Evidence map›Paper›PMID 36585459›Full record

ArticleBone marrow transplantation2023

Reduced post-transplant cyclophosphamide doses in haploidentical hematopoietic cell transplantation for elderly patients with hematological malignancies.

Rémy Duléry, Claire Goudet, Daniele Mannina, Antonio Bianchessi, Angela Granata, Samia Harbi, Valerio Maisano, Christian Chabannon, Florent Malard, Eolia Brissot and 11 more

Abstract read
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In one paragraph

Article in Bone marrow transplantation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
9.6field-weighted citation impact, top 1% 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

31 citing papers in PubMed, 61 citations in OpenAlex.

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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

21 authors at 7 institutions in 2 countries.

Rémy DuléryDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France. remy.dulery@aphp.fr.ORCID 0000-0002-5024-1713
Claire GoudetTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli Calmettes, Marseille, France.
Daniele ManninaDepartment of Hematology - Bone Marrow Transplant and Cell Therapy Unit, IRCSS Humanitas Clinical and Research Center, Milan, Italy.
Antonio BianchessiDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Angela GranataTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli Calmettes, Marseille, France.
Samia HarbiTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli Calmettes, Marseille, France.
Valerio MaisanoTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli Calmettes, Marseille, France.
Christian ChabannonCell Therapy Unit, Institut Paoli Calmettes, Marseille, France.ORCID 0000-0002-3755-4889
Florent MalardDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Eolia BrissotDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.ORCID 0000-0003-4471-418X
Simona SestiliDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Anne BanetDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Zoé Van de WyngaertDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Ramdane BelhocineDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Stéphane EderhyDepartment of Cardiology, UNICO - GRECO cardio oncology Program, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Luca CastagnaBone Marrow Unit, Ospedale Villa Sofia Cervello, Palermo, Italy.
Stefania BramantiDepartment of Hematology - Bone Marrow Transplant and Cell Therapy Unit, IRCSS Humanitas Clinical and Research Center, Milan, Italy.
Didier BlaiseTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli Calmettes, Marseille, France.ORCID 0000-0002-5684-9447
Mohamad MohtyDepartment of Clinical Hematology and Cellular Therapy, Sorbonne University, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.ORCID 0000-0002-7264-808X
Sabine FürstTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli Calmettes, Marseille, France.
Raynier DevillierTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli Calmettes, Marseille, France.ORCID 0000-0002-4045-8310
Inserm · FRInstitut Paoli-Calmettes · FRAix-Marseille Université · FRSorbonne Université · FRHumanitas University · ITOspedale Vincenzo Cervello · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although post-transplant cyclophosphamide (PT-Cy) is effective for graft-versus-host disease (GVHD) prophylaxis, it is associated with toxicities, which might be dose-dependent. We compared the outcomes with PT-Cy at 80 mg/kg to those with PT-Cy at 100 mg/kg in elderly patients undergoing haploidentical hematopoietic cell transplantation (HCT). Inclusion criteria included peripheral blood stem cells, hematological malignancy, and age>65 years (or age>60 years if cardiac event history). Thirty-eight patients received PT-Cy at 80 mg/kg and 55 100 mg/kg, divided in two doses. The cumulative incidences (CI) of acute grade II-IV, acute grade III-IV, and moderate/severe chronic GVHD were 32%, 16%, and 13% with PT-Cy at 80 mg/kg compared to 33%, 13%, and 16% with 100 mg/kg, respectively. In multivariable analysis, reducing PT-Cy dose had no significant impact on GVHD. Neutrophil and platelet engraftments were significantly improved, and CI of BK virus-associated hemorrhagic cystitis was reduced with 80 mg/kg of PT-Cy compared to 100 mg/kg. At 2 years, non-relapse mortality was 16% and 31%, progression-free survival 65% and 49%, overall survival 70% and 56%, and GVHD-free, relapse-free survival 52% and 36% with 80 mg/kg and 100 mg/kg, respectively. Reducing PT-Cy dose to 80 mg/kg is safe and associated with improved hematological recovery and lower CI of hemorrhagic cystitis in elderly patients undergoing haploidentical HCT.

Indexed as

Graft vs Host DiseaseHematologic NeoplasmsHematopoietic Stem Cell TransplantationAgedCyclophosphamideHumansMiddle AgedNeoplasm Recurrence, LocalTransplantation ConditioningCyclophosphamide

Identifiers

PMID36585459
OpenAlexW4313454993

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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.