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Melanoma (Skin)Phase 2NCT00085059

Boron Neutron Capture Therapy Using Boronophenylalanine-Fructose Complex in Treating Patients With Metastatic Melanoma

A Phase 2 study testing boronophenylalanine-fructose complex in people with Melanoma (Skin), run by European Organisation for Research and Treatment of Cancer - EORTC at 1 site in Germany.

Terminated

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

Official record
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Trial summary

RATIONALE: Boron neutron capture therapy using boronophenylalanine-fructose complex may kill tumor cells without harming normal tissue. PURPOSE: This phase II trial is studying how well boron neutron capture therapy using boronophenylalanine-fructose complex works in treating patients with metastatic melanoma. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Melanoma (Skin)
What is being tested?
boronophenylalanine-fructose complex
How many people
4 participants
Where
1 siteGermany
Study dates
Apr 2004to Oct 2006
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 confirmed melanoma
  • Metastatic disease
  • Brain metastases, skin metastases, or soft tissue metastases of the head and neck or the extremities
  • Accessible lesion(s) for boron neutron capture therapy (BNCT)
  • No clear progression of disease at other sites than the ones intended for treatment with surgery and/or BNCT
  • Measurable disease by MRI within the past 4 weeks
  • Lesion(s) ≥ 10 mm in diameter
  • Indication for palliative radiotherapy that is intended to be delivered as BNCT

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Performance status

  • Karnofsky 70-100%

Life expectancy

  • Not specified

Hematopoietic

  • Neutrophil count ≥ 2,000/mm^3
  • Platelet count ≥ 100,000/mm^3
  • Hemoglobin ≥ 10 g/dL

Hepatic

  • Bilirubin ≤ 2.5 times upper limit of normal (ULN)*
  • Transaminases ≤ 2.5 times ULN*
  • Alkaline phosphatase ≤ 2.5 times ULN* NOTE: *Unless due to reversible reaction to antiseizure medication

Renal

  • Creatinine ≤ 2.5 times ULN
  • Blood urea nitrogen ≤ 2.5 times ULN

Cardiovascular

  • No congestive heart failure
  • No newly diagnosed or unstable angina pectoris
  • No uncontrolled arrhythmias
  • No uncontrolled conduction defects
  • No recent coronary artery disease
  • No other severe heart disease

Pulmonary

  • No severe pulmonary disease, including severe obstructive or restrictive lung disease

Other

  • No history of phenylketonuria
  • No severe gastrointestinal disease
  • No active peptic ulcer disease
  • No uncontrolled endocrine disease
  • No pre-existing serious mental or organic brain disease (e.g., epilepsy)
  • No psychological, familial, sociological, or geographical condition that would preclude study compliance
  • Able to travel to the Netherlands via public transportation
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • No concurrent immunologic or biologic therapy
  • No concurrent colony-stimulating factors (e.g., epoetin alfa or filgrastim [G-CSF])

Chemotherapy

  • No concurrent chemotherapy

Endocrine therapy

  • No concurrent hormonal therapy

Radiotherapy

  • No prior radiotherapy to site(s) proposed for study treatment
  • No other concurrent radiotherapy

Surgery

  • See Disease Characteristics

Other

  • Recovered from all prior anti-tumor therapy (excluding alopecia and sensitive peripheral neuropathy ≤ grade 2)
  • No other concurrent anticancer therapy
  • No other concurrent investigational drugs

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Universitaetsklinikum Essen

    Essen, D-45122

Other trials in Germany

About this study

Official title: Early Phase II Study On BNCT In Metastatic Malignant Melanoma Using The Boron Carrier BPA

RATIONALE: Boron neutron capture therapy using boronophenylalanine-fructose complex may kill tumor cells without harming normal tissue.

PURPOSE: This phase II trial is studying how well boron neutron capture therapy using boronophenylalanine-fructose complex works in treating patients with metastatic melanoma.

Read the detailed description

OBJECTIVES:

Primary

  • Determine the therapeutic activity and efficacy of boron neutron capture therapy using boronophenylalanine-fructose complex in patients with metastatic melanoma.
  • Determine the objective local response in patients treated with this regimen.

Secondary

  • Determine the overall survival of patients treated with this regimen.
  • Determine the duration of local response and time to local progression in patients treated with this regimen.
  • Determine the dose-response relationship at the per-lesion level in patients treated with this regimen.
  • Determine the safety of this regimen in these patients.
  • Determine the toxicity of this regimen in these patients.

OUTLINE: This is an open-label study.

Patients receive boronophenylalanine-fructose complex IV over 90 minutes followed by boron neutron capture therapy on days 1 and 2.

Patients are followed at 1 and 6 weeks and then every 8 weeks thereafter. In the event of disease progression, patients are followed every 3 months for survival.

PROJECTED ACCRUAL: A total of 16-24 patients will be accrued for this study.

Conditions
Melanoma (Skin)
Being tested
boronophenylalanine-fructose complex
Keywords
stage IV melanoma, recurrent melanoma
Medical subject headings
Melanoma

What participants receive

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

  • boronophenylalanine-fructose complexDrug

What is being measured

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

  1. Best response to treatment as measured by RECIST every 8 weeks at completion of study treatment

Secondary outcomes (5)
  1. Overall survival as measured every 8 weeks at completion of study treatment

  2. Duration of local response as measured by Kaplan Meier every 8 weeks after completion of study treatment

  3. Time to local progression measured every 8 weeks after completion of study treatment

  4. Acute toxicity as measured by Common Toxicity Criteria AE v 3.0 1- 6 weeks after completion of treatment

  5. Late toxicity as measured by RTOG and EORTC week 6 and thereafter upon completion of study treatment

Timeline

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

  1. First posted11 Jun 2004 (estimated)
  2. Study startApr 2004
  3. Primary completionOct 2006

Why it stopped: low accrual

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
Masking
None (open label)
Enrolment
4 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00085059
Sponsor's protocol ID
EORTC-11011
Other IDs
EORTC-11011
Status last verified
Jul 2012
First submitted
10 Jun 2004
Last updated
18 Jul 2012
Results posted
No

Publications

  • Wittig A, Moss RL, Stecher-Rasmussen F, Appelman K, Rassow J, Roca A, Sauerwein W. Neutron activation of patients following boron neutron capture therapy of brain tumors at the high flux reactor (HFR) Petten (EORTC Trials 11961 and 11011). Strahlenther Onkol. 2005 Dec;181(12):774-82. doi: 10.1007/s00066-005-1433-4.

    PubMed 16362787

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing boronophenylalanine-fructose complex in people with Melanoma (Skin), run by European Organisation for Research and Treatment of Cancer - EORTC at 1 site in Germany.

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 18 Jul 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. 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. 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: low accrual). 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?

Best response to treatment as measured by RECIST every 8 weeks at completion of study treatment. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00085059, which also lists 1 linked publication.

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 18 Jul 2012.

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