TY - JOUR
T1 - An economic evaluation of eribulin for advanced breast cancer treatment based on the Southeast Netherlands advanced breast cancer registry
AU - Pouwels, Xavier G. L.
AU - Ramaekers, Bram L. T.
AU - Geurts, Sandra M. E.
AU - Erdkamp, Frans
AU - Vriens, Birgit E. P. J.
AU - Aaldering, Kirsten N. A.
AU - van de Wouw, Agnes J.
AU - Dercksen, M. W.
AU - Smilde, Tineke J.
AU - Peters, Natascha A. J. B.
AU - van Riel, J. M. G. H.
AU - Pepels, Manon J.
AU - Heijnen-Mommers, Jose
AU - Tjan-Heijnen, Vivianne C. G.
AU - de Boer, Maaike
AU - Joore, Manuela A.
N1 - Funding Information:
The SONABRE Registry is supported by the Netherlands Organisation for Health Research and Development [ZonMw: 80-82500-98-8003], Eisai, Novartis BV, Roche, Pfizer and Eli Lilly. The authors thank all registration clerks of the SONABRE Registry for their involvement in the data collection process. We also thank Ben Wijnen, health economist at the Clinical Epidemiology and Medical Technology Assessment department of the Maastricht University Medical Centre+, for acting as an external reviewer of the model.
Publisher Copyright:
© 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Background: In 2013, eribulin was reimbursed under a coverage with evidence development (CED) as third or later chemotherapy line for advanced breast cancer (ABC) patients in the Netherlands because of uncertain cost effectiveness. In 2016, the final decision of reimbursing eribulin was taken without considering the evidence collected during CED research. We analysed the cost effectiveness of eribulin versus non-eribulin chemotherapy, using real-world data. Methods: A three health states (progression-free, progressed disease, dead) partitioned survival model was developed. The SOuth East Netherlands Advanced BREast Cancer (SONABRE) registry informed the effectiveness and costs inputs. Health state utility values were obtained from the literature. Incremental cost-effectiveness ratio (ICER) between the eribulin and matched non-eribulin chemotherapy was estimated. Deterministic and probabilistic sensitivity analyses and scenario analyses were performed. The financial risk (i.e., the expected value of perfect information (EVPI) plus the expected monetary loss (eML) associated with reimbursing eribulin) and budget impact associated with reimbursing eribulin were calculated. Results: Eribulin led to higher health benefits (0.07 quality-adjusted life year (QALY)) and costs (€15,321) compared with non-eribulin chemotherapy. This resulted in an ICER of €220,608. At a €80,000 per QALY threshold, the risk of reimbursing eribulin was €9,791 per patient (EVPI €13, eML €9,778). Scaled up to the Dutch population, the estimated annual budget impact was €1.9 million and the annual risk of reimbursing eribulin was €2.7 million. Conclusion: From a Dutch societal perspective, eribulin is not cost effective when considering its list price as third and later chemotherapy line for ABC patients.
AB - Background: In 2013, eribulin was reimbursed under a coverage with evidence development (CED) as third or later chemotherapy line for advanced breast cancer (ABC) patients in the Netherlands because of uncertain cost effectiveness. In 2016, the final decision of reimbursing eribulin was taken without considering the evidence collected during CED research. We analysed the cost effectiveness of eribulin versus non-eribulin chemotherapy, using real-world data. Methods: A three health states (progression-free, progressed disease, dead) partitioned survival model was developed. The SOuth East Netherlands Advanced BREast Cancer (SONABRE) registry informed the effectiveness and costs inputs. Health state utility values were obtained from the literature. Incremental cost-effectiveness ratio (ICER) between the eribulin and matched non-eribulin chemotherapy was estimated. Deterministic and probabilistic sensitivity analyses and scenario analyses were performed. The financial risk (i.e., the expected value of perfect information (EVPI) plus the expected monetary loss (eML) associated with reimbursing eribulin) and budget impact associated with reimbursing eribulin were calculated. Results: Eribulin led to higher health benefits (0.07 quality-adjusted life year (QALY)) and costs (€15,321) compared with non-eribulin chemotherapy. This resulted in an ICER of €220,608. At a €80,000 per QALY threshold, the risk of reimbursing eribulin was €9,791 per patient (EVPI €13, eML €9,778). Scaled up to the Dutch population, the estimated annual budget impact was €1.9 million and the annual risk of reimbursing eribulin was €2.7 million. Conclusion: From a Dutch societal perspective, eribulin is not cost effective when considering its list price as third and later chemotherapy line for ABC patients.
KW - COST-EFFECTIVENESS
KW - PRICE
U2 - 10.1080/0284186X.2020.1775289
DO - 10.1080/0284186X.2020.1775289
M3 - Article
C2 - 32544366
SN - 0284-186X
VL - 59
SP - 1123
EP - 1130
JO - Acta Oncologica
JF - Acta Oncologica
IS - 9
ER -