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Focused Ultrasound and RadioTHERapy for non-invasive palliative pain treatment in patients with bone metastasis: a study protocol for the three armed randomized controlled FURTHER trial

Slotman Derk J; Bartels Marcia MTJ; Ferrer Cyril J; Bos Clemens; Bartels Lambertus W.; Boomsma Martijn F.; Phernambucq Erik C. J.; Nijholt Ingrid M.; Morganti Alessio G.; Siepe Giambattista; Buwenge Milly; Grüll Holger; Bratke Grischa; Yeo Sin Yuin; Blanco Sequeiros Roberto; Minn Heikki; Huhtala Mira; Napoli Alessandro; De Felice Francesca; Catalano Carlo; Bazzocchi Alberto; Gasperini Chiara; Campanacci Laura; Simões Corrêa Galendi Julia; Müller Dirk; Braat Manon N. G. J. A.; Moonen Chrit; Verkooijen Helena M.; FURTHER consortium

Focused Ultrasound and RadioTHERapy for non-invasive palliative pain treatment in patients with bone metastasis: a study protocol for the three armed randomized controlled FURTHER trial

Slotman Derk J
Bartels Marcia MTJ
Ferrer Cyril J
Bos Clemens
Bartels Lambertus W.
Boomsma Martijn F.
Phernambucq Erik C. J.
Nijholt Ingrid M.
Morganti Alessio G.
Siepe Giambattista
Buwenge Milly
Grüll Holger
Bratke Grischa
Yeo Sin Yuin
Blanco Sequeiros Roberto
Minn Heikki
Huhtala Mira
Napoli Alessandro
De Felice Francesca
Catalano Carlo
Bazzocchi Alberto
Gasperini Chiara
Campanacci Laura
Simões Corrêa Galendi Julia
Müller Dirk
Braat Manon N. G. J. A.
Moonen Chrit
Verkooijen Helena M.
FURTHER consortium
Katso/Avaa
s13063-022-06942-1.pdf (971.0Kb)
Lataukset: 

BMC
doi:10.1186/s13063-022-06942-1
URI
https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-022-06942-1
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2023020225519
Tiivistelmä

Background

Cancer-induced bone pain (CIBP), caused by bone metastases, is a common complication of cancer and strongly impairs quality of life (QoL). External beam radiotherapy (EBRT) is the current standard of care for treatment of CIBP. However, approximately 45% of patients have no adequate pain response after EBRT. Magnetic resonance image-guided high-intensity focused ultrasound (MR-HIFU) may improve pain palliation in this patient population. The main objective of this trial was to compare MR-HIFU, EBRT, and MR-HIFU + EBRT for the palliative treatment of bone metastases.

Methods/design

The FURTHER trial is an international multicenter, three-armed randomized controlled trial. A total of 216 patients with painful bone metastases will be randomized in a 1:1:1 ratio to receive EBRT only, MR-HIFU only, or combined treatment with EBRT followed by MR-HIFU. During a follow-up period of 6 months, patients will be contacted at eight time points to retrieve information about their level of pain, QoL, and the occurrence of (serious) adverse events. The primary outcome of the trial is pain response at 14 days after start of treatment. Secondary outcomes include pain response at 14 days after trial enrolment, pain scores (daily until the 21st day and at 4, 6, 12 and 24 weeks), toxicity, adverse events, QoL, and survival. Cost-effectiveness and cost-utility analysis will be conducted.

Discussion

The FURTHER trial aims to evaluate the effectiveness and cost-effectiveness of MR-HIFU—alone or in combination with EBRT—compared to EBRT to relieve CIBP. The trial will be performed in six hospitals in four European countries, all of which are partners in the FURTHER consortium.

Trial registration

The FURTHER trial is registered under the Netherlands Trials Register number NL71303.041.19 and ClinicalTrials.gov registration number NCT04307914. Date of trial registration is 13–01-2020.

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