Evidence map›Paper›PMID 32227210›Full record

ArticleBlood advances2020

Checkpoint inhibition before haploidentical transplantation with posttransplant cyclophosphamide in Hodgkin lymphoma.

Chiara De Philippis, Faezeh Legrand-Izadifar, Stefania Bramanti, Laura Giordano, Catalina Montes de Oca, Rémy Duléry, Reda Bouabdallah, Angela Granata, Raynier Devillier, Jacopo Mariotti and 13 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Allogeneic Hematopoietic Cell Transplantation for Relapsed/Refractory Hodgkin Lymphoma: A Multicenter Real-World ExperienceTurkish journal of haematology : official journal of Turkish Society of Haematology · 2026
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  7. When to use stem cell transplantation for classical Hodgkin lymphoma.Hematology. American Society of Hematology. Education Program · 2024
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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

23 authors at 4 institutions in 2 countries.

Chiara De PhilippisDepartment of Hematology, Humanitas Clinical and Research Center-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rozzano, Italy.
Faezeh Legrand-IzadifarDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Stefania BramantiDepartment of Hematology, Humanitas Clinical and Research Center-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rozzano, Italy.
Laura GiordanoBiostatistic Unit, Humanitas Clinical and Research Center-IRCCS, Rozzano, Italy; and.
Catalina Montes de OcaDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Rémy DuléryDepartment of Hematology, Hospital Saint-Antoine, Paris, France.
Reda BouabdallahDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Angela GranataDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Raynier DevillierDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Jacopo MariottiDepartment of Hematology, Humanitas Clinical and Research Center-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rozzano, Italy.
Barbara SarinaDepartment of Hematology, Humanitas Clinical and Research Center-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rozzano, Italy.
Samia HarbiDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Valerio MaisanoDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Sabine FurstDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Thomas PagliardiniDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Pierre-Jean WeillerDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Claude LemarieDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Boris CalmelsDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Christian ChabannonDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Armando SantoroDepartment of Hematology, Humanitas Clinical and Research Center-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rozzano, Italy.
Mohamad MohtyDepartment of Hematology, Hospital Saint-Antoine, Paris, France.
Didier BlaiseDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Luca CastagnaDepartment of Hematology, Humanitas Clinical and Research Center-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rozzano, Italy.
Institut Paoli-Calmettes · FRIstituti di Ricovero e Cura a Carattere Scientifico · ITSorbonne Université · FRHumanitas University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report on 59 Hodgkin lymphoma patients undergoing haploidentical stem cell transplantation (SCT; haplo-SCT) with posttransplant cyclophosphamide (PTCy) as graft-versus-host disease (GVHD) prophylaxis, comparing outcomes based on pretransplant exposure to checkpoint inhibitors (CPIs). Considering pretransplant characteristics, the 2 cohorts (CPI = 29 patients vs no-CPI = 30 patients) were similar, except for the number of prior lines of therapy (6 vs 4; P < .001). With a median follow-up of 26 months (range, 7.5-55 months), by univariate analysis, the 100-day cumulative incidence of grade 2-4 acute GVHD was 41% in the CPI group vs 33% in the no-CPI group (P = .456), whereas the 1-year cumulative incidence of moderate to severe chronic GVHD was 7% vs 8%, respectively (P = .673). In the CPI cohort, the 2-year cumulative incidence of relapse appeared lower compared with the no-CPI cohort (0 vs 20%; P = .054). No differences were observed in terms of overall survival (OS), progression-free survival (PFS), and nonrelapse mortality (NRM) (at 2 years, 77% vs 71% [P = .599], 78% vs 53% [P = .066], and 15% vs 21% [P = .578], respectively). By multivariable analysis, CPI before SCT was an independent protective factor for PFS (hazard ratio [HR], 0.32; P = .037). Stable disease (SD)/progressive disease (PD) was an independent negative prognostic factor for both OS and PFS (HR, 14.3; P < .001 and HR, 14.1; P < .001, respectively) . In conclusion, CPI as a bridge to haplo-SCT seems to improve PFS, with no impact on toxicity profile.

Indexed as

Graft vs Host DiseaseHodgkin DiseaseCyclophosphamideHumansNeoplasm Recurrence, LocalTransplantation, HaploidenticalCyclophosphamide

Identifiers

PMID32227210
PMCPMC7160255
OpenAlexW3013641988

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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.