TY - JOUR
T1 - Cetuximab as first-line treatment for metastatic colorectal cancer (mCRC)
T2 - a model-based economic evaluation in Indonesia setting
AU - Putri, Septiara
AU - Saldi, Siti Rizny F.
AU - Khoe, Levina Chandra
AU - Setiawan, Ery
AU - Megraini, Amila
AU - Santatiwongchai, Benjarin
AU - Nugraha, Ryan R.
AU - Permanasari, Vetty Y.
AU - Nadjib, Mardiati
AU - Sastroasmoro, Sudigdo
AU - Armansyah, Armansyah
N1 - Funding Information:
The authors would like to thank the Indonesian Health Technology Assessment Committee (InaHTAC): Prof. Purwantyastuti, MSc, Sp.FK; Prof. Dr. Sri Suryawati, Apt; Prof Budi Hidayat, SKM, MPPM, PhD; and Dr. Santoso Soeroso, Sp A(K), MARS, who have consistently provided their valuable inputs and advice for study’s completion. We also thank Dr. Kalsum Komaryani, MPPM from Center for Health Financing and Insurance, Ministry of Health, Republic of Indonesia for supporting the whole process in terms of assessment on health technologies. We are grateful for the outstanding support from the Indonesian Society of Hematology and Medical Oncology (PERHOMPEDIN) and our experts panel Dr. Ronald A. Hukom and Dr. Agustinus Taolin. We would also like to thank all the hospitals’ management staff, enumerators/data collectors/interviewers that fully supported our research. We also thank for the great technical assistance from Health Intervention and Technology Assessment Program (HITAP) Thailand: Dr. Yot Teerawattananon, Dr. Thunyarata Anothaisintawee, and Ms. Waranya Rattanavipapong. This study is also part of the collaboration between the Ministry of Health Republic of Indonesia and HITAP through the International Decision Support Initiative (iDSI).
Funding Information:
This study was funded by the Indonesian Health Security Agency (BPJS Kesehatan) Indonesia with agreement number: 208/UN2.F10.PKEKK/HKP.5/2017. The research activities were fully supported and supervised by the Center for Health Financing and Insurance, Ministry of Health, Republic of Indonesia. BPJS Kesehatan had no intervention on study design, data collection, analysis, and interpretation. The funder also had no role for influencing the result and discussion in this paper. All authors worked independently for this study.
Publisher Copyright:
© 2023, BioMed Central Ltd., part of Springer Nature.
PY - 2023/12
Y1 - 2023/12
N2 - Objectives: To assess the cost-effectiveness of cetuximab in combination with chemotherapy fluorouracil, oxaliplatin, and leucovorin (FOLFOX) or fluorouracil, irinotecan and leucovorin (FOLFIRI) compared to standard chemotherapy alone as a first-line treatment for metastatic colorectal cancer (mCRC) with positive KRAS wild type patients in Indonesia. Methods: A cost-utility analysis applying Markov model was constructed, with a societal perspective. Clinical evidence was derived from published clinical trials. Direct medical costs were gathered from hospital billings. Meanwhile, direct non-medical costs, indirect costs, and utility data were collected by directly interviewing patients. We applied 3% discount rate for both costs and outcomes. Probabilistic sensitivity analysis was performed to explore the model’s uncertainty. Additionally, using payer perspective, budget impact analysis was estimated to project the financial impact of treatment coverage. Results: There was no significant difference in life years gained (LYG) between cetuximab plus FOLFOX/FOLFIRI and chemotherapy alone. The incremental QALY was only one month, and the incremental cost-effectiveness ratio (ICER) was approximately IDR 3 billion/QALY for cetuximab plus chemotherapy. Using 1–3 GDP per capita (IDR 215 million or USD 14,350) as the current threshold, the cetuximab plus chemotherapy was not cost-effective. The budget impact analysis resulted that if cetuximab plus chemotherapy remain included in the benefits package under the Indonesian national health insurance (NHI) system, the payer would need more than IDR 1 trillion for five years. Conclusions: The combination of cetuximab and chemotherapy for mCRC is unlikely cost-effective and has a substantial financial impact on the system.
AB - Objectives: To assess the cost-effectiveness of cetuximab in combination with chemotherapy fluorouracil, oxaliplatin, and leucovorin (FOLFOX) or fluorouracil, irinotecan and leucovorin (FOLFIRI) compared to standard chemotherapy alone as a first-line treatment for metastatic colorectal cancer (mCRC) with positive KRAS wild type patients in Indonesia. Methods: A cost-utility analysis applying Markov model was constructed, with a societal perspective. Clinical evidence was derived from published clinical trials. Direct medical costs were gathered from hospital billings. Meanwhile, direct non-medical costs, indirect costs, and utility data were collected by directly interviewing patients. We applied 3% discount rate for both costs and outcomes. Probabilistic sensitivity analysis was performed to explore the model’s uncertainty. Additionally, using payer perspective, budget impact analysis was estimated to project the financial impact of treatment coverage. Results: There was no significant difference in life years gained (LYG) between cetuximab plus FOLFOX/FOLFIRI and chemotherapy alone. The incremental QALY was only one month, and the incremental cost-effectiveness ratio (ICER) was approximately IDR 3 billion/QALY for cetuximab plus chemotherapy. Using 1–3 GDP per capita (IDR 215 million or USD 14,350) as the current threshold, the cetuximab plus chemotherapy was not cost-effective. The budget impact analysis resulted that if cetuximab plus chemotherapy remain included in the benefits package under the Indonesian national health insurance (NHI) system, the payer would need more than IDR 1 trillion for five years. Conclusions: The combination of cetuximab and chemotherapy for mCRC is unlikely cost-effective and has a substantial financial impact on the system.
KW - Cetuximab
KW - Colorectal cancer
KW - Cost utility analysis
KW - Economic evaluation
UR - http://www.scopus.com/inward/record.url?scp=85167372166&partnerID=8YFLogxK
U2 - 10.1186/s12885-023-11253-y
DO - 10.1186/s12885-023-11253-y
M3 - Article
C2 - 37553566
AN - SCOPUS:85167372166
SN - 1471-2407
VL - 23
JO - BMC Cancer
JF - BMC Cancer
IS - 1
M1 - 731
ER -