Ignite Creation Date:
2024-05-05 @ 11:59 AM
Last Modification Date:
2024-10-26 @ 9:18 AM
Study NCT ID:
NCT00203931
Status:
TERMINATED
Last Update Posted:
2014-03-31
First Post:
2005-09-12
Brief Title:
Trial Comparing Cetuximab With PemetrexedCetuximab Therapy for Non-Small Cell Lung Cancer
Sponsor:
University of Chicago
Organization:
University of Chicago
Study Overview
Official Title:
A Randomized Phase II Trial Comparing Cetuximab With Concurrent PemetrexedCetuximab Therapy for Non-Small Cell Lung Cancer Refractory to Primary Treatment
Status:
TERMINATED
Status Verified Date:
2014-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Slow accrual and evidence from other studies showing benefit of early initiation of pemetrexed after first-line therapy
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of the study is to determine in patients with Non Small Cell Lung Cancer refractory to previous chemotherapy whether concomitant treatment with cetuximab and pemetrexed improves progression-free survival compared with cetuximab monotherapy
Detailed Description:
While EGFR inhibitors have demonstrated activity against NSCLC their integration into first-line therapy in combination with standard agents has yielded disappointing results There are many potential reasons for the disappointing results in these first-line studies A single-arm Phase I trial of cetuximab in combination with docetaxel suggested better efficacy in second-line therapy for NSCLC than docetaxel alone but this comes at the expense of some increased toxicity Preliminary data indicate that cetuximab has single agent activity in this setting The confidence intervals for this activity overlap the median time to progression of the current second-line cytotoxic therapy options compared in the Hanna study A clinically relevant question is- does concurrent cetuximab and pemetrexed significantly improve upon outcomes of cetuximab monotherapy followed by pemetrexed monotherapy
Many patients who receive EGFR inhibitors develop an acneiform rash and the severity of the rash is associated with good outcomes from treatment Several of these studies have demonstrated no correlation between the intensity or percentage of tumor cells staining for EFUR expression and response to therapy However a Phase II study at the University of Colorado of cetuximab added to standard first-line treatment of NSCLC revealed 610 responders developed the rash within 2 weeks of initiating treatment Personal Communication Dugan et al BMS Therefore early development of rash may be a clinically useful marker of subsequent response and novel approaches to the identification of biological markers for this phenotype prior to initiation of therapy may be helpful in subsequent determination of which patients will most likely benefit from EGFR inhibitor therapy
To address these issues we propose a phase I randomized study of concurrent pemetrexedcetuximab compared to sequential cetuximabpemetrexed therapy for the second-line treatment of advanced NSCLC Patients will be randomized at study entry Regarding prospective analysis of the rapid-rash forming phenotype all patients will receive 2 weeks of initial treatment with cetuximab and undergo formal rash evaluation serum and skin collection According to the initial randomization half of the study subjects will continue with cetuximab monotherapy while the remainder will receive concurrent cetuximab and pemetrexed The primary study endpoint of freedom from progression and secondary endpoint of objective response rate will be based on the comparison of patients in he concurrent therapy group with patients treated with cetuximab monotherapy with Day-14 first receipt of cetuximab as the reference treatment start date Overall survival will be analyzed as a secondary endpoint to assess the efficacy of concomitant treatment with cetuximab and pemetrexed compared to sequential treatment with cetuximab followed by pemetrexed upon disease progression As patients in both treatment arms receive cetuximab correlative studies will be performed on all enrolled patients For serum proteomic studies designed to identify a serum polypeptide signature associated with response to cetuximab-based therapy serum samples shall be collected at enrollment and just prior to receiving the third dose of cetuximab therapy To provide the opportunity to perform retrospective pharmacogenomic studies whole blood DNA will be collected from each patient at enrollment and subsequently analyzed for candidate gene polymorphisms once outcome data is available Finally an alternative approach to identification of markers for responsiveness to EGFR inhibition already in progress at the University of Chicago entails collection of skin biopsies before and after treatment with an EGFR inhibitor
