Clinician brief
Half a page, built to be read before an appointment. If something here would not change a clinical decision or the next conversation, it is not on it. The full record, source documents and structured data sit behind the links at the bottom.
Diagnosis
Sites of disease Lungs · mediastinal lymph nodes · liver segment VII (new, Jul 2026).
Also Smouldering myeloma (diagnosed end of 2021, under haematology surveillance); Gilbert's syndrome (can raise bilirubin). Original pathology Clinician letter
Molecular
Key detected tumour alterations APC p.S1415Rfs*4; TP53 p.R342*; PTEN reported, not specified Commercial sequencing
Platform Oncomine Comprehensive Plus, 517-gene targeted panel, hg19. Not whole genome or whole exome. Reported tumour-only.
Treatment lines
| Dec 21–Feb 22 | Neoadjuvant XELOX ×4 · good partial response |
| Mar–Oct 22 | Primary resected · liver met resected (R0) · adjuvant CAPOX |
| Oct 22–Apr 23 | Lung mets appear, progress · SABR 55 Gy/5 |
| Jun & Aug 24 | Lung ablations (1 left, then 1 left + 4 right) |
| Feb 25 | EBUS confirms mediastinal nodal disease |
| Apr–Jul 25 | FOLFIRI + cetuximab ×6 · good partial response |
| Feb–May 26 | Rechallenge ×6 · excellent partial response |
| Jul–Aug 26 | Progression during the break · FOLFIRI + cetuximab restarted 19 Aug |
Current regimen
| Chemo day | Standard pre-meds (Akynzeo, dexamethasone, chlorphenamine, atropine) · pegfilgrastim 24h after |
| Supportive | Dexamethasone ×3 days · domperidone · loperamide · doxycycline + Plazon (skin) · Laxido · antihistamine · zopiclone PRN |
| Other | Citalopram 30 mg (breakfast) · melatonin 60 mg (evening) · loratadine 10 mg |
Planned changes
As at 2 October 2026 · Source Proposed by my integrative oncologist (private). Not yet discussed with my primary oncologist or the NHS team. Each step is subject to tolerance. Nothing here is agreed with my treating oncologist yet. Patient-reported
Latest imaging
CEA
Bloods out of range
Open questions
- Which alteration is the driving event? The panel reports APC p.S1415Rfs*4 and TP53 p.R342* as detected, but it does not designate a driver and no clinician has characterised one on my file. If a driver were formally called, would it change anything actionable?
- NHS whole genome sequencing referral — the testing to date is a 517-gene panel, not WGS or WES.
- Matched tumour/normal sequencing — the tumour panel is reported tumour-only.
- Platelet count from 29 Sep 2026 — unreadable on my copy of the report, not yet confirmed.
Treating team
Named identifiers are not published here. A version carrying them is sent to clinicians directly on request.
Patient-maintained, checked against source documents. Not medical advice.
Sequencing — tumour DNA and RNA, liquid biopsy, germline and exosomal transcriptome, Astron / EXACTA (Astron Health), August 2025 — is set out in full, with the raw variant files, at
fcancerwith.ai/full-record. Germline data is not published openly.
Full record: fcancerwith.ai/full-record ·
Structured data: /data/profile.json ·
Corrections: fcancerwith.ai/corrections