EHA Library - The official digital education library of European Hematology Association (EHA)

THE HIDDEN IMPACT OF PATIENT GENERAL CONDITION ON THE OVERALL SURVIVAL OF MYELODYSPLASTIC SYNDROMES AND RELATED DISEASES (CHRONIC MYELOMONOCYTIC LEUKEMIA AND ACUTE MYELOID LEUKEMIA)
Author(s): ,
Paola González Carmona
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
,
Violeta Martínez-Robles
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
,
Seila Cerdá
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
,
Javier Sánchez-del-Real
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
,
Saad Jacoubi
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
,
Filomeno Rondón
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
,
Nakaire Bonache
Affiliations:
Internal Medicine,Hospital Universitario de León,León,Spain
,
María Lavinia Villalobos
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
,
Jose Antonio Rodríguez-García
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
Fernando Ramos
Affiliations:
Hematology,Hospital Universitario de León,León,Spain
(Abstract release date: 05/17/18) EHA Library. González Carmona P. 06/14/18; 216356; PB2089
Paola González Carmona
Paola González Carmona
Contributions
Abstract

Abstract: PB2089

Type: Publication Only

Background

Patient clinical situation at diagnosis (Dx) of MDS is a function of general condition (GC) before Dx and the impact of the new disease. ECOG performance status probably depends on both of them, and consequently may be highly dependent on the very moment that it is measured. GC at baseline can be measured by Lee Index (LIx) for Older Adults (Lee SJ et al, 2006), a 12-item validated scale that has been shown to predict 4-year mortality among community-dwelling adults in USA and also to predict overall survival (OS) in a prospective and molecularly annotated cohort of Spanish MDS patients (Ramos F et al, 2017). To our knowledge, LIx has not been applied yet to MDS-related conditions (CMML and AML).

Aims

To analyze whether patient GC before Dx can be considered an independent determinant of OS in a heterogenous population of Pts diagnosed with MDS and related diseases.

Methods

We have reviewed the clinical charts of 132 pts (84 M, 48 F), median age 79y (IQR 73-82y), diagnosed in our center with MDS (n=88), CMML (17) or AML (27), whose GC had been evaluated by means of the LIx. The study was approved by our Institutional Review Board. All Pts were Dx and classified according to WHO 2008 and stratified prognostically (Px) according to disease-specific criteria (IPSS-R in MDS, CPSS in CMML and MRC/LRF scoring system in AML). ECOG was 0 in 23 Pts (17.4%), 1-2 in 93 (70.4%), 3-4 in 15 (11.4%) and NA in 1 (0.75%). Twenty-two Pts (16.7%) had received therapy known to prolong OS, while the rest had received only supportive care. After a median follow-up of 38.1 months (IQR 37.7-71.6), 70 Pts (53.0%) had died, 45 (34.1%) were alive, and 17 (12.9%) were lost to follow-up. The proportion of Pts that received disease-modifying therapy was similar across the Dx and Px groups. OS was evaluated by Log-rank tests (for trend, as appropriate) and Cox regression models.

Results

OS was longest for CMML Pts (median NR), intermediate for MDS (53.4 months, IQR 29.1-77.7) and shortest for AML (8.5, IQR 0-19.1), p<0.001 (Log-rank). As expected, it was also progressively shorter as the disease-specific Px categories were worse (p<0.001, Log-rank for trend). ECOG categories were strongly associated with both LIx and Px categories (Chi-Square for trend 10.84, p=0.001 and 7.94, p=0.006, respectively), but not to the Dx category (p=0.55).

LIx score ranged 0-19 points (median 8, IQR 6-10). Fifty-three Pts (40.2%) were included in the Q1 (score 0-5), 45 Pts (34.1%) in Q2 (6-9), 25 (18.9%) in Q3 (10-13) and 9 (6.8%) in Q4 (score 14+). As expected, LIx categories were associated neither with the Dx nor with the Px categories (p=0.15 and p=0.36, respectively). At first sight, we observed a non-significant univariate trend towards a shorter OS as the LIx was higher: Q1 68.2 months (IQR 25.6-110.9), Q2+Q3 45.2 (IQR 14.9-75.4) and Q4 16.2 (IQR 0-41.8); p=0.211, Log-rank for trend. Interestingly, multivariate models disclosed that LIx score was an independent determinant of OS in this heterogeneous population, whether the type of treatment is included in the model (p= 0.019) or not (p=0.034).

