Bolus high dose interleukin-2 for the treatment of malignant melanoma
High dose interleukin-2 therapy, administered in bolus, is considered to be a reasonable treatment option in a selected group of patients with metastatic malignant melanoma. To present our experience using this mode of therapy in 21 patients with metastatic melanoma. The 21 patients in our study gro...
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Veröffentlicht in: | The Israel Medical Association journal 2001-03, Vol.3 (3), p.169 |
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description | High dose interleukin-2 therapy, administered in bolus, is considered to be a reasonable treatment option in a selected group of patients with metastatic malignant melanoma.
To present our experience using this mode of therapy in 21 patients with metastatic melanoma.
The 21 patients in our study group comprised 13 men and 8 women with a mean age of 46 years (range 29-63). Their metastatic disease was present in all extracranial sites, dermal and sub-dermal metastases being the most common (15 patients had at least one site, in addition to other locations of metastases). Patients with intracranial disease were excluded due to the poor effectivity of IL-2 at this site. Treatment comprised a course of 2 weeks of therapy with a 1 week rest interval between. Radiological and physical evaluation was performed 6-8 weeks after the first course. If a response was achieved a second course of therapy was given. Patients received up to 14 planned doses of IL-2 in each week, 720,000 IU/kg of IL-2 per dose i.v. in 15 minutes. All treatments were given in the surgical ward, and only one patient was hospitalized in the intensive care unit.
Of the 21 patients, one had a complete response that has lasted for 17 months and 5 patients had a partial response (range 3 months to 3 years). One patient died during treatment, and one patient who refused further treatment because of no response died a few days after completion of treatment. Prior to therapy three of the responders had received autologous vaccines with good immunological response (P = 0.115). Toxic side effects were significant, but they were treated successfully with no residual damage.
High dose IL-2 can be administered safely in a surgical department. The response rates achieved in this series justify the use of high dose IL-2 in a selected group of patients. To improve response rates, a combination of autologous vaccines prior to high dose IL-2 may be recommended. |
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To present our experience using this mode of therapy in 21 patients with metastatic melanoma.
The 21 patients in our study group comprised 13 men and 8 women with a mean age of 46 years (range 29-63). Their metastatic disease was present in all extracranial sites, dermal and sub-dermal metastases being the most common (15 patients had at least one site, in addition to other locations of metastases). Patients with intracranial disease were excluded due to the poor effectivity of IL-2 at this site. Treatment comprised a course of 2 weeks of therapy with a 1 week rest interval between. Radiological and physical evaluation was performed 6-8 weeks after the first course. If a response was achieved a second course of therapy was given. Patients received up to 14 planned doses of IL-2 in each week, 720,000 IU/kg of IL-2 per dose i.v. in 15 minutes. All treatments were given in the surgical ward, and only one patient was hospitalized in the intensive care unit.
Of the 21 patients, one had a complete response that has lasted for 17 months and 5 patients had a partial response (range 3 months to 3 years). One patient died during treatment, and one patient who refused further treatment because of no response died a few days after completion of treatment. Prior to therapy three of the responders had received autologous vaccines with good immunological response (P = 0.115). Toxic side effects were significant, but they were treated successfully with no residual damage.
High dose IL-2 can be administered safely in a surgical department. The response rates achieved in this series justify the use of high dose IL-2 in a selected group of patients. To improve response rates, a combination of autologous vaccines prior to high dose IL-2 may be recommended.</description><identifier>ISSN: 1565-1088</identifier><identifier>PMID: 11303372</identifier><language>eng</language><publisher>Israel</publisher><subject>Adult ; Aged ; Drug Administration Schedule ; Female ; Humans ; Infusions, Intravenous ; Injections, Intravenous ; Interleukin-2 - immunology ; Interleukin-2 - pharmacology ; Interleukin-2 - therapeutic use ; Liver Neoplasms - diagnosis ; Liver Neoplasms - secondary ; Liver Neoplasms - therapy ; Lung Neoplasms - diagnosis ; Lung Neoplasms - secondary ; Lung Neoplasms - therapy ; Male ; Melanoma - pathology ; Middle Aged ; Pelvic Neoplasms - diagnosis ; Pelvic Neoplasms - secondary ; Pelvic Neoplasms - therapy ; Peritoneal Neoplasms - diagnosis ; Peritoneal Neoplasms - secondary ; Peritoneal Neoplasms - therapy ; Remission Induction ; Skin Neoplasms - diagnosis ; Skin Neoplasms - secondary ; Skin Neoplasms - therapy ; Time Factors ; Tomography, Emission-Computed ; Tomography, X-Ray Computed ; Treatment Outcome</subject><ispartof>The Israel Medical Association journal, 2001-03, Vol.3 (3), p.169</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11303372$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pappo, I</creatorcontrib><creatorcontrib>Lotem, M</creatorcontrib><creatorcontrib>Klein, M</creatorcontrib><creatorcontrib>Orda, R</creatorcontrib><title>Bolus high dose interleukin-2 for the treatment of malignant melanoma</title><title>The Israel Medical Association journal</title><addtitle>Isr Med Assoc J</addtitle><description>High dose interleukin-2 therapy, administered in bolus, is considered to be a reasonable treatment option in a selected group of patients with metastatic malignant melanoma.
