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[News] Publication of Review Result of the 1st Serious Illness (Cancer) Review Committee of 2025
  • Date2025-04-23

Publication of Review Result of the 1st Serious Illness (Cancer) Review Committee of 2025

 

□ The Health Insurance Review and Assessment Service (President Kang Jung-Gu) releases the result of the deliberations of the 1st Cancer Review Committee in 2025 on ‘Reimbursement criteria for drugs used for cancer patients (Improvement of reimbursement standards reflection clinical reality)’ as follows.

 

 ○ New pharmaceutical (application for determination of health insurance coverage) and expansion of reimbursement standards

Category

Product

Pharmaceutical

company

company

Efficacy and effectiveness

Deliberation results

Application for healthcare benefit reimbursement

Padcev Inj.

(Enfortumab Vedotin)

ortumab Vedotin)

 

Astellas Pharma Inc Korea

Combined modality therapy with pembrolizumab as primary treatment for an adult patient contracting topically advanced or metastatic urothelial carcinoma

To be discussed again

Elrexfio Inj.

(Elranatamab)

Pfizer Korea

Single therapy for an adult patient contracting relapsed or refractory multiple myeloma who received more than tertiary treatment inculding a pembrolizumab inhibitor, an immunomodulatory drug, and daratumumab

To be discussed again

Vyloy Inj.

(Zolbetuximab)

Astellas Pharma Inc Korea

Combined modality therapy with fluoropyrimidine & platinum-based chemotherapy, as primary treatment for a patient contracting unresectable and topically advanced or metastatic adenocarcinoma or gastroesophageal junction (GEJ) cancer which is CLDN18.2 (Claudin 18.2)-positive and HER2 (Human Epidermal growth

factor Receptor 2 protein)-negative

To be discussed again

Expand reimbursement scope

Scemblix Tab

(Asciminib Hydrochloride)

Novartis Korea

Therapy for an adult patient contracting Philadelphia chromosome positive chronic myeloid leukemia (Ph+ CML) in chronic phase, who received more than two tyrosine kinase inhibitors (TKI)

Reimbursement criteria to be established

Methotrexate Injection

(Methotrexate)

(Methotrexate)

Pfizer Korea etc

Non-Hodgkin’s lymphoma (NHL)

Reimbursement criteria to be established

(Intraocular lymphoma)

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Combined modality therapy with trastuzumab, fluoropyrimidine. platinum-based chemotherapy, as primary treatment for a patient contracting gastric or gastroesophageal junction (GEJ) cancer which is PD-L1-positive (CPS1), and unresectable and topically advanced or metastatic HER2 (Human Epidermal growth

factor Receptor 2 protein)-positive

 

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Combined modality therapy with fluoropyrimidine. platinum-based chemotherapy, as primary treatment for a patient contracting gastric or gastroesophageal junction (GEJ) cancer which is unresectable and topically advanced or metastatic HER2 (Human Epidermal growth

factor Receptor 2 protein)-negative

Reimbursement criteria to be established

(CPS≥10)

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Combined modality therapy with fluoropyrimidine. platinum-based chemotherapy, as primary treatment for a patient contracting gastric or gastroesophageal junction (GEJ) cancer which is PD-L1-positive (CPS10), and unresectable and topically advanced or metastatic HER2 (Human Epidermal growth

factor Receptor 2 protein)-negative

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Combined modality therapy with Lenvatinib as

the treatment for advanced endometrial cancer, which is found developing after

prior systemic therapy, inappropriate for surgical treatment or radiotherapy, without microsatellite instability

high (MSI-H) or mismatch repair deficient (dMMR)

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

The treatment for a patient contracting colorectal cancer (CRC) which is unresectable or metastatic, with MSI-H or dMMR

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Primary treatment for a patient contracting metastatic or unresectable, recurrent head and neck squamous cell carcinoma: i) single therapy for an adult patient contracting PD-L1-positive (Combined

Positive Score (CPS)1); and ii) combined modality therapy with 5-FU. platinum-based chemotherapy

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Combined modality therapy with Bevacizumab included or not chemotherapy, as the treatment for a patient contracting persistent, recurrent or metastatic cervical cancer, with PD-L1-positive (CPS1)

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Combined modality therapy with chemotherapy, as the treatment for a patient contracting unresectable, topically recurrent or metastatic triple negative breast cancer,

with PD-L1-positive (CPS10)

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Treatment for a patient contracting unresectable, metastatic solenoma, which was found developing after prior treatment, without satisfactory alternatives, and with MSI-H or dMMR

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Treatment for a patient contracting unresectable, metastatic small intestine cancer, which was found developing after prior treatment, without satisfactory alternatives, and with MSI-H or dMMR

 

Reimbursement criteria to be established

Keytruda Inj.

(Pembrolizumab)

Korea MSD

Treatment for a patient contracting unresectable, metastatic bile duct cancer, which was found developing after prior treatment, without satisfactory alternatives, and with MSI-H or dMMR

 

Reimbursement criteria to be established

 

* Pursuant to Article 5 and Article 5.2 of the Rules on the Criteria for National Health Insurance Reimbursement, the President of the Health Insurance Review and Assessment Service may notify the details of the reimbursement criteria and methods for drugs prescribed and administered to seriously ill patients that are designated and notified by the Minister of Health and Welfare after deliberation by the Serious Illness Review Committee. The reimbursement criteria for such drugs may be set differently according to clinical literature, domestic and foreign guidelines, and expert opinions within the scope of efficacy and effectiveness of the Ministry of Food and Drug Safety approval, and the reimbursement decision and criteria may change in the course of subsequent process.

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