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Poster session 06

2074P - Oral cannabidiol for prevention of chemotherapy-induced peripheral neuropathy

Date

21 Oct 2023

Session

Poster session 06

Topics

Supportive Care and Symptom Management

Tumour Site

Presenters

Sebastian Nielsen

Citation

Annals of Oncology (2023) 34 (suppl_2): S1080-S1134. 10.1016/S0923-7534(23)01268-1

Authors

S.W. Nielsen1, S. Dyring Hasselsteen2, H. Sylow Dominiak2, D. Labudovic2, J. Herrstedt3

Author affiliations

  • 1 Klinisk Onkologisk Afdeling Og Palliative Enheder, Sjællands Universitets Hospital, 4700 - Naestved/DK
  • 2 Department Of Clinical Oncology And Palliative Care, University Hospital Sjællands Roskilde, 4000 - Roskilde/DK
  • 3 Clinical Oncology Department, ZUH - Zealand University Hospital Roskilde - Region Sjaelland, 4000 - Roskilde/DK

Resources

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Abstract 2074P

Background

Chemotherapy-induced peripheral neuropathy (CIPN) is experienced by 37–84% of patients during and/or after end-of-treatment and often results in discontinuation of anti-neoplastic treatment and impairment of health-related quality of life. Cannabidiol (CBD) has shown preventive effects in CIPN animal models without compromising chemotherapy efficacy.

Methods

Patients with cancer referred for adjuvant treatment with capecitabine and oxaliplatin (CAPOX) or carboplatin and paclitaxel (Carbo-Tax) were recruited to participate in the CINCAN-2 study. CBD oil was self-administered two times daily (300 mg daily oral dose) for 8 days total at each cycle of chemotherapy, beginning 24 hours before start of chemotherapy. Patient reported outcomes (EORTC-CIPN20) were captured before start of chemotherapy and at follow-up until one year after end-of-chemotherapy. Vibration Perception Thresholds (VPTs) were collected at 32, 125 and 250Hz on patient dominant hand and at 8, 32, and 125Hz on the patient dominant foot. Controls were obtained from a similar cohort (CINCAN-1) receiving the same chemotherapy regimens, but no CBD.

Results

From March to December 2021, 54 out of 65 eligible patients were recruited. CINCAN-2 patients were significantly older (median age 64 vs 57 years, p=0.004) compared to the CINCAN-1 cohort. Patients treated with CBD showed significantly better VPT scores than patients not receiving CBD at 3, 6 and 12 months follow-up. The largest VTP difference was found in patients treated with Carbo-Tax and CBD at 32Hz in metatarsal V at 12 months with -1.86 Z-score, CI-95=[-3.16;-0.49] compared to patients who did not receive CBD. Patients treated with CAPOX and CBD scored significantly better in PRO scores at 3 and 6 month follow-up (-6.75 [-11.54;-1.98] and -9.25 [-13.91;-4.58] points respectively compared to patients treated with CAPOX only. No difference in PRO scores was observed for patients treated with Carbo-Tax. Patients receiving Carbo-Tax and CBD received significantly higher cumulative doses of paclitaxel (1737mg vs 1194mg, p=0.027) compared to patients receiving Carbo-Tax only.

Conclusions

Patients treated CBD showed better long term PRO and VPT outcomes than controls. A randomized trial is warranted.

Clinical trial identification

NCT04582591.

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Nordic Cannabis Research Council - Glostrup Pharmacy.

Disclosure

All authors have declared no conflicts of interest.

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