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B SYMPTOMS AND ELEVATED ESR AS PREDICTORS OF OVERALL SURVIVAL IN HODGKIN LYMPHOMA. A 20 YEAR FOLLOW UP MULTICENTER ANALYSIS.
Author(s): ,
Rolando Vallansot
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Lourdes Escoda
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Carmen Talarn
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Marta Cervera
Affiliations:
Haematology Department.,Hospital Universitari Joan XXIII.,Tarragona,Spain
,
Janilson Do Nascimento
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Josep Gumà
Affiliations:
Oncology Department,Hospital Universitari Sant Joan,Reus,Spain
,
María José Miranda
Affiliations:
Oncology Department,Hospital Universitari Sant Joan,Reus,Spain
,
Francisca Martínez
Affiliations:
Oncology Department,Hospital Universitari Sant Joan,Reus,Spain
,
María José Herranz
Affiliations:
Haematology Department,Hospital Sant Pau i Santa Tecla,Tarragona,Spain
,
Margarita Prats
Affiliations:
Haematology Department,Hospital Sant Pau i Santa Tecla,Tarragona,Spain
,
Xavier Ortín
Affiliations:
Haematology Department,Hospital Verge de la Cinta,Tortosa,Spain
,
Reyes Aguinaco
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Teresa Gimenez
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Carmen Araguás
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Ada Esteban
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
,
Alexandra Martínez
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
Josep Sarrá
Affiliations:
Haematology Department,Hospital Universitari Joan XXIII,Tarragona,Spain
(Abstract release date: 05/18/17) EHA Library. O. Vallansot R. 05/18/17; 182575; PB1861
Rolando O. Vallansot
Rolando O. Vallansot
Contributions
Abstract

Abstract: PB1861

Type: Publication Only

Background

The prognosis of Hodgkin lymphoma (HL) has improved significantly with the implementation of a risk-adapted treatment that combines chemo and radiotherapy. Altough this approach has led to the greatest advance in disease response, the benefit in terms of overall survival (OS) has been jeopardized by long term toxicity.
The identification of risk factors is crucial to assign each patient to a well defined risk group and prevent under or overtreatment, minimizing the risk of relapse and long term toxicity.

Aims
To analyze the risk factors associated with survival in HL treated with an ABVD based regimen that restricted radiotherapy only to bulky disease.

Methods

We retrospectively analyzed HL patients diagnosed in 4 centers in Tarragona area (Catalonia, Spain), between 1995 and 2015, treated uniformly according to a local protocol.
Patients were assigned into 4 groups: G1: favorable early stage: ABVDx6 cycles, G2: Bulky early stage without other risk factors: ABVDx6 + IFRDT. G3: unfavorable early stage (B symptoms) and advanced stage without bulky disease: ABVDx8, G4: Bulky advanced stage: AVBDx8 + IFRDT

Results

A total of 183 patients were analyzed with a median follow up of 82 months [range 1-244]. Male/female ratio was 1,29. Median age was 36 years [range 16-82]. Complete response was achieved in 160 patients (87,4%). The estimated OS at 20 years for the whole group was 62.7%.
Kaplan–Meier method and log rank test were used for survival analysis. Cox proportional hazard model was used for univariate analysis to identify predictive factors for OS. Factors with significance (p <0.05) were considered for multivariate Cox regression.
In univariate analysis, worse OS was found in patients with increased LDH, non-NS subtype, albumin <3,5 g/dL, B symptoms, HIV+, advance stage and ESR >50 mm (log rank p=0,012; p=0,049; p=0,024; p=0,002; p=0,005; p=0,004 and p=0,001 respectively).
The multivariate Cox regression analysis identified B symptoms and ESR >50 mm as independent prognostic factors for OS (p=0,002; p=0,006 respectively).
These variables allowed us to identify 3 patient groups: low (no risk factors), intermediate (either B symtoms or ESR>50 mm) and high risk (both risk factors), with significant differences in OS. Estimation for OS was uniformly analyzed at 216 months (18 years), which is the shortest follow up period for patients in the low risk group.
Patients in the low, intermediate and high risk groups had an estimated OS of 85.7%, 65% and 40.1% (p<0.001)

Conclusion
B symptoms and ESR>50mm are independently associated with OS. The combination of these factors can stratify patients in low, intermediate and high risk groups with significant differences in OS, regardless their clinical stage.

Session topic: 17. Hodgkin lymphoma - Clinical

Keyword(s): Survival prediction, Risk factor, Hodgkin's Lymphoma

Abstract: PB1861

Type: Publication Only

Background

The prognosis of Hodgkin lymphoma (HL) has improved significantly with the implementation of a risk-adapted treatment that combines chemo and radiotherapy. Altough this approach has led to the greatest advance in disease response, the benefit in terms of overall survival (OS) has been jeopardized by long term toxicity.
The identification of risk factors is crucial to assign each patient to a well defined risk group and prevent under or overtreatment, minimizing the risk of relapse and long term toxicity.

Aims
To analyze the risk factors associated with survival in HL treated with an ABVD based regimen that restricted radiotherapy only to bulky disease.

Methods

We retrospectively analyzed HL patients diagnosed in 4 centers in Tarragona area (Catalonia, Spain), between 1995 and 2015, treated uniformly according to a local protocol.
Patients were assigned into 4 groups: G1: favorable early stage: ABVDx6 cycles, G2: Bulky early stage without other risk factors: ABVDx6 + IFRDT. G3: unfavorable early stage (B symptoms) and advanced stage without bulky disease: ABVDx8, G4: Bulky advanced stage: AVBDx8 + IFRDT

Results

A total of 183 patients were analyzed with a median follow up of 82 months [range 1-244]. Male/female ratio was 1,29. Median age was 36 years [range 16-82]. Complete response was achieved in 160 patients (87,4%). The estimated OS at 20 years for the whole group was 62.7%.
Kaplan–Meier method and log rank test were used for survival analysis. Cox proportional hazard model was used for univariate analysis to identify predictive factors for OS. Factors with significance (p <0.05) were considered for multivariate Cox regression.
In univariate analysis, worse OS was found in patients with increased LDH, non-NS subtype, albumin <3,5 g/dL, B symptoms, HIV+, advance stage and ESR >50 mm (log rank p=0,012; p=0,049; p=0,024; p=0,002; p=0,005; p=0,004 and p=0,001 respectively).
The multivariate Cox regression analysis identified B symptoms and ESR >50 mm as independent prognostic factors for OS (p=0,002; p=0,006 respectively).
These variables allowed us to identify 3 patient groups: low (no risk factors), intermediate (either B symtoms or ESR>50 mm) and high risk (both risk factors), with significant differences in OS. Estimation for OS was uniformly analyzed at 216 months (18 years), which is the shortest follow up period for patients in the low risk group.
Patients in the low, intermediate and high risk groups had an estimated OS of 85.7%, 65% and 40.1% (p<0.001)

Conclusion
B symptoms and ESR>50mm are independently associated with OS. The combination of these factors can stratify patients in low, intermediate and high risk groups with significant differences in OS, regardless their clinical stage.

Session topic: 17. Hodgkin lymphoma - Clinical

Keyword(s): Survival prediction, Risk factor, Hodgkin's Lymphoma

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