Combination chemotherapy plus low-dose involved-field radiotherapy for early clinical stage Hodgkin's lymphoma

To present our long-term experience regarding the use of chemotherapy plus low-dose involved-field radiotherapy (IFRT) for clinical Stage I-IIA Hodgkin's lymphoma. We analyzed the data of 368 patients. Of these, 66 received mechlorethamine, vincristine, procarbazine, and prednisone (MOPP) and 3...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2004-07, Vol.59 (3), p.765-781
Hauptverfasser: Vassilakopoulos, Theodoros P., Angelopoulou, Maria K., Siakantaris, Marina P., Kontopidou, Flora N., Dimopoulou, Maria N., Kokoris, Styliani I., Kyrtsonis, Marie Christine, Tsaftaridis, Panayiotis, Karkantaris, Christos, Anargyrou, Konstantinos, Boutsis, Dimitrios E., Variamis, Eleni, Michalopoulos, Thymios, Boussiotis, Vassiliki A., Panayiotidis, Panayiotis, Papavassiliou, Constantinos, Pangalis, Gerassimos A.
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container_issue 3
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container_title International journal of radiation oncology, biology, physics
container_volume 59
creator Vassilakopoulos, Theodoros P.
Angelopoulou, Maria K.
Siakantaris, Marina P.
Kontopidou, Flora N.
Dimopoulou, Maria N.
Kokoris, Styliani I.
Kyrtsonis, Marie Christine
Tsaftaridis, Panayiotis
Karkantaris, Christos
Anargyrou, Konstantinos
Boutsis, Dimitrios E.
Variamis, Eleni
Michalopoulos, Thymios
Boussiotis, Vassiliki A.
Panayiotidis, Panayiotis
Papavassiliou, Constantinos
Pangalis, Gerassimos A.
description To present our long-term experience regarding the use of chemotherapy plus low-dose involved-field radiotherapy (IFRT) for clinical Stage I-IIA Hodgkin's lymphoma. We analyzed the data of 368 patients. Of these, 66 received mechlorethamine, vincristine, procarbazine, and prednisone (MOPP) and 302 received doxorubicin (or epirubicin), bleomycin, vinblastine, and dacarbazine [A(E)BVD]. Patients with complete remission or very good partial remission were scheduled for low-dose IFRT (≤3200 cGy). The 10-year failure-free survival (FFS) and overall survival (OS) rate was 85% and 86%, respectively. A(E)BVD-treated patients had superior 10-year FFS and OS rates compared with MOPP-treated patients (87% vs. 75%, p = 0.009; and 93% vs. 71%, p = 0.0004, respectively). Only 10 of 41 relapses had any infield (irradiated) component. Of the complete responders/very good partial responders treated with low-dose IFRT, those who received
doi_str_mv 10.1016/j.ijrobp.2003.11.029
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We analyzed the data of 368 patients. Of these, 66 received mechlorethamine, vincristine, procarbazine, and prednisone (MOPP) and 302 received doxorubicin (or epirubicin), bleomycin, vinblastine, and dacarbazine [A(E)BVD]. Patients with complete remission or very good partial remission were scheduled for low-dose IFRT (≤3200 cGy). The 10-year failure-free survival (FFS) and overall survival (OS) rate was 85% and 86%, respectively. A(E)BVD-treated patients had superior 10-year FFS and OS rates compared with MOPP-treated patients (87% vs. 75%, p = 0.009; and 93% vs. 71%, p = 0.0004, respectively). Only 10 of 41 relapses had any infield (irradiated) component. Of the complete responders/very good partial responders treated with low-dose IFRT, those who received &lt;2800 cGy had inferior FFS but similar OS as those who received 2800–3200 cGy. Adverse prognostic factors for FFS included age ≥45 years, leukocytosis ≥10 × 10 9/L, and extranodal extension. Secondary acute leukemia developed after MOPP with or without salvage therapy ( n = 6) or after ABVD plus salvage therapy ( n = 2). None of the nine secondary solid tumors developed within the RT fields. IFRT at a dose of 2800–3000 cGy is highly effective in clinical Stage I-IIA HL patients who achieved a complete response or very good partial response with A(E)BVD. 