Decreasing Risk of Leukemia with Prolonged Follow-up after Chemotherapy and Radiotherapy for Hodgkin's Disease
Acute nonlymphocytic leukemia is a recognized complication of combined chemotherapy and radiation treatment of patients with Hodgkin's disease. Previous studies have suggested that the risk of leukemia in these patients increases with time after treatment. We analyzed the occurrence of second n...
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Veröffentlicht in: | The New England journal of medicine 1987-03, Vol.316 (12), p.710-714 |
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description | Acute nonlymphocytic leukemia is a recognized complication of combined chemotherapy and radiation treatment of patients with Hodgkin's disease. Previous studies have suggested that the risk of leukemia in these patients increases with time after treatment. We analyzed the occurrence of second neoplasms among 192 patients with Hodgkin's disease who were followed for a median of over 15 years. We originally planned to identify prospectively the morphologic changes in bone marrow that precede the development of acute leukemia. All 63 patients consenting to bone marrow aspiration had normal marrow morphology, and no case of acute leukemia occurred more than 11 years after treatment. Actuarial analysis revealed that the peak onset of leukemia-related complications was between three and nine years after first treatment.
We conclude that there appears to be a period of increased risk in patients treated with chemotherapy and radiation, after which the risk of secondary leukemia decreases. Patients surviving for more than 11 years after treatment appear to be at no increased risk of acute leukemia. (N Engl J Med 1987; 316:710–4.)
THE introduction of megavoltage radiation therapy and the MOPP regimen (mechlorethamine [Mustargen], vincristine [Oncovin], procarbazine, and prednisone) for Hodgkin's disease
1
,
2
has resulted in impressive long-term survival among patients in whom such tumors had previously been fatal.
3
Approximately 70 percent of all patients and 50 percent of patients with advanced disease can be cured by radiation therapy alone, radiation therapy plus combination chemotherapy, or in those with advanced disease, combination chemotherapy alone. This success has resulted in the survival of a large number of patients who formerly were destined to die in less than five years, and these survivors are available . . . |
doi_str_mv | 10.1056/NEJM198703193161203 |
format | Article |
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We conclude that there appears to be a period of increased risk in patients treated with chemotherapy and radiation, after which the risk of secondary leukemia decreases. Patients surviving for more than 11 years after treatment appear to be at no increased risk of acute leukemia. (N Engl J Med 1987; 316:710–4.)
THE introduction of megavoltage radiation therapy and the MOPP regimen (mechlorethamine [Mustargen], vincristine [Oncovin], procarbazine, and prednisone) for Hodgkin's disease
1
,
2
has resulted in impressive long-term survival among patients in whom such tumors had previously been fatal.
3
Approximately 70 percent of all patients and 50 percent of patients with advanced disease can be cured by radiation therapy alone, radiation therapy plus combination chemotherapy, or in those with advanced disease, combination chemotherapy alone. This success has resulted in the survival of a large number of patients who formerly were destined to die in less than five years, and these survivors are available . . .</description><identifier>ISSN: 0028-4793</identifier><identifier>EISSN: 1533-4406</identifier><identifier>DOI: 10.1056/NEJM198703193161203</identifier><identifier>PMID: 3821809</identifier><identifier>CODEN: NEJMAG</identifier><language>eng</language><publisher>Boston, MA: Massachusetts Medical Society</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Biological and medical sciences ; Bone marrow ; Bone Marrow - pathology ; Cancer therapies ; Chemotherapy ; Combined Modality Therapy ; Female ; Hematologic and hematopoietic diseases ; Hodgkin Disease - therapy ; Humans ; Leukemia ; Leukemia - epidemiology ; Leukemia - etiology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Mechlorethamine - adverse effects ; Medical sciences ; Middle Aged ; Myelodysplastic Syndromes - etiology ; Neoplasms, Multiple Primary ; Patients ; Prednisone - adverse effects ; Procarbazine - adverse effects ; Radiation therapy ; Radiotherapy - adverse effects ; Risk ; Time Factors ; Vincristine - adverse effects</subject><ispartof>The New England journal of medicine, 1987-03, Vol.316 (12), p.710-714</ispartof><rights>1987 INIST-CNRS</rights><rights>Copyright Massachusetts Medical Society Mar 19, 1987</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-164b1c701b1cf11268ec5990d8f282ed48132cd9090970dddb819ac8a7fd4f682</citedby><cites>FETCH-LOGICAL-c431t-164b1c701b1cf11268ec5990d8f282ed48132cd9090970dddb819ac8a7fd4f682</cites></display><links><openurl>$$Topenurl_article</openurl><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8272307$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3821809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blayney, Douglas W</creatorcontrib><creatorcontrib>Longo, Dan L</creatorcontrib><creatorcontrib>Young, Robert C</creatorcontrib><creatorcontrib>Greene, Mark H</creatorcontrib><creatorcontrib>Hubbard, Susan M</creatorcontrib><creatorcontrib>Postal, Marcia G</creatorcontrib><creatorcontrib>Duffey, Patricia L</creatorcontrib><creatorcontrib>DeVita, Vincent T</creatorcontrib><title>Decreasing Risk of Leukemia with Prolonged Follow-up after Chemotherapy and Radiotherapy for Hodgkin's Disease</title><title>The New England journal of medicine</title><addtitle>N Engl J Med</addtitle><description>Acute nonlymphocytic leukemia is a recognized complication of combined chemotherapy and radiation treatment of patients with Hodgkin's disease. Previous studies have suggested that the risk of leukemia in these patients increases with time after treatment. We analyzed the occurrence of second neoplasms among 192 patients with Hodgkin's disease who were followed for a median of over 15 years. We originally planned to identify prospectively the morphologic changes in bone marrow that precede the development of acute leukemia. All 63 patients consenting to bone marrow aspiration had normal marrow morphology, and no case of acute leukemia occurred more than 11 years after treatment. Actuarial analysis revealed that the peak onset of leukemia-related complications was between three and nine years after first treatment.
