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Status unknownNCT02887651C-O-METUpdated Mar 22, 2022

Cavity Boost Radiation Therapy vs. Observation in Cerebral Metastases After Complete Surgical Resection

An interventional study of Cavity boost radiation in Cerebral Metastases and Surgery, sponsored by Heinrich-Heine University, Duesseldorf. Status unknown at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-03-22.

Sponsored by Heinrich-Heine University, Duesseldorf · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2022), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
108
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to determine whether a local fractionated radiation therapy achieves a better local tumor control after complete surgical metastases resection at 6 month as compared to observation alone. Further it should be evaluated if cognitive functioning and quality of life is similar in both groups.

Read the detailed description

The surgical resection of cerebral metastases as a key element in a multimodal therapeutic concept of brain metastatic patients is included in the common recommendations and international guidelines (level I evidence). These recommendations are based on a series of prospective, randomized and controlled studies which addressed the impact of the surgical metastases resection combined with a whole-brain radiation therapy (WBRT) in comparison to WBRT alone. Achieving local tumor control is the major goal of surgery and local tumor control rate after surgery alone has been addressed in few studies: A prospective, randomized American multicenter study revealed a local recurrence rate of 46% by median follow-up of 43 weeks for patients who underwent surgery alone without an adjuvant radiation therapy. Similarly, the 2-year local recurrence rate after metastases resection alone was 53.1% in a retrospective Korean study and 59% in the prospective, randomized and controlled EORTC 22952-26001 study.

In conclusion, standard surgery alone is not sufficient to achieve local control in about 50% of patients (evidence level I). Therefore, surgery of cerebral metastases is often followed by an adjuvant radiation therapy, which is an important part of a multi-modal therapy. Evidence for an additional adjuvant whole-brain radiation therapy (WBRT) after surgical resection was gained from a first prospective, randomized study in 1998: Patients treated by surgery followed by adjuvant WBRT had a significant lower local in-brain progression rate as compared to patients randomized to surgery alone (46% with a median follow-up of 48 weeks in the observation group vs. 10% with a median follow-up of 43 weeks). This result was recently confirmed by the EORTC 22952-26001 study: The 2-year local in-brain progression rate after surgical resection was reduced by a WBRT from 59% to 27%. But despite the lower local and also lower distant in-brain progression rate, the WBRT had no significant influence on the overall survival. The additional analysis of the quality of life data of the EORTC 22952-26001 study showed, that a WBRT negatively impacts the health-related quality of life with a statistically relevant and clinically significant impairment of the physical functioning (at 8 weeks), cognitive functioning and of the global health status. In conclusion, WBRT after surgery of cerebral metastases significantly reduces the incidence of local recurrences but has no impact on the overall survival and has a significant negative impact on the patient´s quality of life and cognitive function. Therefore, WBRT is not mandatory as adjuvant concept after surgical metastases resection and does not have an additional oncological impact in comparison to observation.

A local fractionated radiation therapy in analogy to the WBRT might achieve a similar local tumor control than observation alone but might be associated with an improved cognitive functioning as compared to WBRT. The purpose of this study is to determine whether a local fractionated radiation therapy achieves a better local tumor control after complete surgical metastases resection at 6 month as compared to observation alone. Further it should be evaluated if cognitive functioning and quality of life is similar in both groups.

02

Conditions studied

  • Cerebral Metastases
  • Surgery

Keywords

  • cerebrale metastases
  • radiotherapy
  • surgery
  • complete surgical resection
  • resection
  • cavity boost radiation therapy
  • observation
03

In context

Lead sponsor

Heinrich-Heine University, Duesseldorf is the lead sponsor of 180 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • histologically confirmed metastasis of carcinoma (except small cell carcinoma) or malignant melanoma
  • 1-3 metastases in the preoperative MRI
  • Karnofsky Performance Status (KPS) ≥ 70
  • Age > / = 18 years
  • Recursive partitioning analysis (RPA) 1-2
  • life expectation ≥ 6 months
  • no previous irradiation of the brain
  • MRI examinations possible
  • start of the radiation therapy possible within 6 weeks after surgery
  • informed consent

Exclusion criteria

Exclusion Criteria:

