Palliative Radiotherapy in Symptomatic Pelvic Soft Tissue Tumors
Recruiting now · Not applicable
Conditions studied: Gastrointestinal Cancer, Urologic Cancer, Gynecologic Cancer
In brief
PALLSOFT is a randomized, open-label, non-inferiority phase III, multicenter, national trial that will investigate whether the patient-reported symptomatic effect of palliative radiotherapy delivered in 1-2 fractions is non-inferior to palliative radiotherapy delivered in five fractions in patients with pelvic soft tissue tumors from either gastrointestinal, urological or gynecological cancer. Health-related quality of life, toxicities, survival and prognostic and predictive biomarkers will be assessed as secondary and explorative endpoints.
Key facts
- Study ID
- NCT06398314
- Run by
- Sykehuset Telemark
- People needed
- 200
- Starts
- 2024-12-10
- Expected to finish
- 2030-12-01
- Last updated by the study team
- 2025-05-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients unsuitable for curative treatment due to either advanced disease or medical contradictions (i.e comorbidity, old age, poor general condition)
- Histologically verified primary cancer originated from gastrointestinal, urological or gynecological organs (histological verification can be performed on other lesions than the symptomatic pelvic tumor)
- Primary, residual, recurrent or metastatic pelvic tumor from the above-mentioned cancers not amenable for curative treatment
- Tumor-related symptoms including within the 5 defined categories pain, bleeding, bowel/lower urinary/vaginal dysfunction
- Considered candidate for palliative radiotherapy according to both study arms
- Patient reported severity of symptoms ≥4 on a NRS- scale of 0-10
- ≥18 years of age
- Speaks and understands Norwegian or English
- Ability to understand and willing to sign a written informed consent
- ECOG performance status 0-3
- Expected survival > 12 weeks
- Able to pause systemic cancer treatment for one week prior to, during, and one week after the radiotherapy treatment
- Women of childbearing potential (WOCBP) should have a negative highly sensitive serum pregnancy test within 72 hours prior to study intervention. WOCBP must agree to the use of highly effective birth control methods or abstain from heterosexual sexual activity from randomization and until completed study intervention
You may not qualify if…
- Neuroendocrine histology of any kind
- Sarcoma or sarcomal components in the histology
- Tumors that originate from bony metastases without a soft tissue component
- Unable to comply with study questionnaires
- Ongoing treatment with an investigational drug at inclusion
- Planned inclusion in another interventional clinical trial within 4 weeks after radiotherapy
- Patients who are pregnant due to risk of teratogenic and abortifacient effects of radiotherapy
Where it is running
- Helse Møre og Romsdal — Ålesund, Norway (enrolling)
- Haukeland universitetssykehus — Bergen, Norway (enrolling)
- Nordlandssykehuset Bodø — Bodø, Norway (enrolling)
- Vestre Viken HF — Drammen, Norway (enrolling)
- Sykehuset Innlandet HF — Gjøvik, Norway (enrolling)
- Sørlandet sykehus HF — Kristiansand, Norway (enrolling)
- Oslo Universitetssykehus — Oslo, Norway (enrolling)
- Sykehuset Telemark HF — Skien, Norway (enrolling)
- Stavanger Universitetssykehus — Stavanger, Norway (enrolling)
- Universitetssykehuset i Nord-Norge — Tromsø, Norway (enrolling)
- St. Olavs Hospital HF — Trondheim, Norway (enrolling)
Full record on ClinicalTrials.gov
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