Krebs
Studienlage · Detail Pilot Phase-I-Studie · Krebs · 2006

A pilot clinical study of Delta9-tetrahydrocannabinol in patients with recurrent glioblastoma multiforme.

Gemischt GRADE Moderat 362 Zitate
Stichproben = 9 Pat.
DauerMediane Überlebenszeit 24 Wochen
EndpunktSicherheit der…
Verblindungn.a.
DesignPilot Phase-I-Studie
Cannabinoidthc
Applikationinhalativ
Kernaussage

Intratumorales THC war sicher applizierbar und zeigte erste antiproliferative Hinweise, ohne formalen Wirksamkeitsnachweis.

Zusammenfassung

Erste klinische Pilotstudie (n=9, rezidivierendes Glioblastom), intratumorale THC-Gabe nach Versagen Standardtherapie. Primärendpunkt Sicherheit: Cannabis-Delivery sicher, keine offensichtlichen psychoaktiven Effekte. Medianes Überleben ab Therapiebeginn 24 Wochen (95% CI: 15-33). THC inhibierte Tumorzell-Proliferation in vitro; Ki67-Immunfärbung bei 2 Patienten reduziert. Kein Kontrollarm; Phase I ohne Wirksamkeitsnachweis.

P
PopulationPatienten mit rezidivierendem Glioblastoma multiforme nach Versagen von Standardtherapie (Operation und Radiotherapie), n=9
I
InterventionDelta-9-Tetrahydrocannabinol (THC) intratumoral, Dosiseskalationsschema
O
OutcomeIntrakranielle THC-Gabe war sicher ohne manifeste psychoaktive Effekte; mediane Überlebenszeit ab Cannabinoidgabe 24 Wochen (95%-KI: 15–33); Hemmung der Tumorzellproliferation in vitro und Reduktion von Ki67-Immunfärbung bei zwei Patienten
Vertrauen in die Evidenz
Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe
Verblindung
Effektstärke Gemischt
Zitate / Jahr
Autoren
Guzmán M, Duarte MJ, Blázquez C, Ravina J, Rosa MC, Galve-Roperh I, Sánchez C, Velasco G, González-Feria L.
DOI 10.1038/sj.bjc.6603236
Design: Pilot Phase-I-Studie
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Abstract
Delta(9)-Tetrahydrocannabinol (THC) and other cannabinoids inhibit tumour growth and angiogenesis in animal models, so their potential application as antitumoral drugs has been suggested. However, the antitumoral effect of cannabinoids has never been tested in humans. Here we report the first clinical study aimed at assessing cannabinoid antitumoral action, specifically a pilot phase I trial in which nine patients with recurrent glioblastoma multiforme were administered THC intratumoraly. The patients had previously failed standard therapy (surgery and radiotherapy) and had clear evidence of tumour progression. The primary end point of the study was to determine the safety of intracranial THC administration. We also evaluated THC action on the length of survival and various tumour-cell parameters. A dose escalation regimen for THC administration was assessed. Cannabinoid delivery was safe and could be achieved without overt psychoactive effects. Median survival of the cohort from the beginning of cannabinoid administration was 24 weeks (95% confidence interval: 15-33). Delta(9)-Tetrahydrocannabinol inhibited tumour-cell proliferation in vitro and decreased tumour-cell Ki67 immunostaining when administered to two patients. The fair safety profile of THC, together with its possible antiproliferative action on tumour cells reported here and in other studies, may set the basis for future trials aimed at evaluating the potential antitumoral activity of cannabinoids.

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