Evidence map›Paper›PMID 35911683›Full record

ArticleFrontiers in immunology2022

Case Report: Subtotal Lymphoid and Total Marrow Irradiation as Bridge Therapy to CD19-Directed CAR T Cells in a Chemorefractory DLBCL With Leukemic Involvement.

Simonetta Saldi, Vincenzo Maria Perriello, Lorenza Falini, Loredana Ruggeri, Christian Fulcheri, Sara Ciardelli, Alessandra Innocente, Stelvio Ballanti, Nicodemo Baffa, Leonardo Flenghi and 3 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

13 authors at 2 institutions in 1 country.

Simonetta SaldiRadiation Oncology Section, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
Vincenzo Maria PerrielloHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Lorenza FaliniHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Loredana RuggeriHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Christian FulcheriHealth Physics Department, Ospedale S. Maria della Misericordia, Perugia, Italy.
Sara CiardelliHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Alessandra InnocenteHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Stelvio BallantiHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Nicodemo BaffaNuclear Medicine, Ospedale S. Maria della Misericordia, Perugia, Italy.
Leonardo FlenghiHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Antonio PieriniRadiation Oncology Section, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
Cynthia AristeiHematology Section, Department of Medicine and Surgery, Center for Hemato-Oncological Research, University of Perugia, Perugia, Italy.
Brunangelo FaliniRadiation Oncology Section, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
University of Perugia · ITOspedale Santa Maria · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CAR T cell therapy has transformed the salvage approach for relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). Maintaining disease control before CAR T cell infusion during product manufacturing (so-called bridging therapy) is an important step to optimizing outcome. Among possible bridging therapies, radiation therapy (RT) represents a valuable option, particularly when the disease is limited. Here, we report for the first time on a patient with chemorefractory-transformed DLBCL showing nodal, extranodal, and massive bone marrow (BM) lymphoma infiltration associated with leukemic involvement, a successful bridge therapy to CD19-directed CAR T cell therapy by subtotal lymphoid/total marrow irradiation plus thiothepa followed by reinfusion of CD34+ autologous hematopoietic stem cells. Such a novel bridging regimen allowed a significant reduction of nodal and BM tumor volume while improving blood cell count before CAR T cell infusion. The PET-CT scan and BM evaluation performed at 1, 3, and 6 months after treatment showed complete remission of the disease. A relapse occurred at almost 1 year in lymph nodes because of CD19 antigen escape while the BM remained free of disease. This extended radiotherapy approach may be an effective bridging therapy for chemorefractory DLBCL patients eligible for CAR T cells who present with a high tumor burden, including massive BM involvement associated with leukemic involvement. This preliminary evidence is worth confirming in additional patients.

Indexed as

Bone MarrowLymphoma, Large B-Cell, DiffuseAntigens, CD19HumansNeoplasm Recurrence, LocalPositron Emission Tomography Computed TomographyT-LymphocytesAntigens, CD19bridge therapyCAR (chimeric antigen receptor) T cellsdiffuse large B-cell lymphomagene therapyradiotherapy

Identifiers

PMID35911683
PMCPMC9330448
OpenAlexW4285387047

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.