Hodgkin lymphoma: A review and update on recent progress
- PMID: 29194581
- PMCID: PMC5842098
- DOI: 10.3322/caac.21438
Hodgkin lymphoma: A review and update on recent progress
Abstract
Hodgkin lymphoma (HL) is a unique hematopoietic neoplasm characterized by cancerous Reed-Sternberg cells in an inflammatory background. Patients are commonly diagnosed with HL in their 20s and 30s, and they present with supradiaphragmatic lymphadenopathy, often with systemic B symptoms. Even in advanced-stage disease, HL is highly curable with combination chemotherapy, radiation, or combined-modality treatment. Although the same doxorubicin, bleomycin, vinblastine, and dacarbazine chemotherapeutic regimen has been the mainstay of therapy over the last 30 years, risk-adapted approaches have helped de-escalate therapy in low-risk patients while intensifying treatment for higher risk patients. Even patients who are not cured with initial therapy can often be salvaged with alternate chemotherapy combinations, the novel antibody-drug conjugate brentuximab, or high-dose autologous or allogeneic hematopoietic stem cell transplantation. The programmed death-1 inhibitors nivolumab and pembrolizumab have both demonstrated high response rates and durable remissions in patients with relapsed/refractory HL. Alternate donor sources and reduced-intensity conditioning have made allogeneic hematopoietic stem cell transplantation a viable option for more patients. Future research will look to integrate novel strategies into earlier lines of therapy to improve the HL cure rate and minimize long-term treatment toxicities. CA Cancer J Clin 2018;68:116-132. © 2017 American Cancer Society.
Keywords: Hodgkin lymphoma; allogeneic stem cell transplantation; antibody-drug conjugate; brentuximab; immunotherapy; positron emission tomography (PET)-adapted therapy; programmed death 1 (PD-1) inhibitor.
© 2017 American Cancer Society.
Conflict of interest statement
Conflict of Interest Disclosure:
Satish Shanbhag – none
Richard Ambinder – support from Bristol Myers Squib, Celgene
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References
-
- Jaffe ES, H N, Stein H, Vardiman JW. World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. IARC; Lyon: 2001.
-
- Siegel RL, Miller KD, Jemal A. Cancer statistics, 2017. CA: a cancer journal for clinicians. 2017;67(1):7–30. - PubMed
-
- Howlader N, N A, Krapcho M, Miller D, Bishop K, Kosary CL, Yu M, Ruhl J, Tatalovich Z, Mariotto A, Lewis DR, Chen HS, Feuer EJ, Cronin KA, editors. SEER Cancer Statistics Review, 1975-2014. National Cancer Institute; Bethesda, MD: based on November 2016 SEER data submission, posted to the SEER web site, April 2017.; https://seer.cancer.gov/csr/1975_2014/
-
- Ambinder RF, Browning PJ, Lorenzana I, et al. Epstein-Barr virus and childhood Hodgkin’s disease in Honduras and the United States. Blood. 1993;81(2):462–467. - PubMed
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