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Evolent Level 1 Medical Oncology

Pathways and Low-Value Regimens

Hodgkin's Lymphoma

Regimen Options
Last Updated: 02/07/2025 See Details

NOTE: FOR RITUXIMAB, THE USE OF A BIOSIMILAR OR THE REFERENCE PRODUCT IS ON PATHWAY

 

Evolent Pathways Febrile Neutropenic Risk Emetogenic Risk References
Classical Hodgkin Lymphoma (CHL)

Primary or Initial Therapy

ABVD (doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Intermediate High
 

nivolumab + AVD (doxorubicin, vinblastine sulfate, and dacarbazine)

Intermediate High

Relapsed/Refractory

ABVD (doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Intermediate High
 

ICE (ifosfamide, carboplatin and etoposide)

High High
 

GCD (gemcitabine, carboplatin and dexamethasone)

Low High
 

DHAP (dexamethasone, cytarabine and cisplatin)

High Moderate
 

GVD (gemcitabine, vinorelbine and doxil)

Low Moderate
 

MINI-BEAM (carmustine, etoposide, cytarabine and melphalan)

High Moderate
 

MINE (mesna, ifosfamide, novantrone and etoposide)

High Moderate
 

pembrolizumab

Low Low
 

Best Supportive Care or Clinical Trial

Not Applicable Not applicable

Consolidation/Maintenance therapy after autologous hematopoietic stem-cell transplantation (auto-HSCT), in patients at high risk of relapse or progression

brentuximab vedotin (up to 16 cycles)

Low Low
Nodular Lymphocyte-Predominant Hodgkin Lymphoma (NLPHL)

Primary or Initial Therapy

R-ABVD (rituximab, doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Intermediate High
 

R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone)

Intermediate High
 

R-CVP (rituximab, cyclophosphamide, vincristine, prednisone)

Low Moderate

Relapsed/Refractory

R-ABVD (rituximab, doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Intermediate High
 

R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone)

Intermediate High
 

R-CVP (rituximab, cyclophosphamide, vincristine, prednisone)

Low Moderate
 

R-DHAP (rituximab, dexamethasone, cytarabine and cisplatin)

High Moderate
 

R-ICE (rituximab, iosfamide, carboplatin and etoposide)

High High
 

rituximab

Low Low
 

Best Supportive Care or Clinical Trial

Not Applicable Not applicable
Classical Hodgkin Lymphoma (CHL)

Primary or Initial Therapy

Evolent Pathways

ABVD (doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Febrile Neutropenic Risk
intermediate
Emetogenic Risk
high
Evolent Pathways

nivolumab + AVD (doxorubicin, vinblastine sulfate, and dacarbazine)

Febrile Neutropenic Risk
intermediate
Emetogenic Risk
high

Relapsed/Refractory

Evolent Pathways

ABVD (doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Febrile Neutropenic Risk
intermediate
Emetogenic Risk
high
Evolent Pathways

ICE (ifosfamide, carboplatin and etoposide)

Febrile Neutropenic Risk
high
Emetogenic Risk
high
Evolent Pathways

GCD (gemcitabine, carboplatin and dexamethasone)

Febrile Neutropenic Risk
low
Emetogenic Risk
high
Evolent Pathways

DHAP (dexamethasone, cytarabine and cisplatin)

Febrile Neutropenic Risk
high
Emetogenic Risk
moderate
Evolent Pathways

GVD (gemcitabine, vinorelbine and doxil)

Febrile Neutropenic Risk
low
Emetogenic Risk
moderate
Evolent Pathways

MINI-BEAM (carmustine, etoposide, cytarabine and melphalan)

Febrile Neutropenic Risk
high
Emetogenic Risk
moderate
Evolent Pathways

MINE (mesna, ifosfamide, novantrone and etoposide)

Febrile Neutropenic Risk
high
Emetogenic Risk
moderate
Evolent Pathways

pembrolizumab

Febrile Neutropenic Risk
low
Emetogenic Risk
low
Evolent Pathways

Best Supportive Care or Clinical Trial

Febrile Neutropenic Risk
na
Emetogenic Risk
na

Consolidation/Maintenance therapy after autologous hematopoietic stem-cell transplantation (auto-HSCT), in patients at high risk of relapse or progression

Nodular Lymphocyte-Predominant Hodgkin Lymphoma (NLPHL)

Primary or Initial Therapy

Evolent Pathways

R-ABVD (rituximab, doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Febrile Neutropenic Risk
intermediate
Emetogenic Risk
high
Evolent Pathways

R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone)

Febrile Neutropenic Risk
intermediate
Emetogenic Risk
high
Evolent Pathways

R-CVP (rituximab, cyclophosphamide, vincristine, prednisone)

Febrile Neutropenic Risk
low
Emetogenic Risk
moderate

Relapsed/Refractory

Evolent Pathways

R-ABVD (rituximab, doxorubicin, bleomycin sulfate, vinblastine sulfate, and dacarbazine)

Febrile Neutropenic Risk
intermediate
Emetogenic Risk
high
Evolent Pathways

R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone)

Febrile Neutropenic Risk
intermediate
Emetogenic Risk
high
Evolent Pathways

R-CVP (rituximab, cyclophosphamide, vincristine, prednisone)

Febrile Neutropenic Risk
low
Emetogenic Risk
moderate
Evolent Pathways

R-DHAP (rituximab, dexamethasone, cytarabine and cisplatin)

Febrile Neutropenic Risk
high
Emetogenic Risk
moderate
Evolent Pathways

R-ICE (rituximab, iosfamide, carboplatin and etoposide)

Febrile Neutropenic Risk
high
Emetogenic Risk
high
Evolent Pathways

rituximab

Febrile Neutropenic Risk
low
Emetogenic Risk
low
Evolent Pathways

Best Supportive Care or Clinical Trial

Febrile Neutropenic Risk
na
Emetogenic Risk
na
Regimen Alternative References
LOW VALUE REGIMENS (NON-PATHWAY) WITH SUPERIOR ALTERNATIVES

Subsequent Therapy

** brentuximab vedotin and nivolumab **

Alternative: brentuximab vedotin or nivolumab

LOW VALUE REGIMENS (NON-PATHWAY) WITH SUPERIOR ALTERNATIVES

Subsequent Therapy

Regimen

** brentuximab vedotin and nivolumab **