Evidence map›Paper›PMID 35106962›Full record

Trial reportCancer medicine2022

Isatuximab monotherapy in patients with refractory T-acute lymphoblastic leukemia or T-lymphoblastic lymphoma: Phase 2 study.

Nicolas Boissel, Patrice Chevallier, Vadim Doronin, Laimonas Griskevicius, Alexey Maschan, James McCloskey, Alessandro Rambaldi, Giuseppe Rossi, Andrey Sokolov, Ulla Wartiovaara-Kautto and 5 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Cancer medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02999633 (Phase 2, Safety and Efficacy Study of Isatuximab, an Anti-CD38 Monoclonal Antibody, Administered by Intravenous), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 7% 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.

NCT02999633 phase2terminatednot on this map

Phase 2, Safety and Efficacy Study of Isatuximab, an Anti-CD38 Monoclonal Antibody, Administered by Intravenous (IV) Infusion in Patients With Relapsed or Refractory T-acute Lymphoblastic Leukemia (T-ALL) or T-lymphoblastic Lymphoma (T-LBL)

TypeinterventionalSponsorSanofiRan2017 to 2017Enrolled14ConditionsT-cell Type Acute Leukemia-Precursor, T-lymphoblastic Lymphoma/LeukaemiaArmsIsatuximab SAR650984, dexamethasone, acetaminophen, ranitidine, diphenhydramine
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Molecularly targeted therapy and immunotherapy in leukemias.Journal of hematology & oncology · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Treatment of Relapsed Acute Lymphocytic Leukemia in Adult Patients.Current treatment options in oncology · 2024
    Review
  7. Novel Biomarkers and Molecular Targets in ALL.Current hematologic malignancy reports · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. A Bright Horizon: Immunotherapy for Pediatric T-Cell Malignancies.International journal of molecular sciences · 2022
    Review
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

15 authors at 13 institutions in 7 countries.

Nicolas BoisselDepartment of Adult Hematology, Saint-Louis Hospital, Institut de Recherche Saint-Louis, University of Paris, Paris, France.
Patrice ChevallierCHU Hôtel-Dieu, Service d'Hématologie Clinique, Nantes, France.ORCID 0000-0003-3142-5581
Vadim DoroninMunicipal Clinical Hospital, Moscow, Russian Federation.
Laimonas GriskeviciusHematology, Oncology and Transfusion Medicine Center, Vilnius University Hospital Santaros Klinikos, Vilnius University, Vilnius, Lithuania.
Alexey MaschanFederal Research Center for Pediatric Hematology, Oncology, and Immunology, Moscow, Russian Federation.
James McCloskeyDivision of Leukemia, John Theurer Cancer Center at Hackensack University Medical Center, Hackensack, New Jersey, USA.
Alessandro RambaldiUniversità Statale di Milano, Milan and Azienda Socio Sanitaria Territoriale, Bergamo, Italy.
Giuseppe RossiDivisione di Ematologia, ASST Spedali Civili, Brescia, Italy.
Andrey SokolovNational Research Center for Hematology of the Russian Ministry of Health, Moscow, Russian Federation.
Ulla Wartiovaara-KauttoComprehensive Cancer Center, Department of Hematology, Helsinki University Hospital, Helsinki, Finland.
Corina OpreaSanofi, Vitry-sur-Seine, France.
Giovanni AbbadessaSanofi, Cambridge, Massachusetts, USA.
Alice GosselinSanofi, Vitry-sur-Seine, France.
Sandrine MacéSanofi, Vitry-sur-Seine, France.
Xavier ThomasHematology Department, Hospices Civils de Lyon, Lyon-Sud University Hospital, Pierre Bénite, France.
Sanofi (France) · FRAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITCentre d'Investigation Clinique de Nantes · FRCity Clinical Hospital · RUHackensack University Medical Center · USHelsinki University Hospital · FIHospices Civils de Lyon · FRMinistry of Health of the Russian Federation · RUNational Medical Research Center for Hematology · RUSanofi (United States) · USUniversité Paris Cité · FRUniversity of Milan · ITVilnius University · LT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The poor prognosis of acute T-cell lymphoblastic leukemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LBL) in older adults and patients with relapsed/refractory illness is an unmet clinical need, as there is no defined standard of care and there are few treatment options. Abnormally elevated CD38 expression in T-ALL and T-LBL is associated with tumor expansion and disease development, making CD38 a potential target for anti-T-ALL and T-LBL treatment. Isatuximab is a monoclonal antibody that binds to a specific epitope on CD38. The purpose of the study was to assess the efficacy and safety of isatuximab monotherapy in a phase 2, multicenter, one-arm, open-label study in patients with relapsed or refractory T-ALL or T-LBL (Clinical Trials.gov identifier NCT02999633). The primary endpoint was to assess the efficacy of isatuximab by overall response rate (ORR). An interim analysis based on the efficacy and safety of isatuximab in the first 19 patients enrolled was scheduled, however only 14 patients were enrolled in the study. No patient achieved complete response (CR) or CR with incomplete peripheral recovery. Most patients (11 [78.6%]) developed progressive disease and had progressive disease as their best response. A total of 10 (71.4%) patients had treatment emergent adverse events considered treatment-related, with infusion reactions as the most frequent drug-related TEAE, occurring in 8 (57.1%) patients. Despite the low efficacy of isatuximab in the current study, it is likely that the use of immunotherapy medication in T-ALL will be expanded through logically targeted approaches, together with advances in the design of T-cell therapy and clinical experience and will provide restorative options beyond chemotherapy and targeted treatments.

Indexed as

Antibodies, Monoclonal, HumanizedLymphoma, Non-HodgkinPrecursor T-Cell Lymphoblastic Leukemia-LymphomaAgedHumansAntibodies, Monoclonal, Humanizedisatuximabacute lymphoblastic leukemiaisatuximabmonoclonal antibodiesmonotherapyT lymphoblastic lymphoma

Identifiers

PMID35106962
PMCPMC8894690
OpenAlexW4210247426

What OpenQuestion holds

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Registered trials

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.