NCT00948675

Brief Summary

The purpose of this study is to compare the regimens of pemetrexed, carboplatin with pemetrexed maintenance and paclitaxel, carboplatin, bevacizumab with bevacizumab maintenance in participants with Stage IV nonsquamous non-small cell lung cancer.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
361

participants targeted

Target at P50-P75 for phase_3

Timeline
Completed

Started Sep 2009

Longer than P75 for phase_3

Geographic Reach
1 country

45 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 28, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

July 29, 2009

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2009

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2013

Completed
1.2 years until next milestone

Results Posted

Study results publicly available

April 2, 2014

Completed
6.6 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 6, 2020

Completed
Last Updated

October 29, 2021

Status Verified

October 1, 2021

Enrollment Period

3.4 years

First QC Date

July 28, 2009

Results QC Date

January 14, 2014

Last Update Submit

October 18, 2021

Conditions

Keywords

Advanced Non-Small Cell Lung Cancer of Nonsquamous HistologyAdvanced Lung CancerNon-Small Cell Lung CancerLung Cancer

Outcome Measures

Primary Outcomes (1)

  • Progression Free Survival Without Grade 4 Toxicity (G4PFS) as Measured by the Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0

    G4PFS was defined as the duration from the date of randomization to the earliest occurrence date of one of the following three events: Common Terminology Criteria (CTC) grade 4 adverse events (G4AEs), or progressive disease (PD) or death from any cause, whichever occurred earlier. PD was determined using Response Evaluation Criteria In Solid Tumors (RECIST) criteria version 1.0. PD is ≥20% increase in sum of longest diameter of target lesions or the appearance of new lesions. For participants who had no G4AEs, or PD, or death at the time of the data inclusion cutoff, PFS was censored at their last objective progression-free disease assessment prior to the cutoff date or the date of initiation of subsequent systemic anticancer therapy.

    Randomization to measured progressive disease or treatment discontinuation up to 39.49 months

Secondary Outcomes (4)

  • Progression Free Survival (PFS)

    Randomization to measured progressive disease up to 39.49 months

  • Overall Survival (OS)

    Randomization to date of death from any cause up to 39.49 months

  • Percentage of Participants With Complete Response or Partial Response (Overall Tumor Response Rate)

    Baseline to date of objective progressive disease up to 39.49 months

  • Disease Control Rates Defined as Complete Response (CR), Partial Response (PR), and Stable Disease (SD)

    Baseline to date of objective progressive disease up to 39.49 months

Study Arms (2)

Pemetrexed + Carboplatin + Pemetrexed

EXPERIMENTAL

Pemetrexed and Carboplatin followed by Pemetrexed

Drug: PemetrexedDrug: Carboplatin

Paclitaxel + Carboplatin + Bevacizumab

ACTIVE COMPARATOR

Paclitaxel, Carboplatin, and Bevacizumab followed by Bevacizumab

Drug: CarboplatinDrug: PaclitaxelBiological: Bevacizumab

Interventions

Induction therapy: 500 milligrams/square meter (mg/m²) given intravenously every 21 days for 4 cycles. Maintenance therapy: 500 mg/m² given intravenously every 21 days until disease progression or treatment discontinuation.

Also known as: ALIMTA, LY231514
Pemetrexed + Carboplatin + Pemetrexed

Induction Therapy (every 21 days for 4 cycles): Area Under the Curve (AUC) 6 \[maximum possible dose of 900 milligrams (mg)\] intravenously infused over 30 minutes.

Paclitaxel + Carboplatin + BevacizumabPemetrexed + Carboplatin + Pemetrexed

Induction Therapy (every 21 days for 4 cycles): 200 mg/m² intravenously infused over 3 hours

Paclitaxel + Carboplatin + Bevacizumab
BevacizumabBIOLOGICAL

Induction therapy: 15 milligrams/kilogram (mg/kg) given intravenously every 21 days for 4 cycles. Maintenance therapy: 15 mg/kg given intravenously every 21 days until disease progression or treatment discontinuation.

Paclitaxel + Carboplatin + Bevacizumab

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • a histologic or cytologic diagnosis of advanced non-small cell lung cancer (NSCLC) \[Stage IV from the American Joint Committee on Cancer Staging Criteria (AJCC) staging system, version 7.0, including both M1a and M1b\], other than predominantly squamous cell histology, that is not amenable to curative therapy. Participants may not have received any prior systemic chemotherapy, immunotherapy, targeted therapy, or biological therapy, including adjuvant therapy, for any stage of NSCLC.
  • prior radiation therapy is allowed to \< 25% of the bone marrow; however, prior radiation to the whole pelvis not allowed.
  • good performance status.
  • adequate organ function.
  • estimated life expectancy of at least 12 weeks.

You may not qualify if:

  • known central nervous system (CNS) disease, other than treated brain metastasis.
  • major surgical procedure, open biopsy, open pleurodesis, or significant traumatic injury within 28 days prior to study or have an anticipated need for major surgery during the study.
  • core biopsy or other minor surgical procedure, excluding placement of vascular access device, closed pleurodesis, thoracentesis, and mediastinoscopy, within 7 days prior to study.
  • history of gastrointestinal fistula, perforation, or abscess, inflammatory bowel disease, or diverticulitis.
  • currently receiving ongoing treatment with full-dose warfarin or equivalent
  • significant vascular disease within 6 months prior to Day 1 of Cycle 1.
  • evidence of bleeding diathesis or coagulopathy.
  • serious concomitant systemic disorder that, in the opinion of the investigator, would compromise the participant's ability to adhere to the protocol.
  • serious cardiac condition, such as myocardial infarction, angina, or heart disease.
  • inadequately controlled hypertension.
  • any prior history of hypertensive crisis or hypertensive encephalopathy.
  • serious, nonhealing wound, active ulcer, or untreated bone fracture.
  • another active malignancy, other than superficial basal cell and superficial squamous (skin) cell, or carcinoma in situ of the cervix within the last 5 years.
  • previously received treatment with paclitaxel, carboplatin, pemetrexed, or bevacizumab (prior intravitreal administration of bevacizumab does not preclude study participation).
  • pregnant or breast-feeding.
  • +6 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (45)

