# Radiotherapy in addition to systemic therapy reduces the early mortality of angioimmunoblastic T-cell lymphoma

**Authors:** Yaobin Lin, Qiong Lin, Qizhen Xu, Shenghong Shi, Daxin Huang, Gaoda Ju, Shan Liu, Jianyuan Song, Qingliang Lin, Jianwu Chen

PMC · DOI: 10.1007/s00277-026-06796-6 · Annals of Hematology · 2026-01-23

## TL;DR

Adding radiotherapy to chemotherapy can reduce early deaths in a rare type of T-cell lymphoma called AITL, especially in certain patient groups.

## Contribution

This study identifies radiotherapy as a treatment that can lower early mortality in AITL patients when combined with chemotherapy.

## Key findings

- Early mortality in AITL patients was 46.6% overall and 39.7% lymphoma-specific.
- Combining chemotherapy with radiotherapy reduced early mortality in male patients aged 40–69 with localized or regional disease.
- Age, sex, and treatment type were significant risk factors for early mortality in AITL.

## Abstract

Angioimmunoblastic T-cell lymphoma (AITL) is a rare and aggressive peripheral T-cell lymphoma that is prone to early progression and recurrence and has a poor overall prognosis. Notably, early mortality (EM) and risk factors for AITL are currently unclear. We performed a retrospective analysis of AITL data from 2000 to 2021 in the Surveillance, Epidemiology, and End Results databases. Early death was defined as death within two years from the date of diagnosis. Histograms and pie charts were used to present the distribution of overall early mortality (O-EM) and lymphoma-specific early mortality (LS-EM). Cox regression model was used to screen the risk factors. Cumulative event rate curves were used to analyze the effect of treatment on EM. In total, 2,413 patients diagnosed with AITL were included in this study. Among the deceased patients, the O-EM was 46.6%, with an LS-EM of 39.7%. EM increased significantly with age, was higher among white person than among other racial groups, and was higher among males than among females. Significant independent risk factors for both O-EM and LS-EM included sex, age, SEER historic stage, radiation therapy, and chemotherapy. The combination of chemotherapy and radiotherapy can decrease O-EM and LS-EM rates in males, aged 40–69 years, and patients with localized and regional SEER historic stages. AITL demonstrates elevated EM. However, the integration of radiotherapy with chemotherapy can significantly reduce the EM among male patients aged 40–69 years with SEER historical stage as localized and regional.

The online version contains supplementary material available at 10.1007/s00277-026-06796-6.

## Linked entities

- **Diseases:** angioimmunoblastic T-cell lymphoma (MONDO:0004977), AITL (MONDO:0004977)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, IDH2 (isocitrate dehydrogenase (NADP(+)) 2) [NCBI Gene 3418] {aka D2HGA2, ICD-M, IDH, IDH-2, IDHM, IDP}, DNMT3A (DNA methyltransferase 3 alpha) [NCBI Gene 1788] {aka DNMT3A2, HESJAS, M.HsaIIIA, TBRS}, TET2 (tet methylcytosine dioxygenase 2) [NCBI Gene 54790] {aka IMD75, KIAA1546, MDS}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}
- **Diseases:** O (MESH:C535508), central nervous system tumors (MESH:D016543), hematological malignancies (MESH:D019337), extranodal NK/T-cell lymphoma (MESH:D054391), non-Hodgkin lymphomas (MESH:D008228), metastases (MESH:D009362), SMN (MESH:D016609), acute myeloid leukemia (MESH:D015470), EM (MESH:D003643), LS (MESH:D007888), Nasopharyngeal carcinoma (MESH:D000077274), lymphadenopathy (MESH:D008206), EBV infection (MESH:D020031), itchy rashes (MESH:D005076), Ann-Arbor stage III- (MESH:D062706), autoimmune phenomena (MESH:D001327), lymph node metastasis (MESH:D008207), PTCL (MESH:D016411), multiple myeloma (MESH:D009101), vascular hyperplasia (MESH:D006965), hematological diseases (MESH:D006402), immune dysregulation (OMIM:614878), diffuse large B-cell lymphoma (MESH:D016403), AITL (MESH:D016399), Cancer (MESH:D009369), toxicity (MESH:D064420), autoimmune manifestations (MESH:D012877), lymphoma (MESH:D008223)
- **Chemicals:** rituximab (MESH:D000069283), oxygen (MESH:D010100), obinutuzumab (MESH:C543332), cyclophosphamide (MESH:D003520), azacitidine (MESH:D001374), chidamide (MESH:C547816), CHOP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12830441