Monoclonal antibodies attached to microspheres containing magnetic compounds, used to remove neuroblastoma cells from bone marrow taken for autologous transplantation

1982 ◽  
Vol 18 (10) ◽  
pp. 1043 ◽  
1989 ◽  
Vol 59 (6) ◽  
pp. 844-847 ◽  
Author(s):  
V Combaret ◽  
MC Favrot ◽  
B Kremens ◽  
I Philip ◽  
C Bailly ◽  
...  

The Lancet ◽  
1984 ◽  
Vol 323 (8368) ◽  
pp. 70-73 ◽  
Author(s):  
J.G Treleaven ◽  
J Ugelstad ◽  
T Philip ◽  
F.M Gibson ◽  
A Rembaum ◽  
...  

1986 ◽  
Vol 4 (3) ◽  
pp. 363-369 ◽  
Author(s):  
N K Cheung ◽  
D D Von Hoff ◽  
S E Strandjord ◽  
P F Coccia

Three murine monoclonal antibodies (Mab) against a cell surface antigen, the disialoganglioside GD2, were investigated for detecting bone marrow metastasis in patients with neuroblastoma (NB) by indirect immunofluorescence (IF). As few as 0.01% NB cells could be detected. No Mab reactivity was found in 60 non-NB marrows. Thirty-five marrows from patients with stage III and stage IV NB at diagnosis were examined during the course of their disease. Tumor involvement was found in 74% by Mab, 55% by the two-layer soft agar clonogenic assay (CA), and 27% by conventional histochemical stains. All marrows containing NB histologically were positive for tumor by Mab; 71% were also positive by CA. Of histologically negative marrows, 63% were Mab positive, the majority (78%) of which were also positive by CA. All Mab nonreactive samples were negative histologically and by CA. We conclude that these antibodies are highly sensitive and specific in detecting NB metastasis in bone marrow.


Hybridoma ◽  
1982 ◽  
Vol 1 (4) ◽  
pp. 349-368 ◽  
Author(s):  
ZDENKA L. JONAK ◽  
ROGER H. KENNETT ◽  
KATHLEEN B. BECHTOL

Diagnostics ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 649
Author(s):  
Christos Sachpekidis ◽  
Matthias Türk ◽  
Antonia Dimitrakopoulou-Strauss

We report on a 52-year-old patient with an initial diagnosis of smoldering myeloma (SMM), who was monitored by means of dynamic and static positron emission tomography/computed tomography (PET/CT) with the radiotracer 1⁸F-fluorodeoxyglucose (18F-FDG). Baseline PET/CT revealed no pathological signs. Six months later, a transition to symptomatic, multiple myeloma (MM) was diagnosed. The transition was not accompanied by focal, hypermetabolic lesions on PET/CT. However, a diffusely increased 18F-FDG uptake in the bone marrow, accompanied by a marked increase of semi-quantitative (standardized uptake value, SUV) and quantitative, pharmacokinetic 18F-FDG parameters, was demonstrated. After successful treatment, including tandem autologous transplantation, the diffuse uptake in the bone marrow as well as the semi-quantitative and quantitative parameters showed a marked remission. This response was also confirmed by the clinical follow-up of the patient. These findings suggest that in MM a diffuse 18F-FDG uptake in the bone marrow may indeed reflect an actual bone marrow infiltration by plasma cells. Moreover, SUV values and kinetic parameters, not only from myeloma lesions but also from random bone marrow samples, may be used for MM monitoring. This could be particularly helpful in the follow-up of myeloma patients negative for 18F-FDG-avid focal lesions.


Sign in / Sign up

Export Citation Format

Share Document