Skip to main content
Top
Published in: Supportive Care in Cancer 10/2012

01-10-2012 | Original Article

Carmustine infusion reactions are more common with rapid administration

Authors: Brett Janson, Pia Van Koeverden, Sing Wang Kevin Yip, Arti Thakerar, James D. Mellor

Published in: Supportive Care in Cancer | Issue 10/2012

Login to get access

Abstract

Purpose

Carmustine is a nitrosurea alkylating agent predominantly used at Peter MacCallum Cancer Centre as part of the autologous stem cell transplant induction regimens Stanford BCNU and BEAM. Acute infusion reactions were anecdotally reported to be higher than the reported rates of 10%, and it was suggested that the rate of infusion being employed was excessive. Some references suggest maximum infusion rates of 3 mg/m2/min for carmustine, a rate which is exceeded in the 2-h infusions used for Stanford BCNU, but not with BEAM.

Methods

A retrospective audit was conducted in 64 patients (57 Stanford BCNU, 7 BEAM) who had received these regimens between January 2009 and November 2010.

Results

Rates of infusion reaction to carmustine were higher than literature values, with reactions in Stanford BCNU (94.7%) being significantly higher than for BEAM (28.6%; P = 0.0003). These findings have resulted in a change of administration of carmustine in Stanford BCNU from 2 to 3 h. Further studies plan to compare the incidence of infusion reactions before and after the change in administration rates.

