A Study for Patients With Recurrent or Metastatic Squamous Cell Head and Neck Cancer

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Eli Lilly and Company
ClinicalTrials.gov Identifier:
NCT01087970
First received: March 15, 2010
Last updated: August 27, 2013
Last verified: August 2013

March 15, 2010
August 27, 2013
August 2010
August 2013   (final data collection date for primary outcome measure)
Progression-free Survival [ Time Frame: From enrollment to the first date of objectively determined progressive disease or death from any cause (tumor assessments performed every other cycle during study treatment, and then every 6 weeks during follow-up period) ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01087970 on ClinicalTrials.gov Archive Site
  • Overall survival [ Time Frame: From enrollment to the date of death from any cause (assessment completed during trial period at least every 3 months) ] [ Designated as safety issue: No ]
  • Proportion of patients having a confirmed Partial Response (PR) or Complete Response (CR) [ Time Frame: From enrollment to objectively determined progressive disease (tumor assessments during study treatment completed at every other cycle untill progressive disease) ] [ Designated as safety issue: No ]
  • Change in Patient-reported health status (EuroQol EQ-5D) [ Time Frame: Baseline, day 1 of every cycle, 30 day follow up ] [ Designated as safety issue: No ]
  • Change from Baseline in Performance Status Scale for Head and Neck Cancer (PSS-HNC) [ Time Frame: Baseline, Day 1 of every cycle, 30 day follow up ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
A Study for Patients With Recurrent or Metastatic Squamous Cell Head and Neck Cancer
Phase 2 Study of Pemetrexed in Combination With Carboplatin or Cisplatin and Cetuximab in Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck

The purpose of this study is to look for an improvement in progression free survival with the combination of pemetrexed, carboplatin (or cisplatin) and cetuximab in patients with recurrent or metastatic squamous cell carcinoma of the head and neck.

Not Provided
Interventional
Phase 2
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Head and Neck Neoplasms
  • Drug: Pemetrexed
    Administered intravenously, for maximum of 6 cycles
    Other Names:
    • Alimta
    • LY231514
  • Drug: Cetuximab
    Administered intravenously, for a maximum of 6 cycles
  • Drug: Carboplatin
    Administered intravenously, for a maximum of 6 cycles
  • Drug: Cisplatin
    Administered intravenously, for a maximum of 6 cycles
Experimental: Triplet Combination Therapy

Cycle 1:

Week 1 - Cetuximab 400mg/m2 on day 1; Pemetrexed 500 mg/m2 on day 1; Carboplatin AUC 5 on day 1 or Cisplatin 75 mg/m2 on day 1

Week 2 - Cetuximab 250 mg/m2 on day 1

Week 3 - Cetuximab 250 mg/m2 on day 1

Cycle 2-6:

Week 1 - Cetuximab 250 mg/m2 on day 1; Pemetrexed 500 mg/m2 on day 1; Carboplatin AUC 5 on day 1 or Cisplatin 75 mg/m2 on day 1

Week 2 - Cetuximab 250 mg/m2 on day 1

Week 3 - Cetuximab 250 mg/m2 on day 1

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

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
108
August 2013
August 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Histologic or cytologic diagnosis of squamous cell head and neck cancer

    • Recurrent disease (locally advanced or metastatic)that is not amenable to local therapy, (i) with at least 6 months since completion of systemic therapy (chemotherapy or biological anticancer therapy), and (ii) with no more than 1 prior multimodal therapy (such as concurrent chemoradiation with or without sequential chemotherapy) for locally advanced HNC tumor, and (iii) with no prior systemic therapy (chemotherapy or biological anticancer therapy) for metastatic disease; OR
    • Newly diagnosed distant metastatic disease (Stage IVc)
  • Prior therapies:

