Abstract
The major progress in controlling chemotherapy-induced emesis benefits thousands of patients each day. Antiemetic efficacy is found with agents of many different classes, including phenothiazines, butyrophenones, cannabinoids, corticosteroids, substituted benzamides, and serotonin receptor antagonists. To date, the most effective antiemetic regimens are combinations of serotoninreceptor antagonists with corticosteroids.
Most antiemetic studies with cannabinoids have methodological difficulties and can be difficult to interpret. If one concentrates on the better-conducted trials, however, it is clear that cannabinoids possess antiemetic properties in patients receiving cancer chemotherapy. The degree of antiemetic activity demonstrated by cannabinoids is not as high as that seen with several other classes of agents. The side effects associated with cannabinoid use are tolerable, but greater that those seen with other classes of agents.
Studies have not demonstrated an advantage of one tested cannabinoid over another. Results of trials with synthetic cannabinoids, such as levonantradol or nabilone, do not indicate a superior therapeutic index over naturally occurring cannabinoids. Only limited data from well-designed trials can be found comparing inhalant marihuana with other cannabinoids. From that which exists, there is no clear advantage for either inhalant marihuana or for oral THC. Additionally, there is no demonstration that the inhalant agent results in an improved pharmacokinetic profile, an advantage in self titration, or in a different pattern of side effects.
Further studies with cannabinoids, using accepted methodology, could more accurately outline their activity. Decisions should be made whether or not the current moderate degree of efficacy and moderate amount of associated side effects with all tested cannabinoid antiemetics warrant such trials in the context of substantially more active agents that have more favorable toxicity profiles.
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References
Coates, A., Abraham, S., Laye, S. B., et al. (1983) On the receiving end-patient perception of the side-effects of cancer chemotherapy. Eur. J. Cancer Clin. Oncol. 19, 203–208.
Griffin, A. M., Butow, P. N., Coates, A. S., et al. (1996) On the receiving end V: patient perceptions of the side effects of cancer chemotherapy in 1993. Ann. Oncol. 7, 189–195.
Gralla, R. J., Itri, L. M., Pisko, S. E., et al. (1981) Antiemetic efficacy of high dose metoclopramide: randomized trials with placebo and prochlorperazine in patients with chemotherapy-induced nausea vomiting. N. Engl. J. Med. 305, 905–909.
Roila, F., Tonato, M., Cognetti, F., et al. (1991) Prevention of cisplatin-induced emesis: a double-blind multicenter randomized crossover study comparing ondansetron and ondansetron plus dexamethasone. J. Clin. Oncol. 9, 674–678.
Steele, N., Gralla. J., and Braun, D. W., Jr. (1980) Double-blind comparison of the antiemetic effects of nabilone and prochlorperazine on chemotherapy-induced emesis. Cancer Treat. Rep. 64, 219–224.
Tyson, L. B., Gralla, R. J., Clark, R. A., et al. (1985) Phase I trial of levonantradol in chemotherapy-induced emesis. Am. J. Clin. Oncol. 8, 528–532.
Sallan, S. E., Zinberg, N. E., and Frei, E. (1975) Antiemetic effect of delta-9-tetrahydrocannabinol in patients receiving cancer chemotherapy. N. Engl. J. Med. 293, 795–797, 1975.
Chang, A. E., Shiling, D. J., Stillman, R. C., et al. (1979) Delta-9-tetrahydrocannabinol as an antiemetic in patients receiving high-dose methotrexate: a prospective, randomized evaluation. Ann. Intern. Med. 91, 819–824.
Chang, E. A., Shiling, D. J., Stillman, R. C., et al. (1981) A prospective evaluation of delta-9-tetrahydrocannabinol as an antiemetic in patients receiving adriamycin and cytoxan chemotherapy. Cancer 47, 1746–1751.
Frytak, S., Moertel, C. G., O’Fallon, J., et al. (1979) Delta-9-tetrahydrocannabinol as an antiemetic in patients treated with cancer chemotherapy: a double comparison with prochlorperazine and a placebo. Ann. Intern. Med. 91, 825–830.
Sallan, S. E., Cronin, C. M., Zelen, M., et al. (1980) Antiemetics in patients receiving chemotherapy for cancer: a randomized comparison of delta-9-tetrahydrocannabinol and prochlorperazine. N. Engl. J. Med. 302, 135–138.
Orr, L. E., McKerman, J. F., and Bloone, B. (1980) Antiemetic effect of tetrahydrocannabinol. Arch. Intern. Med. 140, 1431–1433.
Levitt, M., Faiman, C., Hawks, R., et al: (1984) Randomized double blind comparison of delta-9-tetahydrocannabinol (THC) and marihuana as chemotherapy antiemetics. Proc. Am. Soc. Clin. Oncol. 3, 91.
Gralla, R. J., Tyson, L. B., Borden, L. B., et al. Antiemetic therapy: a review of recent studies and a report of a random assignment trial comparing metoclopramide with delta-9-tetrahydrocannabinol. Cancer Treat Rep 68: 163–172, 1984.
Borison, H. L., Mc Carthy, L. E. (1983) Neuropharmacology of chemotherapy induced emesis. Drugs 25, 8–17.
Fozard, J. R. (1984) Neuronal 5-HT receptors in the periphery. Neuropharmacology 23, 1473–1486.
