Abstract 1554P
Background
In India public spending on health is 1.5% of the GDP, which is far lower than most countries in the world. The poor public expenditure on health has led to mushrooming of private care, with 60% of hospitalization and 70% outpatient care being offered now by the private hospitals. Private treatment is expensive leading to OOP and catastrophic expenditure. Furthermore, insurance penetration in India is less than 20% adding to the financial woes. Those insured also have to resort to OOP for outpatient services, rehabilitation, supportive care, drugs, disposables and copayments. Copayments vary according to disease, type of policy, age of insured, drug administered, premium limit among other factors.
Methods
All adult insured patients who underwent treatment in the Department of Medical Oncology from April 1 2023 to March 31 2024 were included in the study. This is a retrospective cross sectional observational study.
Results
A total of 236 patients were included in the study comprising 79 (33.4%) males and 157 (66.6%) females. Commonest cancers were Breast (29.6%) and Lung (11%). Most patients were in the age group 41-60 (43.2%) and 61-80 (40.6%) respectively. Co payment was calculated as: amount spent by patient / total insurance approved amount x 100. Average insurance approved amount was 947 USD. Average co payment was 151 USD (16% of approved amount). 105 patients had < 1% (44.4%), while 87 patients (36.8%) had 1-20% co payment. 6.35% had more than 60% co payment expenditure. 50 patients (21.1%) had their claims completely taken care of. Classified for gender copayments amongst men vs women were 61 (77.21%) vs 125 (79.6%) respectively. 96% patients taking Immunotherapy resorted to OOP. Their copayments were almost double of the average (291 USD), while their approved amounts were less than the mean (864 USD).
Conclusions
Insurance for Cancer patients is essential to ensure access to care. Copayments lead to OOP in insured patients. In our study 78% patients had some form of copayment. While most patients had < 1% copayment, 15% had more than 60% OOP. Average copayment was 16% of the total approved amount. OOP was higher among Immunotherapy patients with lesser approved amounts. Measures to reduce copayments and OOP for insured patients is essential to maintain continuity of Cancer care.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1594P - Cancer mortality in young population and estimated radon areas in Spain
Presenter: Miquel Ferriol-Galmés
Session: Poster session 10
1598P - Xaluritamig, a STEAP1 x CD3 XmAb 2+1 immune therapy, in patients (pts) with metastatic castration-resistant prostate cancer (mCRPC): Initial results from dose expansion cohorts in a phase I study
Presenter: William Kelly
Session: Poster session 10
1600P - Phase II trial of pembrolizumab and lenvatinib in advanced neuroendocrine prostate cancer (NEPC)
Presenter: Ulka Vaishampayan
Session: Poster session 10
1601P - First results from ZZFIRST: A randomized phase II trial of enzalutamide (EZ) with or without talazoparib (TALA) in metastatic hormone-naïve prostate cancer (mHNPC)
Presenter: Joaquin Mateo
Session: Poster session 10
1602P - CBP-1018, Bi-ligand-drug conjugate (Bi-XDC) drug treated for metastatic castration resistant prostate cancer (mCRPC) patients from phase I study results
Presenter: Kaiwen Li
Session: Poster session 10
1603P - Updated safety and efficacy of tazemetostat (TAZ) plus enzalutamide (ENZ) in patients with metastatic castration-resistant prostate cancer (mCRPC)
Presenter: Wassim Abida
Session: Poster session 10
1604P - PSMA-targeted radioligand therapy (RLT) with 131I-LNTH-1095 (1095) plus enzalutamide (enza) vs enza alone in chemotherapy-naïve patients (pts) whose piflufolastat F 18-avid metastatic castration-resistant prostate cancer (mCRPC) progressed on abiraterone (abi): ARROW
Presenter: Evan Yu
Session: Poster session 10
1605P - Opevesostat (MK-5684/ODM-208), an oral CYP11A1 inhibitor, in metastatic castration-resistant prostate cancer (mCRPC): Updated CYPIDES phase II results
Presenter: Karim Fizazi
Session: Poster session 10
1606P - Mature follow up of phase I dose finding trial of pembrolizumab (pembro) with AR inhibitors (ARI) and priming tumour-targeted radiation with anti-PSMA alpha emitter 225Ac-J591
Presenter: Aaron Holmes
Session: Poster session 10