Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Original Article
  • Published:

Anti-Emetics

Prospective evaluation of antiemetic outcome following high-dose chemotherapy with hematopoietic stem cell support

Abstract

Considerable progress has been made in improving the control of chemotherapy-induced emesis. The impact of available antiemetic options for patients receiving stem cell transplants is unclear, as few prospective data have been collected. We prospectively evaluated antiemetic outcome in patients receiving stem cell transplantation over a 7-day period following the initiation of chemotherapy. The primary endpoints were the number of emetic episodes and the extent of nausea measured on a four-point scale. Eighty-two patients were evaluated. Ninety-five percent of patients had nausea during the first week of treatment; 80% had at least one emetic episode. The percentage of patients with emesis was as follows: day 1: 13%, day 2: 21%, day 3: 30%, day 4: 38%, day 5: 44%, day 6: 39%, day 7: 18%. In multivariate analysis, gender, emesis with prior chemotherapy, history of morning or motion sickness, type of transplant (auto vs allo), use of total body irradiation, or use of dexamethasone did not effect emesis control. Most patients receiving high-dose chemotherapy experience incompletely controlled emesis. Control of nausea and emesis progressively worsened with each subsequent day following initiation of chemotherapy, reaching a nadir on day 5. New treatment approaches are needed to improve emesis control in this patient population.

Bone Marrow Transplantation (2001) 28, 1061–1066.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1
Figure 2

Similar content being viewed by others

References

  1. Thomas ED, Clift RA, Fefer A et al. Marrow transplantation for the treatment of chronic myelogenous leukemia Ann Intern Med 1986 104: 155–163

    Article  CAS  Google Scholar 

  2. Krivit W, Whitley CB . Bone marrow transplantation for genetic disease New Engl J Med 1987 316: 1085–1087

    Article  CAS  Google Scholar 

  3. Lucarelli G, Galimberti M, Polchi P et al. Marrow transplantation in patients with advanced thalassemia New Engl J Med 1987 316: 1050–1055

    Article  CAS  Google Scholar 

  4. Mickelson E, Petersdorf EW . Histocompatibility. In: ED Thomas, KG Blume, SJ Forman (eds). Hematopoietic Cell Transplantation, 2nd edn Blackwell Science: Massachusetts 1999 p 28

  5. Storb R, Deeg HJ, Whitehead J et al. Methotrexate and cyclosporine compared with cyclosporine alone for prophylaxis of acute graft versus host disease after marrow transplantation for leukemia New Engl J Med 1986 314: 729–735

    Article  CAS  Google Scholar 

  6. Goodrich JM, Mori M, Gleaves CA et al. Early treatment with ganciclovir to prevent cytomegalovirus disease after allogeneic bone marrow transplantation New Engl J Med 1991 325: 1601–1607

    Article  CAS  Google Scholar 

  7. Rubinstein P, Carrier C, Scaradavou A et al. Outcomes among 562 recipients of placental blood transplants from unrelated donors New Engl J Med 1998 339: 1565–1577

    Article  CAS  Google Scholar 

  8. Coates A, Abraham S, Kaye SB et al. On the receiving end: patient perception of the side-effects of cancer chemotherapy Eur J Cancer Clin Oncol 1983 19: 203–208

    Article  CAS  Google Scholar 

  9. Griffin AM, Burtow PN, Coates AS et al. On the receiving end V: patient perceptions of the side effects of the cancer chemotherapy in 1993 Ann Oncol 1996 7: 189–195

    Article  CAS  Google Scholar 

  10. Navari RM, Kaplan HG, Gralla RJ et al. Efficacy and safety of granisetron, a selective 5-hydroxytryptamine-3 receptor antagonist, in the prevention of nausea and vomiting induced by high-dose cisplatin J Clin Oncol 1994 12: 2204–2210

    Article  CAS  Google Scholar 

  11. Riviere A . Dose finding study of granisetron in patients receiving high-dose cisplatin chemotherapy Br J Cancer 1994 69: 967–971

    Article  CAS  Google Scholar 

  12. Gralla RJ, Navari RM, Hesketh PJ et al. Single-dose oral granisetron has equivalent antiemetic efficacy to intravenous ondansetron for highly emetogenic cisplatin-based chemotherapy J Clin Oncol 1998 16: 1568–1573

    Article  CAS  Google Scholar 

  13. Hesketh PJ, Navari R, Grote T et al. Double-blind, randomized comparison of the antiemetic efficacy of intravenous dolasetron mesylate and intravenous ondansetron in the prevention of acute cisplaitin-induced emesis in patients with cancer J Clin Oncol 1996 14: 2242–2249

    Article  CAS  Google Scholar 

  14. Hesketh PJ, Plagge P, Bryson JC . Single-dose ondansetron for prevention of acute cisplatin-induced emesis: analysis of efficacy and prognostic factors. In: Bianchi AL, Grelot L, Miller AD et al (eds) Mechanisms and Control of Emesis Libbey: London 1992 pp 25–26

