Adcetris is a cancer medicine used to treat adults with certain lymphomas (cancers of lymphocytes, white blood cells that are part of the immune system). It is used when the cancer cells have a protein called CD30 on their surface (CD30-positive). For Hodgkin’s lymphoma (HL), it is given: - together with doxorubicin, vinblastine and dacarbazine (other cancer medicines) in patients whose cancer is advanced (stage III or IV disease) and has not been treated before; - together with etoposide, cyclophosphamide, doxorubicin, dacarbazine (other cancer medicines) and dexamethasone (a corticosteroid) in patients whose cancer is advanced (stage IIB, stage III or stage IV) and has not been treated before; - when the cancer has come back or has not responded to an autologous stem cell transplant (a transplant of the patient's own blood-producing cells); - if the cancer is likely to come back or get worse after an autologous stem cell transplant; - when the cancer has come back or has not responded to at least two other therapies and when autologous stem cell transplant or multi-agent chemotherapy (a combination of cancer medicines) cannot be used. In non-Hodgkin’s lymphoma, Adcetris is used for: - systemic anaplastic large cell lymphoma (sALCL, a cancer of lymphocytes called T-cells) when the cancer has never been treated before; Adcetris is used together with cyclophosphamide, doxorubicin and prednisone. It is also used when the cancer has come back or when other treatments have not worked; - cutaneous T-cell lymphoma (CTCL), a lymphoma of T-cells that initially affects the skin, in patients who have received at least one previous treatment. These diseases are rare, and Adcetris was designated an ‘orphan medicine’ (a medicine used in rare diseases). Further information on the orphan designations can be found on the European Medicines Agency’s website ( [Hodgkin’s lymphoma](https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu308596): 15 January 2009; [cutaneous T-cell lymphoma](https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu311939): 11 January 2012; [peripheral T-cell lymphoma](https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu308595): 21 August 2019). Adcetris contains the active substance brentuximab vedotin.
Therapeutic Indication
### Therapeutic indication **Hodgkin lymphoma** Adcetris is indicated for adult patients with previously untreated CD30+ Stage IV Hodgkin lymphoma (HL) in combination with doxorubicin, vinblastine and dacarbazine (AVD). Adcetris is indicated for adult patients with previously untreated CD30+ Stage IIB with risk factors, Stage III or Stage IV HL in combination with etoposide, cyclophosphamide, doxorubicin, dacarbazine, dexamethasone (BrECADD). Adcetris is indicated for the treatment of adult patients with CD30+ HL at increased risk of relapse or progression following autologous stem cell transplant (ASCT). Adcetris is indicated for the treatment of adult patients with relapsed or refractory CD30+ Hodgkin lymphoma (HL): \- following ASCT, or \- following at least two prior therapies when ASCT or multi-agent chemotherapy is not a treatment option. **Systemic anaplastic large cell lymphoma** Adcetris in combination with cyclophosphamide, doxorubicin and prednisone (CHP) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (sALCL). Adcetris is indicated for the treatment of adult patients with relapsed or refractory sALCL. **Cutaneous T-cell lymphoma** Adcetris is indicated for the treatment of adult patients with CD30+ cutaneous T-cell lymphoma (CTCL) after at least 1 prior systemic therapy.
Therapeutic Area (MeSH)
ATC Code
L01FX05
ATC Item
brentuximab vedotin
Pharmacotherapeutic Group
Antineoplastic agents
Active Substance (Summary)
INN / Common Names
| Substance | CAS | Monograph |
|---|---|---|
| Brentuximab vedotin | N/A | 雅诗力冻晶注射剂 |
EMA Name
Adcetris
Medicine Name
Adcetris
Aliases
N/A