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Short-term palliative radiation for painful irresectable pancreatic cancer (PainPanc): a prospective phase 2 study

Short-term palliative radiation for painful irresectable pancreatic cancer (PainPanc): a prospective phase 2 study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON20425
Enrollment
30
Registered
2015-03-27
Start date
2015-07-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Painful Locally advanced or locally recurrent pancreatic cancer

Interventions

radiotherapy 3 X 8 Gy, once per week.

Sponsors

Academic Medical Center Meibergdreef 9 1105 AZ Amsterdam, the Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pain with a NRS ¡Ý 2 as a result of pancreatic cancer, not sufficiently responding to oral, transdermal pain medication or celiac plexus blockade. 2. Primarily irresectable or locally recurrent pancreatic cancer with or without metastases 3. Preferably histological or cytological confirmed adenocarcinoma of the pancreas 4. WHO performance status ¡Ü 2 5. Diagnostic CT-scan not older than 3 months before study entry 6. Age ¡Ý 18 years 7. If the patient is or was treated with chemotherapy, time interval between the course of chemotherapy and start of radiation should at least be 14 days. 8. Written informed consent 9. The ability to answer and fill out the questionnaires

Exclusion criteria

Exclusion criteria: 1. Resectable or borderline resectable tumors without distant metastases 2. Endocrine pancreatic cancer or suspicion of metastasis in the pancreas 3. Pregnant woman

Design outcomes

Primary

MeasureTime frame
To evaluate whether pain relief is successful 4 weeks after the last radiation (7 weeks after start of treatment) . A short course of radiation (3 x 8 Gy) will be given in patients with painful irresectable pancreatic cancer, primary or recurrent.

Secondary

MeasureTime frame
• To determine the effect on pain free interval • To determine the reducing effect on (opiod) pain medication • To evaluate the effect on acute toxicity • To evaluate the correlation of radiation volume with acute toxicity • To evaluate the effect on quality of life • To evaluate the overall survival

Contacts

Public ContactG. van Tienhoven

Academic Medical Center - Meibergdreef 9

G.vantienhoven@amc.nl+31205665591

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)