Table 1.

Summary of treatment recommendations for autologous HCT for Hodgkin lymphoma

Recommendation
Autologous HCT should be offered as first-line therapy for patients who fail to achieve CR. 
Autologous HCT should be offered as salvage therapy over nontransplantation (except for localized disease, in which IFRT may be considered, or for patients with low-stage disease and late relapse, in which chemotherapy may be considered). 
Several salvage chemotherapy regimens may be considered prior to autologous HCT in adult patients. 
BEAM or CBV are the most common conditioning regimens for autologous HCT in standard-risk patients. 
IFRT should be considered in patients with bulky disease not previously irradiated. 
Tandem autologous HCT is not routinely recommended in standard-risk patients. 
Maintenance therapy with brentuximab vedotin post autologous HCT is recommended in high-risk patients.a Additional maintenance therapies incorporating CPI are under investigation. 
Chemosensitive disease and negative functional imaging are associated with improved outcomes. 
Recent data with novel agents + chemotherapy +/− radiation in the second line suggests that in a highly selected population, some patients may not need to proceed with autologous HCT if they achieve a complete response. 
Recommendation
Autologous HCT should be offered as first-line therapy for patients who fail to achieve CR. 
Autologous HCT should be offered as salvage therapy over nontransplantation (except for localized disease, in which IFRT may be considered, or for patients with low-stage disease and late relapse, in which chemotherapy may be considered). 
Several salvage chemotherapy regimens may be considered prior to autologous HCT in adult patients. 
BEAM or CBV are the most common conditioning regimens for autologous HCT in standard-risk patients. 
IFRT should be considered in patients with bulky disease not previously irradiated. 
Tandem autologous HCT is not routinely recommended in standard-risk patients. 
Maintenance therapy with brentuximab vedotin post autologous HCT is recommended in high-risk patients.a Additional maintenance therapies incorporating CPI are under investigation. 
Chemosensitive disease and negative functional imaging are associated with improved outcomes. 
Recent data with novel agents + chemotherapy +/− radiation in the second line suggests that in a highly selected population, some patients may not need to proceed with autologous HCT if they achieve a complete response. 
a

High-risk patients were defined in the AETHERA trial as having 1 of the following: refractory to frontline therapy, relapse less than 12 months after frontline therapy, or relapse 12 months or more after frontline therapy with extranodal disease.

BEAM, BCNU, etoposide, cytarabine, melphalan; CBV, cyclophosphamide, carmustine (BCNU), etoposide; GVD, gemcitabine, vinorelbine, and liposomal doxorubicin.

Adapted with permission from Perales et al.9 

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