Inflammatory myofibroblastic tumour (IMT)
Prepared with OnCo (onco.cc/prep/inflammatory-myofibroblastic-tumour/). Orientation, not medical advice; your team knows your case.
My details
What I know, what is unclear, changes to discuss
Saved in this browserMy questions
14 on the sheet- 1.What is my exact diagnosis, stage, and grade, and which tests established them?
- 2.Which biomarkers have been tested on my tumour (for example ALK immunohistochemistry and FISH or RNA fusion panel, ROS1, NTRK, PDGFRB, RET fusions in ALK-negative tumours, Inflammatory markersas systemic markers, Site and resectability), and what were the results?
- 3.Which subtype is my cancer, and does that change the recommended treatment?
- 4.Is germline (inherited) genetic testing recommended for me or my family?
- 5.For my situation (resectable), which of the standard options do you recommend and why?
- 6.For my situation (unresectable, recurrent or metastatic, alk-positive), which of the standard options do you recommend and why?
- 7.Am I a candidate for Crizotinib, Alectinib, Lorlatinib or related drugs, and what side effects should I expect?
- 8.For my situation (unresectable, alk-negative with other fusion), which of the standard options do you recommend and why?
- 9.Am I a candidate for Entrectinib, Larotrectinib, Imatinib or related drugs, and what side effects should I expect?
- 10.Are there clinical trials I could join, for example of Crizotinib, Lorlatinib, Repotrectinib?
- 11.Would a second opinion at a high-volume centre change anything, and can you help arrange it?
- 12.What supportive care (symptom control, nutrition, exercise, mental health, financial help) is available from the start?
- 13.I read that “How long to continue ALK inhibition in children with complete response, and whether surgery after response can allow stopping”. How does that affect my plan?
- 14.I read that “The fusion-negative minority: RNA sequencing to find drivers”. How does that affect my plan?
The words I may hear
- RACE for Children Act: A US law that makes drug companies test new targeted cancer drugs in children whenever the drug's target matters in a childhood cancer, instead of letting them skip children because their cancers are rare.
- Gene fusion: A gene fusion is two genes broken and joined together, creating a hybrid protein that can drive cancer.
- Rare cancers: Rare cancers are those with fewer than about 6 new cases per 100,000 people per year.
Tests and results to bring
Biomarker results to ask for: ALK immunohistochemistry and FISH or RNA fusion panel, ROS1, NTRK, PDGFRB, RET fusions in ALK-negative tumours, Inflammatory markers (anaemia, raised CRP) as systemic markers, Site and resectability.
Scans and tests linked to this cancer: Comprehensive genomic profiling, RNA sequencing & expression profiling.
Bring copies of scan reports, pathology and blood results, and a list of every medicine and supplement.
The treatments I may be offered
- Resectable: Complete surgical excision; no adjuvant therapy in most cases, surveillance imaging for recurrence. (Limb-salvage surgery and endoprosthetic reconstruction)
- Unresectable, recurrent or metastatic, ALK-positive: Crizotinib (FDA approval July 2022, children 1 year and older and adults); alectinib, ceritinib or lorlatinib at progression. (Crizotinib, Alectinib, Lorlatinib, Ceritinib)
- Unresectable, ALK-negative with other fusion: Match to fusion: entrectinib or crizotinib for ROS1, larotrectinib or entrectinib for NTRK, imatinib for PDGFRB; steroids or NSAIDs for symptom control in indolent disease. (Entrectinib, Larotrectinib, Imatinib, Repotrectinib)
From the standard of care recorded for this cancer; which apply depends on your stage and biomarkers. Ask which the team recommends and why.