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Lung CancerPhase 2TACTICNCT00554775

WBRT & Erlotinib in Advanced NSCLC and Brain Metastases

A Phase 2 study testing erlotinib hydrochloride in people with Lung Cancer and Metastatic Cancer, run by University College, London at 7 sites in United Kingdom.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

RATIONALE: Radiation therapy uses high energy x-rays to kill tumor cells. Erlotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Erlotinib may also make tumor cells more sensitive to radiation therapy. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Lung Cancer, Metastatic Cancer
What is being tested?
erlotinib hydrochloride
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
80 participants
Where
7 sitesUnited Kingdom
Study dates
Jan 2008to Nov 2010
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed advanced non-small cell lung cancer (NSCLC) meeting 1 of the following criteria:
  • Newly diagnosed multiple brain metastases not suitable for first-line chemotherapy
  • Relapsed NSCLC with newly diagnosed multiple brain metastases
  • Relapsed after second-line chemotherapy with newly diagnosed multiple brain metastases NOTE: *Biopsy of brain metastases is not required
  • Diagnosis of brain metastases must be confirmed by contrast CT scan or MRI within the past 4 weeks
  • Symptoms attributable to brain metastases
  • Patients who have undergone craniotomy with incomplete resection are eligible
  • Clinician certain that whole-brain radiotherapy (WBRT) will be beneficial
  • No evidence of solitary brain metastasis on MRI that can be treated with surgical resection, radiosurgery, or stereotactic radiotherapy
  • No more than 3 sites (organ systems) of extracranial metastases
  • No liver metastases

PATIENT CHARACTERISTICS:

  • Karnofsky performance status 70-100%
  • RTOG recursive partitioning analysis (RPA) class I or II
  • Serum bilirubin < 2 times upper limit of normal (ULN)
  • AST and ALT < 2 times ULN (< 5 times ULN if liver metastases are present)
  • Creatinine < 5 times ULN
  • Able to take oral medication
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • Caretaker able and willing to participate in the study
  • Patient and caretaker have access to a telephone and willing to respond to telephone interview
  • No other prior or concurrent malignant disease likely to interfere with study treatment or comparisons
  • No evidence of other significant laboratory finding or concurrent uncontrolled medical illness, that in the opinion of the investigator, would interfere with study treatment or results comparison or render the patient at high risk for treatment complications including, but not limited to, any of the following:
  • Severe uncontrolled infection
  • Unstable angina
  • Myocardial infarction within the past month
  • Uncontrolled inflammatory bowel disease (e.g., Crohn's disease or ulcerative colitis)
  • Acute renal failure

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • At least 28 days since prior chemotherapy (for relapsed patients originally treated with chemotherapy)
  • No prior cranial radiotherapy
  • No prior anti-cancer EGFR therapy (e.g., erlotinib, gefitinib, or cetuximab)
  • No prior treatment for brain metastases (e.g., radiosurgery, radiotherapy, or chemotherapy)
  • Prior radiotherapy to the primary tumor and/or systemic treatment to metastatic sites of disease allowed
  • No concurrent cyclooxygenase-2 (COX-2) inhibitors

Trial locations and contacts

7 sites in 1 country.

7 sites in 1 country

United Kingdom7 sites
  • Charing Cross Hospital

    London, England, W6 8RF

  • University College of London Hospitals

    London, England, WIT 3AA

  • Christie Hospital

    Manchester, England, M20 4BX

  • Glan Clwyd Hospital

    Rhyl, Denbighshire, Wales, LL18 5UJ

  • Salisbury District Hospital

    Salisbury, England, SP2 8BJ

  • Southampton General Hospital

    Southampton, England, SO16 6YD

  • South West Wales Cancer Institute

    Swansea, Wales, SA2 8QA

Other trials in United Kingdom

About this study

Official title: A Randomised Phase II Double Blind Placebo Controlled Trial of Whole Brain Radiotherapy (WBRT) and Tarceva (OSI-774, Erlotinib) in Patients With Advanced Non-Small Cell Lung Cancer (NSCLC) With Multiple Brain Metastases [TACTIC]

RATIONALE: Radiation therapy uses high energy x-rays to kill tumor cells. Erlotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Erlotinib may also make tumor cells more sensitive to radiation therapy. It is not yet known whether giving whole-brain radiation therapy together with erlotinib is more effective than whole-brain radiation therapy alone in treating patients with non-small cell lung cancer and brain metastases.

