In this study, patients with malignant epidural spinal cord compression (MESCC), Bilsky
grade 1c, 2 and 3 who are ambulatory with or without aid (rollator, cane, one persons
help) will be treated by separation surgery followed by SABR (5x 8.0 Gy postoperative)
(control arm) or SABR alone (5x 8.0 Gy) (study arm). The primary objective of the study
is investigating the effect of SABR compared to separation surgery followed by SABR in
ambulatory patients with MESCC on retaining ambulatory function. The primary endpoint of
the study is ambulatory function 3 months post treatment defined as: being able to walk
10m without aid; being able to walk 10m with aid (cane, rollator, one persons help, ...);
not being able to walk. Secondary outcomes are local control, progression free survival,
early and late adverse effects, quality of life, effect on pain and need for
reintervention.
For each participant, the study starts once written informed consent is provided and is
composed by 4 study phases: a screening phase, randomisation, a treatment phase and a
follow-up phase.
The screening phase will allow for assessment of subject eligibility before randomisation
and treatment. Demographic data, disease and spinal metastases characteristics and
previous anticancer therapies will be recorded. Once all screening procedures are
completed, eligibility will be determined according to the inclusion/exclusion criteria.
Randomisation will be performed in a 1:1 ratio to the control arm (separation surgery
followed by SABR) and the study arm (SABR) using an electronic randomisation tool in the
eCRF.
Treatment will be aimed to start as soon as possible, but certainly within 21 days after
randomisation (surgery or upfront SABR). Surgical planning is done by the treating
neurosurgeon in the participating center where the patient was included. Image-guided
fractionated SABR using a SIB technique to the high-dose PTV will be delivered in 5
fractions of 8 Gy to a total of 40 Gy and to the conventional-dose PTV delivered
simultaneously in 5 fractions of 4 Gy to a total of 20 Gy.
At 6 weeks (+/-1 week) after the last RT session following information will be obtained
(preferentially by digital consult):
Ambulatory status defined as: being able to walk 10m without aid, being able to walk
10m with aid (cane, rollator, one persons help, ...), not being able to walk
WHO performance status
Acute and late toxicity assessment: as measured with CTCAE version 5.0
Need for re-intervention, date and type of reintervention (surgery or radiotherapy),
reason (wound infection, neurologic decline, loss of ability to walk or other)
Pain response: VAS pain score
Survival data (survival status, date of death, primary cause of death)
At 3 and 6 months (+/-3 weeks) after the last RT session following information will be
obtained by physical or digital consult:
Ambulatory status defined as: being able to walk 10m without aid, being able to walk
10m with aid (cane, rollator, one persons help, ...), not being able to walk
WHO performance status
Concomitant medications and systemic anticancer therapies
QoL according to the EORTC QLQ-C15 & BM22 questionnaires
Acute and late toxicity assessment: as measured with CTCAE version 5.0
Need for re-intervention, date and type of reintervention (surgery or radiotherapy),
reason (wound infection, neurologic decline, loss of ability to walk or other) 6.
Pain response: VAS pain score 7. Physical examination: body weight 8. Local control
- Survival data (survival status, date of death, primary cause of death)
At 12 and 24 months (+/-3 weeks) after the last RT session following information will be
obtained (preferentially by digital consult):
Ambulatory status defined as: being able to walk 10m without aid, being able to walk
10m with aid (cane, rollator, one persons help, ...), not being able to walk
Need for re-intervention, type of reintervention
Survival data (survival status, date of death, primary cause of death)
Local control (only if information is available in medical record as per standard of
care)