# Autologous Stem Cell Transplantation in HIV-Positive and HIV-Negative Patients with Lymphoma: A Propensity Score-Matched Comparative Analysis

**Authors:** Alessandro Re, Margherita Oberti, Armando Stabile, Angelo Andreini, Chiara Cattaneo, Chiara Pagani, Salvatore Casari, Maria Antonia Forleo, Cristina Tecchio, Camillo Almici, Alessandra Tucci, Francesco Castelli, Giuseppe Rossi, Mauro Krampera

PMC · DOI: 10.3390/cancers18040584 · Cancers · 2026-02-10

## TL;DR

This study shows that autologous stem cell transplantation is more effective for HIV-positive lymphoma patients compared to HIV-negative patients, with better survival and lower relapse rates.

## Contribution

The study is the first to demonstrate better progression-free survival and lower relapse rates in HIV-positive patients after stem cell transplantation compared to HIV-negative patients.

## Key findings

- HIV-positive patients had significantly higher 4-year progression-free survival (81%) compared to HIV-negative patients (51%).
- Relapse rates were significantly lower in HIV-positive patients (23%) compared to HIV-negative patients (36%).
- Four-year overall survival was 81% in HIV-positive and 67% in HIV-negative patients, though not statistically significant.

## Abstract

Treatment of HIV-associated lymphoma (HIV-Ly) with autologous stem cell transplantation (ASCT) has shown to be feasible and effective. In this study we compare the clinical outcomes of HIV-Ly and lymphomas of the general population receiving ASCT, analyzing two series of consecutive HIV-positive and HIV-negative patients, based on a 1:1 propensity score match analysis. Forty-four patients were identified in both groups. Progression-free survival (PFS), defined as the time from ASCT to relapse, progression or death for any cause, was significantly higher in HIV-positive patients (4-year PFS 81% and 51%, in HIV-positive and HIV-negative patients, respectively, p = 0.027). The 4-year OS was 81% in HIV-positive and 67% in HIV-negative patients (p = 0.15). The relapse rate was significantly higher in HIV-negative patients (36% vs. 23%) (p = 0.04). Our results increase the awareness of ASCT as an effective curative option for HIV-Ly and show for the first time better PFS and a low relapse rate after ASCT in patients with HIV compared to patients without, in a statistically reliable manner.

Background/Objectives: Treatment of HIV-associated lymphoma (HIV-Ly) with autologous stem cell transplantation (ASCT) has shown a surprisingly low relapse rate in several series. The aim of this study was to compare the clinical outcomes of HIV-Ly and lymphomas in the general population receiving ASCT. Methods: We compared two series of consecutive HIV-positive and HIV-negative patients, based on a 1:1 propensity score analysis, matching for age, sex, histology, disease status and prior therapies. Results: After propensity matching we identified a final population of 88 patients (44 HIV-positive vs. 44 HIV-negative). All HIV-positive patients received combination antiretroviral therapy (cART). With a median follow-up of 51 months, PFS was significantly higher in HIV-positive patients (4-year PFS 81% and 51%, in HIV-positive and HIV-negative patients, respectively, p = 0.027). Four-year OS was 81% for HIV-positive and 67% in HIV-negative patients (p = 0.15). The relapse rate was significantly higher in HIV-negative patients (36% vs. 23%) (p = 0.04). Conclusions: Our results clearly show that ASCT is an effective curative option for HIV-Ly, with better PFS and a lower relapse rate compared to patients without HIV. A favorable effect of ASCT on HIV infection and immune system recovery, potential off-target effects of cART or other yet unknown factors may account for this observation.

## Linked entities

- **Diseases:** lymphoma (MONDO:0003659)

## Full-text entities

- **Genes:** CD34 (CD34 molecule) [NCBI Gene 947], CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** CMV (MESH:D003586), diarrhea (MESH:D003967), Rhinovirus pneumonia (MESH:D011014), Hodgkin Lymphoma (MESH:D006689), HIV viremia (MESH:D014766), fever (MESH:D005334), hematologic malignancies (MESH:D019337), seizure (MESH:D012640), HHV-6 infection (MESH:D020031), injury to (MESH:D014947), HL (MESH:C538324), chemo-s disease (MESH:D004194), inflammation (MESH:D007249), pancreatic adenocarcinoma (MESH:D010190), Plasmablastic Lymphoma (MESH:D000069293), cancer (MESH:D009369), Peripheral T-cell Lymphoma (MESH:D016411), adult T-cell leukemia (MESH:D015459), hepatitis B (MESH:D006509), neutropenic (MESH:D044504), invasive pulmonary aspergillosis (MESH:D055744), Primary Mediastinal B-cell Lymphoma (MESH:D016393), enteritis (MESH:D004751), PLWH (MESH:C000719191), Lymphoma (MESH:D008223), bacterial infection (MESH:D001424), NHL (MESH:D008228), hepatic toxicity (MESH:D056486), herpes zoster (MESH:D006562), HIV (MESH:D015658), Diffuse Large B-cell Lymphoma (MESH:D016403), sepsis (MESH:D018805), chronic (MESH:D002908), Infectious (MESH:D003141), HIV-Ly (MESH:D016483), Co-infection (MESH:D060085), Follicular Lymphoma (MESH:D008224), viral infections (MESH:D014777), C.parapsilosis (OMIM:211750), LSM (MESH:D003643), immunodeficiency (MESH:D007153), gastrointestinal toxicity (MESH:D005767), Infections (MESH:D007239), febrile events (MESH:D002318), oral mucositis (MESH:D013280), Toxicity (MESH:D064420)
- **Chemicals:** Levofloxacin (MESH:D064704), acyclovir (MESH:D000212), fluconazole (MESH:D015725), nucleoside (MESH:D009705), trimethoprim sulfamethoxazole (MESH:D015662), zidovudine (MESH:D015215)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], hepatitis C virus [taxon 11103], Human betaherpesvirus 6 (species) [taxon 10368], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939142/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939142/full.md

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Source: https://tomesphere.com/paper/PMC12939142