Evidence map›Paper›PMID 41203978›Full record

ArticleAnnals of hematology2025

Efficacy of venetoclax in the treatment of relapsed/refractory light-chain amyloidosis.

Xin-Yi Xiong, Ai Guan, Yi Xu, Cheng-Yang Xu, Kai-Ni Shen, Jian Li

Abstract read
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Xin-Yi XiongDepartment of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID http://orcid.org/0009-0008-9123-393X
Ai GuanDepartment of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yi XuDepartment of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Cheng-Yang XuDepartment of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Kai-Ni ShenDepartment of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. shenkaini3@sina.com.
Jian LiDepartment of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. lijian@pumch.cn.

Funding

National High Level Hospital Clinical Research Funding 2022-PUMCH-C-051National Natural Science Foundation of China 82200230National Natural Science Foundation of China 82470202Peking Union Medical College Hospital Talent Cultivation Program UHB11543Post-Marketing Clinical Research Special Program for Innovative Drugs WKZX2024CX105204
6 · The paper itself

Abstract

Few studies have reported that venetoclax, a selective BCL2 inhibitor, has shown promising efficacy in relapsed/refractory AL amyloidosis (RRAL), especially among patients harboring t(11;14). We retrospectively reviewed 29 RRAL patients treated with venetoclax between July 2022 and January 2025. Treatment was given for suboptimal prior response (45%), hematologic progression (38%), or rising involved free light chain not meeting progression criteria (17%). Venetoclax induced rapid and deep responses: 79% achieved very good partial response (VGPR) or complete response (CR), and 52% achieved stringent FLC response. High t(11;14) (> 10%) patients achieved ≥ VGPR in 91% versus 33% in low t(11;14) (p = 0.008). Cardiac responses occurred in 59% of evaluable patients. At a median follow-up of 19.7 months, one-year overall survival and event-free survival were 96.6% and 82.6%, respectively; two deaths were due to cardiac progression. Venetoclax was well tolerated, with mostly grade 1-2 adverse events, except one grade 3 leukopenia/neutropenia with grade 3 infection. These results support venetoclax as an effective and safe therapy for RRAL, particularly in t(11;14) patients, and highlight the need for prospective studies to refine patient selection and optimize treatment strategies.

Indexed as

Antineoplastic AgentsImmunoglobulin Light-chain AmyloidosisAdultAgedBridged Bicyclo Compounds, HeterocyclicFemaleHumansMaleMiddle AgedRetrospective StudiesSulfonamidesAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicSulfonamidesvenetoclaxHematologic responseLight chain amyloidosisRelapsed/refractoryT(11;14)Venetoclax

Identifiers

PMID41203978
PMCPMC12672616

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.