To present our experience using this mode of therapy in 21 patients with metastatic melanoma.
The 21 patients in our study group comprised 13 men and 8 women with a mean age of 46 years (range 29-63). Their metastatic disease was present in all extracranial sites, dermal and sub-dermal metastases being the most common (15 patients had at least one site, in addition to other locations of metastases). Patients with intracranial disease were excluded due to the poor effectivity of IL-2 at this site. Treatment comprised a course of 2 weeks of therapy with a 1 week rest interval between. Radiological and physical evaluation was performed 6-8 weeks after the first course. If a response was achieved a second course of therapy was given. Patients received up to 14 planned doses of IL-2 in each week, 720,000 IU/kg of IL-2 per dose i.v. in 15 minutes. All treatments were given in the surgical ward, and only one patient was hospitalized in the intensive care unit.
Of the 21 patients, one had a complete response that has lasted for 17 months and 5 patients had a partial response (range 3 months to 3 years). One patient died during treatment, and one patient who refused further treatment because of no response died a few days after completion of treatment. Prior to therapy three of the responders had received autologous vaccines with good immunological response (P = 0.115). Toxic side effects were significant, but they were treated successfully with no residual damage.
High dose IL-2 can be administered safely in a surgical department. The response rates achieved in this series justify the use of high dose IL-2 in a selected group of patients. To improve response rates, a combination of autologous vaccines prior to high dose IL-2 may be recommended.</description><subject>Adult</subject><subject>Aged</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>Injections, Intravenous</subject><subject>Interleukin-2 - immunology</subject><subject>Interleukin-2 - pharmacology</subject><subject>Interleukin-2 - therapeutic use</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - secondary</subject><subject>Liver Neoplasms - therapy</subject><subject>Lung Neoplasms - diagnosis</subject><subject>Lung Neoplasms - secondary</subject><subject>Lung Neoplasms - therapy</subject><subject>Male</subject><subject>Melanoma - pathology</subject><subject>Middle Aged</subject><subject>Pelvic Neoplasms - diagnosis</subject><subject>Pelvic Neoplasms - secondary</subject><subject>Pelvic Neoplasms - therapy</subject><subject>Peritoneal Neoplasms - diagnosis</subject><subject>Peritoneal Neoplasms - secondary</subject><subject>Peritoneal Neoplasms - therapy</subject><subject>Remission Induction</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - secondary</subject><subject>Skin Neoplasms - therapy</subject><subject>Time Factors</subject><subject>Tomography, Emission-Computed</subject><subject>Tomography, X-Ray Computed</subject><subject>Treatment Outcome</subject><issn>1565-1088</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j8tqwzAURLVoadI0v1D0AwZdPSxp2Yb0AYFs2nW4jq9jp5ZtJHnRv6-hLQwMZzOcuWFrMKUpQDi3YvcpXYWQxgh_x1YASihl5Zrtn8d-TrztLi2vx0S8GzLFnuavbigkb8bIc0s8R8IcaMh8bHjAvrsMuECgHocx4AO7bbBPtP3rDft82X_s3orD8fV993QoJilsLmS5GDllHDqUqMHpc-MqbYwFDSUoJTzWpIWwlT0b732tJfglUClHqNWGPf7uTnMVqD5NsQsYv0__f9QPXEJEFg</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Pappo, I</creator><creator>Lotem, M</creator><creator>Klein, M</creator><creator>Orda, R</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20010301</creationdate><title>Bolus high dose interleukin-2 for the treatment of malignant melanoma</title><author>Pappo, I ; Lotem, M ; Klein, M ; Orda, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p207t-261568358a8a2a4184cf8b4557141613309ade4007b7c5999d42192191b38ea43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Humans</topic><topic>Infusions, Intravenous</topic><topic>Injections, Intravenous</topic><topic>Interleukin-2 - immunology</topic><topic>Interleukin-2 - pharmacology</topic><topic>Interleukin-2 - therapeutic use</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - secondary</topic><topic>Liver Neoplasms - therapy</topic><topic>Lung Neoplasms - diagnosis</topic><topic>Lung Neoplasms - secondary</topic><topic>Lung Neoplasms - therapy</topic><topic>Male</topic><topic>Melanoma - pathology</topic><topic>Middle Aged</topic><topic>Pelvic Neoplasms - diagnosis</topic><topic>Pelvic Neoplasms - secondary</topic><topic>Pelvic Neoplasms - therapy</topic><topic>Peritoneal Neoplasms - diagnosis</topic><topic>Peritoneal Neoplasms - secondary</topic><topic>Peritoneal Neoplasms - therapy</topic><topic>Remission Induction</topic><topic>Skin Neoplasms - diagnosis</topic><topic>Skin Neoplasms - secondary</topic><topic>Skin Neoplasms - therapy</topic><topic>Time Factors</topic><topic>Tomography, Emission-Computed</topic><topic>Tomography, X-Ray Computed</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pappo, I</creatorcontrib><creatorcontrib>Lotem, M</creatorcontrib><creatorcontrib>Klein, M</creatorcontrib><creatorcontrib>Orda, R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>The Israel Medical Association journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pappo, I</au><au>Lotem, M</au><au>Klein, M</au><au>Orda, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bolus high dose interleukin-2 for the treatment of malignant melanoma</atitle><jtitle>The Israel Medical Association journal</jtitle><addtitle>Isr Med Assoc J</addtitle><date>2001-03-01</date><risdate>2001</risdate><volume>3</volume><issue>3</issue><spage>169</spage><pages>169-</pages><issn>1565-1088</issn><abstract>High dose interleukin-2 therapy, administered in bolus, is considered to be a reasonable treatment option in a selected group of patients with metastatic malignant melanoma.
To present our experience using this mode of therapy in 21 patients with metastatic melanoma.
The 21 patients in our study group comprised 13 men and 8 women with a mean age of 46 years (range 29-63). Their metastatic disease was present in all extracranial sites, dermal and sub-dermal metastases being the most common (15 patients had at least one site, in addition to other locations of metastases). Patients with intracranial disease were excluded due to the poor effectivity of IL-2 at this site. Treatment comprised a course of 2 weeks of therapy with a 1 week rest interval between. Radiological and physical evaluation was performed 6-8 weeks after the first course. If a response was achieved a second course of therapy was given. Patients received up to 14 planned doses of IL-2 in each week, 720,000 IU/kg of IL-2 per dose i.v. in 15 minutes. All treatments were given in the surgical ward, and only one patient was hospitalized in the intensive care unit.
Of the 21 patients, one had a complete response that has lasted for 17 months and 5 patients had a partial response (range 3 months to 3 years). One patient died during treatment, and one patient who refused further treatment because of no response died a few days after completion of treatment. Prior to therapy three of the responders had received autologous vaccines with good immunological response (P = 0.115). Toxic side effects were significant, but they were treated successfully with no residual damage.
High dose IL-2 can be administered safely in a surgical department. The response rates achieved in this series justify the use of high dose IL-2 in a selected group of patients. To improve response rates, a combination of autologous vaccines prior to high dose IL-2 may be recommended.</abstract><cop>Israel</cop><pmid>11303372</pmid></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Adult Aged Drug Administration Schedule Female Humans Infusions, Intravenous Injections, Intravenous Interleukin-2 - immunology Interleukin-2 - pharmacology Interleukin-2 - therapeutic use Liver Neoplasms - diagnosis Liver Neoplasms - secondary Liver Neoplasms - therapy Lung Neoplasms - diagnosis Lung Neoplasms - secondary Lung Neoplasms - therapy Male Melanoma - pathology Middle Aged Pelvic Neoplasms - diagnosis Pelvic Neoplasms - secondary Pelvic Neoplasms - therapy Peritoneal Neoplasms - diagnosis Peritoneal Neoplasms - secondary Peritoneal Neoplasms - therapy Remission Induction Skin Neoplasms - diagnosis Skin Neoplasms - secondary Skin Neoplasms - therapy Time Factors Tomography, Emission-Computed Tomography, X-Ray Computed Treatment Outcome |
title | Bolus high dose interleukin-2 for the treatment of malignant melanoma |
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