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Scottsdale, Arizona, 85259, United States

Location

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Tucson, Arizona, 85715, United States

Location

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Mission Hills, California, 91345, United States

Location

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Aventura, Florida, 33180, United States

Location

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Daytona Beach, Florida, 32114, United States

Location

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Fort Myers, Florida, 33916, United States

Location

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Gainesville, Florida, 32610, United States

Location

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Jacksonville, Florida, 32256, United States

Location

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Port Saint Lucie, Florida, 34952, United States

Location

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Athens, Georgia, 30607, United States

Location

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Augusta, Georgia, 30901, United States

Location

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Macon, Georgia, 31201, United States

Location

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Marietta, Georgia, 30060, United States

Location

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Post Falls, Idaho, 83854, United States

Location

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Gurnee, Illinois, 60031, United States

Location

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Joliet, Illinois, 60435, United States

Location

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Goshen, Indiana, 46526, United States

Location

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New Albany, Indiana, 47150, United States

Location

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Sioux City, Iowa, 51101, United States

Location

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Mount Sterling, Kentucky, 40353, United States

Location

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Ann Arbor, Michigan, 48106, United States

Location

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Lansing, Michigan, 48910, United States

Location

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Southfield, Michigan, 48075, United States

Location

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Rochester, Minnesota, 55905, United States

Location

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Branson, Missouri, 65616, United States

Location

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Billings, Montana, 59107, United States

Location

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Great Falls, Montana, 59405, United States

Location

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Albuquerque, New Mexico, 87106, United States

Location

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Burlington, North Carolina, 27215, United States

Location

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High Point, North Carolina, 27262, United States

Location

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Bismarck, North Dakota, 58501, United States

Location

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Fargo, North Dakota, 58122, United States

Location

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Cincinnati, Ohio, 45242, United States

Location

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Tulsa, Oklahoma, 74136, United States

Location

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DuBois, Pennsylvania, 15801, United States

Location

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Philadelphia, Pennsylvania, 19107, United States

Location

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Columbia, South Carolina, 29210, United States

Location

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Chattanooga, Tennessee, 37404, United States

Location

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Memphis, Tennessee, 38119, United States

Location

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Nashville, Tennessee, 37203, United States

Location

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Fort Worth, Texas, 76104, United States

Location

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Houston, Texas, 77030, United States

Location

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Salt Lake City, Utah, 84106, United States

Location

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Richmond, Virginia, 23230, United States

Location

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Kennewick, Washington, 99336, United States

Location

Related Publications (1)

  • Zinner RG, Obasaju CK, Spigel DR, Weaver RW, Beck JT, Waterhouse DM, Modiano MR, Hrinczenko B, Nikolinakos PG, Liu J, Koustenis AG, Winfree KB, Melemed SA, Guba SC, Ortuzar WI, Desaiah D, Treat JA, Govindan R, Ross HJ. PRONOUNCE: randomized, open-label, phase III study of first-line pemetrexed + carboplatin followed by maintenance pemetrexed versus paclitaxel + carboplatin + bevacizumab followed by maintenance bevacizumab in patients ith advanced nonsquamous non-small-cell lung cancer. J Thorac Oncol. 2015 Jan;10(1):134-42. doi: 10.1097/JTO.0000000000000366.

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell LungLung Neoplasms

Interventions

PemetrexedCarboplatinPaclitaxelBevacizumab

Condition Hierarchy (Ancestors)

Carcinoma, BronchogenicBronchial NeoplasmsRespiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract Diseases

Intervention Hierarchy (Ancestors)

GuanineHypoxanthinesPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic CompoundsGlutamatesAmino Acids, AcidicAmino AcidsAmino Acids, Peptides, and ProteinsAmino Acids, DicarboxylicCoordination ComplexesOrganic ChemicalsTaxoidsCyclodecanesCycloparaffinsHydrocarbons, AlicyclicHydrocarbons, CyclicHydrocarbonsDiterpenesTerpenesAntibodies, Monoclonal, HumanizedAntibodies, MonoclonalAntibodiesImmunoglobulinsImmunoproteinsBlood ProteinsProteinsSerum GlobulinsGlobulins

Results Point of Contact

Title
Chief Medical Officer
Organization
Eli Lilly and Company

Study Officials

  • Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

    Eli Lilly and Company

    STUDY DIRECTOR

Publication Agreements

PI is Sponsor Employee
No
Restriction Type
GT60
Restrictive Agreement
Yes

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 28, 2009

First Posted

July 29, 2009

Study Start

September 1, 2009

Primary Completion

January 31, 2013

Study Completion

November 6, 2020

Last Updated

October 29, 2021

Results First Posted

April 2, 2014

Record last verified: 2021-10

Data Sharing

IPD Sharing
Will share

Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.

Shared Documents
STUDY PROTOCOL, SAP, CSR
Time Frame
Data are available 6 months after the primary publication and approval of the indication studied in the US and EU, whichever is later. Data will be indefinitely available for requesting.
Access Criteria
A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.
More information

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