Evidence map›Paper›PMID 40841802›Full record

ReviewImmunotherapy2025

Pure red cell aplasia due to Parvovirus B19 infection and atezolizumab: case report and literature review.

Dante Pio Pallotta, Bernardo Stefanini, Agnese Pratelli, Cristina Papayannidis, Clara Bertuzzi, Maria Boe, Francesca Girolami, Francesco Tovoli, Alessandro Granito

Abstract readCase ReportsReview
In one paragraph

Review in Immunotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Dante Pio PallottaUnit of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedalie-ro-Universitaria di Bologna, Bologna, Italy.
Bernardo StefaniniUnit of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedalie-ro-Universitaria di Bologna, Bologna, Italy.
Agnese PratelliUnit of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedalie-ro-Universitaria di Bologna, Bologna, Italy.
Cristina PapayannidisDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Clara BertuzziHaemolymphopathology Unit, IRCCS - Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Maria BoeUnit of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedalie-ro-Universitaria di Bologna, Bologna, Italy.
Francesca GirolamiDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Francesco TovoliUnit of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedalie-ro-Universitaria di Bologna, Bologna, Italy.
Alessandro GranitoUnit of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedalie-ro-Universitaria di Bologna, Bologna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The benefits of immune checkpoint inhibitor (ICI)-based treatment are tempered by immune-related adverse events (irAEs). However, various aspects of the pathogenesis of these events remain unclear. Here, we report the case of a 69-year-old patient with advanced hepatocellular carcinoma (HCC) developing severe anemia after 15 cycles of atezolizumab/bevacizumab. The initial workup based on bone marrow aspirate demonstrated selective deficiency of the erythroid line, CD8+ T-cell infiltrate, and Parvovirus B19 PCR (PVB19) positivity, suggesting a pure-red cell aplasia (PRCA) secondary to PVB19 infection. The patient received blood transfusion, intravenous immunoglobulin, and temporary atezolizumab/bevacizumab treatment interruption. After discharge, due to good clinical condition and stable Hb values, atezolizumab/bevacizumab therapy was resumed; however, after three cycles of re-treatment, a recurrence of anemia necessitating blood transfusions every 10 days and hyporeticulocytaemia was observed. The bone marrow aspirate was reassessed, and pure ICI-related red blood cell aplasia was suspected. Prednisone treatment (1 mg/kg per day) was initiated, resulting in progressive improvement of hemoglobin levels without the need for blood transfusion. After resolution of the anemia, treatment with atezolizumab was resumed without recurrence of anemia. This case highlights the potential for atezolizumab to be associated with hematological adverse events, possibly in conjunction with a PVB19 infection.

Indexed as

Antibodies, Monoclonal, HumanizedCarcinoma, HepatocellularImmune Checkpoint InhibitorsLiver NeoplasmsParvoviridae InfectionsParvovirus B19, HumanRed-Cell Aplasia, PureAgedBevacizumabHumansAntibodies, Monoclonal, HumanizedatezolizumabBevacizumabImmune Checkpoint Inhibitorsimmune checkpoint inhibitorsimmune-related adverse eventsimmunotherapyParvovirus B19Pure red cell aplasia

Identifiers

PMID40841802
PMCPMC12439566

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.