Evidence map›Paper›PMID 33031541›Full record

ArticleBlood advances2020

Safety of venetoclax rapid dose escalation in CLL patients previously treated with B-cell receptor signaling antagonists.

Kristin L Koenig, Ying Huang, Emily K Dotson, Shane Sheredy, Seema A Bhat, John C Byrd, Emily Desmond, Jill Ford, Shauna Iarocci, Jeffrey A Jones and 6 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.8field-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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Review
  8. Treatment with Venetoclax for Chronic Lymphocytic Leukemia with the Highest Known White Blood Cell Count: Safe and EffectiveTurkish journal of haematology : official journal of Turkish Society of Haematology · 2021
    Article
  9. 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

16 authors at 2 institutions in 1 country.

Kristin L KoenigDivision of Hematology and.
Ying HuangDivision of Hematology and.
Emily K DotsonDepartment of Pharmacy, The Ohio State University, Columbus, OH; and.
Shane SheredyDepartment of Pharmacy, The Ohio State University, Columbus, OH; and.
Seema A BhatDivision of Hematology and.
John C ByrdDivision of Hematology and.
Emily DesmondDivision of Hematology and.
Jill FordDivision of Hematology and.
Shauna IarocciDivision of Hematology and.
Jeffrey A JonesDivision of Hematology and.
Margaret S LucasDivision of Hematology and.
Mollie E MoranDivision of Hematology and.
Tracy E WiczerDepartment of Pharmacy, The Ohio State University, Columbus, OH; and.
Jennifer A WoyachDivision of Hematology and.
Farrukh T AwanDivision of Hematology and Oncology, University of Texas Southwestern Medical Center, Dallas, TX.
Kerry A RogersDivision of Hematology and.
The Ohio State University · USThe University of Texas Southwestern Medical Center · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
NCI NIH HHS P30 CA016058
6 · The paper itself

Abstract

Venetoclax has efficacy in patients relapsing after B-cell receptor pathway inhibitors (BCRis); however, because of the risk of tumor lysis syndrome (TLS), a 5-week dose ramp-up is required to attain the target dose. Patients relapsing after BCRis frequently have proliferative disease, requiring a faster time to target dose than this scheme allows. This limitation can potentially be overcome with rapid dose escalation (RDE). We analyzed 33 chronic lymphocytic leukemia patients who underwent venetoclax RDE after prior BTKi treatment. Median time to target dose was 9 days. Seventeen patients (52%) developed laboratory TLS, and 5 (15%) developed clinical TLS, all as a result of renal injury. TLS was seen in more patients with a higher initial tumor burden. TLS occurred at all dose levels, with most episodes occurring at the 50- and 100-mg doses. Most interestingly, a decrease in absolute lymphocyte count (ALC) from pre-venetoclax dose to 24 hours post-venetoclax dose of 10 × 103/μL was associated with an increased risk of TLS (hazard ratio, 1.32; P = .02), after controlling for venetoclax dose level. Venetoclax RDE with close in-hospital monitoring at experienced centers and in select patients is feasible. The rapidity with which ALC drops helps predict TLS and could help guide dose-escalation decisions.

Indexed as

Antineoplastic AgentsLeukemia, Lymphocytic, Chronic, B-CellBridged Bicyclo Compounds, HeterocyclicHumansReceptors, Antigen, B-CellSulfonamidesAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicReceptors, Antigen, B-CellSulfonamidesvenetoclax

Identifiers

PMID33031541
PMCPMC7556146
OpenAlexW3092565633

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.