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Brain MetastasesRECARENCT04084431

Supportive Care With or Without Repeated Whole Brain Radiotherapy in Patients With Recurrent Brain Metastases

A study testing Radiation and OSC in people with Brain Metastases, run by University Hospital Heidelberg at 1 site in Germany.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

Patients with solid cancers may develop cerebral metastases, requiring whole brain radiotherapy (WBRT). Furthermore, in several cases, a secondary course of WBRT might be required due to intracerebral recurrence and limited options for alternative treatments, besides optimal supportive care (OSC). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Brain Metastases
What is being tested?
Radiation and OSC
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
1 siteGermany
Study dates
1 Jul 2019to 1 Jul 2025
Phase
Interventional
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

Who may be able to join

  • histologically confirmed malignancy
  • previous WBRT or prophylactic whole brain irradiation (PCI)
  • MR- or CT-imaging confirmed recurrent cerebral metastases (>10)
  • Or: MR- or CT-imaging confirmed recurrent cerebral metastases (1-10) and inability to perform SRS or surgery (e.g. meningeal carcinomatosis), concluded by interdisciplinary conference
  • age ≥ 18 years
  • Time between initial WBRT/PCI and recurrent WBRT >3 months
Show all 10Show fewer
  • WHO performance score ≤3
  • For women with childbearing potential, (and men) adequate contraception.
  • Ability of subject to understand character and individual consequences of the clinical trial
  • Written informed consent (must be available before enrolment in the trial)

Who cannot join

  • • refusal to take part in the study
  • Pregnant or lactating women
  • Participation in another competing clinical study or observation period of competing trials, respectively
  • Ability to perform SRS or surgery on brain metastases as a treatment alternative
  • Systemic anticancer treatment <4 weeks for chemotherapy and <1 week for TKIs and targeted therapies before randomisation.
  • Persons who are in a relationship of dependence/employment with the investigators
  • Cerebral lymphomas, metastases of germ cell tumours

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • University Hospital

    Heidelberg, 69120

Other trials in Germany

About this study

Official title: Supportive Care With or Without Repeated Whole Brain Radiotherapy in Patients With Recurrent Brain Metastases Unsuitable for Resection or Stereotactic Radiotherapy.

Patients with solid cancers may develop cerebral metastases, requiring whole brain radiotherapy (WBRT). Furthermore, in several cases, a secondary course of WBRT might be required due to intracerebral recurrence and limited options for alternative treatments, besides optimal supportive care (OSC). There have been few reports on re-irradiation of the whole brain, but further evaluation especially of the optimal dose concept is warranted. Especially, the efficacy compared to OSC has to date not been evaluated.

The present trial aims at evaluating the efficacy of a repeated WBRT with a total dose of 20 Gy in 10 fractions compared to OSC.

Read more

Primary endpoint is time to WHO performance status (PS) deterioration to more than 3 (duration of functional independence).

Secondary endpoints are quality of life, overall survival, radiation-induced toxicity and functional independence assessed by the Barthel Index of Activities of Daily Living (ADL)1.

Read the detailed description

According to Nussbaum et al., 24-45% of cancer patients develop cerebral metastases during their disease. Brain metastases are generally associated with a poor prognosis and high morbidity2. Published median survival rates after WBRT are between 2 and 7 months3. Standard of care in multiple BM is WBRT delivered as total dose of 30 Gy in 10 fractions, leading to modest palliation with a median survival of 3 to 5 months 4-6. Prognostic factors include the RPA-classification, performance status, response to steroids and evidence of systemic disease3,6.

