This trial is active, not recruiting.

Condition lung cancer
Treatments seneca valley virus-001, placebo
Phase phase 2
Sponsor Alliance for Clinical Trials in Oncology
Collaborator National Cancer Institute (NCI)
Start date January 2010
End date January 2013
Trial size 99 participants
Trial identifier NCT01017601, CDR0000659547, NCCTG-N0923, NCI-2011-01991


RATIONALE: A virus called Seneca Valley virus-001 (NTX-010) may be able to kill tumor cells without damaging normal cells. It is not yet known whether NTX-010 is more effective than a placebo in treating small cell lung cancer.

PURPOSE: This randomized phase II trial is studying NTX-010 to see how well it works compared with a placebo when given after chemotherapy in treating patients with extensive-stage small cell lung cancer.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Intervention model parallel assignment
Masking double blind (subject, investigator)
Primary purpose treatment
Patients receive a single dose of Seneca Valley virus-001 (NTX-010) IV over 1 hour on day 1.
seneca valley virus-001
Given IV
(Placebo Comparator)
Patients receive a single dose of placebo IV over 1 hour on day 1.
Given IV

Primary Outcomes

Progression-free survival
time frame: Up to 5 years

Secondary Outcomes

Overall survival
time frame: Up to 5 years
Response rate (complete response and partial response) as assessed by RECIST criteria
time frame: Up to 5 years
Duration of response
time frame: Up to 5 years
Time-to-disease progression
time frame: Up to 5 years
Toxicity as assessed by NCI CTCAE v3.0
time frame: Up to 5 years
Quality of life as assessed by the single-item Linear Analogue Self Assessment
time frame: Up to 5 years

Eligibility Criteria

Male or female participants at least 18 years old.

DISEASE CHARACTERISTICS: - Histologically confirmed diagnosis of extensive-stage small cell lung cancer (SCLC) - No mixed histology - Presence of ≥ 1 neuroendocrine marker (synaptophysin, chromogranin, or CD56) in tumor tissue - Achieved partial response (PR), complete response (CR), or stable disease (SD) ≤ 12 weeks of completing 4-6 courses of platinum-based chemotherapy regimen for extensive-stage SCLC - Patients with PR or SD must have measurable disease, defined as ≥ 1 lesion whose longest diameter can be accurately measured as ≥ 2.0 cm but < 10 cm by chest x-ray OR as ≥ 1.0 cm but < 10 cm by CT scan, CT component of a PET/CT scan, or MRI - If CT scan is used, it must be used for both pre- and post-treatment tumor assessments - Measurable disease is not required for patients with CR - Brain metastases allowed provided they have been stable for ≥ 4 weeks after completion of prior radiotherapy PATIENT CHARACTERISTICS: - ECOG performance status 0 or 1 - Life expectancy of ≥ 8 weeks - ANC ≥ 1,500/μL - Platelet count ≥ 100,000/μL - Hemoglobin ≥ 9 g/dL - Total bilirubin ≤ 1.5 times upper limit of normal (ULN) OR direct bilirubin normal - AST ≤ 3 times ULN (≤ 5 times ULN if liver has tumor involvement) - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use adequate contraception - Able to comply with study procedures to minimize virus exposure to others - Willing to provide required biologic specimens - Willing to return to NCCTG/CTSU enrolling institution for follow-up - Adequate lung function (i.e., not oxygen dependent) - The patient is eligible if not on a 24-hour oxygen schedule - No second primary malignancy within the past 5 years, except for the following: - Carcinoma in situ of the cervix - Non-melanomatous skin cancer - History of low-grade (Gleason score ≤ 6) localized prostate cancer (even if diagnosed < 5 years prior to study entry) - Stage I breast cancer that was treated ≥ 5 years before study entry - Transitional cell carcinoma of the bladder (in situ) - No active hepatitis B or hepatitis C - No clinically significant infection - No significant traumatic injury within the past 4 weeks - No concurrent uncontrolled illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situation that would limit compliance with study requirements PRIOR CONCURRENT THERAPY: - See Disease Characteristics - More than 4 weeks since prior radiotherapy (2 weeks for palliative radiotherapy to skeletal metastases) - Other prior radiation therapy (including WBRT, PCI, or Gamma Knife) is permitted as long as the following are true: - Recovered from prior radiotherapy (alopecia allowed) - No prior consolidation radiation therapy to the chest - No prior radiotherapy to > 25% of bone marrow - For patients without brain metastases, WBRT or standard of care PCI completed ≥ 2 weeks before administration of NTX- 010/placebo - More than 365 days since prior immunotherapy or biologic therapy - More than 4 weeks since prior major surgery* (i.e., laparotomy) or open biopsy - More than 2 weeks since prior minor surgery* - No prior exposure to the Seneca Valley virus (NTX-010), as determined by negative serum antibodies - No concurrent combination antiretroviral therapy for HIV-positive patients NOTE: *Insertion of a vascular access device is not considered major or minor surgery.

Additional Information

Official title A Randomized Double-Blinded Phase II Study of NTX-010, a Replication-Competent Picornavirus, After Standard Platinum-Containing Cytoreductive Induction Chemotherapy in Patients With Extensive Stage Small Cell Lung Cancer
Description OBJECTIVES: Primary - To compare the progression-free survival (PFS) of patients with extensive-stage small cell lung cancer treated with Seneca Valley virus-001 (NTX-010) vs placebo. Secondary - To compare the overall survival (OS) of patients treated with NTX-010 vs placebo. - To describe the adverse events profile and safety of NTX-010 in this patient population. - To determine the antitumor response rate, as assessed by RECIST criteria, and duration of tumor response in this patient population. - To assess the quality of life of this patient population. Exploratory - To determine the relationship between the presence of neutralizing antibodies and PFS. - To assess whether or not a slow viral clearance is associated with better response as determined by PFS. - To determine any potential impact of the presence of one or several neuroendocrine markers in the tumor sample (synaptophysin, chromogranin, or CD56) on PFS and OS. - To determine any potential relationship between presence of cell surface determinants of NTX-010 tropism in the tumor tissue and clinical outcomes such as improved PFS and OS. - To determine any potential relationship between the loss of integrity of IFN signaling in the tumor tissue and clinical outcomes such as improved PFS and OS. - To assess whether or not the presence of circulating tumor cells permissive to NTX-010 is associated with better clinical outcomes as determined by PFS and OS. OUTLINE: This is a multicenter study. Patients are stratified according to ECOG performance status (0 vs 1), tumor response to standard chemotherapy (partial response vs stable disease vs complete response), and time between completion of chemotherapy to randomization 1 month (≤1 month) vs 2 months (>1 month but ≤ 2 months) vs 3 months (> 2 months but ≤ 3 months). Patients are randomized to 1 of 2 treatment arms. - Arm I: Patients receive a single dose of Seneca Valley virus-001 (NTX-010) IV over 1 hour on day 1. - Arm II: Patients receive a single dose of placebo IV over 1 hour on day 1. In both arms, patients may also undergo prophylactic cranial irradiation (PCI) daily on days 22-35 if they have not previously undergone PCI or whole-brain radiotherapy. Quality of life is assessed at baseline and then periodically during the study. Blood samples are collected periodically for viral clearance and antiviral neutralizing antibody levels, circulating tumor cells, and other biomarker laboratory studies. After completion of study therapy, patients are followed up periodically for up to 5 years.
Trial information was received from ClinicalTrials.gov and was last updated in August 2016.
Information provided to ClinicalTrials.gov by Alliance for Clinical Trials in Oncology.