-Author name in bold denotes the presenting author
-Asterisk * with author name denotes a Non-ASH member
Clinically Relevant Abstract denotes an abstract that is clinically relevant.

PhD Trainee denotes that this is a recommended PHD Trainee Session.

Ticketed Session denotes that this is a ticketed session.

4454 Prognostic Factors and Treatment Strategy in Patients with Hodgkin Lymphoma and HIV Infection Treated with ABVD and CART: A Retrospective Study from Spanish Group Geltamo

Program: Oral and Poster Abstracts
Session: 624. Hodgkin Lymphomas and T/NK cell Lymphomas: Clinical and Epidemiological: Poster III
Hematology Disease Topics & Pathways:
Hodgkin lymphoma, Lymphomas, Diseases, Lymphoid Malignancies
Monday, December 11, 2023, 6:00 PM-8:00 PM

Maria Huguet, MD1*, Aleix Méndez2*, Blanca Sanchez-Gonzalez3*, Mariana Bastos-Oreiro, MD4*, Ramon Garcia-Sanz, MD, PhD5*, Samuel Romero, MD6*, María-Jesús Vidal-Manceñido7*, Antonio Gutiérrez, MD, PhD8*, Paola Villafuerte Gutierrez, MD9*, Ana Garcia Noblejas, MD10*, Gustavo Tapia11*, Juan-Manuel Sancho, MD, PhD12*, Josep-Maria Ribera, MD, PhD13 and José-Tomás Navarro2*

1Hematology Department, ICO Badalona, Germans Trias i Pujol University Hospital. Universitat Autònoma de Barcelona. Josep Carreras Leukemia Research Institute, Barcelona, AL, Spain
2Hematology Department, ICO Badalona, Germans Trias i Pujol University Hospital. Universitat Autònoma de Barcelona. Josep Carreras Leukemia Research Institute, Badalona, Spain
3Hematology Department, Hospital del Mar, Barcelona, Spain
4Hematology Department, Hospital General Gregorio Marañon, Madrid, Spain
5University Hospital of Salamanca, Salamanca, Spain
6Hematology Research Group, Instituto de Investigación Sanitaria La Fe, Valencia, Spain
7Hematology Department, Hospital de León, León, Spain
8Hematology Department, Hospital Universitario Son Espases, Palma de Mallorca, Spain
9Hematology Department, Hospital Universitario Principe de Asturias, Madrid, ESP
10Hematology Department, Hospital Universitario La Princesa, Madrid, Spain
11Department of Pathology, Germans Trias i Pujol University Hospital, Universitat Autònoma de Barcelona, Badalona, Spain
12Hematology Department, ICO Badalona, Germans Trias i Pujol University Hospital. Universitat Autònoma de Barcelona. Josep Carreras Leukemia Research Institute, Barcelona, Spain
13ICO-Hospital Germans Trias i Pujol, Institut de Recerca contra la Leucèmia Josep Carreras (IJC), Universitat Autònoma de Barcelona, Badalona, Spain

Background

Hodgkin lymphoma (HL) is one of the most frequent non-AIDS defining neoplasm in people living with HIV (PLWH). Since the widespread use of combined antiretroviral therapy (cART), the incidence of most types of non-Hodgkin lymphoma affecting PLWH have decreased, but the incidence of HL has increased.

The International Prognostic Score (IPS) is the most widely used score for HL. However, its implementation in PLWH is still controversial. Current HL treatment guidelines consider early and advanced stage. In function of the presence of unfavorable risk factors in early stages, an interim PET-CT can be used to guide therapeutic strategy. Unfavorable risk factors have been described by international groups (EORT, GHSG, NCI-C, and NCCN), which are: ≥3-4 involved lymph node areas, elevated RDW, age ≥50 years, ≥1 extranodal involvement and presence of B symptoms. There is a lack of evidence of the impact of this strategy in patients with HIV.

Methods

Retrospective multicentric study of patients with HIV infection diagnosed with HL in 9 hospitals from the GELTAMO group in Spain, from 1995 to 2022. All patients were treated with ABVD and cART +/- radiotherapy. The main clinical and biological variables were collected. Peripheral absolute neutrophil, lymphocyte and monocyte counts were studied, including L/M ratio and CD4+ lymphocyte count. Moreover, serum lactate dehydrogenase (LDH), albumin and RDW were evaluated. Univariable and multivariable analysis were performed using the binary logistic regression model for complete response (CR) rate and Cox proportional-hazards regression model for overall survival (OS) and progression-free survival (PFS). Survival curves were plotted by the Kaplan-Meier method and compared by the log-rank test.

Results

Ninety patients were retrospectively analyzed with a median follow up of 5.89 [0,4;24,78] years. The characteristics of the patients are summarized in Table 1. Extranodal involvement, hemoglobin <105 g/L, leucocytosis, high RDW, hypoalbuminemia and high LDH were associated with worse probabilities of complete response (CR) achievement. In the univariate analysis, bone marrow involvement and monocytes count ≥0.6 x10^9/L were associated with shorter overall survival (OS) and progression free survival (PFR) probabilities. A lymphocyte/monocyte (L/M) ratio <1.09 was associated with shorter PFR probabilities. By multivariable analysis, only monocyte count ≥0.6 x10^9/L emerged as an unfavorable prognostic factor for OS and PFS (Figure 1). Data about treatment strategy and CR achievement is described in Table 1. Most patients (74%) presented advanced stage and the presence of unfavorable prognostic factors (described by international groups) was detected in most of the patients with localized stages (Table 1).

Conclusions

High monocyte count is a strong prognostic factor which can be used in PLWH with HL. Most patients with HL and HIV infection present an advanced stage at diagnosis or a localized stage with unfavorable prognosis factors. In patients with localized stage, interim PET-CT guided strategy seems to be feasible.

Disclosures: Garcia-Sanz: Roche: Consultancy, Honoraria; BMS/Celgene: Consultancy, Honoraria, Other: TRAVEL, ACCOMMODATIONS, EXPENSES; Janssen: Consultancy, Honoraria, Other: TRAVEL, ACCOMMODATIONS, EXPENSES, Research Funding, Speakers Bureau; Gilead/Kite: Consultancy, Honoraria, Other: TRAVEL, ACCOMMODATIONS, EXPENSES, Research Funding; Takeda: Consultancy, Honoraria, Other: TRAVEL, ACCOMODATIONS, EXPENSES, Research Funding, Speakers Bureau; Eusa Pharma: Honoraria; Novartis: Consultancy, Honoraria; Kyowa Kirin: Consultancy; Incyte: Consultancy, Honoraria; Lilly: Consultancy; ADC Therapeutics America: Consultancy; Miltenyi: Consultancy; Ideogen: Consultancy; Abbvie: Consultancy; BeiGene: Consultancy, Honoraria, Other: TRAVEL, ACCOMODATIONS, EXPENSES, Speakers Bureau; invivo scribe (IVS): Patents & Royalties. Ribera: Pfizer: Consultancy, Research Funding; Novartis: Consultancy; AMGEN: Research Funding; Takeda: Consultancy; Bristol Myers Squibb: Consultancy; Incyte: Consultancy, Research Funding.

*signifies non-member of ASH