Health economic impact of high-dose versus standard-dose cytarabine induction chemotherapy for acute myeloid leukaemia
- PMID: 24863325
- DOI: 10.1111/imj.12478
Health economic impact of high-dose versus standard-dose cytarabine induction chemotherapy for acute myeloid leukaemia
Abstract
Background: Induction chemotherapy for acute myeloid leukaemia (AML) is one of the most resource-intensive cancer therapies delivered in hospitals.
Aims: To assess the health resource impact of different chemotherapy approaches for AML commonly used in Australia.
Methods: A retrospective analysis was undertaken in 63 patients aged 18-55 years with AML given induction with either 7 + 3 (cytarabine 100 mg/m(2) days 1-7 and idarubicin 12 mg/m(2) days 1-3) or HiDAC-3 (high-dose cytarabine 3 g/m(2) twice daily days 1, 3, 5 and 7 and idarubicin 12 mg/m(2) days 1-3) chemotherapy. Average costs of hospitalisation, pathology, radiology, chemotherapy and ancillary drugs were calculated and compared with current Victorian casemix funding. Two consolidation approaches, HiDAC (cytarabine 3 g/m(2) twice daily days 1, 3, 5 and 7) × either three or four cycles (following 7 + 3) and IcE (idarubicin 12,mg/m(2) days 1-2, cytarabine 100 mg/m(2) × 5 days and etoposide 75 mg/m(2) × 5 days) × 2 cycles (following HiDAC-3) were modelled, using a policy of discharge following completion of chemotherapy with outpatient monitoring.
Results: The cost (in AUD) of induction was similar between 7 + 3 ($58,037) and HiDAC-3 ($56,902), with bed day costs accounting for 61-62% of the total expense. Blood bank costs ranked second, accounting for 15%. Accumulated costs for HiDAC consolidation were $44,289 for a three-cycle protocol and $59,052 for four cycles ($14,763 per cycle) versus $31,456 for two cycles of IcE consolidation ($15,728 per cycle). Overall, the classical 7 + 3 → HiDAC approach ($102,326/$117,089 for three or four consolidation cycles) incurs a greater cost than a HiDAC-3 → IcE × 2 approach ($88,358). For patients requiring complete hospitalisation until neutrophil recovery, the estimated costs of treatment will be even higher, ranging between $122,282 for HiDAC-3 → IcE × 2, $153,212 for 7 + 3 → HiDAC × 3 and $184,937 for 7 + 3 → HiDAC × 4. State-based casemix funding for non-complicated AML therapy is currently $74,013 for 7 + 3 → HiDAC × 4, $64,177 for 7 + 3 → HiDAC × 3 and $54,340 for HiDAC-3 → IcE × 2 based on outpatient recovery after consolidation chemotherapy. These calculations do not take into account additional resource implications associated with complications of consolidation chemotherapy or reinduction for treatment failure.
Conclusion: Regimens minimising the total number of chemotherapy cycles may represent the most efficient use of limited health resources for the treatment of AML.
Keywords: HiDAC; acute myeloid leukaemia; cost effectiveness; cytarabine.
© 2014 The Authors; Internal Medicine Journal © 2014 Royal Australasian College of Physicians.
Similar articles
-
High-dose cytarabine (24 g/m2) in combination with idarubicin (HiDAC-3) results in high first-cycle response with limited gastrointestinal toxicity in adult acute myeloid leukaemia.Intern Med J. 2013 Mar;43(3):294-7. doi: 10.1111/j.1445-5994.2012.02868.x. Intern Med J. 2013. PMID: 22757980 Review.
-
A phase I/II study of intensive dose escalation of cytarabine in combination with idarubicin and etoposide in induction and consolidation treatment of adult acute myeloid leukemia. Australian Leukaemia Study Group (ALSG).Leuk Lymphoma. 1999 Aug;34(5-6):501-10. doi: 10.3109/10428199909058477. Leuk Lymphoma. 1999. PMID: 10492073 Clinical Trial.
-
A new combination of carboplatin, high-dose cytarabine and cross-over mitoxantrone or idarubicin for refractory and relapsed acute myeloid leukemia.Haematologica. 1998 May;83(5):422-7. Haematologica. 1998. PMID: 9658726 Clinical Trial.
-
High-dose cytarabine in induction treatment improves the outcome of adult patients younger than age 46 years with acute myeloid leukemia: results of the EORTC-GIMEMA AML-12 trial.J Clin Oncol. 2014 Jan 20;32(3):219-28. doi: 10.1200/JCO.2013.51.8571. Epub 2013 Dec 2. J Clin Oncol. 2014. PMID: 24297940 Clinical Trial.
-
High risk of relapse with intermediate dose cytarabine for consolidation in young favourable-risk acute myeloid leukaemia patients following induction with 7+3: a retrospective multicentre analysis and critical review of the literature.Br J Haematol. 2021 Jul;194(1):140-144. doi: 10.1111/bjh.17462. Epub 2021 Apr 11. Br J Haematol. 2021. PMID: 33843048 Review.
Cited by
-
Comparison of Hospital Length of Stay and Supportive Care Utilization Between Patients Treated with CPX-351 and 7+3 for Therapy-Related Acute Myeloid Leukemia or Acute Myeloid Leukemia with Myelodysplasia-Related Changes.Clinicoecon Outcomes Res. 2022 Jan 8;14:21-34. doi: 10.2147/CEOR.S342303. eCollection 2022. Clinicoecon Outcomes Res. 2022. PMID: 35035224 Free PMC article.
-
A genomics-informed computational biology platform prospectively predicts treatment responses in AML and MDS patients.Blood Adv. 2019 Jun 25;3(12):1837-1847. doi: 10.1182/bloodadvances.2018028316. Blood Adv. 2019. PMID: 31208955 Free PMC article. Clinical Trial.
-
Comparison of in-patient costs for children treated on the AAML0531 clinical trial: A report from the Children's Oncology Group.Pediatr Blood Cancer. 2015 Oct;62(10):1775-81. doi: 10.1002/pbc.25569. Epub 2015 May 6. Pediatr Blood Cancer. 2015. PMID: 25946708 Free PMC article. Clinical Trial.
-
Trends in Clinical Benefits and Costs of Novel Therapeutics in AML: at What Price Does Progress Come?Curr Hematol Malig Rep. 2019 Jun;14(3):171-178. doi: 10.1007/s11899-019-00510-2. Curr Hematol Malig Rep. 2019. PMID: 31079354 Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical