PET scans may help guide chemo for rare abdominal cancer
NCT ID NCT04224948
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether PET scans can detect early response to chemotherapy in people with retroperitoneal sarcoma, a rare cancer in the abdomen. 18 participants received extra PET scans before and after their first chemo cycle. The goal was to see if PET could predict tumor shrinkage better than standard CT scans, which take longer to show results.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PET MRI scan
- What this could lead to
- If PET scans prove reliable, doctors could adjust chemotherapy earlier for sarcoma patients, potentially improving outcomes.
- What could go wrong
- This is a very small, early study (18 people) focused on imaging accuracy, not treatment. It may not change practice or benefit patients directly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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18 people
The number who actually took part.
- Started
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Jan 2020
- Finished
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Dec 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Tumour-related criteria * Primary soft tissue sarcoma of retroperitoneal space or infra-peritoneal spaces of pelvis * Sarcoma not originated from bone structure, abdominal or gynecological viscera * Unifocal tumour (not multifocal disease) * Absence of extension through the sciatic notch or across the diaphragm * Histologically-proven RPS (local pathologist/ imaging-guided or surgical biopsy), only including the following histological sub-types: * High grade Leiomyosarcoma * High grade Dedifferentiated Liposarcoma * Tumour not previously treated (no previous surgery -excluding diagnosis biopsy-, radiotherapy or systemic therapy) * Tumour both operable and suitable for chemotherapy (This will be based on pretreatment CT scan/MRI and multidisciplinary consultation with surgeon medical oncologist and radiologist (anticipated macroscopically complete resection, R0/R1resection) * Patients for whom surgery is expected to be R2 on the CT-scan before randomization are not eligible * Patients must have American Society of Anesthesiologist (ASA) score ≤ 2 (see Appendix G) * The criteria for non-resectability are: * (i) involvement of superior mesenteric artery * (ii) involvement of aorta * (iii) involvement of bone * distant metastatic disease * Patient must have radiologically measurable disease (RECIST 1.1) Patient-related criteria * ≥ 18 years' old * WHO performance status ≤ 2 (see Appendix C) * Absence of history of bowel obstruction or mesenteric ischemia or severe chronic inflammatory bowel disease * Normal renal function: * Calculated creatinine clearance within normal value Functional contra-lateral kidney to the side involved by the RPS as assessed by intravenous pyelogram (done during the baseline CT-scan) or differential renal isotope scan * Normal bone marrow and hepatic function: * White Blood cells ≥ 2.5 x10 9 cells/L * Platelets ≥ 80 x10 9 cells/L * Total bilirubin \< 1.5 time the institutional upper limit normal of value (ULN) * Adequate cardiac function: less or equal to NYHA II * Normal 12 lead ECG (without clinically significant abnormalities) * No co-existing malignancy within the last 5 years except for adequately treated basal cell carcinoma of the skin or carcinoma in situ of the cervix * No prior abdominal or pelvic irradiation for other prior malignancy or other disease * Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule * Excluding patients who presented after incomplete resection and underwent immediate completion surgery. Exclusion Criteria: * Age\< 18 years * Recurrent tumour * Benign retroperitoneal tumours * Presence of second active cancer * Serious psychiatric disease that precludes informed consent or limits compliance * impossible to ensure adequate follow up
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University Health Network and The Sinai Health System
Toronto, Ontario, M5G 1X5, Canada
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Other studies related to the condition(s) this trial covers.
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