Evidence map›Paper›PMID 35123433›Full record

ArticleBMC cancer2022

Real world risk of infusion reactions and effectiveness of front-line obinutuzumab plus chlorambucil compared with other frontline treatments for chronic lymphocytic leukemia.

Nicole Bourrier, Ivan Landego, Oliver Bucher, Mandy Squires, Erin Streu, Irena Hibbert, Theresa Whiteside, Spencer B Gibson, Marc Geirnaert, James B Johnston and 2 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in BMC cancer, 2022. 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
0.8field-weighted citation impact, top 29% 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, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
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

12 authors at 2 institutions in 1 country.

Nicole BourrierMax Rady College of Medicine, 727 McDermot Ave, Winnipeg, MB, R3E 3P5, Canada.
Ivan LandegoDepartment of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, 727 McDermot Ave, Winnipeg, MB, R3E 3P5, Canada.
Oliver BucherDepartment of Epidemiology, CancerCare Manitoba, 675 McDermot Ave, Winnipeg, MB, R3E 0V9, Canada.
Mandy SquiresCancerCare Manitoba Research Institute, 675 McDermot Ave, Winnipeg, MB, R3E 0V9, Canada.
Erin StreuDepartment of Nursing, CancerCare Manitoba, 675 McDermot Ave, Winnipeg, MB, R3E 0V9, Canada.
Irena HibbertDepartment of Nursing, CancerCare Manitoba, 675 McDermot Ave, Winnipeg, MB, R3E 0V9, Canada.
Theresa WhitesideDepartment of Nursing, CancerCare Manitoba, 675 McDermot Ave, Winnipeg, MB, R3E 0V9, Canada.
Spencer B GibsonCancerCare Manitoba Research Institute, 675 McDermot Ave, Winnipeg, MB, R3E 0V9, Canada.
Marc GeirnaertProvincial Oncology Drug Program, CancerCare Manitoba, 675 McDermot Ave, Winnipeg, MB, R3E 0V9, Canada.
James B JohnstonDepartment of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, 727 McDermot Ave, Winnipeg, MB, R3E 3P5, Canada.
David E DaweDepartment of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, 727 McDermot Ave, Winnipeg, MB, R3E 3P5, Canada.
Versha BanerjiMax Rady College of Medicine, 727 McDermot Ave, Winnipeg, MB, R3E 3P5, Canada. vbanerji@cancercare.mb.ca.
CancerCare Manitoba · CAUniversity of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic lymphocytic leukemia (CLL) is the most common type of leukemia in North America. Previous studies have shown improved progression free survival (PFS) and response rates in unfit patients treated with obinutuzumab compared to other regimens. The aim of this study was to evaluate the obinutuzumab-chlorambucil regimen in the context of historical treatments and first-dose infusion reactions at CancerCare Manitoba (CCMB).

methodsA retrospective chart review was conducted for patients treated with obinutuzumab from January 1, 2014 to December 31, 2017 at CCMB. A minimum data set was extracted for patients treated with other front-line therapies. Descriptive statistics were used to evaluate patient demographics, toxicity, duration and dosing of obinutuzumab treatment. Kaplan-Meier curves were used to evaluate time-to-next-treatment (TTNT), overall survival (OS) and PFS for patients treated with obinutuzumab. A multivariable logistic regression model was used to investigate associations between infusion related reactions (IRRs) and age at treatment, pre-treatment lymphocyte count, cumulative illness rating scale (CIRS) and receipt of prior chemotherapy.

resultsForty seven percent of patients receiving frontline therapy received chlorambucil and obinutuzumab. Sixty-seven patients were treated with obinutuzumab and consisted of 36 males (53.7%) and 31 females (46.3%) with 29 patients (43.3%) over age 75 years. Rates of grade 3 and 4 obinutuzumab IRRs were lower (6%) compared to the CLL11 clinical trial (20%) due to local practices including slower infusion rates and using chlorambucil before starting obinutuzumab treatment. Many patients had difficulty tolerating the full dosage of chlorambucil. Only 26 patients (38.8%) had their dose of chlorambucil escalated to the full dose of 0.5 mg/kg. In addition, only 18 patients (26.9%) received all doses of obinutuzumab and all 12 doses of chlorambucil.

conclusionsIn summary, first dose infusion reactions with obinutuzumab can be markedly reduced by using chlorambucil to decrease the lymphocyte count before obinutuzumab and by using a very slow initial obinutuzumab infusion rate. Modifications in chlorambucil dosing and obinutuzumab administration can improve tolerance without significant loss in efficacy.

Indexed as

AgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsChlorambucilFemaleHumansInjection Site ReactionLeukemia, Lymphocytic, Chronic, B-CellMaleManitobaMiddle AgedRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedChlorambucilobinutuzumabChronic lymphocytic leukemiaCLLFront-line therapyObinutuzumabRetrospective cohort study

Identifiers

PMID35123433
PMCPMC8818183
OpenAlexW4210796934

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.