Docetaxel and Bortezomib in Treating Patients With Progressive or Recurrent Non-Small Cell Lung Cancer

Non-small Cell Lung Cancer Clinical Trial

Official title:

Randomized Phase II Trial of Sequential Versus Concurrent Docetaxel and PS-341 (NSC 681239) in Previously Treated Non-Small Cell Lung Cancer (NSCLC)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00362882
• Other study ID #: NCI-2009-00123
• Secondary ID: PHII-70N01CM1710
• Status: Completed
• Phase: Phase 2
• First received: August 10, 2006
• Last updated: October 31, 2017
• Start date: July 2006
• Est. completion date: July 2010

Study information

• Verified date: October 2017
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This trial is studying two different schedules of docetaxel and bortezomib to compare how well they work in treating patients with progressive or recurrent non-small cell lung cancer. Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving docetaxel together with bortezomib may kill more tumor cells

Description:

PRIMARY OBJECTIVE:

I. To compare the efficacy and tolerability of sequential vs concurrent docetaxel and bortezomib in patients with previously treated, progressive or recurrent, advanced non-small cell lung cancer (NSCLC).

SECOND OBJECTIVES:

I. To compare time to progression in patients with previously treated NSCLC treated with these regimens.

II. To compare 1-year and overall survival of patients treated with these regimens.

III. To compare the toxicity of these regimens in these patients. IV. To determine the pharmacokinetics of docetaxel in the context of this study.

TERTIARY OBJECTIVE:

I. To determine levels of expression of molecular markers regulated by docetaxel and bortezomib and correlate with clinical response and overall survival of these patients.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to ECOG performance status (0 vs 1) and number of prior chemotherapy treatments (1 vs >1). Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive docetaxel IV over 60 minutes on day 1 and bortezomib IV over 3-5 seconds on days 1 and 8. Treatment repeats every 21 days for up to 8 courses in the absence of disease progression or unacceptable toxicity.

ARM II: Patients receive docetaxel as in arm I and bortezomib IV over 3-5 seconds on days 2 and 8. Treatment repeats every 21 days for up to 8 courses in the absence of disease progression or unacceptable toxicity.

After completion of study therapy, patients are followed periodically.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 81
• Est. completion date: July 2010
• Est. primary completion date: July 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 120 Years

Eligibility

Criteria:

• No other prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated stage I or II cancer for which the patient is currently in complete remission, or any other cancer for which the patient has been disease-free for 5 years.

• Histologically or cytologically confirmed non-small cell lung cancer (NSCLC).

• Progressive or recurrent NSCLC after treatment with 1 prior platinum-based chemotherapy regimen for metastatic disease. Prior neoadjuvant/adjuvant chemotherapy and/or concurrent chemoradiation for early-stage disease allowed.

• At least 4 weeks since prior chemotherapy (6 weeks for mitomycin C or nitrosoureas) and recovered.

• No prior docetaxel or bortezomib

• Prior epidermal growth factor receptor inhibitor therapy allowed.

• Prior paclitaxel allowed

• At least 4 weeks since prior major surgery and recovered.

• At least 2 weeks since prior and no concurrent enzyme-inducing anticonvulsants.

• No concurrent hormonal therapy, biologic therapy, or radiotherapy to measurable lesions. Concurrent palliative radiotherapy to small-field nonindicator lesions (e.g., painful bony metastases) allowed.

• Measurable disease* with >= 1 unidimensionally objectively measurable lesion, including any of the following:

• Lung mass (measurable on chest x-ray, tomograms, or CT scan)

• Enlarged lymph nodes

• Liver metastasis (measurable as a discrete focal lesion on radionuclide or CT scan, or ultrasound)

• Metastatic abdominal mass (measurable on CT scan with >= 1 perpendicular diameter = the distance between cuts)

• Measurable disease must be outside the previous radiation field or a new lesion must be present.

• Life expectancy >= 12 weeks

• Progressive disease within a previously radiated field allowed.

• [Note: *Measurable disease DOES NOT include bone metastases or non-focal liver metastases].

• No symptomatic or untreated brain metastasis requiring steroids. Asymptomatic, previously treated (surgical resection or radiotherapy) brain metastasis allowed provided they are neurologically stable and >= 4 weeks since prior steroids.

• Creatinine clearance >= 50 mL/min

• Creatinine =< 1.6 mg/dL

• Bilirubin normal

• AST =< 2 times upper limit of normal

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No peripheral neuropathy >= grade 2

• Absolute granulocyte count >= 1,500/mm³

• Platelet count >= 100,000/mm³

• Cutaneous nodule

• ECOG performance status 0-1

• At least 4 weeks since prior radiotherapy and recovered.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms
• Non-small Cell Lung Cancer
• Recurrent Non-small Cell Lung Cancer
• Stage IV Non-small Cell Lung Cancer

Intervention

Drug:
• docetaxel
Given IV
• bortezomib
Given IV

Other:
• laboratory biomarker analysis
correlative study
• immunoenzyme technique
correlative study
• immunohistochemistry staining method
correlative study
• pharmacological study
correlative study

Locations

Country	Name	City	State
United States	City of Hope Medical Center	Duarte	California

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Response Rate	Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by CT, MRI or X-ray: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR	Up to 4 years
Secondary	Overall Survival	Will be estimated using the product-limit method of Kaplan and Meier.	From first day of treatment to time of death due to any cause, up to 4 years
Secondary	Disease Control Rate	Disease control rate was defined as the rate of partial response (PR) plus stable disease (SD; for at least 2 cycles).	Up to 4 years
Secondary	Progression-free Survival @ 6 Months	Estimated using the product-limit method of Kaplan and Meier. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.	6 months