# Ewing sarcoma-related pain: potential role of medical cannabis monotherapy in symptom management – a case report

**Authors:** Cesare De Virgilio Suglia, Felice Antonio Spaccavento, Fabio Turco, Angela De Trizio, Rossella Giannuzzi, Silvio Tafuri

PMC · DOI: 10.1186/s42238-026-00388-x · Journal of Cannabis Research · 2026-01-23

## TL;DR

A patient with severe Ewing sarcoma pain and infection found relief using medical cannabis, reducing opioid use and improving symptoms.

## Contribution

This case report suggests medical cannabis monotherapy may manage complex oncologic pain and inflammation.

## Key findings

- Medical cannabis reduced pain from VAS 9–10 to 2–3 and enabled opioid discontinuation.
- Chronic fistula closed and inflammation markers dropped during cannabis therapy.
- No significant adverse effects were observed over nine months of treatment.

## Abstract

Persistent, multimodal cancer pain remains a challenge, particularly in long-term survivors facing treatment-related complications. The management of high-dose opioid dependence concurrent with chronic, multi-drug resistant (MDR) periprosthetic infection presents a critical unmet need. This case reports the potential use and sustained efficacy of medical cannabis monotherapy, highlighting an unexpected temporal association with the resolution of inflammatory and infectious symptoms in a highly complex oncologic setting.

A 27-year-old male, a long-term survivor of high-risk Ewing Sarcoma of the proximal tibia, presented with intractable mixed pain (VAS 9–10) secondary to chronic, recurrent MDR periprosthetic osteomyelitis and multiple surgical revisions (2013–2024). Despite continuous use of high-dose opioids (up to 120 mg/day morphine equivalents), pain levels remained moderate-to-severe (VAS 6–7) and functional status was poor. The patient had previously found temporary relief with self-administered cannabis. In January 2025, after refusing limb amputation, supervised medical cannabis therapy (Bedrocan®, 22% THC, 1% CBD, 1 g/day) was initiated. Pain levels gradually stabilized at VAS 2–3, coinciding with complete opioid discontinuation within four weeks. Over nine months of follow-up, the patient maintained full autonomy and an active lifestyle. Notably, sustained cannabis monotherapy was associated with the complete closure of the chronic draining fistula and a reduction in systemic inflammatory markers (CRP from 9.6 to 2.3 mg/dL). No significant adverse effects were reported.

This case suggests that THC-rich medical cannabis may represent a feasible strategy for achieving opioid-free analgesia in selected patients with refractory oncologic pain. While causality cannot be established from a single observation, the correlation between cannabis initiation and the resolution of severe chronic inflammatory and infectious symptoms is intriguing and suggests a potential pleiotropic role extending beyond traditional pain management. While these findings align with emerging evidence highlighting the potent immunomodulatory and anti-inflammatory properties of cannabinoids, they contrast with some recent neutral meta-analyses in broader populations, an this would justify warrant urgent controlled investigation into the potential mechanisms of cannabinoids in complex inflammatory pain states and their role as a possible adjunct in managing long-term oncological complications.

## Linked entities

- **Chemicals:** THC (PubChem CID 16078), CBD (PubChem CID 644019), morphine (PubChem CID 5288826)
- **Diseases:** Ewing Sarcoma (MONDO:0012817)

## Full-text entities

- **Genes:** EWSR1 (EWS RNA binding protein 1) [NCBI Gene 2130] {aka EWS, EWS-FLI1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** cognitive dulling (MESH:D003072), ischemia (MESH:D007511), cardiovascular symptoms (MESH:D002318), injury (MESH:D014947), hepatic intolerance (MESH:D056486), Swelling (MESH:D004487), nausea (MESH:D009325), depressive symptoms (MESH:D003866), dizziness (MESH:D004244), septic (MESH:D001170), anxiety (MESH:D001007), chronic inflammation (MESH:D007249), necrosis (MESH:D009336), Pain (MESH:D010146), opioid dependence (MESH:D009293), sleep fragmentation (MESH:D012892), nerve injury (MESH:D000080902), psychomotor slowing (MESH:D011596), cancer pain (MESH:D000072716), tenderness (MESH:D063806), psychiatric (MESH:D001523), osteomyelitis (MESH:D010019), Chronic infection (MESH:D000088562), fistula (MESH:D005402), infection (MESH:D007239), erythema (MESH:D004890), leukocytosis (MESH:D007964), periprosthetic infection (MESH:D057068), cytotoxicity (MESH:D064420), neuropathic (MESH:D009437), Ewing Sarcoma (MESH:D012512), analgesia (MESH:D000699), peripheral neuropathy (MESH:D010523), fatigue (MESH:D005221), chronic pain (MESH:D059350), nausea and vomiting (MESH:D020250), infectious (MESH:D003141), fibrosis (MESH:D005355), cancer (MESH:D009369)
- **Chemicals:** busulfan (MESH:D002066), nabiximols (MESH:C587251), methicillin (MESH:D008712), teicoplanin (MESH:D017334), codeine (MESH:D003061), dalbavancin (MESH:C469289), rifampicin (MESH:D012293), melphalan (MESH:D008558), levofloxacin (MESH:D064704), daptomycin (MESH:D017576), morphine (MESH:D009020), paracetamol (MESH:D000082), ifosfamide (MESH:D007069), macrolides (MESH:D018942), minocycline (MESH:D008911), oxycodone (MESH:D010098), beta-lactams (MESH:D047090), Delta9-tetrahydrocannabinol (MESH:D013759), cannabinoid (MESH:D002186), linezolid (MESH:D000069349), CBD (MESH:D002185), Bedrocan (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Corynebacterium striatum (species) [taxon 43770], Acinetobacter baumannii (species) [taxon 470], Staphylococcus aureus (species) [taxon 1280], Enterococcus faecalis (species) [taxon 1351]
- **Mutations:** A2A
- **Cell lines:** TC-71 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_S882), A-673 — Homo sapiens (Human), Ewing sarcoma, Cancer cell line (CVCL_0080)

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12879326/full.md

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Source: https://tomesphere.com/paper/PMC12879326