Bevacizumab, Pemetrexed Disodium, and Cisplatin or Erlotinib Hydrochloride and Bevacizumab in Treating Patients With Stage IV Non-Small Cell Lung Cancer. A Multicenter Phase II Trial Including Biopsy at Progression (BIO-PRO Trial).

May 13, 2019 updated by: Swiss Group for Clinical Cancer Research

Bevacizumab, Pemetrexed and Cisplatin, or Erlotinib and Bevacizumab for Advanced Non-Squamous NSCLC Stratified by EGFR Mutation Status. A Multicenter Phase II Trial Including Biopsy at Progression (BIO-PRO Trial).

RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy, such as pemetrexed disodium and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether bevacizumab given together with pemetrexed disodium and cisplatin is more effective than erlotinib hydrochloride given together with bevacizumab in treating patients with non-small cell lung cancer.

PURPOSE: This phase II trial is studying giving bevacizumab together with pemetrexed disodium and cisplatin to see how well it works compared with giving erlotinib hydrochloride together with bevacizumab in treating patients with stage IV non-small cell lung cancer.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

OBJECTIVES:

Primary

  • To demonstrate that tailored therapy, according to tumor histology and EGFR-mutation status, and the introduction of novel drug combinations in the frontline treatment of patients with stage IV non-squamous non-small cell lung cancer, is promising for further investigation.

Secondary

  • To prospectively explore molecular markers of clinical outcomes.

OUTLINE: This is a multicenter study. Patients are stratified according to EGFR(epidermal growth factor receptor)-mutation status (mutated vs wildtype). Patients are assigned to 1 of 2 groups.

  • mutEGFR (mutated epidermal growth factor receptor) group: Patients receive bevacizumab IV over 30-90 minutes on day 1 and oral erlotinib hydrochloride once daily on days 1-21. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

  • wtEGFR (wildtype epidermal growth factor receptor) group cohort 1:

    • Induction chemotherapy: Patients receive bevacizumab IV over 30-90 minutes, pemetrexed disodium IV over 10 minutes, and cisplatin IV over 60 minutes on day 1. Treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity.
    • Maintenance therapy: Patients without progressive disease receive bevacizumab IV over 30-90 minutes and pemetrexed disodium IV over 10 minutes on day 1. Treatment repeats every 21 days in the absence of disease progression.

Blood and tissue specimens are collected for EGFR and molecular markers analysis, including gene expression, mutation, and pharmacogenomic analyses.

After completion of study treatment, patients are followed every 3 months.

  • wtEGFR (wildtype epidermal growth factor receptor) group cohort 2:

    • Induction chemotherapy: Patients receive pemetrexed disodium IV over 10 minutes, and cisplatin IV over 60 minutes on day 1. Treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity.
    • Maintenance therapy: Patients without progressive disease receive pemetrexed disodium IV over 10 minutes on day 1. Treatment repeats every 21 days in the absence of disease progression.

Blood and tissue specimens are collected for EGFR and molecular markers analysis, including gene expression, mutation, and pharmacogenomic analyses.

After completion of study treatment, patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 129 evaluable patients (77 in cohort 1 and 52 in cohort 2) with wtEGFR status and 20 patients with mutEGFR status will be accrued for this study.

Study Type

Interventional

Enrollment (Anticipated)

