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

Primary Purpose

Brain Metastases

Status
Suspended
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Radiation
OSC
Sponsored by
University Hospital Heidelberg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Metastases focused on measuring repeated whole brain radiation therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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
  • 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)

Exclusion Criteria:

  • • 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

Sites / Locations

  • University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

WBRT (10 x 2 Gy) + OSC

Optimal Supportive Care (OSC) alone

Arm Description

Whole brain radiotherapy will be applied with a total dose of 20 Gy in 10 fractions (single dose of 2 Gy). OSC as needed.

Symptomatic treatment including steroids, pain medication, nutritional support, etc

Outcomes

Primary Outcome Measures

Time to WHO PS to more than 3
WHO Performance status

Secondary Outcome Measures

OS
Overall survival

Full Information

First Posted
August 27, 2019
Last Updated
September 28, 2021
Sponsor
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT04084431
Brief Title
Supportive Care With or Without Repeated Whole Brain Radiotherapy in Patients With Recurrent Brain Metastases
Acronym
RECARE
Official Title
Supportive Care With or Without Repeated Whole Brain Radiotherapy in Patients With Recurrent Brain Metastases Unsuitable for Resection or Stereotactic Radiotherapy.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Suspended
Why Stopped
organizational reasons
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
July 1, 2024 (Anticipated)
Study Completion Date
July 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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). 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. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastases
Keywords
repeated whole brain radiation therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, randomized 2-armed Phase II Pilot-Trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
WBRT (10 x 2 Gy) + OSC
Arm Type
Active Comparator
Arm Description
Whole brain radiotherapy will be applied with a total dose of 20 Gy in 10 fractions (single dose of 2 Gy). OSC as needed.
Arm Title
Optimal Supportive Care (OSC) alone
Arm Type
Experimental
Arm Description
Symptomatic treatment including steroids, pain medication, nutritional support, etc
Intervention Type
Radiation
Intervention Name(s)
Radiation
Intervention Description
WBRT will be applied in 10 fractions with single doses of 2 Gy (Arm 1) to the whole brain
Intervention Type
Other
Intervention Name(s)
OSC
Intervention Description
optimal supportive Care (OSC) alone
Primary Outcome Measure Information:
Title
Time to WHO PS to more than 3
Description
WHO Performance status
Time Frame
up to 4 years or from date of randomization unitl the date of documented date of death from any cause
Secondary Outcome Measure Information:
Title
OS
Description
Overall survival
Time Frame
up to 4 years or from date of randomization unitl the date of documented date of death from any cause

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 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) Exclusion Criteria: • 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
Facility Information:
Facility Name
University Hospital
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No

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

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