Active Ingredient: Epcoritamab
Epcoritamab as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) after two or more lines of systemic therapy.
For this indication, competent medicine agencies globally authorize below treatments:
For:
Subcutaneous, 0.16 milligrams epcoritamab, one dose, over the duration of 1 week. Afterwards, subcutaneous, 0.8 milligrams epcoritamab, one dose, over the duration of 1 week. Afterwards, subcutaneous, 3 milligrams epcoritamab, one dose, over the duration of 1 week. Afterwards, subcutaneous, 48 milligrams epcoritamab, one dose, over the duration of 1 week. Afterwards, subcutaneous, 48 milligrams epcoritamab, once weekly, over the duration of 4 weeks. This step is repeated 2 times. Afterwards, subcutaneous, 48 milligrams epcoritamab, once every 2 weeks, over the duration of 4 weeks. This step is repeated 6 times. Afterwards, subcutaneous, 48 milligrams epcoritamab, once every 4 weeks.
Epcoritamab should be administered according to the following step-up dose schedule in 28-day cycles which is outlined in Table 1 for patients with follicular lymphoma.
Table 1. Epcoritamab 3-step step-up dose schedule for patients with follicular lymphoma:
| Dosing schedule | Cycle of treatment | Days | Epcoritamab dose (mg)a |
|---|---|---|---|
| Weekly | Cycle 1 | 1 | 0.16 mg (Step-up dose 1) |
| 8 0.8 mg | (Step-up dose 2) | ||
| 15 3 mg | (Step-up dose 3) | ||
| 22 48 mg | (First full dose) | ||
| Weekly | Cycles 2 – 3 | 1, 8, 15, 22 | 48 mg |
| Every two weeks | Cycles 4 – 9 1, 15 | 48 mg | |
| Every four weeks | Cycles 10 + 1 | 48 mg |
a 0.16 mg is a priming dose, 0.8 mg is an intermediate dose, 3 mg is a second intermediate dose and 48 mg is a full dose.
Epcoritamab should be administered until disease progression or unacceptable toxicity.
Details on recommended pre-medication for cytokine release syndrome (CRS) are shown in Table 2.
Table 2. Epcoritamab pre-medication:
| Cycle | Patient requiring pre-medication | Pre-medication | Administration |
|---|---|---|---|
| Cycle 1 | All patients | Dexamethasoneb (15 mg oral or intravenous) or Prednisolone (100 mg oral or intravenous) or equivalent | • 30-120 minutes prior to each weekly administration of epcoritamab • And for three consecutive days following each weekly administration of epcoritamab in Cycle 1 |
| • Diphenhydramine (50 mg oral or intravenous) or equivalent • Paracetamol (650 to 1 000 mg oral) | • 30-120 minutes prior to each weekly administration of epcoritamab | ||
| Cycle 2 and beyond | Patients who experienced Grade 2 or 3a CRS with previous dose | Dexamethasoneb (15 mg oral or intravenous) or Prednisolone (100 mg oral or intravenous) or equivalent | • 30-120 minutes prior to next administration of epcoritamab after a grade 2 or 3a CRS event • And for three consecutive days following the next administration of epcoritamab until epcoritamab is given without subsequent any grade of CRS |
a Patients will be permanently discontinued from epcoritamab after a Grade 4 CRS event.
b Dexamethasone is the preferred corticosteroid for CRS prophylaxis based on the GCT 3013-01 Optimisation study.
Prophylaxis against Pneumocystis jirovecii pneumonia (PCP) and herpes virus infections is strongly recommended especially during concurrent use of steroids.
Epcoritamab should be administered to adequately hydrated patients.
It is strongly recommended that all patients adhere to the following fluid guidelines during Cycle 1, unless medically contraindicated:
Patients at an increased risk for clinical tumour lysis syndrome (CTLS) are recommended to receive hydration and prophylactic treatment with a uric acid lowering agent.
Patients should be monitored for signs and symptoms of CRS and/or immune effector cell-associated neurotoxicity syndrome (ICANS) and managed per current practice guidelines following epcoritamab administration. Patients should be counselled on the signs and symptoms associated with CRS and ICANS and on seeking immediate medical attention should signs or symptoms occur at any time.
It should be administered by subcutaneous injection only, preferably in the lower part of the abdomen or the thigh. Change of injection site from left to right side or vice versa is recommended especially during the weekly administration schedule (i.e., Cycles 1-3).
Liability Disclaimer : RxReasoner has utilized reasonable care in providing content and services that are accurate, complete and up to date. However, RxReasoner does not accept any responsibility or liability about it. The content and services of RxReasoner are for informational purposes only and they are not intended to be a substitute for the knowledge, expertise, skill, and judgment of physicians, pharmacists, nurses, or other healthcare professionals involved in patient care. RxReasoner offers no medical advice. Users are responsible for the use of the provided content. A shown indication or treatment should not be construed to indicate that the medication is safe, appropriate, or effective in any given patient or under any particular circumstances. The absence of an indication or treatment should not roule out the existence of other appropriate medications. Always seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition or medicament. RxReasoner is not liable for any damages allegedly sustained arising out of the use of its content and services.
