Evidence map›Paper›PMID 42394711›Full record

ArticleFrontiers in oncology2026

Real-world effectiveness and safety of carfilzomib, pomalidomide, and dexamethasone in relapsed/refractory multiple myeloma: a retrospective analysis from China.

Wei Jiang, Wei Zhong, Jingdi Yu, Yufei Tang, Qunyi Guo

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. 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

5 authors.

Wei JiangDepartment of Hematology, Shangyu People's Hospital of Shaoxing, Shaoxing, China.
Wei ZhongDepartment of Hematology, Shangyu People's Hospital of Shaoxing, Shaoxing, China.
Jingdi YuDepartment of Hematology, Shangyu People's Hospital of Shaoxing, Shaoxing, China.
Yufei TangDepartment of Hematology, Shangyu People's Hospital of Shaoxing, Shaoxing, China.
Qunyi GuoDepartment of Hematology, Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, Linhai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pomalidomide, a next-generation immunomodulatory drug (IMiD), and carfilzomib, a novel proteasome inhibitor (PI), have been separately approved in combination regimens for relapsed/refractory multiple myeloma (RRMM). However, real-world data, particularly for Chinese RRMM patients with prior-line treatment, including lenalidomide and bortezomib, remain limited. Methods: We retrospectively analyzed RRMM patients treated with KPd between October 2022 and December 2024 at two Chinese centers. Results: This study included 34 patients who received KPd. The median age was 65 years. All patients were bortezomib-exposed, 91.2% were lenalidomide-exposed (and refractory), and 50.0% were daratumumab-exposed. The overall response rate (ORR) was 82.4% and was significantly influenced by high-risk cytogenetics, prior daratumumab exposure, and the receipt of ≥ 3 prior lines of therapy. The median progression-free survival (PFS) was 13 months, with a 2-year PFS rate of 40.3%. Hematologic toxicities were the most common adverse events (AEs) (73.5%), and grade 3/4 AEs occurred in 58.8% of patients. Conclusions: KPd exhibited substantial effectiveness in this real-world cohort of heavily pretreated Chinese RRMM patients, including those with lenalidomide-refractory disease. However, the high incidence of hematologic toxicities necessitates careful monitoring and management.

Indexed as

carfilzomibdexamethasonemultiple myelomapomalidomidereal-world

Identifiers

PMID42394711
PMCPMC13322894

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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.