Conclusion

Patient general condition, as evaluated multidimensionally by the Lee Index for Older Adults, is an independent determinant of OS in patients with MDS, CMML and AML. This statement is now being evaluated in a larger and prospective patient cohort.

Session topic: 10. Myelodysplastic syndromes – Clinical

Keyword(s): Acute Myeloid Leukemia, Chronic myelomonocytic leukemia, Myelodysplasia, Survival

Abstract: PB2089

Type: Publication Only

Background

Patient clinical situation at diagnosis (Dx) of MDS is a function of general condition (GC) before Dx and the impact of the new disease. ECOG performance status probably depends on both of them, and consequently may be highly dependent on the very moment that it is measured. GC at baseline can be measured by Lee Index (LIx) for Older Adults (Lee SJ et al, 2006), a 12-item validated scale that has been shown to predict 4-year mortality among community-dwelling adults in USA and also to predict overall survival (OS) in a prospective and molecularly annotated cohort of Spanish MDS patients (Ramos F et al, 2017). To our knowledge, LIx has not been applied yet to MDS-related conditions (CMML and AML).

Aims

To analyze whether patient GC before Dx can be considered an independent determinant of OS in a heterogenous population of Pts diagnosed with MDS and related diseases.

Methods

We have reviewed the clinical charts of 132 pts (84 M, 48 F), median age 79y (IQR 73-82y), diagnosed in our center with MDS (n=88), CMML (17) or AML (27), whose GC had been evaluated by means of the LIx. The study was approved by our Institutional Review Board. All Pts were Dx and classified according to WHO 2008 and stratified prognostically (Px) according to disease-specific criteria (IPSS-R in MDS, CPSS in CMML and MRC/LRF scoring system in AML). ECOG was 0 in 23 Pts (17.4%), 1-2 in 93 (70.4%), 3-4 in 15 (11.4%) and NA in 1 (0.75%). Twenty-two Pts (16.7%) had received therapy known to prolong OS, while the rest had received only supportive care. After a median follow-up of 38.1 months (IQR 37.7-71.6), 70 Pts (53.0%) had died, 45 (34.1%) were alive, and 17 (12.9%) were lost to follow-up. The proportion of Pts that received disease-modifying therapy was similar across the Dx and Px groups. OS was evaluated by Log-rank tests (for trend, as appropriate) and Cox regression models.

Results

OS was longest for CMML Pts (median NR), intermediate for MDS (53.4 months, IQR 29.1-77.7) and shortest for AML (8.5, IQR 0-19.1), p<0.001 (Log-rank). As expected, it was also progressively shorter as the disease-specific Px categories were worse (p<0.001, Log-rank for trend). ECOG categories were strongly associated with both LIx and Px categories (Chi-Square for trend 10.84, p=0.001 and 7.94, p=0.006, respectively), but not to the Dx category (p=0.55).

LIx score ranged 0-19 points (median 8, IQR 6-10). Fifty-three Pts (40.2%) were included in the Q1 (score 0-5), 45 Pts (34.1%) in Q2 (6-9), 25 (18.9%) in Q3 (10-13) and 9 (6.8%) in Q4 (score 14+). As expected, LIx categories were associated neither with the Dx nor with the Px categories (p=0.15 and p=0.36, respectively). At first sight, we observed a non-significant univariate trend towards a shorter OS as the LIx was higher: Q1 68.2 months (IQR 25.6-110.9), Q2+Q3 45.2 (IQR 14.9-75.4) and Q4 16.2 (IQR 0-41.8); p=0.211, Log-rank for trend. Interestingly, multivariate models disclosed that LIx score was an independent determinant of OS in this heterogeneous population, whether the type of treatment is included in the model (p= 0.019) or not (p=0.034).

Conclusion

Patient general condition, as evaluated multidimensionally by the Lee Index for Older Adults, is an independent determinant of OS in patients with MDS, CMML and AML. This statement is now being evaluated in a larger and prospective patient cohort.

Session topic: 10. Myelodysplastic syndromes – Clinical

Keyword(s): Acute Myeloid Leukemia, Chronic myelomonocytic leukemia, Myelodysplasia, Survival

By clicking “Accept Terms & all Cookies” or by continuing to browse, you agree to the storing of third-party cookies on your device to enhance your user experience and agree to the user terms and conditions of this learning management system (LMS).

Cookie Settings
Accept Terms & all Cookies