149

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Switzerland
      • Aarau, Switzerland, CH-5001
        • Kantonsspital Aarau
      • Baden, Switzerland, 5404
        • Kantonsspital Baden
      • Basel, Switzerland, CH-4016
        • Saint Claraspital AG
      • Basel, Switzerland, CH-4031
        • Clinical Cancer Research Center at University Hospital Basel
      • Bellinzona, Switzerland, CH-6500
        • Istituto Oncologico della Svizzera Italiana - Ospedale San Giovanni
      • Bern, Switzerland, CH-3010
        • Inselspital Bern
      • Biel, Switzerland, CH-2501
        • Spitalzentrum Biel
      • Bruderholz, Switzerland, CH-4101
        • Kantonsspital Bruderholz
      • Chur, Switzerland, CH-7000
        • Kantonsspital Graubuenden
      • Freiburg, Switzerland, 1700
        • Kantonsspital Freiburg
      • Geneva, Switzerland, CH-1211
        • Hôpital Cantonal Universitaire de Genève
      • Lausanne, Switzerland, 1011
        • Centre Pluridisciplinaire d' Oncologie
      • Liestal, Switzerland, CH-4410
        • Kantonsspital Liestal
      • Luzerne, Switzerland, CH-6000
        • Kantonsspital Luzern
      • Olten, Switzerland, 4600
        • Kantonsspital Olten
      • St. Gallen, Switzerland, CH-9007
        • Kantonsspital - St. Gallen
      • Thun, Switzerland, 3600
        • Regionalspital
      • Uster, Switzerland, 8610
        • Spital Uster
      • Winterthur, Switzerland, CH-8401
        • Kantonsspital Winterthur
      • Zurich, Switzerland, CH-8063
        • City Hospital Triemli
      • Zurich, Switzerland, CH-8044
        • Universitaetsspital Zuerich
      • Zürich, Switzerland, 8008
        • Onkozentrum Hirslanden

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

DISEASE CHARACTERISTICS:

  • Histologically confirmed non-small cell lung cancer of the following non-squamous subtypes:

    • Adenocarcinoma
    • Bronchioloalveolar carcinoma
    • Large cell carcinoma

  • Stage IV disease including any of the following:

    • M1a (separate tumor nodule in a contralateral lobe, tumor with pleural nodules, or malignant pleural or pericardial effusion)
    • M1b (distant metastasis)
  • Measurable disease, defined as ≥ 1 lesion (outside of irradiated areas) that can be measured in ≥ 1 dimension as ≥ 10 mm (≥ 15 mm in case of lymph nodes) according to RECIST 1.1
  • Paraffin-embedded or formalin-fixed diagnostic biopsy collected in the past 2 months must be available
  • Must have EGFR-mutation status (mutated or wild type) confirmed by the central pathologist in Basel
  • Must consent to tumor biopsy at progression
  • No intrathoracic tumors invading or abutting major blood vessels
  • No CNS metastases by mandatory CT scan (MRI within the past 3 weeks is acceptable)

PATIENT CHARACTERISTICS:

  • WHO performance status 0-1
  • Hemoglobin ≥ 100 g/L
  • ANC ≥ 1,500/mm³
  • Platelet count ≥ 100,000/mm³
  • Bilirubin ≤ 1.5 times upper limit of normal (ULN)
  • ALT ≤ 3 times ULN (≤ 5 times ULN if liver metastases are present)
  • Alkaline phosphatase ≤ 3 times ULN (≤ 5 times ULN if liver metastases are present)
  • Calculated creatinine clearance ≥ 60 mL/min
  • Urine dipstick for proteinuria < 2+
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 12 months after completion of study therapy
  • Must be compliant and have geographic proximity to allow proper staging and follow-up

  • No active bleeding, including hemoptysis ≥ grade 2 (defined as bright red blood of ≥ 5 mL per episode within the past 4 weeks)

    • Minor hemoptysis is allowed
  • No prior malignancy within the past 5 years, except adequately treated cervical carcinoma in situ or localized non-melanoma skin cancer
  • No psychiatric disorder precluding understanding of information on trial-related topics, giving informed consent, or interfering with compliance for oral drug intake

  • No other medical condition that would impair the ability of the patient to participate in the trial or might preclude therapy with trial drugs, including any of the following:

    • Unstable or uncompensated respiratory, cardiac, hepatic, or renal disease
    • Active infection
    • Uncontrolled diabetes mellitus
    • Uncontrolled arterial hypertension (i.e., BP ≥ 150/100 mm Hg despite optimal medical therapy)
    • History of myocardial infarction in the last 3 months
    • History of hemorrhagic disorders
    • Non-healing wound, ulcer, or bone fracture
    • Significant traumatic injury within the past 28 days
  • No known hypersensitivity to trial drugs or to any other component of the trial drugs

