TY - JOUR
T1 - Rapid and sustained symptom reduction following psilocybin treatment for anxiety and depression in patients with life-threatening cancer
T2 - A randomized controlled trial
AU - Ross, Stephen
AU - Bossis, Anthony
AU - Guss, Jeffrey
AU - Agin-Liebes, Gabrielle
AU - Malone, Tara
AU - Cohen, Barry
AU - Mennenga, Sarah E.
AU - Belser, Alexander
AU - Kalliontzi, Krystallia
AU - Babb, James
AU - Su, Zhe
AU - Corby, Patricia
AU - Schmidt, Brian L.
N1 - Publisher Copyright:
© The Author(s) 2016.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Background: Clinically significant anxiety and depression are common in patients with cancer, and are associated with poor psychiatric and medical outcomes. Historical and recent research suggests a role for psilocybin to treat cancer-related anxiety and depression. Methods: In this double-blind, placebo-controlled, crossover trial, 29 patients with cancer-related anxiety and depression were randomly assigned and received treatment with single-dose psilocybin (0.3 mg/kg) or niacin, both in conjunction with psychotherapy. The primary outcomes were anxiety and depression assessed between groups prior to the crossover at 7 weeks. Results: Prior to the crossover, psilocybin produced immediate, substantial, and sustained improvements in anxiety and depression and led to decreases in cancer-related demoralization and hopelessness, improved spiritual wellbeing, and increased quality of life. At the 6.5-month follow-up, psilocybin was associated with enduring anxiolytic and anti-depressant effects (approximately 60-80% of participants continued with clinically significant reductions in depression or anxiety), sustained benefits in existential distress and quality of life, as well as improved attitudes towards death. The psilocybin-induced mystical experience mediated the therapeutic effect of psilocybin on anxiety and depression. Conclusions: In conjunction with psychotherapy, single moderate-dose psilocybin produced rapid, robust and enduring anxiolytic and anti-depressant effects in patients with cancer-related psychological distress. Trial Registration: ClinicalTrials.gov Identifier: NCT00957359.
AB - Background: Clinically significant anxiety and depression are common in patients with cancer, and are associated with poor psychiatric and medical outcomes. Historical and recent research suggests a role for psilocybin to treat cancer-related anxiety and depression. Methods: In this double-blind, placebo-controlled, crossover trial, 29 patients with cancer-related anxiety and depression were randomly assigned and received treatment with single-dose psilocybin (0.3 mg/kg) or niacin, both in conjunction with psychotherapy. The primary outcomes were anxiety and depression assessed between groups prior to the crossover at 7 weeks. Results: Prior to the crossover, psilocybin produced immediate, substantial, and sustained improvements in anxiety and depression and led to decreases in cancer-related demoralization and hopelessness, improved spiritual wellbeing, and increased quality of life. At the 6.5-month follow-up, psilocybin was associated with enduring anxiolytic and anti-depressant effects (approximately 60-80% of participants continued with clinically significant reductions in depression or anxiety), sustained benefits in existential distress and quality of life, as well as improved attitudes towards death. The psilocybin-induced mystical experience mediated the therapeutic effect of psilocybin on anxiety and depression. Conclusions: In conjunction with psychotherapy, single moderate-dose psilocybin produced rapid, robust and enduring anxiolytic and anti-depressant effects in patients with cancer-related psychological distress. Trial Registration: ClinicalTrials.gov Identifier: NCT00957359.
KW - Psilocybin
KW - anxiety
KW - cancer
KW - depression
KW - mystical experience
KW - psychedelic
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U2 - 10.1177/0269881116675512
DO - 10.1177/0269881116675512
M3 - Article
C2 - 27909164
AN - SCOPUS:85002808787
SN - 0269-8811
VL - 30
SP - 1165
EP - 1180
JO - Journal of Psychopharmacology
JF - Journal of Psychopharmacology
IS - 12
ER -