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ArticleScientific reports2024

HALP score as a novel prognostic factor for patients with myelodysplastic syndromes.

Vildan Gursoy, Sevil Sadri, Hatice Demirci Kucukelyas, Fazıl Cagri Hunutlu, Ibrahim Ethem Pinar, Zafer Serenli Yegen, Nihan Alkış, Tuba Ersal, Ridvan Ali, Vildan Ozkocaman and 1 more

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

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12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Vildan GursoyDepartment of Hematology, Bursa City Hospital, Bursa, Turkey. vildanterzioglu@hotmail.com.ORCID 0000-0002-3645-9345
Sevil SadriDepartment of Hematology, Bursa City Hospital, Bursa, Turkey.
Hatice Demirci KucukelyasDepartment of Internal Medicine, Bursa City Hospital, Bursa, Turkey.
Fazıl Cagri HunutluDepartment of Hematology, Uludag University Medical Faculty, Bursa, Turkey.
Ibrahim Ethem PinarDepartment of Hematology, Isparta City Hospital, Isparta, Turkey.
Zafer Serenli YegenDepartment of Hematology, Bursa City Hospital, Bursa, Turkey.
Nihan AlkışDepartment of Hematology, Bursa City Hospital, Bursa, Turkey.
Tuba ErsalDepartment of Hematology, Uludag University Medical Faculty, Bursa, Turkey.
Ridvan AliDepartment of Hematology, Uludag University Medical Faculty, Bursa, Turkey.
Vildan OzkocamanDepartment of Hematology, Uludag University Medical Faculty, Bursa, Turkey.
Fahir OzkalemkasDepartment of Hematology, Uludag University Medical Faculty, Bursa, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelodysplastic syndrome (MDS) is a heterogeneous spectrum of clonal hematopoietic disorders with varying degrees of cytopenia and morphologic dysplasia. The hemoglobin, albumin, lymphocyte, and platelet (HALP) score is a prognostic marker in several types of malignant tumors. Prognostic value of HALP score remains unclear for MDS. To determine the prognostic value of baseline HALP score in MDS. We retrospectively analyzed data from 130 newly diagnosed MDS patients evaluated and classified under HALP score. By the receiver operating characteristic (ROC) analysis, the optimal cut-off value of HALP was > 67.5 in predicting mortality. Patients were divided into two groups: with low and high HALP scores, and the characteristics were compared between both groups. Patients' median age was 68 (19-84) years, and 79 (60.8%) were male. Higher HALP score was detected in MDS patients with intermediate-risk under IPSS score, and at high and very high risks under IPSS-R score, and those receiving azacitidine (AZA) treatment. The survival rates of those with a HALP score > 67.5 were significantly lower than those with low HALP score at 17.77 ± 3.98 (median ± SE) (p < 0.001). The 3-, 5- and 10-years survival rates of individuals with HALP scores > 67.5 were found as 25, 18, and 11%, respectively. Median overall survival (OS) was also determined as 33.10 (95% CI 16.34-49.88) months by the Kaplan-Meier method. HALP score has shown an ability to be a useful prognostic biomarker in various cancers, including MDS. The meaningful cut-off value of HALP is disease-specific and largely study-specific. High HALP score is associated with unfavorable clinicopathological characteristics. Also, it may be useful in predicting OS and mortality of MDS.

Indexed as

Myelodysplastic SyndromesAdultAgedAged, 80 and overBlood PlateletsFemaleHemoglobinsHumansLymphocytesMaleMiddle AgedPlatelet CountPrognosisRetrospective StudiesROC CurveYoung AdultHemoglobinsAlbuminHemoglobinLymphocyteMyelodysplastic syndromePlateletPrognostic factor

Identifiers

PMID38879594
PMCPMC11180126

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