Hodgkin lymphoma: A review and update on recent progress
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 adva...
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description | 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. |
doi_str_mv | 10.3322/caac.21438 |
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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. 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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.</description><subject>allogeneic stem cell transplantation</subject><subject>antibody‐drug conjugate</subject><subject>Antineoplastic Combined Chemotherapy Protocols</subject><subject>Biomarkers, Tumor - blood</subject><subject>brentuximab</subject><subject>Combined Modality Therapy</subject><subject>Diagnosis, Differential</subject><subject>Diagnostic Imaging</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hodgkin Disease - diagnosis</subject><subject>Hodgkin Disease - mortality</subject><subject>Hodgkin Disease - pathology</subject><subject>Hodgkin Disease - therapy</subject><subject>Hodgkin lymphoma</subject><subject>Humans</subject><subject>immunotherapy</subject><subject>Neoplasm Staging</subject><subject>positron emission tomography (PET)‐adapted therapy</subject><subject>Prognosis</subject><subject>programmed death 1 (PD‐1) inhibitor</subject><subject>Risk Factors</subject><subject>Survival Analysis</subject><subject>Transplantation Conditioning - trends</subject><issn>0007-9235</issn><issn>1542-4863</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqWw4QNQ1kgpftYOC6QoAopUiQ2sLTu220BesvtQ_74JgQo2rEYzc-fM1QXgGsEpIRjf5UrlU4woESdgjBjFMRUzcgrGEEIeJ5iwEbgI4QP2PefnYIQTlFAm0BiIeWOWn0UdlfuqXTWVuo_SyNttYXeRqk20aY1a26ipu2Fu63XU-mbpbQiX4MypMtir7zoB70-Pb9k8Xrw-v2TpIs47EyJ2imCntcHOcj5LkIYacmaQQCR3SnPGtKMCGg4TJDRTjiiqbYIcodB0fskEPAzcdqMra3oPXpWy9UWl_F42qpB_N3WxkstmK5mgGCaiA9wOgNw3IXjrjrcIyj4_2ecnv_LrxDe_vx2lP4F1AjQIdkVp9_-gZJam2QA9ANZ2e5U</recordid><startdate>201803</startdate><enddate>201803</enddate><creator>Shanbhag, Satish</creator><creator>Ambinder, Richard F.</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0663-6221</orcidid></search><sort><creationdate>201803</creationdate><title>Hodgkin lymphoma: A review and update on recent progress</title><author>Shanbhag, Satish ; Ambinder, Richard F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4868-fa32fbbd2fe77691b0b075d1813cfab755bf480d70918b5af3a4be91f340d0003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>allogeneic stem cell transplantation</topic><topic>antibody‐drug conjugate</topic><topic>Antineoplastic Combined Chemotherapy Protocols</topic><topic>Biomarkers, Tumor - blood</topic><topic>brentuximab</topic><topic>Combined Modality Therapy</topic><topic>Diagnosis, Differential</topic><topic>Diagnostic Imaging</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hodgkin Disease - diagnosis</topic><topic>Hodgkin Disease - mortality</topic><topic>Hodgkin Disease - pathology</topic><topic>Hodgkin Disease - therapy</topic><topic>Hodgkin lymphoma</topic><topic>Humans</topic><topic>immunotherapy</topic><topic>Neoplasm Staging</topic><topic>positron emission tomography (PET)‐adapted therapy</topic><topic>Prognosis</topic><topic>programmed death 1 (PD‐1) inhibitor</topic><topic>Risk Factors</topic><topic>Survival Analysis</topic><topic>Transplantation Conditioning - trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shanbhag, Satish</creatorcontrib><creatorcontrib>Ambinder, Richard F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>CA: a cancer journal for clinicians</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Shanbhag, Satish</au><au>Ambinder, Richard F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hodgkin lymphoma: A review and update on recent progress</atitle><jtitle>CA: a cancer journal for clinicians</jtitle><addtitle>CA Cancer J Clin</addtitle><date>2018-03</date><risdate>2018</risdate><volume>68</volume><issue>2</issue><spage>116</spage><epage>132</epage><pages>116-132</pages><issn>0007-9235</issn><eissn>1542-4863</eissn><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.</abstract><cop>United States</cop><pmid>29194581</pmid><doi>10.3322/caac.21438</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-0663-6221</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | allogeneic stem cell transplantation antibody‐drug conjugate Antineoplastic Combined Chemotherapy Protocols Biomarkers, Tumor - blood brentuximab Combined Modality Therapy Diagnosis, Differential Diagnostic Imaging Hematopoietic Stem Cell Transplantation Hodgkin Disease - diagnosis Hodgkin Disease - mortality Hodgkin Disease - pathology Hodgkin Disease - therapy Hodgkin lymphoma Humans immunotherapy Neoplasm Staging positron emission tomography (PET)‐adapted therapy Prognosis programmed death 1 (PD‐1) inhibitor Risk Factors Survival Analysis Transplantation Conditioning - trends |
title | Hodgkin lymphoma: A review and update on recent progress |
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