Evidence map›Paper›PMID 38790976›Full record

ArticleBiomedicines2024

Exploring the Impact of Cytogenetic Abnormalities on Treatment Responses and Survival Outcomes in Multiple Myeloma: A Single-Centre Experience of 13 Years of Follow-Up.

Mehmet Ali Kazgı, Ertugrul Bayram, Tolga Kosecı, Burak Mete, Tugba Toyran, Melek Ergin, Ismail Oguz Kara

Abstract read
In one paragraph

Article in Biomedicines, 2024. 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. 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

7 authors.

Mehmet Ali KazgıDepartment of Internal Medicine, Faculty of Medicine, Cukurova University, Adana 01250, Turkey.
Ertugrul BayramDepartment of Medical Oncology, Faculty of Medicine, Cukurova University, Adana 01250, Turkey.ORCID 0000-0001-8713-7613
Tolga KosecıDepartment of Medical Oncology, Faculty of Medicine, Cukurova University, Adana 01250, Turkey.
Burak MeteDepartment of Public Health, Faculty of Medicine, Cukurova University, Adana 01250, Turkey.ORCID 0000-0002-0780-6176
Tugba ToyranDepartment of Medical Pathology, Faculty of Medicine, Cukurova University, Adana 01250, Turkey.
Melek ErginDepartment of Medical Pathology, Faculty of Medicine, Cukurova University, Adana 01250, Turkey.
Ismail Oguz KaraDepartment of Medical Oncology, Faculty of Medicine, Cukurova University, Adana 01250, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: The introduction of novel therapies has led to a considerable evolution in the management of Multiple Myeloma, and chromosomal abnormalities predict the success of treatment. We aimed to characterize cytogenetic abnormalities for risk stratification in the patient population and to evaluate the predictive and prognostic value of the specified abnormalities in distinct treatment modalities. (2) Methods: This study included patients with Multiple Myeloma who applied to the Internal Medicine Clinic of the Cukurova University Faculty of Medicine. Between 2010 and 2023, 98 cases with cytogenetic abnormality data were identified. We analysed the effects of cytogenetic abnormalities on survival and response rates to first chemotherapies. (3) Results: P53 del was the most prevalent abnormality, and t(11;14) was the most common translocation. There was no significant difference in the mean survival and treatment response rates for specific cytogenetic abnormalities. When chemotherapies based on lenalidomide were initiated, patients' life-death statuses differed significantly from those of treatments without lenalidomide. Regardless of the type of chromosomal aberration, lenalidomide-based treatments independently enhanced average survival 14-fold, while there was no significant difference in overall survival among treatments. (4) Conclusions: In individuals with cytogenetic abnormalities, lenalidomide-based treatments should be started regardless of the chemotherapy to be used for the condition.

Indexed as

cytogenetic abnormalitiesimmunomodulatorsmultiple myeloma

Identifiers

PMID38790976
PMCPMC11117921

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