    Google Scholar 

  15. Beck TM, Hesketh PJ, Madajewicz S et al. Stratified, randomized, double-blind comparison of intravenous ondansetron administered as a multiple-dose regimen versus two single-dose regimens in the prevention of cisplatin-induced nausea and vomiting J Clin Oncol 1992 10: 1969–1975

    Article  CAS  Google Scholar 

  16. Trovato JA, Stull DM, Finley RS . Outcomes of antiemetic therapy after the administration of high-dose antineoplastic agents Am J Health Syst Pharm 1998 55: 1269–1274

    CAS  PubMed  Google Scholar 

  17. Perez EA, Tiemeier T, Solberg LA . Antiemetic therapy for high-dose chemotherapy with transplantation: report of a retrospective analysis of a 5-HT3 regimen and literature review Support Care Cancer 1999 7: 413–424

    Article  CAS  Google Scholar 

  18. Armitage P, Berry G . Statistical Methods in Medical Research, 3rd edn Blackwell: Boston 1994 pp 422–436

  19. Gralla RJ, Osoba D, Kris MG et al. Recommendations for the use of antiemetics: evidence-based, clinical practice guidelines J Clin Oncol 1999 17: 2971–2994

    Article  CAS  Google Scholar 

  20. Abbott B, Ippoliti C, Bruton J et al. Antiemetic efficacy of granisetron plus dexamethasone in bone marrow transplant patients receiving chemotherapy and total body irradiation Bone Marrow Transplant 1999 23: 265–269

    Article  CAS  Google Scholar 

  21. Osowksi CL, Dix SP, Lynn M et al. An open-label dose comparison study of ondansetron for the prevention of emesis associated with chemotherapy prior to bone marrow transplantation Support Care Cancer 1998 6: 511–517

    Article  Google Scholar 

  22. Abbott B, Ippoliti C, Hecth D et al. Granisetron (Kytril) plus dexamethasone for antiemetic control in bone marrow transplant patients receiving highly emetogenic chemotherapy with or without total body irradiation Bone Marrow Transplant 2000 25: 1279–1283

    Article  CAS  Google Scholar 

  23. Orchard PJ, Rogosheske J, Burns L et al. A prospective randomized trial of the anti-emetic efficacy of ondansetron and granisetron during bone marrow transplantation Biol Blood Marrow Transplant 1999 5: 386–393

    Article  CAS  Google Scholar 

  24. Barbounis V, Koumakis G, Hatzichristou H et al. The anti-emetic efficacy of tropisetron plus dexamethasone in patients treated with high-dose chemotherapy and stem cell transplantation Support Care Cancer 1999 7: 79–83

    Article  CAS  Google Scholar 

  25. Spitzer TR, Friedman CJ, Bushnell W et al. Double-blind, randomized, parallel-group study on the efficacy and safety of oral granisetron and oral ondansetron in the prophylaxis of nausea and vomiting in patients receiving hyperfractionated total body irradiation Bone Marrow Transplant 2000 26: 203–210

    Article  CAS  Google Scholar 

  26. Ioannidis JP, Hesketh PJ, Lau J . Contribution of dexamethasone to control of chemotherapy-induced nausea and vomiting: a meta-analysis of randomized evidence J Clin Oncol 2000 18: 3409–3422

    Article  CAS  Google Scholar 

  27. Bountra C, Bunce K, Dale T et al. Antiemetic profile of a non-peptide neurokinin NK1 receptor antagonist CP-99,994 in ferrets Eur J Pharmacol 1993 249: R3–R4

    Article  CAS  Google Scholar 

  28. Watson JW, Gonsalves SF, Fossa AA et al. The anti-emetic effects of CP-99,994 in the ferret and the dog: role of the NK1 receptor Br J Pharmacol 1995 115: 84–94

    Article  CAS  Google Scholar 

  29. Tattersall FD, Rycroft W, Hill RG, Hargreaves RJ . Enantioselective inhibition of apomorphine-induced emesis in the ferret by the neurokinin1 receptor antagonist CP-99,994 Neuropharmacology 1994 33: 259–260

    Article  CAS  Google Scholar 

  30. Navari RM, Reinhardt RR, Gralla RJ et al. Reduction of cisplatin-induced emesis by selective neurokinin-1-receptor antagonist New Engl J Med 1999 340: 190–195

    Article  CAS  Google Scholar 

  31. Hesketh PH, Gralla RJ, Webb RT et al. Randomized phase II study of the neurokinin 1 receptor antagonist CJ-11,974 in the control of cisplatin-induced emesis J Clin Oncol 1999 17: 338–343

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors thank the outstanding nursing staff of the UMassMemorial Bone Marrow Transplant Unit. The authors thank Carol Perch and Shelly Anderson for their excellent technical assistance.

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ballen, K., Hesketh, A., Heyes, C. et al. Prospective evaluation of antiemetic outcome following high-dose chemotherapy with hematopoietic stem cell support. Bone Marrow Transplant 28, 1061–1066 (2001). https://doi.org/10.1038/sj.bmt.1703280

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.bmt.1703280

Keywords

This article is cited by

Search

Quick links