  • confirmation of residual tumor in the postoperative MRI
  • dementia or disease of central nervous system with a higher risk or radiogenic toxicity
  • contraindication for MRIs or lack of acceptance for a MRI
  • Glasgow Coma Scale \< 12
  • Severe concomitant disease: severe cardiac, pulmonary, renal diseases with an increased risk of surgery and radiation
  • previous therapeutic irradiation of the brain
  • no histological confirmation of carcinoma metastases or malignant melanoma metastases
  • cerebral metastases of small cell cancer, undifferentiate neuro-endocrine carcinoma, lymphoma, leucemia, sarcoma or germ cell tumor
  • leptomeningeal carcinosis
  • distance of the cerebral metastasis to the optic system or radiation sensible brain parts \< 10 mm
  • metastases of the brain stem, Di- or Mesencephalons, Pons oder Medulla oblongata
  • bone marrow dysfunction
  • contrast agent allergy
  • pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
108 participants (estimated)

Study arms

  • No intervention
    observation

    patients in the observation arm receive no adjuvant local radiation therapy after complete surgical resection of a cerebral metastasis

  • Active comparator
    cavity boost radiation therapy

    patients in the intervention arm receive an adjuvant local radiation therapy (cavity boost radiation therapy: 10 x 3 Gy ad 30 Gy; clinical target volume (CTV): resection cavity plus surrounding 5 mm; planning target volume (PTV): CTV + 1mm)

    Radiation: Cavity boost radiation

Interventions

  • RadiationCavity boost radiation

    Cavity boost radiation therapy with 10 x 3 Gy for patients suffering from complete resected cerebral metastases

06

What researchers measure

Primary outcomes

  1. Local tumor control of resected metastases at 6 month

    Primary outcome measure is the local tumor control of resected metastases after local cavity boost radiation therapy or observation at 6 month

    Time frame: 6 month

Secondary outcomes

  1. Local tumor control of resected metastases at 12 and 18 month

    Secondary outcome measure is the local tumor control of resected metastases after local cavity boost radiation therapy or observation at 12 and 18 month

    Time frame: 12, 18 month

  2. Distant tumor control of resected metastases at 6, 12 and 18 month

    Secondary outcome measure is the distant tumor control at 6, 12 and 18 month

    Time frame: 6, 12 and 18 month

  3. Incidence of leptomeningeal carcinosis

    Secondary outcome measure is the incidence of a leptomeningeal carcinosis at 6, 12 and 18 month

    Time frame: 6, 12 and 18 month

  4. Eortc qlq bn20 questionaire

    Secondary outcome measure is the patients quality of life at 3, 6, 9 12, 15, 18 month as assessed by the Eortc qlq bn20 questionaire

    Time frame: 3, 6, 9 12, 15, 18 month

  5. Eortc qlq c30 questionaire

    Secondary outcome measure is the patients quality of life at 3, 6, 9, 12, 15 and 18 month as assessed by the Eortc qlq c30 questionaire

    Time frame: 3, 6, 9, 12, 15, 18 month

  6. Mini-Mental State Examination (MMSE)

    Secondary outcome measure is the patients neurocognitive functioning at 3, 6, 9 12, 15 and 18 month as assessed by the MMSE

    Time frame: 3, 6, 9 12, 15, 18 month

  7. Hopkins Verbal Learning Test (HVLT)

    Secondary outcome measure is the patients neurocognitive functioning at 3, 6, 9, 12, 15 and 18 month as assessed by the Hopkins Verbal Learning Test (HVLT),

    Time frame: 3, 6, 9 12, 15, 18 month

  8. Controlled Oral Word Association (COWA)

    Secondary outcome measure is the patients neurocognitive functioning at 3, 6, 9 12, 15 and 18 month as assessed by the Controlled Oral Word Association (COWA)

    Time frame: 3, 6, 9 12, 15, 18 month

  9. Test and Trail-Making Test (TMT) A & B

    Secondary outcome measure is the patients neurocognitive functioning at 3, 6, 9 12, 15 and 18 month as assessed by the Test and Trail-Making Test (TMT) A \& B

    Time frame: 3, 6, 9 12, 15, 18 month

07

Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02887651
Responsible party
Sponsor
First posted
Sep 2, 2016
Start date
Nov 14, 2016
Primary completion
Dec 2023 (estimated)
Completion
Dec 2024 (estimated)
Last update
Mar 22, 2022

Study contacts

Marcel A. Kamp, MD
Contact
marcelalexander.kamp@med.uni-duesseldorf.de
0049 - 211 - 81 - 07461
Michael Sabel, Prof. Dr.
principal investigator · Department of Neurosurgery
Wilfried Budach, Prof. Dr.
principal investigator · department of radiation oncology

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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