TY - JOUR
T1 - Development and validation of a risk assessment tool for BKPyV Replication in allogeneic stem cell transplant recipients
AU - Abudayyeh, Ala
AU - Lin, Heather
AU - Abdelrahim, Maen
AU - Rondon, Gabriela
AU - Andersson, Borje S.
AU - Martinez, Charles S.
AU - Page, Valda D.
AU - Tarrand, Jeffrey J.
AU - Kontoyiannis, Dimitrios P.
AU - Marin, David
AU - Oran, Betul
AU - Olson, Amanda
AU - Jones, Roy
AU - Popat, Uday
AU - Champlin, Richard E.
AU - Chemaly, Roy F.
AU - Shpall, Elizabeth J.
AU - Rezvani, Katayoun
N1 - Funding Information:
This research was supported by funds from the University Cancer Foundation and the Duncan Family Institute for Cancer Prevention and Risk Assessment via Cancer Survivorship Research Seed Money Grants at The University of Texas MD Anderson Cancer Center. We are grateful to Amy Ninetto from the Department of Scientific Publications at The University of Texas MD Anderson Cancer Center for their valuable contributions.
Publisher Copyright:
© 2020 Wiley Periodicals LLC
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Background: BK polymavirus (BKPyV), a member of the family Polyomaviridae, is associated with increased morbidity and mortality in allogeneic stem cell transplant recipients. Methods: In our previous retrospective study of 2477 stem cell transplant patients, BKPyV replication independently predicted chronic kidney disease and poor survival. In this study, using the same cohort, we derived and validated a risk grading system to identify patients at risk of BKPyV replication after transplantation in a user-friendly modality. We used 3 baseline variables (conditioning regimen, HLA match status, and underlying cancer diagnosis) that significantly predicted BKPyV replication in our initial study in a subdistribution hazard model with death as a competing risk. We also developed a nomogram of the hazard model as a visual aid. The AUC of the ROC of the risk-score-only model was 0.65. We further stratified the patients on the basis of risk score into low-, moderate-, and high-risk groups. Results: The total risk score was significantly associated with BKPyV replication (P <.0001). At 30 days after transplantation, the low-risk (score ≤ 0) patients had a 9% chance of developing symptomatic BKPyV replication, while the high-risk (score ≥ 8) of the population had 56% of developing BKPyV replication. We validated the risk score using a separate cohort of 1478 patients. The AUC of the ROC of the risk-score-only model was 0.59. Both the total risk score and 3-level risk variable were significantly associated with BKPyV replication in this cohort (P <.0001). Conclusions: This grading system for the risk of symptomatic BKPyV replication may help in early monitoring and intervention to prevent BKPyV-associated morbidity, mortality, and kidney function decline.
AB - Background: BK polymavirus (BKPyV), a member of the family Polyomaviridae, is associated with increased morbidity and mortality in allogeneic stem cell transplant recipients. Methods: In our previous retrospective study of 2477 stem cell transplant patients, BKPyV replication independently predicted chronic kidney disease and poor survival. In this study, using the same cohort, we derived and validated a risk grading system to identify patients at risk of BKPyV replication after transplantation in a user-friendly modality. We used 3 baseline variables (conditioning regimen, HLA match status, and underlying cancer diagnosis) that significantly predicted BKPyV replication in our initial study in a subdistribution hazard model with death as a competing risk. We also developed a nomogram of the hazard model as a visual aid. The AUC of the ROC of the risk-score-only model was 0.65. We further stratified the patients on the basis of risk score into low-, moderate-, and high-risk groups. Results: The total risk score was significantly associated with BKPyV replication (P <.0001). At 30 days after transplantation, the low-risk (score ≤ 0) patients had a 9% chance of developing symptomatic BKPyV replication, while the high-risk (score ≥ 8) of the population had 56% of developing BKPyV replication. We validated the risk score using a separate cohort of 1478 patients. The AUC of the ROC of the risk-score-only model was 0.59. Both the total risk score and 3-level risk variable were significantly associated with BKPyV replication in this cohort (P <.0001). Conclusions: This grading system for the risk of symptomatic BKPyV replication may help in early monitoring and intervention to prevent BKPyV-associated morbidity, mortality, and kidney function decline.
KW - BK virus
KW - allogeneic stem cell transplant
KW - grading system
UR - http://www.scopus.com/inward/record.url?scp=85087804065&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85087804065&partnerID=8YFLogxK
U2 - 10.1111/tid.13395
DO - 10.1111/tid.13395
M3 - Article
C2 - 32602954
AN - SCOPUS:85087804065
VL - 22
JO - Transplant Infectious Disease
JF - Transplant Infectious Disease
SN - 1398-2273
IS - 5
M1 - e13395
ER -