Evidence map›Paper›PMID 35836543›Full record

ArticleTranslational cancer research2022

A case report of acquired immunodeficiency syndrome (AIDS)-related refractory Burkitt lymphoma got complete remission by multidisciplinary and multi-target combined therapy.

Renfang Zhang, Jianjun Sun

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In one paragraph

Article in Translational cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Renfang ZhangDepartment of Infection and Immunity, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Jianjun SunDepartment of Infection and Immunity, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Shanghai Public Health Clinical Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The incidence of Burkitt lymphoma among acquired immunodeficiency syndrome (AIDS) patients is significantly higher than that in general populations. It often features high malignancy and a poor prognosis. For patients with AIDS-related Burkitt lymphoma, the guidelines recommend the dose-adjusted EPOCH-R (DA-EPOCH-R) regimen (rituximab + etoposide vincristine + doxorubicin + cyclophosphamide + dexamethasone) as one of the first-line treatment options. If complete or partial responses are not achieved after first-line treatment, then a second-line regimen such as rituximab + gemcitabine + dexamethasone + cisplatin (R-GDP) or rituximab + ifosfamide + carboplatin + etoposide (R-ICE) can be employed instead. Patients without response to the second line regimen often have poor prognosis. However, with our growing understanding of the pathogenic mechanism of Burkitt lymphoma, it has become apparent that patients with Burkitt lymphoma who have a poor response to first- and second-line regimens require personalized treatment, such as immune checkpoint inhibitors [programmed death 1 (PD-1) inhibitors] or new small-molecule inhibitors [e.g., Bruton tyrosine kinase (BTK) inhibitors: ibrutinib and zanubrutinib; B-cell lymphoma-2 (BCL-2) inhibitors: venetoclax]. For the efficacy of the personalized treatment, the publication is scarce. Case Description: This report describes a patient with AIDS-related Burkitt lymphoma who did not achieve complete remission after first- and second-line treatment but eventually reached complete remission after combined therapy that included chemotherapy with small-molecule inhibitors, radiotherapy, and PD-1 inhibitors. During the multidisciplinary and multi-target combined therapy, patient has good tolerance. After 14 months' follow-up, patients' condition is stable. Conclusions: In addition to traditional chemotherapy and radiotherapy, the combined use of novel targeted therapies and early anti-HIV treatment maybe a choice to improve the prognosis of patients with AIDS-related refractory Burkitt lymphoma.

Indexed as

Acquired immunodeficiency syndrome (AIDS)Burkitt lymphomacase reportmulti-targetrefractory

Identifiers

PMID35836543
PMCPMC9273674
OpenAlexW4285542157

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.