year post adjuvant therapy.
  • Subjects with measurable disease.
  • Subjects with ECOG performance status 0-1.
  • Subjects with asymptomatic brain metastasis are eligible; however, they must have completed radiotherapy/radiosurgery at least 2 weeks prior to enrollment and be off steroids.
  • Radiotherapy must have been completed > 2 weeks prior to enrollment and the subject must have recovered from all adverse effects of prior radiotherapy. No previous irradiation to the only area of measurable disease. New lesions that developed in a previously irradiated area will be allowed.
  • If diagnostic tissue or slides are available for a subject, these must be submitted for testing of EGFR status.
  • Subjects ≥18 years of age.
  • Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy throughout the study and for up to 4 weeks after the study in such a manner that the risk of pregnancy is minimized. WOCBP include any female who has experienced menarche and who has not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation or bilateral oophorectomy) or is not postmenopausal [defined as amenorrhea ≥12 consecutive months; or women on hormone replacement therapy (HRT) with documented serum follicle stimulating hormone (FSH) level >35mIU/mL]. Even women who are using oral, implanted or injectable contraceptive hormones or mechanical products such as an intrauterine device or barrier methods (diaphragm, condoms, spermicides) to prevent pregnancy or practicing abstinence or where partner is sterile (e.g., vasectomy), should be considered to be of child bearing potential. WOCBP must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 72 hours prior to the start of study medication.

  • Subjects with adequate hematologic function defined as: ANC ≥1,500/mm 3 ; WBC

    ≥3,000/mm 3 ; platelets ≥100,000/mm 3 ; and hemoglobin ≥9 g/dL.

  • Subjects with adequate hepatic function defined as: total bilirubin ≤1.5 x upper limit of normal (ULN) or AST ≤2.5 x ULN.
  • Subjects with adequate renal function defined as a serum creatinine level ≤1.5 mg/dL or a creatinine clearance ≥60 cc/minute.

Exclusion Criteria:

Any of the following criteria will make the subject ineligible to participate in this study.

  • WOCBP who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to 4 weeks after the study. Subjects who are men must also agree to use effective contraception.
  • WOCBP using a prohibited contraceptive method.
  • Women who are pregnant or breastfeeding.
  • Women with a positive pregnancy test on enrollment or prior to study drug administration.
  • Subjects who have had prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer for which the subject has been disease-free for 5 years.
  • Subjects with significant history of cardiac disease, i.e., uncontrolled hypertension, unstable angina, uncontrolled congestive heart failure, cardiomyopathy with decreased ejection fraction, myocardial infarction within the past year, or cardiac ventricular arrythmias requiring medication.
  • Subjects with an uncontrolled seizure disorder, or active neurological disease.
  • Subjects with symptomatic brain metastasis. Prohibited Therapies and/or Medications
  • Subjects who have received prior systemic chemotherapy. Subjects with no more than one prior adjuvant regimen for initially diagnosed disease are eligible for the study.
  • Subjects with a history of prior cetuximab or other therapy that specifically and directly targets the EGFR pathway.
  • Subject with prior severe infusion reaction to a monoclonal antibody.
  • Subjects with know allergy to Cremophor EL.
  • Subjects with known peripheral neuropathy (> grade 1).
  • Subjects with prior erythropoietin (i.e., Epogen, Procrit) treatment.
  • Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for treatment of either a psychiatric or physical (e.g., infectious disease) illness.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: Arm A (3-week cycle)

Cetuximab was administered weekly at an initial dose (Week 1) of 400 mg/m2 IV infusion and a weekly maintenance dose of 250 mg/m2 IV infusion.

Paclitaxel 225 mg/m2 infused over 180 minutes on Day 1 and subsequently every 3 weeks.

Carboplatin (AUC = 6) was infused over 30 minutes on Day 1 and subsequently every 3 weeks.
Biologique: Cetuximab

(Week 1) of 400 mg/m2 IV infusion and a weekly maintenance dose of 250 mg/m2 IV infusion.

A cycle of therapy was defined as 3 weeks in Arm A and 4 weeks in Arm B.

Autres noms:
  • Erbitux
Médicament: Carboplatin
(AUC = 6) was infused over 30 minutes on Day 1 and subsequently every 3 weeks (AUC = 6) was infused over 30 minutes on Day 1 and subsequently every 4 weeks.
Autres noms:
  • Paraplatine
Médicament: Paclitaxel
225 mg/m2 infused over 180 minutes on Day 1 and subsequently every 3 weeks. OR 100 mg/m2 infused over 180 minutes on Day 1, Day 8 and Day 15 of a 4-week cycle.
Autres noms:
  • Taxol
Comparateur actif: Arm B (4-week cycle)

Cetuximab was administered weekly at an initial dose (Week 1) of 400 mg/m2 IV infusion and a weekly maintenance dose of 250 mg/m2 IV infusion.

Paclitaxel 100 mg/m2 infused over 180 minutes on Day 1, Day 8 and Day 15 of a 4-week cycle.

Carboplatin (AUC = 6) was infused over 30 minutes on Day 1 and subsequently every 4 weeks.
Biologique: Cetuximab

(Week 1) of 400 mg/m2 IV infusion and a weekly maintenance dose of 250 mg/m2 IV infusion.

A cycle of therapy was defined as 3 weeks in Arm A and 4 weeks in Arm B.

Autres noms:
  • Erbitux
Médicament: Carboplatin
(AUC = 6) was infused over 30 minutes on Day 1 and subsequently every 3 weeks (AUC = 6) was infused over 30 minutes on Day 1 and subsequently every 4 weeks.
Autres noms:
  • Paraplatine
Médicament: Paclitaxel
225 mg/m2 infused over 180 minutes on Day 1 and subsequently every 3 weeks. OR 100 mg/m2 infused over 180 minutes on Day 1, Day 8 and Day 15 of a 4-week cycle.
Autres noms:
  • Taxol

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
To estimate median progression free survival and the progression free survival rate
Délai: 6 months
6 months

Mesures de résultats secondaires

Mesure des résultats
Délai
To estimate the overall response rate in each treatment arm
Délai: 6 months
6 months
To estimate median survival and the survival rate at one year in each treatment arm
Délai: 6 months
6 months
To evaluate the toxicity profile of each treatment arm
Délai: 6 months
6 months
To explore the relationship between EGFR expression and the "clinical benefit" received from each treatment regimen
Délai: 6 months
6 months
To evaluate symptom response rate in each treatment arm using the Lung Cancer Subscale (LCS) of the FACT-L
Délai: 6 months
6 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Eli Lilly and Company

Collaborateurs

Bristol-Myers Squibb

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 novembre 2004

Achèvement primaire (Réel)

1 avril 2007

Achèvement de l'étude (Réel)

1 avril 2007

Dates d'inscription aux études

Première soumission

18 novembre 2004

Première soumission répondant aux critères de contrôle qualité

18 novembre 2004

Première publication (Estimation)

19 novembre 2004

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

9 avril 2010

Dernière mise à jour soumise répondant aux critères de contrôle qualité

8 avril 2010

Dernière vérification

1 avril 2010

Plus d'information

Termes liés à cette étude

Mots clés

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • CA225-058

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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