    • Radiation therapy must be completed at least 4 weeks before study enrollment. For palliative therapy, prior radiation therapy allowed <25% of the bone marrow and prior radiation to the whole pelvis is not allowed. Patients must have recovered from the acute toxic effects of the treatment prior to study enrollment.
    • Surgery (excluding prior diagnostic biopsy) must be completed at least 4 weeks before study enrollment. Patients must have fully recovered from any acute effects of surgery prior to study enrollment.
  • An estimated life expectancy of at least 12 weeks.
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
  • Biological tissue available for biomarker analysis on tumor tissue.
  • Disease status must be measurable as defined by RECIST. The index lesion must not be in a prior irradiated area. Positron emission tomography (PET) scans and ultrasounds may not be used for lesion measurements.
  • Patient compliance and geographic proximity that allow for adequate follow-up.
  • Adequate organ function as defined by the following:

    • Bone marrow reserve: absolute neutrophil (segmented and bands) count (ANC) greater than or equal to 1.5 × 109/L, platelets greater than or equal to 100 × 109/L, and hemoglobin greater than or equal to 9 g/dL.
    • Hepatic: bilirubin less than or equal to 1.5 × the upper limit of normal (ULN); alkaline phosphatase (ALP), aspartate aminotransferase (AST), and alanine aminotransferase (ALT) less than or equal to 3.0 × ULN (ALP, AST, and ALT less than or equal to 5.0 × ULN is acceptable if the liver has tumor involvement).
    • Renal: calculated creatinine clearance (CrCl) greater than or equal to 60 mL/min.
  • For women: Must be surgically sterile, postmenopausal, or compliant with a medically approved contraceptive regimen during and for 6 months after the treatment period; must have a negative serum or urine pregnancy test within 7 days before study enrollment, and must not be breast-feeding. For men: Must be surgically sterile or compliant with a contraceptive regimen during and for 6 months after the treatment period.

Exclusion Criteria:

  • 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.
  • Are receiving concurrent chronic systemic immune therapy, or chemotherapy for a disease other than cancer.
  • Concurrent administration of any other antitumor therapy.
  • Known prior allergic/hypersensitivity reaction to any of the components of the study treatment.
  • Serious concomitant systemic disorder (for example, active infection) or psychiatric disorder that, in the opinion of the investigator, would compromise the patient's ability to complete the study.
  • Have serious cardiac disease, such as symptomatic angina, unstable angina, or the history of myocardial infarction in the previous 12 months.
  • Second primary malignancy that is clinically detectable at the time of consideration for study enrollment.
  • Have had another primary malignancy other than HNC, unless that prior malignancy was treated at least 2 years previously with no evidence of recurrence. Exception: Patients with a history of in situ carcinoma of the cervix, nonmelanoma skin cancer, or low-grade (Gleason score less than or equal to 6) localized prostate cancer will be eligible even if diagnosed and treated less than 2 years previously.
  • Nasopharyngeal, paranasal sinus, lip, or salivary gland cancer.
  • Presence of clinically significant (by physical exam) third-space fluid collections; for example, ascites or pleural effusions that cannot be controlled by drainage or other procedures prior to study entry.
  • Have peripheral neuropathy of Common Terminology Criteria for Adverse Events (CTCAE) Grade 1 or higher.
  • Have central nervous system (CNS) metastases (unless the patient has completed successful local therapy for CNS metastases and has been off corticosteroids for at least 4 weeks before starting study therapy). Brain imaging is required in symptomatic patients to rule out brain metastases, but is not required in asymptomatic patients.
  • Inability to interrupt aspirin or other nonsteroidal anti-inflammatory agents, other than an aspirin dose less than or equal to 1.3 grams per day, for a 5-day period (8-day period for long-acting agents, such as piroxicam).
  • Unable or unwilling to take folic acid, vitamin B12, or prophylactic corticosteroids.
  • Recent (within 30 days before enrollment) or concurrent yellow fever vaccination.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01087970
13491, H3E-MC-S132
No
Eli Lilly and Company
Eli Lilly and Company
Not Provided
Study Director: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9AM - 5 PM Eastern Time (UTC/GMT - 5 hours, EST) Eli Lilly and Company
Eli Lilly and Company
August 2013

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