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • No prior chemotherapy or molecular-targeted therapy for metastatic disease (neoadjuvant or adjuvant chemotherapy allowed if terminated > 6 months ago)
  • No prior radiotherapy to lesion(s) selected for measurement
  • At least 30 days since prior yellow fever vaccination
  • At least 30 days since prior experimental drugs, anticancer therapy, or treatment in a clinical trial
  • More than 28 days since major surgical procedure or open biopsy
  • No concurrent full-dose oral, intravenous, or subcutaneous anticoagulants (low-dose heparin or aspirin [≤ 325 mg p.o. daily] allowed)
  • No concurrent herbal extracts or drugs contraindicated for use with trial drugs
  • No concurrent investigational agents
  • No other concurrent anti-neoplastic or anti-tumor agents, including chemotherapy, immunotherapy, or hormonal anticancer therapy
  • No concurrent Asasantin® (acetylsalicylic acid and dipyridamole) or Plavix® (clopidogrel bisulfate)

Inclusion criteria

  • Before registration, patient must give written informed consent for participation in the trial including tumor biopsy at progression.
  • Patient must have the capability to understand informed consent and information given by the investigator on the trial.
  • Non-small cell lung cancer (NSCLC), predominant non-squamous subtype (adenocarcinoma, bronchioloalveolar carcinoma, and large cell carcinoma) confirmed by the central pathologist in Basel.
  • NSCLC stage IV according to the 7th edition of the TNM classification, including M1a (separate tumor nodule in a contralateral lobe, tumor with pleural nodules or malignant pleural or pericardial effusion) and/or M1b (distant metastasis).
  • Most recent diagnostic biopsy paraffin-embedded or only formalin-fixed and sufficient for further molecular analysis as determined by central pathologist in Basel.
  • EGFR mutation status determined by local or central pathologist in Basel.
  • EDTA blood samples (2 x 5 mL) for translational research projects will be taken before treatment start.
  • WHO performance status 0-1 (see Appendix 4).
  • Age ≥ 18 years and legally competent person.
  • Measurable disease, defined as at least one lesion (outside of irradiated areas) that can be measured in at least one dimension as ≥ 10 mm (≥ 15 mm in case of lymph nodes)according to RECIST v1.1
  • Adequate hematological values: Hemoglobin ≥ 100 g/L, neutrophils ≥ 1.5 x 109/L, platelets ≥ 100 x 109/L
  • Adequate hepatic function: Bilirubin ≤ 1.5 x ULN, ALT and AP ≤ 3 x ULN (≤ 5 x ULN in case of liver metastases)
  • Adequate renal function: Calculated creatinine clearance ≥ 60 mL/min (according to the formula of Cockroft-Gault)
  • Urine dipstick for proteinuria < 2+
  • Women are not breastfeeding. Women with child-bearing potential are using effective contraception (see 9.2.4 and 9.3.5), are not pregnant and agree not to become pregnant during participation in the trial and during the 12 months thereafter. A negative pregnancy test before inclusion into the trial is required for all women with childbearing potential. Men agree not to father a child during participation in the trial or during the 12 months thereafter.
  • Patient compliance and geographic proximity allow proper staging and follow-up.

