Evidence map›Paper›PMID 37831432›Full record

ReviewClinical and experimental medicine2023

Evaluation of Bruton tyrosine kinase inhibitors monotherapy and combination therapy in lymphocytic leukemia.

Xiangxing Liu, Binyi Hu, Nan Peng, Liming Chen, Dingyuan Hu, Jiaojiao Zhang, Lijue Wang, Zhenwei Xie, Suping Niu, Qian Lu and 2 more

Erratum issuedAbstract readReviewNetwork Meta-Analysis
PubMed Publisher
In one paragraph

Review in Clinical and experimental medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Xiangxing LiuDepartment of Clinical Pharmacy, Xuzhou Medical University, 209 Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, China.
Binyi HuDepartment of Clinical Pharmacy, Xuzhou Medical University, 209 Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, China.
Nan Peng *Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, 100044, Beijing, China.
Liming Chen *Nursing Department, Peking University People's Hospital, 100044, Beijing, China.
Dingyuan HuClinical Trial Institution, Peking University People's Hospital, 100044, Beijing, China.
Jiaojiao ZhangDepartment of Clinical Pharmacy, Xuzhou Medical University, 209 Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, China.
Lijue WangClinical Trial Institution, Peking University People's Hospital, 100044, Beijing, China.
Zhenwei XieClinical Trial Institution, Peking University People's Hospital, 100044, Beijing, China.
Suping NiuClinical Trial Institution, Scientific Research Department, Peking University People's Hospital, 100044, Beijing, China.
Qian LuJiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, 209 Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, China.
Jin LuPeking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, 100044, Beijing, China. jin1lu@sina.com.
Yi FangClinical Trial Institution, Peking University People's Hospital, 100044, Beijing, China. phaseistudy@163.com.
Peking University People's Hospital · CNXuzhou Medical College · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BTKi is an effective treatment in chronic lymphocytic leukemia. However, head-to-head clinical trials between BTKi are rare. To explore evidence-based treatment decisions, we conducted this network meta-analysis. We searched in PubMed, Cochrane Library and Embase and selected articles of BTKi treatment in CLL patients, with English restrictions. Objective response rate (ORR), progression-free survival (PFS) and safety were outcomes. Combination therapy and acalabrutinib monotherapy achieved great ORR (greater than 80%). Combination therapy (AO and IR) also performed terrific PFS (> 80%). Compared with ibrutinib monotherapy, zanubrutinib, acalabrutinib and IR showed no significance in overall survival. Diarrhea, hypertension, cardiac events, neutropenia were common adverse events of BTKi therapy. IR had higher incidence of hypertension (0.38, 95% CI 0.28-0.48), and IU was more likely occurred cardiac events. Zanubrutinib monotherapy had lower incidence of total serious adverse reaction (0.42, 95% confidence interval (95% CI): 0.36-0.47),while ibrutinib monotherapy occurred higher adverse reactions of grade ≥ 3 (0.77, 95% CI 0.72-0.82). Although both BTKi monotherapy and combination therapy showed great efficacy, combination therapy did not display priority. Meanwhile, safety of BTKi combination therapy needs to be fully and comprehensively considered.Registration number: CRD42022378732.

Indexed as

Cardiovascular DiseasesHypertensionLeukemia, Lymphocytic, Chronic, B-CellBenzamidesHumansPyrazinesTyrosine Kinase InhibitorsacalabrutinibBenzamidesPyrazinesTyrosine Kinase InhibitorsAcalabrutinibBruton tyrosine kinase inhibitorsChronic lymphocytic leukemiaIbrutinibNetwork meta-analysis

Identifiers

PMID37831432
OpenAlexW4387599766

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.