We conclude that there appears to be a period of increased risk in patients treated with chemotherapy and radiation, after which the risk of secondary leukemia decreases. Patients surviving for more than 11 years after treatment appear to be at no increased risk of acute leukemia. (N Engl J Med 1987; 316:710–4.)
THE introduction of megavoltage radiation therapy and the MOPP regimen (mechlorethamine [Mustargen], vincristine [Oncovin], procarbazine, and prednisone) for Hodgkin's disease
1
,
2
has resulted in impressive long-term survival among patients in whom such tumors had previously been fatal.
3
Approximately 70 percent of all patients and 50 percent of patients with advanced disease can be cured by radiation therapy alone, radiation therapy plus combination chemotherapy, or in those with advanced disease, combination chemotherapy alone. This success has resulted in the survival of a large number of patients who formerly were destined to die in less than five years, and these survivors are available . . .</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Bone marrow</subject><subject>Bone Marrow - pathology</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hodgkin Disease - therapy</subject><subject>Humans</subject><subject>Leukemia</subject><subject>Leukemia - epidemiology</subject><subject>Leukemia - etiology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Mechlorethamine - adverse effects</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myelodysplastic Syndromes - etiology</subject><subject>Neoplasms, Multiple Primary</subject><subject>Patients</subject><subject>Prednisone - adverse effects</subject><subject>Procarbazine - adverse effects</subject><subject>Radiation therapy</subject><subject>Radiotherapy - adverse effects</subject><subject>Risk</subject><subject>Time Factors</subject><subject>Vincristine - adverse effects</subject><issn>0028-4793</issn><issn>1533-4406</issn><fulltext>false</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kN1qGzEQhUVpSR03TxACggZyETbVSPKudFnsJG5x2hDS60XWjy17d-VKu4S8fRRsfFU6AzMw880cOAidA7kBMim__br9-QBSVISBZFACJewDGsGEsYJzUn5EI0KoKHgl2Wd0mtKG5AAuT9AJExQEkSPUzayOViXfrfCTT1scHF7YYWtbr_CL79f4MYYmdCtr8F1omvBSDDusXG8jnq5tG_q1jWr3ilVn8JMy_jhwIeJ5MKut764SnvmUVewX9MmpJtmzQx-jP3e3z9N5sfh9_2P6fVFozqAvoORL0BWBXB0ALYXVEymJEY4Kag0XwKg2kuSsiDFmKUAqLVTlDHeloGP0df93F8Pfwaa-3oQhdlmyBiE4SE6JzBTbUzqGlKJ19S76VsXXGkj9bnH9D4vz1cXh97BsrTneHDzN-8vDXiWtGhdVp306YoJWlJEqY9d7rG1T3dlN-1_RN8Flj0E</recordid><startdate>19870319</startdate><enddate>19870319</enddate><creator>Blayney, Douglas W</creator><creator>Longo, Dan L</creator><creator>Young, Robert C</creator><creator>Greene, Mark H</creator><creator>Hubbard, Susan M</creator><creator>Postal, Marcia G</creator><creator>Duffey, Patricia L</creator><creator>DeVita, Vincent T</creator><general>Massachusetts Medical Society</general><scope>IQODW</scope><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>0TZ</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K0Y</scope><scope>LK8</scope><scope>M0R</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>19870319</creationdate><title>Decreasing Risk of Leukemia with Prolonged Follow-up after Chemotherapy and Radiotherapy for Hodgkin's Disease</title><author>Blayney, Douglas W ; Longo, Dan L ; Young, Robert C ; Greene, Mark H ; Hubbard, Susan M ; Postal, Marcia G ; Duffey, Patricia L ; DeVita, Vincent T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-164b1c701b1cf11268ec5990d8f282ed48132cd9090970dddb819ac8a7fd4f682</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Bone marrow</topic><topic>Bone Marrow - pathology</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hodgkin Disease - therapy</topic><topic>Humans</topic><topic>Leukemia</topic><topic>Leukemia - epidemiology</topic><topic>Leukemia - etiology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Mechlorethamine - adverse effects</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myelodysplastic Syndromes - etiology</topic><topic>Neoplasms, Multiple Primary</topic><topic>Patients</topic><topic>Prednisone - adverse effects</topic><topic>Procarbazine - adverse effects</topic><topic>Radiation therapy</topic><topic>Radiotherapy - adverse effects</topic><topic>Risk</topic><topic>Time