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TerminatedPhase 3NCT00551733
Official study title

Carboplatin With Either Paclitaxel Poliglumex or Paclitaxel in Treating Women With Stage IIIB, Stage IV, or Recurrent Non-Small Cell Lung Cancer

Study summary

RATIONALE: Drugs used in chemotherapy, such as carboplatin, paclitaxel, and paclitaxel poliglumex, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. It is not yet known whether giving carboplatin together with paclitaxel poliglumex is more effective than giving carboplatin together with paclitaxel in treating non-small cell lung cancer. PURPOSE: This randomized phase III trial is studying carboplatin and paclitaxel poliglumex to see how well they work compared with carboplatin and paclitaxel in treating women with stage III, stage IV, or recurrent non-small cell lung cancer.

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Key things to know

Main goalTreatment

This describes the study’s primary purpose.

What is being studiedcarboplatin and paclitaxel

Plus 1 other study approaches.

Who it may be forNon-small cell lung cancer (NSCLC) · Locally advanced · Metastatic or stage IV

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Oct 5, 2020 · Source: ClinicalTrials.gov

Is enrollment open?Terminated

Ask the study team to confirm whether enrollment is open.

What kind of study?Phase 3

Interventional

Where is it offered?41 U.S. locations

Locations may change over time.

Who runs it?CTI BioPharma

Study sponsor

01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 3
Sponsor
CTI BioPharma
Interventions being studied
Drug: carboplatin; Drug: paclitaxel; Drug: paclitaxel poliglumex
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Cancer type
Non-small cell lung cancer (NSCLC)→
Disease setting
Locally advanced→Metastatic or stage IV→Recurrent or relapsed→
Treatment approach
Chemotherapy→
03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • DISEASE CHARACTERISTICS:
  • Histologically or cytologically confirmed diagnosis of non-small cell lung cancer (NSCLC)
  • Cytologic specimens obtained by brushings, washings, or needle aspiration of a defined lesion or from a pleural effusion are acceptable; sputum cytology alone is not acceptable for determining cell type
  • Must meet one of the following criteria:
  • Recurrent disease following completion of radiation or surgery
  • Stage IIIB disease and not a candidate for combined modality therapy (primary radiation therapy or surgery)
  • Stage IV disease
  • Patients may have either measurable or nonmeasurable disease according to RECIST criteria
  • Baseline estradiol \> 30 pg/mL
  • Patients on hormone replacement therapy are eligible provided baseline estradiol \> 30 pg/mL
  • Patients with known brain metastases must have received standard antitumor treatment (e.g. whole brain radiation, stereotactic radioablation, or surgery) for their CNS metastases as defined by the site's institutional standards
  • Neurologic function must have been stable for 2 weeks before randomization and patients must either be off steroid therapy for their brain metastases or on a tapering regimen
  • Patients must have recovered from therapy for their brain metastases with no evidence of significant unstable neurological symptoms within the 4 weeks before study randomization
  • No evidence of small cell carcinoma, carcinoid, or mixed small cell/non-small cell histology PATIENT CHARACTERISTICS:
  • Female
  • ECOG performance score 0-2
  • Life expectancy ≥ 12 weeks
  • Absolute neutrophil count ≥ 1,500/mm³
  • Platelet count ≥ 100,000/mm³
  • Hemoglobin ≥ 10 g/dL (may be achieved with transfusion)
  • Creatinine ≤ 1.5 times upper limit of normal (ULN)
  • Total bilirubin ≤ 1.5 times ULN (CTC grade 1) (patients with Gilbert syndrome or other hereditary bilirubin defects may be included regardless of bilirubin levels)
  • SGOT and SGPT ≤ 2.5 times ULN (CTC grade 0 or 1) (5 times ULN \[CTC grade 0 to 2\] if due to liver metastases)
  • Alkaline phosphatase ≤ 2.5 times ULN except for elevated alkaline phosphatase with laboratory documentation that demonstrates bone origin
  • No pregnant women or nursing mothers
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 6 months after study participation
  • No known hypersensitivity to study drugs or excipients
  • Meets all of the following criteria:
  • No weight loss \> 10% in previous 6 months
  • Lactate dehydrogenase (LDH) ≤ 600 IU/L (central laboratory) regardless of weight loss
  • LDH ≤ 400 IU/L (central laboratory) and no weight loss ≥ 5% in previous 6 months
  • BMI ≤ 35
  • No concurrent primary malignancies except for carcinoma in situ or non-melanoma skin cancer
  • No neuropathy grade 2 or greater
  • No clinically significant active infection for which active therapy is underway
  • No unstable medical conditions including unstable angina or myocardial infarction within the past 6 months
  • Patients with evidence of cardiac conduction abnormalities are eligible if their cardiac status is stable
  • No circumstance that would preclude completion of the study or the required follow-up PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics
  • Recovered from major surgery
  • At least 7 days since prior local palliative radiotherapy
  • At least 30 days since prior radiation therapy with curative intent
  • At least 4 weeks since prior investigational therapy, unless local requirements are more stringent
  • No prior systemic chemotherapy for the treatment of lung cancer, including systemic radiosensitizers used to treat brain metastases or any biologic agents
  • No concurrent non-protocol-specified systemic antitumor therapy
  • No concurrent amifostine, investigational agents, other cytotoxic agents for this disease
  • No concurrent radiotherapy (with the exception of radiotherapy for brain or bone metastases for palliative purposes or radiotherapy for a condition other than NSCLC that was ongoing at the time of randomization)
  • Patients receiving palliative radiotherapy (treatment for symptomatic metastatic disease) may be treated while on study

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Scottsdale Medical SpecialistsScottsdale, Arizona
  • Roy and Patricia Disney Family Cancer Center at Providence Saint Joseph Medical CenterBurbank, California
  • Southwest Cancer Care - EscondidoEscondido, California
  • Clinical Trials and Research Associates, IncorporatedMontebello, California
  • Stanford Cancer CenterStanford, California
  • Broward Oncology AssociatesFort Lauderdale, Florida
  • Horizon Institute for Clinical ResearchHollywood, Florida
  • Rush Cancer Institute at Rush University Medical CenterChicago, Illinois
  • Joliet Oncology-Hematology Associates, Limited - WestJoliet, Illinois
  • Hematology Oncology Consultants - NapervilleNaperville, Illinois
  • Saint James Hospital and Health Centers Comprehensive Cancer Institute - Olympia FieldsOlympia Fields, Illinois
  • Cancer Center of IndianaNew Albany, Indiana

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 5, 2020. Always confirm current availability with the study team.

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