Abstract

Simple SummaryThe cure rate of Hodgkin lymphoma is currently higher than 80% for almost all stages at diagnosis. Despite the particularly good efficacy of chemotherapy and radiotherapy, some late complications such as cardiovascular disease and second malignancies can occur in a small proportion of patients. A major concern nowadays is, therefore, to find the balance between remission and toxicity in the development of new treatments for classical Hodgkin lymphoma. This review focuses on how to best treat first-line advanced Hodgkin lymphomas, considering the acute and long-term consequences of chemotherapy and radiotherapy treatments. New drugs such as brentuximab vedotin and checkpoint inhibitors are also a field of interest.Hodgkin lymphoma (HL) is a lymphoid-type hematologic disease that is derived from B cells. The incidence of this lymphoid malignancy is around 2–3/100,000/year in the western world. Long-term remission rates are linked to a risk-adapted approach, which allows remission rates higher than 80%. The first-line treatment for advanced stage classical HL (cHL) widely used today is doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) or escalated bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPPesc) chemotherapy. Randomized studies comparing these two regimens and a recently performed meta-analysis have demonstrated consistently better disease control with BEACOPPesc. However, this treatment is not the standard of care, as there is an excess of acute hematological toxicities and therapy-related myeloid neoplasms. Moreover, there is a recurrent controversy concerning the impact on overall survival with this regimen. More recently, new drugs such as brentuximab vedotin and checkpoint inhibitors have become available and have been evaluated in combination with doxorubicin, vinblastine, and dacarbazine (AVD) for the first-line treatment of patients with advanced cHL with the objective of tumor control improvement. There are still major debates with respect to first-line treatment of advanced cHL. The use of positron emission tomography-adapted strategies has allowed a reduction in the toxicity of chemotherapy regimens. Incorporation of new drugs into the treatment algorithms requires confirmation.

Highlights

  • Hodgkin lymphoma (HL) is a B-cell lymphoma, accounting for about 10–15% of newly diagnosed lymphoma cases in the United States (8260 of 80,500 cases), and the remainder are non-Hodgkin lymphoma [1]

  • We focus on the management of advanced stage classical Hodgkin lymphoma (cHL) in patients aged between 16 and 60 years, with special attention to the balance between cure and toxicity

  • Advanced stage cHL is usually treated with chemotherapy alone—most commonly, either with escalated bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPPesc ) or doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) chemotherapy

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Summary

Introduction

Hodgkin lymphoma (HL) is a B-cell lymphoma, accounting for about 10–15% of newly diagnosed lymphoma cases in the United States (8260 of 80,500 cases), and the remainder are non-Hodgkin lymphoma [1]. EORTC = European Organization for Research and Treatment of Cancer; ESR = erythrocyte sedimentation rate; GHSG = German Hodgkin Study Group; LYSA = Lymphoma Study Association. Involved-field and involved-node radiotherapy, multi-agent chemotherapy, and combined chemoradiotherapy have improved patient care Recent approaches such as risk-adapted and response-adapted modulation have allowed more personalized treatment. We focus on the management of advanced stage cHL in patients aged between 16 and 60 years, with special attention to the balance between cure and toxicity. It remains one of the main issues in the development of improved treatment strategies for cHL patients

ABVD versus BEACOPP
PET-Adapted Treatment
New Drugs
Brentuximab Vedotin
Kaplan–Meier
Checkpoint Inhibitors
Findings
Conclusions
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