Unfortunately, intracerebral recurrence happens 7-9. For example, in the cohort of Meyners et al. (2010) on WBRT in relatively radio-resistant tumours, median time to recurrence was 4.5 months and the local control rates at 6 and 12 months after radiotherapy were 37% and 15%, respectively10. Furthermore, the treatment of intracerebral recurrence after previous WBRT is challenging. In case of ≤ 3 recurrent BM, surgery or stereotactic radiosurgery (SRS) are options. One other option, especially in case of >3 recurrent BM is repeated WBRT. In this setting, one of the first reports on repeated WBRT was published by Cooper et al. in 199011. The authors reported on repeated WBRT (n=52) consisting of a total dose of 25 Gy in 10 fractions. Response to re-irradiation was seen in about 40% of the patients. Furthermore, the patients improved by at least one level in their neurologic function status. Survival after second therapy averaged 5 months. In the report by Wong et al. (1996) median dose of retreatment (n=86) was 20 Gy12. Resolution of symptoms was achieved in 27% of patients, partial improvement in 43% and no improvement or worsening of symptoms was seen in 29% of patients. The majority of patients had no significant toxicity in consequence of re-irradiation. Five patients had radiographic abnormalities of their brain consistent with radiation-related changes. One patient had symptoms of dementia that was thought to be caused by radiotherapy. Sadikov et al. (2007) reported on 72 patients who underwent repeated WBRT for recurrent or progressive BM13. The median survival after re-irradiation was 4.1 months. One patient was reported having memory impairment and pituitary insufficiency after 5 months of progression-free survival.

In the report by Mayer et al. on re-irradiation tolerance of the human brain (this analysis was focused on recurrent glioma), the authors concluded that radiation-induced brain tissue necrosis is likely to occur at normalized tolerance doses of cumulative > 100 Gy14.

The recent QUARTZ trial investigated the efficacy of WBRT vs. OSC in patients with non-small cell lung cancer and low performance status. The results suggest that WBRT, even in the primary situation, offers no substantial benefit to most patients with brain metastases from NSCLC in terms of improved survival, overall quality of life, or reduction of steroid use in this cohort15.

In the present trial, the primary endpoint (time to WHO PS deterioration to more than 3) as well as the secondary endpoints QoL, overall survival, radiation-induced toxicity and functional independence assessed by the Barthel Index of Activities of Daily Living (ADL) in patients previously treated with WBRT requiring repeated WBRT for intracerebral tumour progression will be evaluated.

Being tested
Radiation, OSC
Keywords
repeated whole brain radiation therapy
Medical subject headings
Brain Neoplasms

What participants receive

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

  • RadiationRadiation

    WBRT will be applied in 10 fractions with single doses of 2 Gy (Arm 1) to the whole brain

  • OSCOther

    optimal supportive Care (OSC) alone

Study groups in NCT04084431
Study groupRoleWhat they receive
WBRT (10 x 2 Gy) + OSCActive comparatorWhole brain radiotherapy will be applied with a total dose of 20 Gy in 10 fractions (single dose of 2 Gy). OSC as needed.
Receives: Radiation: Radiation
Optimal Supportive Care (OSC) aloneExperimentalSymptomatic treatment including steroids, pain medication, nutritional support, etc
Receives: Other: OSC

What is being measured

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

  1. Time to WHO PS to more than 3

    WHO Performance status

    Measured: up to 4 years or from date of randomization unitl the date of documented date of death from any cause

Secondary outcomes (1)
  1. OS

    Overall survival

    Measured: up to 4 years or from date of randomization unitl the date of documented date of death from any cause

Timeline

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

  1. First posted10 Sep 2019
  2. Study start1 Jul 2019
  3. Primary completion1 Jul 2024
  4. Study completion1 Jul 2025

Why it stopped: Organizational Reasons

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 N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Prospective, randomized 2-armed Phase II Pilot-Trial
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04084431
Sponsor's protocol ID
RECARE Trial Version 1.1
Acronym
RECARE
Status last verified
Apr 2026
First submitted
27 Aug 2019
Last updated
5 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Radiation and OSC in people with Brain Metastases, run by University Hospital Heidelberg 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?

The sponsor lists 10 inclusion and 7 exclusion criteria. 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: withdrawn, as of the sponsor's last update on 5 May 2026. 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.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

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?

Time to WHO PS to more than 3 (time frame: up to 4 years or from date of randomization unitl the date of documented date of death from any cause). 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 5 May 2026.

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