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NCT03143322Active, not recruiting

Standard Treatment +/- SBRT in Solid Tumors Patients With Between 1 and 5 Bone-only Metastases

Extracranial Stereotactic Body Radiation Therapy (SBRT) Added to Standard Treatment Versus Standard Treatment Alone in Solid Tumors Patients With Between 1 and 5 Bone-only Metastases

Source: ClinicalTrials.gov · Last updated 26 Nov 2025

Brief summary (registry, in English)

Bone metastases occur frequently during the evolution of solid tumors, either isolated or associated with visceral metastases. The incidence varies between 20 and 85% depending on the primary cancer. Breast, prostate, and lung cancers are responsible for 70% of bone metastases. Cancer with bone metastases compared to other metastatic sites is considered as associated with a better prognosis, particularly for breast and prostate cancer. Bone metastases may be present at diagnosis (synchronous metastasis) or appear at a later time (metachronous metastasis). The concept of "oligometastases" was proposed in patients with about 3 up to 5 metastases (without restriction on the primary site) and associated with an intermediate prognosis. It was hypothesized that local treatment with curative intent, aiming at the few metastatic sites, would yield long-term survival probabilities, along with systemic therapies. Long-term survivors have been reported after curative-intent treatment of metastasis in sarcoma and colorectal cancers with liver or lung metastasis. We chose to focus on bone metastasis because of their high incidence, their impact on the patient's quality of life and autonomy, and their accessibility to potentially curative radiotherapy. The systemic treatment of metastatic cancer includes hormonal therapy (breast and prostate cancer), biologically-targeted drugs and chemotherapy (all cancers). Stereotactic radiotherapy is a highly accurate technique was initially developed for performing the radiosurgery of brain tumors in patients for whom it was deemed be too difficult to proceed to classical excision surgery. In this process, a high total dose of radiation is delivered in a single fraction to a well-defined intra-cranial target. The concept of radiotherapy in stereotactic conditions was extended to one or several fractions delivered to small volumes primary tumors/ metastases in extra-cranial sites (Stereotactic Body RadioTherapy \[SBRT\]). At present, high control rates have been achieved for lung metastases. Similarly, very high local control rates have been reported in bone metastases after stereotactic radiotherapy. In this protocol, our purpose is to demonstrate, via a randomized phase III trial, that high doses of radiotherapy, delivered in stereotactic conditions to the bone metastases (between 1 and 5 metastases) in solid tumor patients is able to improve the survival without progression.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
168 (actual)
First submitted
28 Apr 2017
Start date
24 Jul 2018
Primary completion date
31 Jul 2025
Lead sponsor
UNICANCER
NCT number
NCT03143322

What you commit to

  • Study type: Interventional
  • Participants enrolled: 168
  • From 24 Jul 2018 to the primary completion date, 31 Jul 2025
  • 28 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous systemic therapy for metastasis for patients with metachronous metastasis. Prostate and breast cancer patients remain eligible if hormonal treatment was initiated 6 months before enrollment
  • All bone metastasis requiring surgical treatment (spinal cord compression, fracture…)
  • Previous radiotherapy on bone metastasis (e.g: antalgic radiotherapy)

Other illness

  • Visceral metastases as defined by FDG-PET (F-Choline-PET or PSMA PET-CT for prostate cancer) and cerebral CT or MRI performed.
  • Previous cancer within the 5 years before inclusion (except basal cell carcinoma of the skin, in situ carcinoma of the uterine cervix)
  • Hypersensitivity to the active substance (FDG and NaF or F-Choline or PSMA for prostate cancer) or to any of the excipients
  • Patients deprived of liberty or placed under the authority of a tutor. Patients with any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial. Patients unable to understand the purpose of the study (language, etc.).

Other

  • More than 5 bone metastases as defined by NaF-PET or conventional SPECT-CT scan and spinal MRI (if spinal bone metastases on NaF-PET)
  • Patient enrolled in another therapeutic trial
  • Pregnant women or breast feeding mothers,
  • Contraindication to MRI (in case of spinal metastases)

Who the study is looking for

  • Patients older than 18 years and younger than 75 years
  • Good general condition: WHO performance status ≤ 2
  • Patients with histological proof of breast, non-small cell lung, or prostate cancer Note: Histological proof can be done on the primitive tumour and/or adenopathy and/or metastatic site.
  • Absence of co-morbidity contra-indicating radio-chemotherapy or surgery
  • Primary tumor accessible to curative-intent treatment (surgery, chemoradiation…) for patients with synchronous metastases
  • Patients with between 1 and 5 synchronous or metachronous bone metastases as defined by NaF-PET or conventional SPECT-CT scan and spinal MRI (if necessary) within 6 weeks before randomization)
  • Bones metastases treatable by SBRT
  • Primary cancer considered to be controlled or accessible to curative-intent treatment (surgery, chemoradiation…) in case of locoregional recurrence for metachronous bone oligo-metastatic disease
  • Women of childbearing potential and male patients must agree to use adequate contraception for the duration of study participation and up to 3 months following completion of therapy
  • Patients who have received the information sheet, dated and signed the informed consent form
  • Affiliated to the social security system

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (28)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
ICO - Site Paul Papin
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AngersFranceUnknown status
Hôpital Privé Les Bonnettes
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ArrasFranceUnknown status
Centre Marie Curie
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ArrasFranceUnknown status
Institut Sainte-Catherine
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AvignonFranceUnknown status
Clinique Ambroise Pare
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BeuvryFranceUnknown status
Centre Pierre Curie
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BeuvryFranceUnknown status
Clinique Tivoli-Ducos
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BordeauxFranceUnknown status
Institut Bergonie
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BordeauxFranceUnknown status
Hôpital Métropole Savoie
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ChambéryFranceUnknown status
Pôle Leonard de Vinci
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Chambray-lès-ToursFranceUnknown status
Centre Amethyst CROM
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CreilFranceUnknown status
Hopital Henri Mondor
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CréteilFranceUnknown status
Centre Léonard de Vinci
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DechyFranceUnknown status
Institut de Cancérologie de Bourgogne
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DijonFranceUnknown status
Chu Grenoble
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GrenobleFranceUnknown status
Centre Oscar Lambret
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LilleFranceUnknown status
Hôpital Privé Le Bois
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LilleFranceUnknown status
Centre Leon Berard
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LyonFranceUnknown status
Institut Paoli-Calmettes
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MarseilleFranceUnknown status
Centre de Cancérologie du Grand Montpellier
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MontpellierFranceUnknown status
Institut de cancérologie de Lorraine
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NancyFranceUnknown status
Institut de Cancérologie de l'Ouest
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NantesFranceUnknown status
Centre Catalan d'Oncologie
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PerpignanFranceUnknown status
Institut Jean Godinot
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ReimsFranceUnknown status
Centre Henri Becquerel
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RouenFranceUnknown status
Centre d'oncologie et radiothérapie Saint-Jean
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Saint-DoulchardFranceUnknown status
GCS RISSA - Institut de cancérologie Paris Nord
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SarcellesFranceUnknown status
Clinique des dentellières
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ValenciennesFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.