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Pilot Study of Psilocybin Treatment for Anxiety in Patients With Advanced-Stage Cancer

Gurpreet S Chopra, Marycie Hagerty, Charles S. Grob, Alicia Danforth, Charles R. Mckay, Adam L. Halberstadt, George Greer

Archives of General Psychiatry September 7, 2010 DOI: 10.1001/archgenpsychiatry.2010.116 via OpenAlex

Summary

AI-generated from the abstract

In a double-blind, placebo-controlled study, twelve adults with advanced-stage cancer and anxiety received a moderate dose (0.2 mg/kg) of psilocybin. Safe physiological and psychological responses were documented, with no clinically significant adverse events. The State-Trait Anxiety Inventory trait anxiety subscale showed a significant reduction in anxiety at 1 and 3 months after treatment. The Beck Depression Inventory indicated improved mood that reached significance at 6 months; the Profile of Mood States showed mood improvement that approached but did not reach significance. The results support the need for more research into psilocybin for cancer-related anxiety.

Study at a glance

Characteristics Double-blind, placebo-controlled study Pilot study Peer reviewed
Sample size 12
Population Adults with advanced-stage cancer and anxiety
Intervention Psilocybin
Dose 0.2 mg/kg
Duration 6-month follow-up after treatment
Topics Anxiety Psilocybin
Keywords Mood Psychiatry Clinical psychology Beck depression inventory
Citations 1,220
Registration NCT00302744
Key finding Psilocybin was safe and associated with reduced anxiety and improved mood in patients with advanced-stage cancer and reactive anxiety.

Abstract

CONTEXT: Researchers conducted extensive investigations of hallucinogens in the 1950s and 1960s. By the early 1970s, however, political and cultural pressures forced the cessation of all projects. This investigation reexamines a potentially promising clinical application of hallucinogens in the treatment of anxiety reactive to advanced-stage cancer. OBJECTIVE: To explore the safety and efficacy of psilocybin in patients with advanced-stage cancer and reactive anxiety. DESIGN: A double-blind, placebo-controlled study of patients with advanced-stage cancer and anxiety, with subjects acting as their own control, using a moderate dose (0.2 mg/kg) of psilocybin. SETTING: A clinical research unit within a large public sector academic medical center. PARTICIPANTS: Twelve adults with advanced-stage cancer and anxiety. MAIN OUTCOME MEASURES: In addition to monitoring safety and subjective experience before and during experimental treatment sessions, follow-up data including results from the Beck Depression Inventory, Profile of Mood States, and State-Trait Anxiety Inventory were collected unblinded for 6 months after treatment. RESULTS: Safe physiological and psychological responses were documented during treatment sessions. There were no clinically significant adverse events with psilocybin. The State-Trait Anxiety Inventory trait anxiety subscale demonstrated a significant reduction in anxiety at 1 and 3 months after treatment. The Beck Depression Inventory revealed an improvement of mood that reached significance at 6 months; the Profile of Mood States identified mood improvement after treatment with psilocybin that approached but did not reach significance. CONCLUSIONS: This study established the feasibility and safety of administering moderate doses of psilocybin to patients with advanced-stage cancer and anxiety. Some of the data revealed a positive trend toward improved mood and anxiety. These results support the need for more research in this long-neglected field. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00302744.

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