Conclusion

Patients receiving rapid infusion of carmustine in the Stanford BCNU regimen for stem cell conditioning have a high rate of infusion reaction. A maximum rate of 3 mg/m2/min is recommended.
Literature
2.
go back to reference Stiff PJ, Dahlberg S, Forman SJ et al (1998) Autologous bone marrow transplantation for patients with relapsed or refractory diffuse aggressive non-Hodgkin’s lymphoma: value of augmented preparative regimens—a Southwest Oncology Group trial. J Clin Oncol 16(1):48–55PubMed Stiff PJ, Dahlberg S, Forman SJ et al (1998) Autologous bone marrow transplantation for patients with relapsed or refractory diffuse aggressive non-Hodgkin’s lymphoma: value of augmented preparative regimens—a Southwest Oncology Group trial. J Clin Oncol 16(1):48–55PubMed
3.
go back to reference Horning SJ, Chao NJ, Negrin RS et al (1991) The Stanford experience with high-dose etoposide cytoreductive regimens and autologous bone marrow transplantation in Hodgkin's disease and non-Hodgkin's lymphoma: preliminary data. Ann Onc 2(Supplement 1):47–50 Horning SJ, Chao NJ, Negrin RS et al (1991) The Stanford experience with high-dose etoposide cytoreductive regimens and autologous bone marrow transplantation in Hodgkin's disease and non-Hodgkin's lymphoma: preliminary data. Ann Onc 2(Supplement 1):47–50
4.
go back to reference Gribben JG, Linch DC, Singer CR et al (1989) Successful treatment of refractory Hodgkin's disease by high-dose combination chemotherapy and autologous bone marrow transplantation. Blood 73:340–344PubMed Gribben JG, Linch DC, Singer CR et al (1989) Successful treatment of refractory Hodgkin's disease by high-dose combination chemotherapy and autologous bone marrow transplantation. Blood 73:340–344PubMed
5.
go back to reference Chopra R, McMillan AK, Linch DC et al (1993) The place of high-dose BEAM therapy and autologous bone marrow transplantation in poor-risk Hodgkin's disease. A single-center eight-year study of 155 patients. Blood 81:1137–1145PubMed Chopra R, McMillan AK, Linch DC et al (1993) The place of high-dose BEAM therapy and autologous bone marrow transplantation in poor-risk Hodgkin's disease. A single-center eight-year study of 155 patients. Blood 81:1137–1145PubMed
6.
go back to reference Caballero MD, Rubio V, Rifon J et al (1997) BEAM chemotherapy followed by autologous stem cell support in lymphoma patients: analysis of efficacy, toxicity and prognostic factors. Bone Marrow Transplant 20:451–458PubMedCrossRef Caballero MD, Rubio V, Rifon J et al (1997) BEAM chemotherapy followed by autologous stem cell support in lymphoma patients: analysis of efficacy, toxicity and prognostic factors. Bone Marrow Transplant 20:451–458PubMedCrossRef
7.
go back to reference Bristol-Myers Squibb (2010) BiCNU™ Powder for injection (Carmustine) Approved Product Information. Date of TGA approval (latest amendment) 20 July 2010. Bristol-Myers Squibb (2010) BiCNU™ Powder for injection (Carmustine) Approved Product Information. Date of TGA approval (latest amendment) 20 July 2010.
8.
go back to reference National Cancer Institute (2010) Common Terminology Criteria for Adverse Events, version 4.03, June 2010 National Cancer Institute (2010) Common Terminology Criteria for Adverse Events, version 4.03, June 2010
9.
go back to reference Woo MH, Ippoliti C, Bruton J et al (1997) Headache, circumoral paresthesia, and facial flushing associated with high-dose carmustine infusion. Bone Marrow Transplant 19:845–847PubMedCrossRef Woo MH, Ippoliti C, Bruton J et al (1997) Headache, circumoral paresthesia, and facial flushing associated with high-dose carmustine infusion. Bone Marrow Transplant 19:845–847PubMedCrossRef
10.
go back to reference Takvorian T, Parker LM, Hochberg FH, Canellos GP (1983) Autologous bone-marrow transplantation: host effects of high-dose BCNU. J Clin Oncol 1(10):610–620PubMed Takvorian T, Parker LM, Hochberg FH, Canellos GP (1983) Autologous bone-marrow transplantation: host effects of high-dose BCNU. J Clin Oncol 1(10):610–620PubMed
11.
go back to reference Bearman SI, Overmoyer BA, Bolwell BJ et al (1997) High-dose chemotherapy with autologous peripheral blood progenitor cell support for primary breast cancer in patients with 4–9 involved axillary lymph nodes. Bone Marrow Transplant 20:931–937PubMedCrossRef Bearman SI, Overmoyer BA, Bolwell BJ et al (1997) High-dose chemotherapy with autologous peripheral blood progenitor cell support for primary breast cancer in patients with 4–9 involved axillary lymph nodes. Bone Marrow Transplant 20:931–937PubMedCrossRef
12.
go back to reference Kanj SS, Sharara AI, Shpall EJ, Jones RB, Peters WP (1991) Myocardial ischemia associated with high-dose carmustine infusion. Cancer 68(9):1910–1912PubMedCrossRef Kanj SS, Sharara AI, Shpall EJ, Jones RB, Peters WP (1991) Myocardial ischemia associated with high-dose carmustine infusion. Cancer 68(9):1910–1912PubMedCrossRef
13.
go back to reference Henner WD, Peters WP, Eder JP et al (1986) Pharmacokinetics and immediate effects of high-dose carmustine in man. Cancer Treat Rep 70(7):877–880PubMed Henner WD, Peters WP, Eder JP et al (1986) Pharmacokinetics and immediate effects of high-dose carmustine in man. Cancer Treat Rep 70(7):877–880PubMed
14.
go back to reference Peters WP, Shpall EJ, Jones RB et al (1988) High-dose combination alkylating agents with bone marrow support as initial treatment for metastatic breast cancer. J Clin Oncol 6(9):1368–1376PubMed Peters WP, Shpall EJ, Jones RB et al (1988) High-dose combination alkylating agents with bone marrow support as initial treatment for metastatic breast cancer. J Clin Oncol 6(9):1368–1376PubMed
15.
go back to reference Kwan H, Knight S, Thirlwell S (2010) Beyond nausea & vomiting: monitoring less common reactions to high dose BCNU. Biol Blood Marrow Tr 16(2):S196CrossRef Kwan H, Knight S, Thirlwell S (2010) Beyond nausea & vomiting: monitoring less common reactions to high dose BCNU. Biol Blood Marrow Tr 16(2):S196CrossRef
16.
go back to reference Genet P, Pulik M, Gallet B et al (2002) Acute myocardial ischemia after high-dose therapy with BEAM regimen. Bone Marrow Transplant 30(4):253–254PubMedCrossRef Genet P, Pulik M, Gallet B et al (2002) Acute myocardial ischemia after high-dose therapy with BEAM regimen. Bone Marrow Transplant 30(4):253–254PubMedCrossRef
17.
go back to reference Altura BM, Altura BT (1987) Peripheral and cerebrovascular actions of ethanol, acetaldehyde, and acetate: relationship to divalent cations. Alcohol Clin Exp Res 11(2):99–111PubMedCrossRef Altura BM, Altura BT (1987) Peripheral and cerebrovascular actions of ethanol, acetaldehyde, and acetate: relationship to divalent cations. Alcohol Clin Exp Res 11(2):99–111PubMedCrossRef
Metadata
Title
Carmustine infusion reactions are more common with rapid administration
Authors
Brett Janson
Pia Van Koeverden
Sing Wang Kevin Yip
Arti Thakerar
James D. Mellor
Publication date
01-10-2012
Publisher
Springer-Verlag
Published in
Supportive Care in Cancer / Issue 10/2012
Print ISSN: 0941-4355
Electronic ISSN: 1433-7339
DOI
https://doi.org/10.1007/s00520-011-1377-4

Other articles of this Issue 10/2012

Supportive Care in Cancer 10/2012 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine