Evidence map›Paper›PMID 42187563›Full record

ArticleCurrent oncology (Toronto, Ont.)2026

Outcomes of Double-Hit and Single High-Risk Cytogenetic Newly Diagnosed Myeloma in Transplant-Eligible Patients.

Raeef Rahman, Anas Zayad, Carmel Awadallah, Beining Wang, Jianzheng Wu, Aroog Khaliq, Prerna Mewawalla, Shebli Atrash, Dinesh Pal Mudaranthakam, Joseph McGuirk and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Current oncology (Toronto, Ont.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

18 authors.

Raeef RahmanSchool of Medicine, University of Kansas, Kansas City, KS 66160, USA.
Anas ZayadDepartment of Internal Medicine, Hamad Medical Corporation, Doha P.O. Box 3050, Qatar.ORCID 0009-0006-7537-0112
Carmel AwadallahDivision of Internal Medicine, St John Episcopal Hospital, Far Rockaway, NY 11691, USA.
Beining WangSchool of Medicine at Shanghai Medical College, Fudan University, Shanghai 201399, China.ORCID 0009-0006-5209-4848
Jianzheng WuDivision of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS 66205, USA.
Aroog KhaliqDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Prerna MewawallaDivision of Hematology and Cellular Therapy, Allegheny Health Network Cancer Institute, Pittsburgh, PA 15224, USA.ORCID 0009-0008-7464-6898
Shebli AtrashLevine Cancer Center, Atrium Health, Wake Forest University School of Medicine, Charlotte, NC 28204, USA.ORCID 0000-0003-4547-7534
Dinesh Pal MudaranthakamDivision of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS 66205, USA.ORCID 0000-0001-9767-1158
Joseph McGuirkDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Zahra MahmoudjafariDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.ORCID 0000-0002-3168-2521
Muhammad Umair MushtaqDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Al-Ola AbdallahDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.ORCID 0000-0002-6603-185X
Nausheen AhmedDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Jordan SnyderDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Anita MazloomDivision of Hematology and Oncology, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA.ORCID 0009-0009-7899-7078
Omar AlkharabshehDivision of Hematology and Oncology, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA.ORCID 0000-0002-5299-4233
Mansi R ShahDivision of Hematology, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08901, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHigh-risk multiple myeloma (HRMM) is primarily defined by adverse cytogenetic abnormalities that are associated with inferior outcomes despite contemporary treatment with novel induction agents and autologous stem cell transplantation (ASCT). While the accumulation of high-risk lesions has been proposed to further stratify prognosis, the relative impact of single-hit versus double-hit HRMM on post-transplant outcomes in real-world clinical practice remains incompletely characterized.

methodsWe conducted a multicenter retrospective cohort study of transplant-eligible adults with HRMM undergoing upfront ASCT between 2009 and 2024 at three U.S. academic centers. Patients were categorized as single-hit HRMM or double-hit HRMM based on the number of high-risk cytogenetic abnormalities at diagnosis. Response rates, progression-free survival (PFS), and overall survival (OS) were compared between groups using standard statistical methods.

resultsA total of 154 patients were included, of whom 63 had SH-HRMM, and 91 had DH-HRMM. Following induction therapy, overall response rates (ORR) were high and comparable between groups. After ASCT, ORR was significantly higher in SH-HRMM compared with DH-HRMM (97% vs. 82%,

conclusionsIn this real-world cohort of transplant-treated HRMM, single-hit disease was associated with a higher likelihood of achieving post-ASCT response; however, no significant differences in long-term survival outcomes were observed between single-hit and double-hit HRMM. These findings suggest that cytogenetic hit burden alone may be insufficient to predict post-transplant survival, highlighting the need for refined risk stratification incorporating additional biological and response-based markers.

Indexed as

Multiple MyelomaAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesTransplantation, Autologousautologous stem cell transplantationdouble-hit cytogeneticshigh-risk multiple myelomasurvival outcomes

Identifiers

PMID42187563
PMCPMC13205681

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.