Evidence map›Paper›PMID 26133724›Full record

ArticleLeukemia & lymphoma2016

Radioimmunotherapy consolidation using 131I-tositumomab for patients with chronic lymphocytic leukemia or small lymphocytic lymphoma in first remission.

Mazyar Shadman, Ajay K Gopal, Britt Kammerer, Pamela S Becker, David G Maloney, Barbara Pender, Andrei R Shustov, Oliver W Press, John M Pagel

Abstract read
In one paragraph

Article in Leukemia & lymphoma, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Maintenance therapy for chronic lymphocytic leukaemia.The Cochrane database of systematic reviews · 2024
    Review
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Mazyar Shadmana Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
Ajay K Gopala Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
Britt Kammerera Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
Pamela S Beckerb Department of Medicine , University of Washington , Seattle , WA , USA.
David G Maloneya Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
Barbara Pendera Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
Andrei R Shustovb Department of Medicine , University of Washington , Seattle , WA , USA.
Oliver W Pressa Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
John M Pagela Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

TREATMENT OF B-CELL LYMPHOMAP01CA044991 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BALDWIN, JANELL · 1988 to 2015
$29.3M
RESEARCH TRAINING IN HEMATOLOGYT32HL007093 · NHLBI · UNIVERSITY OF WASHINGTON · PI Janis L Abkowitz · 1985 to 2026
$13.9M
NCI NIH HHS P01 CA044991NHLBI NIH HHS T32 HL007093
6 · The paper itself

Abstract

Despite initial responses to chemoimmunotherapy, relapse and minimal residual disease (MRD) remain major issues in treatment of chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) patients. We administered (131)I-tositumomab to patients in complete response (CR) or partial response (PR) after induction chemotherapy. Toxicities and rate of PR to CR conversion and MRD elimination were assessed three months later. The study stopped prematurely after enrolling 16 patients. Four (25%) were in CR, 12 (75%) in PR, and 12 (75%) had MRD. Three months after treatment with (131)I-tositumomab, CR was achieved (n = 8; 50%) or sustained (n = 4; 25%) in 12 patients and MRD was eliminated in four of 12 patients (33%). Hematologic toxicities were anemia in one patient (6%), neutropenia in 13 (81%), and thrombocytopenia in eight (50%). Two patients (12%) developed MDS 17 and 20 months after consolidation. Consolidation with (131)I-tositumomab for CLL/SLL patients in first remission is feasible and may provide the benefit of converting PR to CR and/or eliminating MRD.

Indexed as

RadioimmunotherapyAdultAgedAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsBiomarkersChromosome AberrationsCombined Modality TherapyDrug Administration ScheduleFemaleHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedMutationNeoplasm StagingAntibodies, MonoclonalBiomarkerstositumomab I-131131I-tositumomabCLLconsolidationminimal residual diseaseradioimmunotherapySLL

Identifiers

PMID26133724
PMCPMC4798884
OpenAlexW1886101999

What OpenQuestion holds

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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.