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Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Recurrence ; Remission Induction ; Technology. Biomaterials. Equipments. Material. Instrumentation ; Treatment Outcome ; Vinblastine - administration & dosage ; Vincristine - administration & dosage]]></subject><ispartof>International journal of radiation oncology, biology, physics, 2004-07, Vol.59 (3), p.765-781</ispartof><rights>2004 Elsevier Inc.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-e382748393380e19dfe270c4957c6c74e03b6e22ab96f5ee5c6c9546f511dd643</citedby><cites>FETCH-LOGICAL-c465t-e382748393380e19dfe270c4957c6c74e03b6e22ab96f5ee5c6c9546f511dd643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0360301603023241$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15862637$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15183480$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vassilakopoulos, Theodoros P.</creatorcontrib><creatorcontrib>Angelopoulou, Maria K.</creatorcontrib><creatorcontrib>Siakantaris, Marina P.</creatorcontrib><creatorcontrib>Kontopidou, Flora N.</creatorcontrib><creatorcontrib>Dimopoulou, Maria N.</creatorcontrib><creatorcontrib>Kokoris, Styliani I.</creatorcontrib><creatorcontrib>Kyrtsonis, Marie Christine</creatorcontrib><creatorcontrib>Tsaftaridis, Panayiotis</creatorcontrib><creatorcontrib>Karkantaris, Christos</creatorcontrib><creatorcontrib>Anargyrou, Konstantinos</creatorcontrib><creatorcontrib>Boutsis, Dimitrios E.</creatorcontrib><creatorcontrib>Variamis, Eleni</creatorcontrib><creatorcontrib>Michalopoulos, Thymios</creatorcontrib><creatorcontrib>Boussiotis, Vassiliki A.</creatorcontrib><creatorcontrib>Panayiotidis, Panayiotis</creatorcontrib><creatorcontrib>Papavassiliou, Constantinos</creatorcontrib><creatorcontrib>Pangalis, Gerassimos A.</creatorcontrib><title>Combination chemotherapy plus low-dose involved-field radiotherapy for early clinical stage Hodgkin's lymphoma</title><title>International journal of radiation oncology, biology, physics</title><addtitle>Int J Radiat Oncol Biol Phys</addtitle><description>To present our long-term experience regarding the use of chemotherapy plus low-dose involved-field radiotherapy (IFRT) for clinical Stage I-IIA Hodgkin's lymphoma. We analyzed the data of 368 patients. Of these, 66 received mechlorethamine, vincristine, procarbazine, and prednisone (MOPP) and 302 received doxorubicin (or epirubicin), bleomycin, vinblastine, and dacarbazine [A(E)BVD]. Patients with complete remission or very good partial remission were scheduled for low-dose IFRT (≤3200 cGy). The 10-year failure-free survival (FFS) and overall survival (OS) rate was 85% and 86%, respectively. A(E)BVD-treated patients had superior 10-year FFS and OS rates compared with MOPP-treated patients (87% vs. 75%, p = 0.009; and 93% vs. 71%, p = 0.0004, respectively). Only 10 of 41 relapses had any infield (irradiated) component. Of the complete responders/very good partial responders treated with low-dose IFRT, those who received &lt;2800 cGy had inferior FFS but similar OS as those who received 2800–3200 cGy. Adverse prognostic factors for FFS included age ≥45 years, leukocytosis ≥10 × 10 9/L, and extranodal extension. Secondary acute leukemia developed after MOPP with or without salvage therapy ( n = 6) or after ABVD plus salvage therapy ( n = 2). None of the nine secondary solid tumors developed within the RT fields. IFRT at a dose of 2800–3000 cGy is highly effective in clinical Stage I-IIA HL patients who achieved a complete response or very good partial response with A(E)BVD. The long-term toxicity with respect to secondary malignancies appears to be acceptable.