We use cookies necessary to giving you a better online experience. By using our website you consent to all cookies in accordance with our Privacy Policy.
Yes, I accept
Menu
Search Opener
Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Sunday
May 08
16:55 - 17:55
Room D3
Oligometastatic disease
Joachim Widder, Austria;
Jonas Willmann, Switzerland
2510
Proffered Papers
Clinical
17:45 - 17:55
Early toxicity after SABR of oligometastatic bony metastases in the BONY M phase II trial
Nicklas Juel Spindler, Denmark
OC-0604

Abstract

Early toxicity after SABR of oligometastatic bony metastases in the BONY M phase II trial
Authors:

Nicklas Juel Spindler1, Mette Van Overeem Felter1, Olfred Hansen2, Tine Bjørn Nielsen3, Morten Hiul Suppli4, Mirjana Josipovic4, Laurids Østergaard Poulsen5, Fatma Gaard-Petersen1, Hella Maria Brøgger Sand5, Tatiana Mikhailovna Abramova6, Marie Johansen6, Josefine Staahl Kornerup7, Mirjam Delange Alsaker7, Eva Serup-Hansen1, Poul Geertsen1, Ivan Richter Vogelius8, Claus Behrens1, Gitte Fredberg Persson9

1Copenhagen University Hospital - Herlev and Gentofte, Department of Oncology, Herlev, Denmark; 2Odense University Hospital, University of Southern Denmark, Department of Oncology, Department of Clinical Research, Odense, Denmark; 3Odense University Hospital, Laboratory of Radiation Physics, Department of Oncology, Odense, Denmark; 4Copenhagen University Hospital - Rigshospitalet, Department of Oncology, Copenhagen, Denmark; 5Aalborg University Hospital, Department of Oncology, Aalborg, Denmark; 6Ålesund Hospital, Department of Radiotherapy, Clinic of Oncology, Ålesund, Norway; 7St. Olavs University hospital, Department of Radiotherapy, Clinic of Oncology, Trondheim, Norway; 8Copenhagen University Hospital - Rigshospitalet, Faculty of Health, University of Copenhagen, Department of Oncology, Department of Clinical Medicine, Copenhagen, Denmark; 9Copenhagen University Hospital - Herlev and Gentofte, Faculty of Health, University of Copenhagen, Department of Oncology, Department of Clinical Medicine, Herlev, Denmark

Show Affiliations
Purpose or Objective

Stereotactic ablative radiotherapy (SABR) of bone metastases is rapidly emerging into standard practice but is still considered investigational and not without risk. When applied to patients with oligometastatic disease (OMD), lasting local control is important. The multicenter prospective phase II trial, BONY-M, evaluated the efficacy and safety of SABR to bone metastases in patients with OMD. Patient characteristics and preliminary early toxicity data are presented.

Material and Methods

Patients eligible for the study had at least one bony metastasis and OMD defined as a maximum of five metastatic lesions or oligo-progressive disease (OPD) defined as a maximum of three metastatic lesions. Maximum diameter of each bone metastasis ≤ 5cm. Ablative treatments, including surgery of all metastatic sites, should be possible and planned. Patients with spinal metastases and a Bilsky score ≥ 1b were excluded. The primary endpoint was 1-year local control rate. Secondary endpoints include toxicity (CTCAE v.5.0), change in pain score, quality of life, efficacy, and survival measures. At least 67 patients were planned to be included. SABR was delivered in three fractions of 37.5Gy or 30Gy to the GTV, with 80% and 67% isodose coverage of CTV and PTV, respectively. Dose distribution within the target area was non-homogenous, with steep dose gradients outside the GTV. Dose constraints to selected organs at risk (OAR) were predefined and prioritized over target coverage. Radiotherapy parameters were accessed through the national radiotherapy collaboration system (DcmCollab), CRF data were accessed through the protocol’s redcap database.

Results

The BONY-M trial opened in December 2019 and finished recruiting the 67 patients in late October 2021. At abstract submission, 66 patients from six centers across Norway and Denmark had finished treatment and had a median follow-up of 6.8 months (range 0.1-22.9). Patient and treatment characteristics are listed in Table 1 and 2. Early CTCAE toxicity records were accessible for 43 patients (64%), of whom five (~7%) experienced treatment-related G2 and one (~1.5%) G3 toxicity. The G3 toxicity was a fractured lumbar vertebra requiring spinal surgery three months post SABR with lumbar stabilization on pain indication. No study-related G4 toxicity or deaths were reported. 


Conclusion

Early toxicity after SABR of oligometastatic bony metastases seems acceptable. Mature toxicity data is required to confirm these early, promising findings.