Evidence map›Paper›PMID 34461632›Full record

Trial reportBlood advances2021

Bortezomib and rituximab in de novo adolescent/adult CD20-positive, Ph-negative pre-B-cell acute lymphoblastic leukemia.

Hasmukh Jain, Manju Sengar, Vasu Babu Goli, Jayashree Thorat, Prashant Tembhare, Dhanlaxmi Shetty, V N Avinash Bonda, Lingaraj Nayak, P G Subramanian, Bhausaheb Bagal and 4 more

Open access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Minimal Residual Disease in the Management of B-Cell Acute Lymphoblastic Leukemia: A Systematic Review of Studies from Indian Settings.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2024
    Review
  4. Review
  5. Review
  6. Review
  7. 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

14 authors at 2 institutions in 2 countries.

Hasmukh JainAdult Hematolymphoid Unit, Department of Medical Oncology.ORCID 0000-0002-9947-7065
Manju SengarAdult Hematolymphoid Unit, Department of Medical Oncology.ORCID 0000-0002-3509-5682
Vasu Babu GoliDepartment of Medical Oncology.ORCID 0000-0003-2343-2503
Jayashree ThoratAdult Hematolymphoid Unit, Department of Medical Oncology.
Prashant TembhareHematopathology Laboratory, ACTREC.ORCID 0000-0002-9030-0415
Dhanlaxmi ShettyDepartment of Cytogenetics, ACTREC.
V N Avinash BondaAdult Hematolymphoid Unit, Department of Medical Oncology.
Lingaraj NayakAdult Hematolymphoid Unit, Department of Medical Oncology.ORCID 0000-0001-9520-795X
P G SubramanianHematopathology Laboratory, ACTREC.ORCID 0000-0001-9107-5937
Bhausaheb BagalAdult Hematolymphoid Unit, Department of Medical Oncology.ORCID 0000-0001-9754-0182
Nikhil PatkarHematopathology Laboratory, ACTREC.ORCID 0000-0001-9234-2857
Neha SharmaAdult Hematolymphoid Unit, Department of Medical Oncology.ORCID 0000-0002-5540-0509
Himanshi GuptaClinical Research Secretariat, Mumbai, and.
Sumeet GujralDepartment of Pathology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, Maharashtra, India.
Ashland Community and Technical College · USHomi Bhabha National Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of CD20 in precursor B-cell acute lymphoblastic leukemia (B-ALL) is associated with poor outcomes. The addition of rituximab to intensive chemotherapy in CD20+ ALL has led to improved outcomes in several studies. However, there is no clear evidence regarding the optimal number of doses and its benefit without an allogeneic stem cell transplant. Achieving measurable residual disease (MRD)-negative status postinduction would reduce the requirement for a transplant. Novel approaches are needed to induce a higher proportion of MRD-negative complete remission in patients with high-risk ALL. Given bortezomib's activity in relapsed ALL and its synergism with rituximab in B-cell lymphomas, the addition of bortezomib to rituximab and chemotherapy may provide an incremental benefit in CD20+ precursor B-ALL. We conducted a phase 2 study to test the activity of bortezomib and rituximab in combination with a pediatric-inspired regimen during induction therapy in newly diagnosed adolescents and adults (aged >14 years) with CD20+, Philadelphia-negative precursor B-ALL; bone marrow MRD negativity at the end of induction was the primary end point. From December 2017 through August 2019, a total of 35 patients were enrolled. End-of-induction MRD-negative status was achieved in 70.9% of patients, as opposed to 51.7% in the historical cohort treated with chemotherapy alone. MRD-negative rates improved to 87.5% post-consolidation. At a median follow-up of 21 months, event-free survival and overall survival rates were 78.8% (95% confidence interval, 66-94) and 78.7% (95% confidence interval, 65.8-94), respectively. There was no significant increase in toxicity with bortezomib and rituximab compared with the historical cohort. The incidence of neuropathy was 26% (all less than grade 3). The combination of bortezomib, rituximab, and a pediatric-inspired ALL regimen was active and well tolerated in de novo CD20+ Philadelphia-negative precursor B-ALL. This trial was registered with the Clinical Trials Registry-India as CTRI/2017/04/008393(http://ctri.nic.in/Clinicaltrials).

Indexed as

Lymphoma, B-CellPrecursor Cell Lymphoblastic Leukemia-LymphomaAdolescentAdultBortezomibChildHumansPrecursor Cells, B-LymphoidRituximabBortezomibRituximab

Identifiers

PMID34461632
PMCPMC8525225
OpenAlexW3197114532

What OpenQuestion 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 OpenQuestion graph.