Exclusion criteria

  • Diagnosis of SCLC, predominantly squamous NSCLC (>50% by central pathology review) or combined SCLC-NSCLC.
  • Patients with intrathoracic tumors invading or abutting major blood vessels.
  • Prior chemotherapy or molecular targeted therapy for metastatic disease, with the exception of neoadjuvant or adjuvant chemotherapy if terminated 6 months before registration. Prior radiotherapy to lesion(s) selected for measurement.
  • CNS metastases by mandatory CT-scan (MRI is acceptable).
  • Anticoagulation, with the exception of low dose heparin or aspirin (≤ 325 mg p.o. daily).
  • Active bleeding, including hemoptysis ≥ grade 2 (defined as bright red blood of at least 5 mL per episode within the last 4 weeks of registration). Minor hemoptysis is allowed.
  • Yellow fever vaccination within the 30 days prior to registration.
  • Previous malignancy within 5 years with the exception of adequately treated cervical carcinoma in situ or localized non-melanoma skin cancer.
  • Psychiatric disorder precluding understanding of information on trial related topics, giving informed consent, or interfering with compliance for oral drug intake.
  • Concurrent treatment with other experimental drugs or other anti-cancer therapy, treatment in a clinical trial within 30 days prior to trial entry.
  • Evidence of other medical condition which would impair the ability of the patient to participate in the trial or might preclude therapy with trial drugs (e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease, active infection, uncontrolled diabetes mellitus; uncontrolled arterial hypertension ≥ 150/100 mmHg, history of myocardial infarction in the last 3 months, history of hemorrhagic disorders, non healing wound, ulcer or bone fracture)
  • Major surgical procedure, open biopsy or significant traumatic injury within 28 days prior to registration
  • Known hypersensitivity to trial drugs or hypersensitivity to any other component of the trial drugs.
  • Any concomitant drugs contraindicated for use with the trial drugs according to the Swissmedic-approved product information.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Stratum mut EGFR
  • Bevacizumab 7.5 mg/kg i.v. every 3 weeks and
  • Erlotinib 150 mg p.o. daily until progression.
Biological: bevacizumab, erlotinib
  • Bevacizumab 7.5 mg/kg i.v. every 3 weeks and
  • Erlotinib 150 mg p.o. daily until progression.
Other Names:
  • erlotinib (Tarceva)
  • bevacizumab (Avastin)
Active Comparator: Stratum wtEGFR

Cohort 1:

Induction chemotherapy with

  • Bevacizumab 7.5 mg/kg i.v. and
  • Pemetrexed 500 mg/m2 i.v. and
  • Cisplatin* 75 mg/m2 i.v. every 3 weeks for a maximum of 4 cycles or until progression.

Followed by maintenance therapy in patients without disease progression with

  • Bevacizumab 7.5 mg/kg i.v. and
  • Pemetrexed 500 mg/m2 i.v. every 3 weeks until progression.

Cohort 2:

Induction chemotherapy with

  • Pemetrexed 500 mg/m2 i.v. and
  • Cisplatin* 75 mg/m2 i.v. every 3 weeks for a maximum of 4 cycles or until progression.

Followed by maintenance therapy in patients without disease progression with

o Pemetrexed 500 mg/m2 i.v. every 3 weeks until progression.
Drug: bevacizumab, pemetrexed, cisplatin

Induction chemotherapy with

  • Bevacizumab 7.5 mg/kg i.v. and
  • Pemetrexed 500 mg/m2 i.v. and
  • Cisplatin* 75 mg/m2 i.v. every 3 weeks for a maximum of 4 cycles or until progression. Followed by maintenance therapy in patients without disease progression with
  • Bevacizumab 7.5 mg/kg i.v. and
  • Pemetrexed 500 mg/m2 i.v. every 3 weeks until progression.
Other Names:
  • Bevacizumab (Avastin)
  • pemetrexed (Alimta)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Progression-free survival at 6 months in stratum wtEGFR cohort 1
Time Frame: at 6 months
at 6 months

Secondary Outcome Measures

Outcome Measure
Time Frame
Progression-free survival
Time Frame: at 6 months
at 6 months
Overall survival
Time Frame: from registration until death
from registration until death
Best response (RECIST 1.1)
Time Frame: up to disease progression or start of new treatment
up to disease progression or start of new treatment
Adverse events (CTCAE v4.0)
Molecular markers in tumor tissue and blood

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Swiss Group for Clinical Cancer Research

Investigators

  • Study Chair: Oliver Gautschi, MD, Luzerner Kantonsspital
  • Principal Investigator: Adrian Ochsenbein, MD, University Hospital Inselspital, Berne
  • Principal Investigator: Nicolas Mach, MD, Hopital Cantonal Universitaire de Geneve HUG
  • Principal Investigator: Sacha Rothschild, MD, University Hospital, Basel, Switzerland

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (Actual)

July 1, 2014

Study Completion (Actual)

May 1, 2016

Study Registration Dates

First Submitted

April 27, 2010

First Submitted That Met QC Criteria

May 3, 2010

First Posted (Estimate)

May 4, 2010

Study Record Updates

Last Update Posted (Actual)

May 15, 2019

Last Update Submitted That Met QC Criteria

May 13, 2019

Last Verified

May 1, 2019

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SAKK 19/09
  • SWS-SAKK-19-09
  • EU-21026

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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