scholarly journals A prospective study comparing quantitative Cytomegalovirus (CMV) polymerase chain reaction in plasma and pp65 antigenemia assay in monitoring patients after allogeneic stem cell transplantation

2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Giuseppe Gentile ◽  
Alessandra Picardi ◽  
Angela Capobianchi ◽  
Alessandra Spagnoli ◽  
Laura Cudillo ◽  
...  
2000 ◽  
Vol 181 (5) ◽  
pp. 1713-1719 ◽  
Author(s):  
Holger Hebart ◽  
Jürgen Löffler ◽  
Christof Meisner ◽  
François Serey ◽  
Diethard Schmidt ◽  
...  

Blood ◽  
2001 ◽  
Vol 97 (6) ◽  
pp. 1560-1565 ◽  
Author(s):  
Eduardo Olavarria ◽  
Edward Kanfer ◽  
Richard Szydlo ◽  
Jaspal Kaeda ◽  
Katayoun Rezvani ◽  
...  

The reverse transcriptase–polymerase chain reaction (RT-PCR) has become widely used for monitoring minimal residual disease after allogeneic stem cell transplantation (SCT) for chronic myeloid leukemia (CML). However, most of these studies were performed using qualitative RT-PCR, and the interpretation of the results obtained has been conflicting. The correlation of a quantitative RT-PCR test performed early after SCT (at 3 to 5 months) and long-term outcome of CML patients surviving for more than 6 months was studied. Between January 1991 and June 1999, data from 138 CML patients who received allografts were evaluated. Early RT-PCR results were classified as (1) negative if there were no BCR-ABLtranscripts detected (n = 61), (2) positive at low level if the total number of BCR-ABL transcripts was less than 100 per μg RNA and/or the BCR-ABL/ABL ratio was less than 0.02% (n = 14), or (3) positive at high level if transcript levels exceeded the thresholds defined above (n = 63). Three years after SCT the cumulative incidence of relapse was 16.7%, 42.9%, and 86.4%, respectively (P = .0001). The relationship betweenBCR-ABL transcript level and probability of relapse was apparent whether patients had received sibling or unrelated donor SCT and also whether or not the transplantation was T cell depleted. The results suggest that quantitative RT-PCR performed early after SCT is useful for predicting outcome and may help to define the need for further treatment.


2006 ◽  
Vol 48 (5) ◽  
pp. 275-278 ◽  
Author(s):  
Sandra Helena Alves Bonon ◽  
Cláudio Lúcio Rossi ◽  
Cármino Antonio de Souza ◽  
Afonso Celso Vigorito ◽  
Sandra Cecília Botelho Costa

Forty-six allogeneic hematopoietic stem cell transplantation (HSCT) patients were monitored for the presence of CMV antibodies, CMV-DNA and CMV antigens after transplantation. Immunoenzymatic serological tests were used to detect IgM and the increase in CMV IgG antibodies (increase IgG), a nested polymerase chain reaction (N-PCR) was used to detect CMV-DNA, and an antigenemia assay (AGM) was used to detect CMV antigens. The presence of CMV-IgM and/or CMV-increase IgG antibodies was detected in 12/46 (26.1%) patients, with a median time between HSCT and the detection of positive serology of 81.5 days. A positive AGM was detected in 24/46 (52.2%) patients, with a median time between HSCT and antigen detection of 62 days. Two or more consecutive positive N-PCR results were detected in 32/46 (69.5%) patients, with a median time between HSCT and the first positive PCR of 50.5 days. These results confirmed that AGM and mainly PCR are superior to serology for the early diagnosis of CMV infection. Six patients had CMV-IgM and/or CMV-increase IgG with a negative AGM (five cases) or N-PCR assay (one case). In five of these cases the serological markers were detected during the first 100 days after HSCT, the period of highest risk. These findings support the idea that serology may be useful for monitoring CMV infections in HSCT patients, especially when PCR is unavailable.


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