Cisplatinum/Pemetrexed Versus Split-dose Cisplatinum/Pemetrexed In NSCLC

NCT01742767 | Unknown Phase 2 DMC

• 1 other identifier: 2011-001963-37
• Study Type: interventional
• Target: N/A
• Locations: 1 country
• Sites: 1

Brief Summary

Cisplatinum and pemetrexed (ALIMTA®) has become an effective first-line regimen for advanced and inoperable non-squamous NSCLC without somatic activating mutations of epidermal growth factor receptor (EGFR). In the standard regimen the cisplatinum dose is 75 mg/m2 on day 1 of a 21-day cycle. Due to the high platinum-dose patients do need a strict hyperhydration and often have to be hospitalized for survey. Split-dose cisplatinum with two administrations on Day 1 and 8 of a 21-day-cycle has already been administered in other platin-containing chemotherapy regimens (cis/gem cis/nav cis/paclitaxel cis/docetaxel) with favourable toxicity profiles and generally with an excellent patient compliance.

Conditions

NSCLC

Keywords

NSCLC; split dose Cisplatinum; Pemetrexed

Outcome Measures

Primary Outcomes (1)

• Response rate

  3 years

Study Arms (2)

Cis (D1) + Pem (D1)

ACTIVE COMPARATOR

Cisplatinum 75 mg/m2 d 1 Pemetrexed 500 mg/m2 d 1 q d 21

Drug: Cisplatinum; Drug: Pemetrexed

CIS (D1+8) + Pem (D!)

EXPERIMENTAL

Cisplatinum 40 mg/m2 d 1 + d 8 Pemetrexed 500 mg/m2 d 1 q d 21

Drug: Cisplatinum; Drug: Pemetrexed

Interventions

Cisplatinum DRUG

CIS (D1+8) + Pem (D!); Cis (D1) + Pem (D1)

Pemetrexed DRUG

CIS (D1+8) + Pem (D!); Cis (D1) + Pem (D1)

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients are eligible to be included in the study only if they meet all of the following criteria:
• Histologically or cytologically confirmed diagnosis of non-squamous-cell non-small cell lung cancer (NSCLC) Stage IV (American Joint Committee on Cancer Staging Criteria \[AJCC\], Version 7, 2009)
• No prior systemic chemotherapy for lung cancer
• At least one unidimensionally measurable lesion meeting Response Evaluation Criteria in Solid Tumours (RECIST; version 1.1, Eisenhauer et al. 2009), longest diameter ≥10 mm with computed tomography (CT) scan \[CT scan slice thickness no greater than 5 mm\] , or ≥ 20 mm with chest x-ray. Positron emission tomography (PET) scans and ultrasounds should not be used.
• ECOG performance status of 0 or 1 (Oken et al. 1982)
• ≥ 18 years of age \< 75 years
• Adequate organ function,
• Prior radiation therapy allowed to \<25% of the bone marrow (Cristy and Eckerman 1987). Prior radiation to the whole pelvis is not allowed. Prior radiotherapy must be completed at least 4 weeks before study enrollment. Patients must have recovered from the acute toxic effects of the treatment prior to study enrollment.
• Patient must understand and sign an informed consent document before the start of specific protocol procedures.
• A pretreatment FFPE tumour biopsy must be available for central biomarker analysis. If consented by the patient and clinically feasible, a fresh pretreatment biopsy is obtained and submitted for central biomarker analysis.
• Female patients with childbearing potential must use highly effective methods of contraception (combined oral contraceptives, hormon-releasing intrauterine contraceptive device, hormonal contraceptive implants, hormonal contraceptive injectables) or have sexual intercourse with a vasectomised partner only during and for 6 months after the study and their pregnancy test must be negative within 7 days prior to study enrollment.
• A female subject is considered to be of childbearing potential unless she is age ≥ 50 years and naturally amenorrhoeic for ≥ 2 year or unless she is surgically sterile.
• Male patients must agree to use condoms during the study and for 6 months after the study if their partner is of childbearing potential and does not use highly effective method of contraception.
• Estimated life expectancy of 12 weeks
• Patient compliance and geographic proximity that allow adequate follow up.

