Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?

<p>Abstract</p> <p>Background</p> <p>Patient selection for phase I trials (PIT) in oncology is challenging. A typical inclusion criterion for PIT is 'life expectancy > 3 months', however the 90 day mortality (90DM) and overall survival (OS) of patients with...

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Main Authors: Bedard Philippe, Chen Eric X, Wang Lisa, Chan Kelvin K, Florescu Ana, Chau Nicole G, Oza Amit M, Siu Lillian L
Format: Article
Language:English
Published: BMC 2011-10-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/11/426
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spelling doaj-ddfd4d311b91470ab57dc2216397c6ec2020-11-25T01:03:06ZengBMCBMC Cancer1471-24072011-10-0111142610.1186/1471-2407-11-426Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?Bedard PhilippeChen Eric XWang LisaChan Kelvin KFlorescu AnaChau Nicole GOza Amit MSiu Lillian L<p>Abstract</p> <p>Background</p> <p>Patient selection for phase I trials (PIT) in oncology is challenging. A typical inclusion criterion for PIT is 'life expectancy > 3 months', however the 90 day mortality (90DM) and overall survival (OS) of patients with advanced solid malignancies are difficult to predict.</p> <p>Methods</p> <p>We analyzed 233 patients who were enrolled in PIT at Princess Margaret Hospital. We assessed the relationship between 17 clinical characteristics and 90DM using univariate and multivariate logistic regression analyses to create a risk score (PMHI). We also applied the Royal Marsden Hospital risk score (RMI), which consists of 3 markers (albumin < 35g/L, > 2 metastatic sites, LDH > ULN).</p> <p>Results</p> <p>Median age was 57 years (range 21-88). The 90DM rate was 14%; median OS was 320 days. Predictors of 90DM were albumin < 35g/L (OR = 8.2, p = 0.01), > 2 metastatic sites (OR = 2.6, p = 0.02), and ECOG > 0 (OR = 6.3, p = 0.001); all 3 factors constitute the PMHI. To predict 90DM, the PMHI performed better than the RMI (AUC = 0.78 vs 0.69). To predict OS, the RMI performed slightly better (RMI ≥ 2, HR = 2.2, p = 0.002 vs PMHI ≥ 2, HR = 1.6, p = 0.05).</p> <p>Conclusions</p> <p>To predict 90DM, the PMHI is helpful. To predict OS, risk models should include ECOG > 0, > 2 metastatic sites, and LDH > ULN. Prospective validation of the PMHI is warranted.</p> http://www.biomedcentral.com/1471-2407/11/426
collection DOAJ
language English
format Article
sources DOAJ
author Bedard Philippe
Chen Eric X
Wang Lisa
Chan Kelvin K
Florescu Ana
Chau Nicole G
Oza Amit M
Siu Lillian L
spellingShingle Bedard Philippe
Chen Eric X
Wang Lisa
Chan Kelvin K
Florescu Ana
Chau Nicole G
Oza Amit M
Siu Lillian L
Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?
BMC Cancer
author_facet Bedard Philippe
Chen Eric X
Wang Lisa
Chan Kelvin K
Florescu Ana
Chau Nicole G
Oza Amit M
Siu Lillian L
author_sort Bedard Philippe
title Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?
title_short Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?
title_full Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?
title_fullStr Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?
title_full_unstemmed Early mortality and overall survival in oncology phase I trial participants: can we improve patient selection?
title_sort early mortality and overall survival in oncology phase i trial participants: can we improve patient selection?
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2011-10-01
description <p>Abstract</p> <p>Background</p> <p>Patient selection for phase I trials (PIT) in oncology is challenging. A typical inclusion criterion for PIT is 'life expectancy > 3 months', however the 90 day mortality (90DM) and overall survival (OS) of patients with advanced solid malignancies are difficult to predict.</p> <p>Methods</p> <p>We analyzed 233 patients who were enrolled in PIT at Princess Margaret Hospital. We assessed the relationship between 17 clinical characteristics and 90DM using univariate and multivariate logistic regression analyses to create a risk score (PMHI). We also applied the Royal Marsden Hospital risk score (RMI), which consists of 3 markers (albumin < 35g/L, > 2 metastatic sites, LDH > ULN).</p> <p>Results</p> <p>Median age was 57 years (range 21-88). The 90DM rate was 14%; median OS was 320 days. Predictors of 90DM were albumin < 35g/L (OR = 8.2, p = 0.01), > 2 metastatic sites (OR = 2.6, p = 0.02), and ECOG > 0 (OR = 6.3, p = 0.001); all 3 factors constitute the PMHI. To predict 90DM, the PMHI performed better than the RMI (AUC = 0.78 vs 0.69). To predict OS, the RMI performed slightly better (RMI ≥ 2, HR = 2.2, p = 0.002 vs PMHI ≥ 2, HR = 1.6, p = 0.05).</p> <p>Conclusions</p> <p>To predict 90DM, the PMHI is helpful. To predict OS, risk models should include ECOG > 0, > 2 metastatic sites, and LDH > ULN. Prospective validation of the PMHI is warranted.</p>
url http://www.biomedcentral.com/1471-2407/11/426
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