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   <subfield code="a">10.1007/BF00172459</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/BF00172459</subfield>
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   <subfield code="a">Treatment of recurrent malignant glioma by repeated intracerebral injections of human recombinant interleukin-2 alone or in combination with systemic interferon-α. Results of a phase I clinical trial</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Randall Merchant, Daniel McVicar, Lynn Merchant, Harold Young]</subfield>
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   <subfield code="a">Summary: Nine patients with a recurrent malignant glioma were treated with repeated intracavitary or intracerebroventricular injections of human recombinant interleukin-2 (rIL-2) alone or in combination with systemic interferon-α (IFN-α). Five patients received only rIL-2 and four were treated with rIL-2 plus subcutaneous injections of IFN-α. Therapy was administered on a Monday, Wednesday, Friday schedule for up to 10 weeks, beginning with a dose of 10,000 IU rIL-2/injection. Doses were escalated every two weeks until some toxicity was apparent. The maximum amount of rIL-2 any one patient in this group received was 580,000 IU. Patients on combination immunotherapy were held at an rIL-2 dosage of 10,000 IU while IFN-α, which began at 3 million IU, was escalated every other week up to 18 million IU/dose. They were then held at that IFN-α dosage and rIL-2 was increased to 50,000 IU. The total amount of rIL-2 and IFN-α any one in this group received was 510,000IU and 417 million IU, respectively. Repeated injections of 10,000 IU rIL-2 were well-tolerated by all nine patients and no change in their functional status was seen. At doses at 50,000 IU. rIL-2, increased edema around the tumor cavity was observed by MRI/CT scand in 3/5 patients and clinical side-effects in the form of somnolence and headache along with some morbidity specifically associated with tumor location were also seen. Patients receiving rIL-2 + IFN-α showed progressive fatigue, muscle weakness, and occasionally nausea. Two of these patients showed increased peritumoral edema on MRI/CT scan. Neither hematological abnormalities nor changes from baseline values were seen in blood samples from any of the patients. MRI/CT scans made at the conclusion of immunotherapy indicated tumor progression in two of the patients treated with rIL-2 alone while no tumor growth at the site of treatment occurred in the other two or in the four treated with the combination of rIL-2 and IFN-α. Further clinical testing of rIL-2 in combination with IFN-α is indicated.</subfield>
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   <subfield code="a">Kluwer Academic Publishers, 1992</subfield>
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   <subfield code="a">IL-2, roferon-A</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">toxicity</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">intracavitary</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">immunotherapy</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">cytokines</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">brain tumor</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Merchant</subfield>
   <subfield code="D">Randall</subfield>
   <subfield code="u">Department of Surgery, Division of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, USA</subfield>
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   <subfield code="a">McVicar</subfield>
   <subfield code="D">Daniel</subfield>
   <subfield code="u">Department of Anatomy, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia, USA</subfield>
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   <subfield code="a">Merchant</subfield>
   <subfield code="D">Lynn</subfield>
   <subfield code="u">Department of Surgery, Division of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, USA</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Young</subfield>
   <subfield code="D">Harold</subfield>
   <subfield code="u">Department of Surgery, Division of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, USA</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Journal of Neuro-Oncology</subfield>
   <subfield code="d">Kluwer Academic Publishers</subfield>
   <subfield code="g">12/1(1992-01-01), 75-83</subfield>
   <subfield code="x">0167-594X</subfield>
   <subfield code="q">12:1&lt;75</subfield>
   <subfield code="1">1992</subfield>
   <subfield code="2">12</subfield>
   <subfield code="o">11060</subfield>
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   <subfield code="u">https://doi.org/10.1007/BF00172459</subfield>
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   <subfield code="B">NATIONALLICENCE</subfield>
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   <subfield code="a">McVicar</subfield>
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   <subfield code="u">Department of Anatomy, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia, USA</subfield>
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   <subfield code="a">Young</subfield>
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   <subfield code="B">NATIONALLICENCE</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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