As in ongoing collaborations with the University of Chicago Section of Dermatology patients in this proposed study will undergo skin biopsies at enrollment and after 2 weeks of cetuximab therapy The investigators will extract mRNA from the fresh frozen skin specimens and perform microarray studies to test the utility of mRNA expression patterns associated with rash and responsiveness to EOFR inhibitors in currently ongoing investigations at the University of Chicago Therefore we expect this study 1 to identify any significant improvement of concurrent cetuximabpemetrexed therapy for second-line treatment of NSCLC over sequential monotherapy 2 through timely minimally invasive collection of serum and exposed skin to provide the opportunity to test previously identified biomarkers for individual responsiveness to cetuximab therapy and 3 to confirm prospectively whether early development of rash on cetuximab treatment predicts responsiveness to either concurrent or sequential therapy
Many patients who receive EGFR inhibitors develop an acneiform rash and the severity of the rash is associated with good outcomes from treatment Several of these studies have demonstrated no correlation between the intensity or percentage of tumor cells staining for EFUR expression and response to therapy However a Phase II study at the University of Colorado of cetuximab added to standard first-line treatment of NSCLC revealed 610 responders developed the rash within 2 weeks of initiating treatment Personal Communication Dugan et al BMS Therefore early development of rash may be a clinically useful marker of subsequent response and novel approaches to the identification of biological markers for this phenotype prior to initiation of therapy may be helpful in subsequent determination of which patients will most likely benefit from EGFR inhibitor therapy
To address these issues we propose a phase I randomized study of concurrent pemetrexedcetuximab compared to sequential cetuximabpemetrexed therapy for the second-line treatment of advanced NSCLC Patients will be randomized at study entry Regarding prospective analysis of the rapid-rash forming phenotype all patients will receive 2 weeks of initial treatment with cetuximab and undergo formal rash evaluation serum and skin collection According to the initial randomization half of the study subjects will continue with cetuximab monotherapy while the remainder will receive concurrent cetuximab and pemetrexed The primary study endpoint of freedom from progression and secondary endpoint of objective response rate will be based on the comparison of patients in he concurrent therapy group with patients treated with cetuximab monotherapy with Day-14 first receipt of cetuximab as the reference treatment start date Overall survival will be analyzed as a secondary endpoint to assess the efficacy of concomitant treatment with cetuximab and pemetrexed compared to sequential treatment with cetuximab followed by pemetrexed upon disease progression As patients in both treatment arms receive cetuximab correlative studies will be performed on all enrolled patients For serum proteomic studies designed to identify a serum polypeptide signature associated with response to cetuximab-based therapy serum samples shall be collected at enrollment and just prior to receiving the third dose of cetuximab therapy To provide the opportunity to perform retrospective pharmacogenomic studies whole blood DNA will be collected from each patient at enrollment and subsequently analyzed for candidate gene polymorphisms once outcome data is available Finally an alternative approach to identification of markers for responsiveness to EGFR inhibition already in progress at the University of Chicago entails collection of skin biopsies before and after treatment with an EGFR inhibitor
As in ongoing collaborations with the University of Chicago Section of Dermatology patients in this proposed study will undergo skin biopsies at enrollment and after 2 weeks of cetuximab therapy The investigators will extract mRNA from the fresh frozen skin specimens and perform microarray studies to test the utility of mRNA expression patterns associated with rash and responsiveness to EOFR inhibitors in currently ongoing investigations at the University of Chicago Therefore we expect this study 1 to identify any significant improvement of concurrent cetuximabpemetrexed therapy for second-line treatment of NSCLC over sequential monotherapy 2 through timely minimally invasive collection of serum and exposed skin to provide the opportunity to test previously identified biomarkers for individual responsiveness to cetuximab therapy and 3 to confirm prospectively whether early development of rash on cetuximab treatment predicts responsiveness to either concurrent or sequential therapy
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None