Factors</topic><topic>Vincristine - adverse effects</topic><toplevel>peer_reviewed</toplevel><creatorcontrib>Blayney, Douglas W</creatorcontrib><creatorcontrib>Longo, Dan L</creatorcontrib><creatorcontrib>Young, Robert C</creatorcontrib><creatorcontrib>Greene, Mark H</creatorcontrib><creatorcontrib>Hubbard, Susan M</creatorcontrib><creatorcontrib>Postal, Marcia G</creatorcontrib><creatorcontrib>Duffey, Patricia L</creatorcontrib><creatorcontrib>DeVita, Vincent T</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>New England Journal of Medicine</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>The New England journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>no_fulltext</fulltext></delivery><addata><au>Blayney, Douglas W</au><au>Longo, Dan L</au><au>Young, Robert C</au><au>Greene, Mark H</au><au>Hubbard, Susan M</au><au>Postal, Marcia G</au><au>Duffey, Patricia L</au><au>DeVita, Vincent T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreasing Risk of Leukemia with Prolonged Follow-up after Chemotherapy and Radiotherapy for Hodgkin's Disease</atitle><jtitle>The New England journal of medicine</jtitle><addtitle>N Engl J Med</addtitle><date>1987-03-19</date><risdate>1987</risdate><volume>316</volume><issue>12</issue><spage>710</spage><epage>714</epage><pages>710-714</pages><issn>0028-4793</issn><eissn>1533-4406</eissn><coden>NEJMAG</coden><abstract>Acute nonlymphocytic leukemia is a recognized complication of combined chemotherapy and radiation treatment of patients with Hodgkin's disease. Previous studies have suggested that the risk of leukemia in these patients increases with time after treatment. We analyzed the occurrence of second neoplasms among 192 patients with Hodgkin's disease who were followed for a median of over 15 years. We originally planned to identify prospectively the morphologic changes in bone marrow that precede the development of acute leukemia. All 63 patients consenting to bone marrow aspiration had normal marrow morphology, and no case of acute leukemia occurred more than 11 years after treatment. Actuarial analysis revealed that the peak onset of leukemia-related complications was between three and nine years after first treatment.
We conclude that there appears to be a period of increased risk in patients treated with chemotherapy and radiation, after which the risk of secondary leukemia decreases. Patients surviving for more than 11 years after treatment appear to be at no increased risk of acute leukemia. (N Engl J Med 1987; 316:710–4.)
THE introduction of megavoltage radiation therapy and the MOPP regimen (mechlorethamine [Mustargen], vincristine [Oncovin], procarbazine, and prednisone) for Hodgkin's disease
1
,
2
has resulted in impressive long-term survival among patients in whom such tumors had previously been fatal.
3
Approximately 70 percent of all patients and 50 percent of patients with advanced disease can be cured by radiation therapy alone, radiation therapy plus combination chemotherapy, or in those with advanced disease, combination chemotherapy alone. This success has resulted in the survival of a large number of patients who formerly were destined to die in less than five years, and these survivors are available . . .</abstract><cop>Boston, MA</cop><pub>Massachusetts Medical Society</pub><pmid>3821809</pmid><doi>10.1056/NEJM198703193161203</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - adverse effects Biological and medical sciences Bone marrow Bone Marrow - pathology Cancer therapies Chemotherapy Combined Modality Therapy Female Hematologic and hematopoietic diseases Hodgkin Disease - therapy Humans Leukemia Leukemia - epidemiology Leukemia - etiology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Mechlorethamine - adverse effects Medical sciences Middle Aged Myelodysplastic Syndromes - etiology Neoplasms, Multiple Primary Patients Prednisone - adverse effects Procarbazine - adverse effects Radiation therapy Radiotherapy - adverse effects Risk Time Factors Vincristine - adverse effects |
title | Decreasing Risk of Leukemia with Prolonged Follow-up after Chemotherapy and Radiotherapy for Hodgkin's Disease |
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