Andrews P. L. R., and Davis CJ. The physiology of emesis induced by anti-cancer therapy. IN: Serotonin and the Scientific Basis of Anti-Emetic Therapy. (Reynolds, D. J. M., Andrews, P. L. R., and Davis, C. J., eds.) Oxford Clinical Communications, Oxford, UK, 1995,pp. 25–49.
Davis C.J. Emesis research: a concise history of the critical concepts and experiments. In: Serotonin and the Scientific Basis of Anti-Emetic Therapy. ( Reynolds D. J. M., Andrews, P. L. R., Davis, C. J., eds.) Oxford Clinical Communications, Oxford, UK, 1995, pp. 9–24.
Gralla, R. J., Clark, R. A., Kris, M. G., and Tyson, L. B.: (1991) Methodology in anti-emetic trials. Eur. J. Cancer 27, S5–8.
Vinciguerra, V., Moore, T., and Brennan, E. (1988) Inhalation marihuana as an antiemetic for cancer chemotherapy. NY State J. Med. 10, 525–527.
Kris, M. G., Gralla, R. J., Clark, R. A., et al. (1987) Antiemetic control and prevention of side effects of anticancer therapy with lorazepam or diphenhydramine when used in combination with metoclopramide plus dexamethasone: a double-blind randomized trial. Cancer 602816–2822.
Perez, E. A., Chawla, S. P., Kaywin, P. K., et al. (1997) Efficacy and safety of oral granisetron versus IV ondansetron in prevention of moderately emetogenic chemotherapy-induced nausea and vomiting. Proc. Am. Soc. Clin. Oncol. 16–43.
Gralla, R. J., Navari, R. M., Hesketh, P. J., et al. (1998) Single-dose oral granisetron has equivalent antiemetic efficacy to intravenous ondansetron for highly emetogenic cisplatin-based chemotherapy. J. Clin. Oncol. 16 1-7.
Clark, R. A., Tyson, L. B., and Frisone, M. (1985) A correlation of objective and subjective parameters in assessing antiemetic regimens. Proc. Tenth Ann. Cong. Oncol. Nurs. Soc. 2, 96.
Gralla, R. J., Braun, T. J., Squillante, A., et al. Metoclopramide: initial clinical studies of high dosage regimens in cisplatin-induced emesis. In: Poster D, ed. The treatment of nausea vomiting induced by cancer chemotherapy. New York, N.Y.: Masson Publishing; 167–176, 1981.
Gralla, R. J. (1983) Metoclopramide. A review of antiemetic trials. Drugs 25: 163–73.
Homesley, H. D., Gainey, J. M., Jobson, V. N., et al. (1982) Double-blind placebo-controlled study of metoclopramide in cisplatin-induced emesis. N. Engl. J. Med. 307250–251.
The Italian Group for Antiemetic Trials (1995) Dexamethasone, granisetron, or both for the prevention of nausea and vomiting during chemotherapy for cancer. N. Engl. J. Med. 332–337.
DeMulder, P. H. M., Seynaeve, C., Vermorker, J. B., et al. (1990) Ondansetron compared with high-dose metoclopramide in prophylaxis of acute and delayed cisplatin-induced nausea and vomiting. A multicenter, randomized, double-blind, crossover study. Ann. Inter. Med. 113, 834–840.
Beck, T. M., Hesketh, P. J., Madajewicz, S., et al. (1992) Stratified, randomized, double-blind comparison on intravenous dose regimens in the prevention of cisplatin-induced nausea and vomiting. J. Clin. Oncol. 10 (12), 1969–75.
Kris, M. G., Gralla, R. J., Tyson, L. B., et al. (1985) Improved control of cisplatin-induced emesis with high-dose metoclopramide and with combinations of metoclopramide, dexamethasone and diphenhydramine: results of consecutive trials in 255 patients. Cancer 55, 527–534.
Gralla, R. J., Rittenberg, C. N., Lettow, L. A., et al. (1995) A unique all-oral, single-dose, combination antiemetic regimen with high efficacy and marked cost saving potential. Proc. Am. Soc. Clin. Oncol. 14, 526.
Kris, M. G., Radford, J. E., Pizzo, B. A., et al. (1997) Use of an NK-1 receptor antagonist to prevent delayed emesis following cisplatin. J. Natl. Cancer Inst. 89, 817–818.
Hesketh, P. A., Gralla, R. J., Webb, R. T., et al. (1998) Randomized Phase II Study of the Neurokinin-1 Antagonist CJ-11,974 for the Control of Cisplatin-Induced Emesis. Proc. Am. Soc. Clin. Oncol. 17
Navari, R. M., Gralla, R. J., Hesketh, P., Kris, M. G., et al. (1998) MK-869, A selective neurokinin-1 antagonist, reduces cisplatin-induced acute and delayed emesis. Proc. Am. Soc. Clin. Oncol. 17
Tyson, L. B., Clark, R. A., and Gralla, R. J. (1982) High-dose metoclopramide: control of dacarbazineinduced emesis in a preliminary trial. Cancer Treat. Rep. 66, 2108.
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Gralla, R.J. (1999). Cannabinoids and the Control of Chemotherapy-Induced Nausea and Vomiting. In: Nahas, G.G., Sutin, K.M., Harvey, D., Agurell, S., Pace, N., Cancro, R. (eds) Marihuana and Medicine. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-710-9_59
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DOI: https://doi.org/10.1007/978-1-59259-710-9_59
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