You may not qualify if:

• Patients will be excluded from the study if they meet any of the following criteria:
• Active participation in other clinical studies or treatment with any experimental drug within 30 days prior to study enrollment or during study participation.
• Patients with known somatic activating mutations of EGFR, as these patients should be offered EGFR- tyrosine kinase inhibitor (EGFR-TKI) treatment as first-line therapy. Detection of EGFR mutations and additional somatic mutations with relation to treatment will be performed centrally at the Universitätsklinikum Essen. In case immediate treatment initiation is required for medical reasons (such as superior vena cava syndrome, severely symptomatic disease) patients may be enrolled before results from EGFR testing are available. As EGFR-TKI treatment is equally effective in second-line therapy, such patients may remain on study treatment if a clinical benefit is derived.
• Peripheral neuropathy of ³CTCAE Grade 1
• Inability to comply with protocol or study procedures
• A serious concomitant systemic disorder that, in the opinion of the investigator, would compromise the patient's ability to complete the study.
• A serious cardiac condition, such as myocardial infarction within 6 months prior to study enrollment, symptomatic coronary artery disease, cardiac arrhythmia, or other heart disease, as defined by the New York Heart Association Class III or IV (functional capacity)
• Second primary malignancy that is clinically detectable at the time of consideration for study enrollment
• Documented brain metastases unless the patient has completed successful local therapy for central nervous system metastases and has been off of corticosteroids for at least 4 weeks before enrollment. Brain imaging is required in symptomatic patients to rule out brain metastases,but is not required in asymptomatic patients
• The effect of third space fluid, such as pleural effusion and ascites, on pemetrexed is unknown. In patients with clinically significant third space fluid, consideration should be given to draining the effusion prior to pemetrexed administration.
• Significant weight loss (that is 10%) over the previous 6 weeks before study entry
• Significant hearing function impairment, especially high-frequency hearing function impairment
• Any active or uncontrolled infection
• Concurrent administration of any other antitumour therapy
• Inability to interrupt aspirin or other nonsteroidal anti-inflammatory agents, other than an aspirin dose \<1.3 grams per day, for a 5-day period (8-day period for long-acting agents, such as piroxicam)

Sponsors & Collaborators

• Universität Duisburg-Essen: lead
• Eli Lilly and Company: collaborator

Study Sites (1)

University hospital essen

Essen, North Rhine-Westphalia, 45122, Germany

RECRUITING

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell Lung

Interventions

Cisplatin; Pemetrexed

Condition Hierarchy (Ancestors)

Carcinoma, Bronchogenic; Bronchial Neoplasms; Lung Neoplasms; Respiratory Tract Neoplasms; Thoracic Neoplasms; Neoplasms by Site; Neoplasms; Lung Diseases; Respiratory Tract Diseases

Intervention Hierarchy (Ancestors)

Chlorine Compounds; Inorganic Chemicals; Nitrogen Compounds; Platinum Compounds; Guanine; Hypoxanthines; Purinones; Purines; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds; Glutamates; Amino Acids, Acidic; Amino Acids; Amino Acids, Peptides, and Proteins; Amino Acids, Dicarboxylic

Study Officials

• Wilfried Eberhardt, MD

  Universital hospital essen

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Wilfried Eberhardt, MD

CONTACT

00492017232011; wilfried.eberhardt@uk-essen.de

Mathias Hoiczyk

CONTACT

00492017232011; mathias.hoiczyk@uk-essen.de

Study Design

• Study Type: interventional
• Phase: phase 2
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Physician

Study Record Dates

• First Submitted: December 3, 2012
• First Posted: December 5, 2012
• Study Start: November 1, 2012
• Primary Completion: May 1, 2014
• Study Completion: April 1, 2015
• Last Updated: December 5, 2012

Record last verified: 2012-12

Locations

DE (1)