PURPOSE: This randomized phase II trial is studying whole-brain radiation therapy and erlotinib to see how well they work compared with whole-brain radiation therapy alone in treating patients with advanced non-small cell lung cancer and brain metastases.

Read the detailed description

OBJECTIVES:

Primary

  • Compare the effect of whole-brain radiotherapy (WBRT) and erlotinib hydrochloride vs WBRT alone on neurological progression-free survival at 2 months in patients with advanced non-small cell lung cancer and multiple brain metastases.

Secondary

  • Compare the toxicity of these regimens.
  • Compare the response rate in these patients.
  • Compare quality of life of these patients.
  • Compare change in performance status in these patients.
  • Compare steroid dosing in these patients.
  • Compare sites of progression (cranial or extracranial) in these patients.

OUTLINE: This is a multicenter study. Patients are stratified by presence of extracranial metastases (yes vs no), RTOG recursive partitioning analysis (RPA) score (I vs II) and treatment center. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients undergo whole-brain radiotherapy (WBRT) once daily for 5 days. Patients also receive oral erlotinib hydrochloride once daily for up to 24 months.
  • Arm II: Patients undergo WBRT as in arm I. Patients also receive oral placebo once daily for up to 24 months.

Quality of life is assessed at baseline, monthly for 12 months, and then at 18 and 24 months.

After completion of study therapy, patients are followed every 1-2 months.

Peer Reviewed and Funded or Endorsed by Cancer Research UK.

Being tested
erlotinib hydrochloride, placebo
Keywords
tumors metastatic to brain, stage IV non-small cell lung cancer, recurrent non-small cell lung cancer
Medical subject headings
Lung Neoplasms, Neoplasm Metastasis, Brain Neoplasms, Carcinoma, Non-Small-Cell Lung

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • erlotinib hydrochlorideDrug

    Also called tarceva, OSI-774

    PO 100 mg daily during WBRT, increasing to 150mg daily after WBRT for up to 24 months

  • placeboDrug

    WBRT plus matched placebo for the same schedule and duration as erlotinib hydrochloride

Study groups in NCT00554775
Study groupRoleWhat they receive
erlotinib hydrochlorideExperimentalWBRT plus Tarceva (OSI-774, erlotinib) PO 100 mg daily during WBRT, increasing to 150mg daily after WBRT for up to 24 months
Receives: Drug: erlotinib hydrochloride
placeboPlacebo comparatorWBRT plus matched placebo for the same schedule and duration as erlotinib hydrochloride arm
Receives: Drug: placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Neurological progression-free survival at 2 months

    Measured: at 2 months

Secondary outcomes (6)
  1. Toxicity

    Measured: during and for 28 days following Tarceva/placebo treatment.

  2. Response rate

    Measured: from date of randomisation to radiological progression

  3. Quality of life

    Measured: completed monthly for the first 12 months and at 18 and 24 months from randomisation

  4. Change in performance status

    Measured: from baseline

  5. Steroid dosing

    Measured: from baseline

  6. Sites of progression (cranial or extracranial)

    Measured: from baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Nov 2007 (estimated)
  2. Study startJan 2008
  3. Primary completionNov 2010
  4. Study completionNov 2010

Why it stopped: IDMC made a recommendation to stop the trial as the target for continuing to the 2nd phase was not met.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
80 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00554775
Sponsor's protocol ID
CDR0000573254
Other IDs
CRUK-UCL-BRD-05-177, BRD/05/177, EUDRACT-2006-000113-38, CRUK-TACTIC, EU-20792, ISRCTN31916843
Acronym
TACTIC
Status last verified
Dec 2011
First submitted
6 Nov 2007
Last updated
12 Dec 2011
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing erlotinib hydrochloride in people with Lung Cancer and Metastatic Cancer, run by University College, London at 7 sites in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 12 Dec 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 7 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was stopped early (reason given: IDMC made a recommendation to stop the trial as the target for continuing to the 2nd phase was not met.). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Neurological progression-free survival at 2 months (time frame: at 2 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Dec 2011.

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