Blood online
Home About Blood Authors Subscriptions Permission Advertising Public Access contact us
 

 
Advanced
Current Issue
First Edition
Future Articles
Archives
Submit to Blood
Search
American Society of Hematology
Meeting Abstracts
Email Alerts
Prepublished online as a Blood First Edition Paper on March 20, 2003; DOI 10.1182/blood-2002-12-3674.

This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2002-12-3674v1
102/2/477    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Right arrow Rights and Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhou, P.
Right arrow Articles by Comenzo, R. L
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhou, P.
Right arrow Articles by Comenzo, R. L
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Submitted December 4, 2002
Accepted March 12, 2003

Melphalan-mobilized blood stem cell components contain minimal clonotypic myeloma cell contamination

Ping Zhou, Yana Zhang, Carmen Martinez, Nagesh Kalakonda, Stephen D Nimer, and Raymond L Comenzo*

Hematology Service, Division of Hematologic Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY, USA
Sloan-Kettering Institute, New York, NY, USA

* Corresponding author; email: comenzor{at}mskcc.org.

Optimal methods of stem cell mobilization in multiple myeloma are undefined, and contaminating clonotypic cells could contribute to disease recurrence. A phase 2 trial of intravenous melphalan (60mg/m2) and G-CSF (10ug/kg/d) for mobilization was performed. To enhance reliability, contamination was assessed with two sensitive methods, immunoglobulin light- and heavy-chain variable region patient-specific limiting-dilution PCR. We evaluated 29 stem cell components (SCC) from fifteen patients; for 9 SCC, only VL PCR was used because of light chain disease or technical problems with VH primers. For 20 SCC, VL and VH PCR results were highly correlated (r2 = 0.93, p << 0.01) with 35% (7/20) having identical estimates. VH PCR gave significantly higher estimates for 8, and VL PCR for 5, SCC, supporting the utility of employing two methods. Estimated clonotypic contamination per SCC was 0.0009% (0-0.1) or 0.5 x 104 clonotypic cells per kg (0-41.2), and contamination correlated with CD34+ cells collected (r2 = 0.42, p << 0.01). Melphalan-mobilized SCC contain minimal clonotypic contamination.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
BloodHome page
R. L. Comenzo, P. Zhou, M. Fleisher, B. Clark, and J. Teruya-Feldstein
Seeking confidence in the diagnosis of systemic AL (Ig light-chain) amyloidosis: patients can have both monoclonal gammopathies and hereditary amyloid proteins
Blood, May 1, 2006; 107(9): 3489 - 3491.
[Abstract] [Full Text] [PDF]



 click for free articles
home about blood authors subscriptions permissions advertising public access contact us
  Copyright © 2003 by American Society of Hematology         Online ISSN: 1528-0020