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  • Articles: DFG German National Licenses  (4)
  • Electronic Resource  (4)
  • Ganglioside  (2)
  • Antibody  (1)
  • Doxorubicin  (1)
  • Immunoscintigraphy  (1)
Source
  • Articles: DFG German National Licenses  (4)
Material
  • Electronic Resource  (4)
Years
  • 1
    ISSN: 1619-7089
    Keywords: Monoclonal antibody ; 3F8 ; Ganglioside ; Small-cell lung cancer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The present study evaluated the ability of the anti-GD2 ganglioside monoclonal antibody 3F8 to target tumor sites in patients with small-cell lung cancer (SCLC). Of 12 patients entered into the trial, ten received intravenous 3F8 labeled with 2 or 10 mCi iodine-131. The first five patients had recurrent or progressive disease after chemotherapy. Subsequent patients were studied before starting chemotherapy. Radionuclide scans were performed on days 1, 2, and 3 post-infusion and once between day 5 and day 7. Four patients underwent single-photon emission tomography (SPET) imaging. Radionuclide scans demonstrated localization to all known sites of disease, other than small brain metastases in one patient. SPET/CT scan fusion images confirmed precise localization. No significant toxicity was observed. Mean serum half-life was 64.2 h. Analysis of specimens from one patient who died of unrelated causes 6 days post-infusion confirmed the scan results. The present study demonstrates that 3F8 targets SCLC sites in patients. Further studies of anti-GD2 antibodies with higher doses of antibody and radionuclide are warranted to evaluate their role in SCLC.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1619-7089
    Keywords: Anaplastic astrocytoma ; Monoclonal antibody ; Ganglioside ; GD2 ; Immunoscintigraphy ; 3F8
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Iodine-131 3F8, a murine IgG3 monoclonal antibody that targets to GD2-bearing tumors, was administered intravenously to 12 patients with brain tumors. Six patients received 2 mCi (0.74 Bq) of131I-3F8, five patients 10 mCi (3.7 Bq)/1.73 m2 of131I-3F8, and one patient 2.6 mCi (0.96 Bq) of124I-3F8, with no side-effects. Nine of 11 malignant gliomas and the single metastatic melanoma showed antibody localization, with the best tumor delineation on single-photon emission tomography (SPET) following 10 mCi (3.7 Bq)/1.73 m2 dose. No nonspecific uptake in the normal craniospinal axis was detected. There was no difference in the pharmacokinetics of low-dose versus the higher-dose antibody groups; plasma and total-body half-lives were 18 h and 49 h, respectively. Surgical sampling and time-activity curves based on quantitative imaging showed peak uptake in high-grade glioma at 39 h, with a half-life of 62 h. Tumor uptake at time of surgery averaged 3.5×10−3 %ID/g and peak activity by the conjugate view method averaged 9.2×10−3 %ID/g (3.5–17.8). Mean radiation absorption dose was 3.9 rad per mCi injected (range 0.7–9.6) or 10.5 cGy/Bq (range 1.9–26). There was agreement on positive sites when immunoscintigraphy was compared with technetium-99m glucoheptonate/diethylene triamine penta-acetic acid planar imaging, thallium-201 SPET, and fluorine-18 fluorodeoxyglucose positron emission tomography. Taken together, these data suggest that quantitative estimates of antibody targeting to intracranial tumors can be made using the modified conjugate view method.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1619-7089
    Keywords: Positron emission tomography ; Antibody ; Iodine-124 ; Glioma ; Microdosimetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We present a method to assess quantitatively the immunological characteristics of tumours using radiolabelled monoclonal antibody and positron emission tomography (PET) to improve dosimetry for radioimunotherapy. This method is illustrated with a glioma patient who was injected with 96.2 MBq of iodine-124 labelled 3F8, a murine antibody (IgG3) specific against the ganglioside GD2. Serial PET scans and plasma samples were taken over 11 days. A three-compartment model was used to estimate the plasma to tumour transfer constant (K 1), the tumour to plasma transfer constant k 2, the association and dissociation constants (k 3, k 4) of antibody binding, and the binding potential. Tumour radioactivity peaked at 18 h at 0.0045% ID/g. The kinetic parameters were estimated to be: K 1 = 0.048 ml h−1 g−1, k 2 = 0.16 h−1, k 3 = 0.03 h−1, k 4 = 0.015 h−1 and BP = 2.25. Based on these kinetic parameters, the amount of tumour-bound radiolabelled monoclonal antibody was calculated. This method permits estimates of both macrodosimetry and microdosimetry at the cellular level based on in vivo non-invasive measurement.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-9686
    Keywords: Interstitial fluid pressure ; Artificial lymphatic system ; Walker 256 ; Sarcoma ; 3F8 ; NMB-7 Neuroblastoma ; Doxorubicin ; Monoclonal antibody ; Cyclophosphamide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract This paper presents findings from uptake studies to evaluate the ability of an “artificial lymphatic system” (ALS) to enhance large and small molecular weight drug transport into solid tumors and the therapeutic effect of the additional drug on their growth. These studies also served to test the effectiveness of an implantable multidrain ALS. Walker 256, Neuroblastoma, and Sarcoma dual-tumor models were used to evaluate the effect of ALS aspiration on the uptake of 3F8 monoclonal antibody, and doxorubicin. A tumor shrinkage experiment using Walker 256 dual tumors was used to evaluate the efficacy of an implantable ALS with cyclophosphamide chemotherapy. Drug uptake significantly increased in all aspirated tumors; 3F8 uptake was enhanced 37.4% in the Walker and 93.1% in the Neuroblastoma tumor lines (p 〈 0.05). Doxorubicin uptake increased 23.2%; in Sarcoma tumor (p 〈 0.05). The shrinkage study demonstrated that one-drain aspirated tumors shrank 90% faster (p 〈 0.01) than control tumors, while three-drain aspirated tumors shrank 123% faster than control tumors (p 〈 0.01). © 2000 Biomedical Engineering Society. PAC00: 8719Tt, 8719Xx, 8780-y, 8719Uv
    Type of Medium: Electronic Resource
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