</description><subject>ABVD</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analysis of Variance</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bleomycin - administration &amp; dosage</subject><subject>Combined Modality Therapy</subject><subject>Dacarbazine - administration &amp; dosage</subject><subject>Disease-Free Survival</subject><subject>Doxorubicin - administration &amp; dosage</subject><subject>Early stage</subject><subject>Epirubicin - administration &amp; dosage</subject><subject>Female</subject><subject>Hodgkin Disease - drug therapy</subject><subject>Hodgkin Disease - pathology</subject><subject>Hodgkin Disease - radiotherapy</subject><subject>Hodgkin's lymphoma</subject><subject>Humans</subject><subject>Male</subject><subject>Mechlorethamine - administration &amp; dosage</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Neoplasms, Second Primary - etiology</subject><subject>Prednisone - administration &amp; dosage</subject><subject>Procarbazine - administration &amp; dosage</subject><subject>Prognosis</subject><subject>Radiotherapy</subject><subject>Radiotherapy Dosage</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Recurrence</subject><subject>Remission Induction</subject><subject>Technology. Biomaterials. Equipments. Material. Instrumentation</subject><subject>Treatment Outcome</subject><subject>Vinblastine - administration &amp; dosage</subject><subject>Vincristine - administration &amp; dosage</subject><issn>0360-3016</issn><issn>1879-355X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFq3DAQhkVpabZp36AEXZqe7EiWLFuXQFjaphDopYHehCyNs9rIkiN5N-zbV2GXtqeeZhi--Wf4EPpISU0JFVfb2m1THOa6IYTVlNakka_QivadrFjb_nqNVoQJUrECn6F3OW8JIZR2_C06oy3tGe_JCoV1nAYX9OJiwGYDU1w2kPR8wLPfZezjc2VjBuzCPvo92Gp04C1O2ro_5BgTBp38ARvvgjPa47zoB8C30T48uvC55BymeRMn_R69GbXP8OFUz9H91y8_17fV3Y9v39c3d5Xhol0qYH3T8Z5JxnoCVNoRmo4YLtvOCNNxIGwQ0DR6kGJsAdoylS0vPaXWCs7O0eUxd07xaQd5UZPLBrzXAeIuKypLlGxEAfkRNCnmnGBUc3KTTgdFiXrxrLbq6Fm9eFaUquK5rF2c8nfDBPbv0klsAT6dAJ2LkDHpYFz-h-tFud4V7vrIQbGxd5BUNg6CAesSmEXZ6P7_yW9EY59U</recordid><startdate>20040701</startdate><enddate>20040701</enddate><creator>Vassilakopoulos, Theodoros P.</creator><creator>Angelopoulou, Maria K.</creator><creator>Siakantaris, Marina P.</creator><creator>Kontopidou, Flora N.</creator><creator>Dimopoulou, Maria N.</creator><creator>Kokoris, Styliani I.</creator><creator>Kyrtsonis, Marie Christine</creator><creator>Tsaftaridis, Panayiotis</creator><creator>Karkantaris, Christos</creator><creator>Anargyrou, Konstantinos</creator><creator>Boutsis, Dimitrios E.</creator><creator>Variamis, Eleni</creator><creator>Michalopoulos, Thymios</creator><creator>Boussiotis, Vassiliki A.</creator><creator>Panayiotidis, Panayiotis</creator><creator>Papavassiliou, Constantinos</creator><creator>Pangalis, Gerassimos A.</creator><general>Elsevier Inc</general><general>Elsevier</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>7T5</scope><scope>H94</scope></search><sort><creationdate>20040701</creationdate><title>Combination chemotherapy plus low-dose involved-field radiotherapy for early clinical stage Hodgkin's lymphoma</title><author>Vassilakopoulos, Theodoros P. ; Angelopoulou, Maria K. ; Siakantaris, Marina P. ; Kontopidou, Flora N. ; Dimopoulou, Maria N. ; Kokoris, Styliani I. ; Kyrtsonis, Marie Christine ; Tsaftaridis, Panayiotis ; Karkantaris, Christos ; Anargyrou, Konstantinos ; Boutsis, Dimitrios E. ; Variamis, Eleni ; Michalopoulos, Thymios ; Boussiotis, Vassiliki A. ; Panayiotidis, Panayiotis ; Papavassiliou, Constantinos ; Pangalis, Gerassimos A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-e382748393380e19dfe270c4957c6c74e03b6e22ab96f5ee5c6c9546f511dd643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>ABVD</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Analysis of Variance</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bleomycin - administration &amp; dosage</topic><topic>Combined