Potential of chemo-immunotherapy and radioimmunotherapy in relapsed primary central nervous system (CNS) lymphoma

被引:33
作者
Doolittle, Nancy D.
Jahnke, Kristoph
Belanger, Richard
Ryan, Deborah A.
Nance, Robert W., Jr.
Lacy, Cynthia A.
Tyson, Rose Marie
Haluska, Marianne
Hedrick, Nancy A.
Varallyay, Csanad
Neuwelt, Edward A.
机构
[1] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97239 USA
[3] Ryan Belanger Assoc, San Diego, CA 92117 USA
[4] Oregon Hlth & Sci Univ, Dept Radiol & Nucl Med, Portland, OR 97239 USA
[5] Oregon Hlth & Sci Univ, Dept Neurosurg, Portland, OR 97239 USA
[6] Vet Affairs Med Ctr, Portland, OR USA
关键词
D O I
10.1080/10428190701493902
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Five patients with relapsed PCNSL were given chemo-immunotherapy (rituximab followed by carboplatin and methotrexate) with osmotic blood-brain barrier (BBB) opening. Four patients achieved CR and one patient had stable disease. Two patients (2/5) had durable responses (survival: 230+, 122+, 82, 42, 38 weeks). One patient later received Indium-111-ibritumomab tiuxetan and Yttrium-90-ibritumomab tiuxetan intravenous, without BBB opening. There was good uptake of Indium-111 ibritumomab tiuxetan in tumor on SPECT scan after 48 h. Estimated radiation doses to brain around and distant from tumor were within safe limits. After Ytrium-90 ibritumomab tiuxetan there was CR in enhancing tumor where the BBB was leaky, but lesions occurred in other brain regions, where the BBB was intact during Yttrium-90 ibritumomab tiuxetan infusion. Imaging and dosimetry with Indium-111 ibritumomab tiuxetan and efficacy with Yttrium-90 ibritumomab tiuxetan suggest the need for future enhanced CNS delivery when using monoclonal or radiolabeled antibodies, as intravenous delivery alone may provide modest clinical benefit due to limited BBB permeability.
引用
收藏
页码:1712 / 1720
页数:9
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