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Status: Bibliographieeintrag

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Verfasst von:Sprave, Tetyana [VerfasserIn]   i
 Verma, Vivek [VerfasserIn]   i
 Förster, Robert [VerfasserIn]   i
 Schlampp, Ingmar [VerfasserIn]   i
 Bruckner, Thomas [VerfasserIn]   i
 Bostel, Tilman [VerfasserIn]   i
 Welte, Stefan Ezechiel [VerfasserIn]   i
 Tonndorf-Martini, Eric [VerfasserIn]   i
 Nicolay, Nils [VerfasserIn]   i
 Debus, Jürgen [VerfasserIn]   i
 Rief, Harald [VerfasserIn]   i
Titel:Randomized phase II trial evaluating pain response in patients with spinal metastases following stereotactic body radiotherapy versus three-dimensional conformal radiotherapy
Verf.angabe:Tanja Sprave, Vivek Verma, Robert Förster, Ingmar Schlampp, Thomas Bruckner, Tilman Bostel, Stefan Ezechiel Welte, Eric Tonndorf-Martini, Nils Henrik Nicolay, Jürgen Debus, Harald Rief
E-Jahr:2018
Jahr:26 May 2018
Umfang:9 S.
Fussnoten:Gesehen am 03.04.2020
Titel Quelle:Enthalten in: Radiotherapy and oncology
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1983
Jahr Quelle:2018
Band/Heft Quelle:128(2018), 2, Seite 274-282
ISSN Quelle:1879-0887
Abstract:BACKGROUND: To report the primary endpoint of a randomized trial comparing pain response following palliative stereotactic body radiation therapy (SBRT) versus conventionally-fractionated 3D-conformal radiotherapy (3DCRT) for previously untreated spinal metastases. - METHODS: Fifty-five patients with histologically/radiologically confirmed painful spinal metastases were analyzed in this single-institutional, non-blinded, randomized explorative trial. Participants were randomly assigned (1:1) to receive single-fraction SBRT (24Gy) or 3DCRT (30Gy in 10 fractions). The primary endpoint was pain relief of >2 points on the visual analog scale (VAS) measured within the irradiated region at 3months following radiotherapy completion. Other recorded parameters included pain response (per International Bone Consensus response definitions), use of concurrent medications and opioid usage (oral morphine equivalent dose, OMED). All parameters were assessed at baseline and at three and six months after RT. Intention-to-treat analysis was applied. This trial is registered with ClinicalTrials.gov, number NCT02358720. - FINDINGS: Despite no significant differences for VAS at 3months between groups (p=0.13), pain values decreased faster within this time period in the SBRT arm (p=0.01). At 6months following RT, significantly lower VAS values were reported in the SBRT group (p=0.002). There were no differences in OMED consumption at 3 (p=0.761) and 6months (p=0.174). There was a trend toward improved pain response in the SBRT arm at 3months (p=0.057), but significantly so after 6months (p=0.003). No patient in the SBRT group experienced grade ≥3 toxicities according to the Common Terminology Criteria for Adverse Events v.4.03. - CONCLUSIONS: This randomized trial demonstrates the utility of palliative SBRT for spinal metastases, which was associated with a quicker and improved pain response. Larger ongoing randomized studies will assist in further addressing these endpoints.
DOI:doi:10.1016/j.radonc.2018.04.030
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.radonc.2018.04.030
 DOI: https://doi.org/10.1016/j.radonc.2018.04.030
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Adolescent
 Adult
 Aged
 Aged, 80 and over
 Bone metastases
 Female
 Humans
 IMRT
 Male
 Middle Aged
 Pain
 Pain Measurement
 Palliative radiotherapy
 Radiosurgery
 Radiotherapy, Conformal
 SBRT
 Spinal Neoplasms
 Spine
 Young Adult
K10plus-PPN:1693993953
Verknüpfungen:→ Zeitschrift

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