Modality Therapy</topic><topic>Dacarbazine - administration &amp; dosage</topic><topic>Disease-Free Survival</topic><topic>Doxorubicin - administration &amp; dosage</topic><topic>Early stage</topic><topic>Epirubicin - administration &amp; dosage</topic><topic>Female</topic><topic>Hodgkin Disease - drug therapy</topic><topic>Hodgkin Disease - pathology</topic><topic>Hodgkin Disease - radiotherapy</topic><topic>Hodgkin's lymphoma</topic><topic>Humans</topic><topic>Male</topic><topic>Mechlorethamine - administration &amp; dosage</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Neoplasms, Second Primary - etiology</topic><topic>Prednisone - administration &amp; dosage</topic><topic>Procarbazine - administration &amp; dosage</topic><topic>Prognosis</topic><topic>Radiotherapy</topic><topic>Radiotherapy Dosage</topic><topic>Radiotherapy. 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We analyzed the data of 368 patients. Of these, 66 received mechlorethamine, vincristine, procarbazine, and prednisone (MOPP) and 302 received doxorubicin (or epirubicin), bleomycin, vinblastine, and dacarbazine [A(E)BVD]. Patients with complete remission or very good partial remission were scheduled for low-dose IFRT (≤3200 cGy). The 10-year failure-free survival (FFS) and overall survival (OS) rate was 85% and 86%, respectively. A(E)BVD-treated patients had superior 10-year FFS and OS rates compared with MOPP-treated patients (87% vs. 75%, p = 0.009; and 93% vs. 71%, p = 0.0004, respectively). Only 10 of 41 relapses had any infield (irradiated) component. Of the complete responders/very good partial responders treated with low-dose IFRT, those who received &lt;2800 cGy had inferior FFS but similar OS as those who received 2800–3200 cGy. Adverse prognostic factors for FFS included age ≥45 years, leukocytosis ≥10 × 10 9/L, and extranodal extension. Secondary acute leukemia developed after MOPP with or without salvage therapy ( n = 6) or after ABVD plus salvage therapy ( n = 2). None of the nine secondary solid tumors developed within the RT fields. IFRT at a dose of 2800–3000 cGy is highly effective in clinical Stage I-IIA HL patients who achieved a complete response or very good partial response with A(E)BVD. The long-term toxicity with respect to secondary malignancies appears to be acceptable.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>15183480</pmid><doi>10.1016/j.ijrobp.2003.11.029</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0360-3016
ispartof International journal of radiation oncology, biology, physics, 2004-07, Vol.59 (3), p.765-781
issn 0360-3016
1879-355X
language eng
recordid cdi_proquest_miscellaneous_19957926
source MEDLINE; Elsevier ScienceDirect Journals
subjects ABVD
Adolescent
Adult
Aged
Aged, 80 and over
Analysis of Variance
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Bleomycin - administration & dosage
Combined Modality Therapy
Dacarbazine - administration & dosage
Disease-Free Survival
Doxorubicin - administration & dosage
Early stage
Epirubicin - administration & dosage
Female
Hodgkin Disease - drug therapy
Hodgkin Disease - pathology
Hodgkin Disease - radiotherapy
Hodgkin's lymphoma
Humans
Male
Mechlorethamine - administration & dosage
Medical sciences
Middle Aged
Neoplasm Staging
Neoplasms, Second Primary - etiology
Prednisone - administration & dosage
Procarbazine - administration & dosage
Prognosis
Radiotherapy
Radiotherapy Dosage
Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
Recurrence
Remission Induction
Technology. Biomaterials. Equipments. Material. Instrumentation
Treatment Outcome
Vinblastine - administration & dosage
Vincristine - administration & dosage
title Combination chemotherapy plus low-dose involved-field radiotherapy for early clinical stage Hodgkin's lymphoma
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