Phase II Study of Combination of Paclitaxel Poliglumex and Alimta for Advanced Non-small Cell Lung Cancer (NSCLC)

NCT ID: NCT00487669

Last Updated: 2014-01-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-10-31
• Study Completion Date: 2009-11-30

Brief Summary

This is a non-randomized, single-arm, single-institution, open label, two-stage phase II and dose-ranging study designed to evaluate the efficacy and safety of paclitaxel poliglumex in combination with pemetrexed in patients with advanced stage IIIB or stage IV NSCLC.

Detailed Description

Primary objective

To evaluate the overall response rate (complete plus partial responses by RECIST criteria) to the combination of paclitaxel poliglumex and pemetrexed as therapy in patients with advanced NSCLC.

Secondary Objectives

To evaluate the safety and adverse event profile of the combination of paclitaxel poliglumex and pemetrexed as therapy in patients with advanced NSCLC.

To evaluate the duration of response, time to progression, and overall survival of advanced NSCLC treated with the combination of paclitaxel poliglumex and pemetrexed.

To compare the overall response rate using three-dimensional reconstruction of target lesions by Medical Metrx Solutions (MMS) and RECIST criteria.

Conditions

Advanced Non-small Cell Lung Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Paclitaxel Poliglumex with Pemetrexed

The first 6 eligible patients will be enrolled at a dose of 135 mg/m2 paclitaxel poliglumex in combination with 500 mg/m2 of pemetrexed. Patients who experience disease progression without dose-limiting adverse events after the initial cycle will be replaced. Dose escalation to the next dose level can occur provided that no more than 1 of 6 patients experience in initial dose limiting toxicity (IDLT) following 2 cycles of therapy. If ≥ 2 of 6 patients experience IDLTs at the 135 mg/m2 dose, the maximally tolerated dose (MTD) was surpassed and the study will be discontinued.

Group Type: EXPERIMENTAL

paclitaxel poliglumex, pemetrexed

Intervention Type: DRUG

The first 6 eligible patients will be enrolled at a dose of 135 mg/m2 paclitaxel poliglumex in combination with 500 mg/m2 of pemetrexed. Patients who experience disease progression without dose-limiting adverse events after the initial cycle will be replaced. Dose escalation to the next dose level can occur provided that no more than 1 of 6 patients experience in initial dose limiting toxicity (IDLT) following 2 cycles of therapy. If ≥ 2 of 6 patients experience IDLTs at the 135 mg/m2 dose, the maximally tolerated dose (MTD) was surpassed and the study will be discontinued

Interventions

paclitaxel poliglumex, pemetrexed

The first 6 eligible patients will be enrolled at a dose of 135 mg/m2 paclitaxel poliglumex in combination with 500 mg/m2 of pemetrexed. Patients who experience disease progression without dose-limiting adverse events after the initial cycle will be replaced. Dose escalation to the next dose level can occur provided that no more than 1 of 6 patients experience in initial dose limiting toxicity (IDLT) following 2 cycles of therapy. If ≥ 2 of 6 patients experience IDLTs at the 135 mg/m2 dose, the maximally tolerated dose (MTD) was surpassed and the study will be discontinued

Intervention Type: DRUG

Other Intervention Names

Xyotax; Alimta

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically confirmed diagnosis of locally advanced and/or metastatic NSCLC (Stage IIIB or IV).
• Bidimensionally measurable lesions or unidimensionally evaluable lesions.
• Age ≥ 18 years.
• At least one measurable target lesion as defined by Response Evaluation Criteria in Solid Tumors (RECIST), which has not been previously treated with local therapy (e.g. radiation therapy, chemoembolization, surgery, etc.).
• May have received prior chemotherapy (including taxanes) for advanced NSCLC.
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
• Life expectancy > 12 weeks.
• No active infections.
• Adequate liver and bone marrow function.
• AST<2.5 x ULN, bilirubin <1.5x ULN, alkaline phosphatase<2.5 x ULN (unless bone origin and no liver metastases are documented).
• ANC ≥ 1,500/uL, platelet count ≥ 100,000/uL.
• Normal PT and PTT.
• Bisphosphates initiated prior to study entry will be permitted. However, initiation of bisphosphonates following study entry is not permitted.
• Patients with treated brain metastases must be neurologically stable.
• At least 3 weeks since last chemotherapy and recovered from treatment-related adverse events ≤ grade 1.
• At least 3 weeks since prior radiation and recovered from treatment-related adverse events ≤ grade 1.
• Women of childbearing potential are eligible for the study, provided they have a negative serum or urine pregnancy test within three days of study entry, and an adequate method of contraception is used. Acceptable methods of birth control include barrier methods (condoms, diaphragms with spermicide) or intrauterine devices (IUD). Women whose sole sexual partner is infertile, or who are not sexually active, are also eligible.
• Able to provide written informed consent.

Exclusion Criteria

• Grade 2 or greater peripheral neuropathy, according to the National Cancer Institute-Common Toxicity Criteria.
• Clinically significant pleural, pericardial or abdominal effusions.
• Untreated brain metastases.
• Patients with previously diagnosed brain metastases will be eligible if they are neurologically stable and have recovered from the effects of radiotherapy or surgery (≤ grade 2).
• Patients with brain metastases must have at least one other site of measurable disease.
• Concurrent radiotherapy.
• Other concurrent cancer treatment-related investigational agent. Investigational supportive care medications are permitted.
• Concurrent treatment with unfractionated heparin or warfarin.
• History of radiotherapy encompassing greater than 50% of the marrow-bearing skeleton.
• Prior bone marrow or stem cell transplant.
• History of other active malignancy within the last year requiring chemotherapy, not including curatively-treated carcinoma in situ of the cervix, or non-melanoma skin cancer (basal cell carcinoma or squamous cell carcinoma).
• Uncontrolled infection.
• Active bleeding, or history of bleeding requiring transfusion within 2 weeks of study entry.
• Active cardiac disease, as defined as:
• Current history of uncontrolled or symptomatic angina.
• History of arrhythmias requiring medications or clinically significant arrhythmias, with the exception of uncomplicated atrial fibrillation.
• Myocardial infarction < 6 months from study entry.
• Any other cardiac conditions, which in the opinion of the treating physician, would make this protocol unreasonably hazardous for the patient.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

CTI BioPharma

INDUSTRY

Sponsor Role: collaborator

Dartmouth-Hitchcock Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

James R Rigas, MD

Role: PRINCIPAL_INVESTIGATOR

Norriss Cotten Cancer Center

Locations

Dartmouth-Hitchcock Medical Center

Lebanon, New Hampshire, United States

Countries

United States

Other Identifiers

D-0433

Identifier Type: -

Identifier Source: org_study_id