Evidence map›Paper›PMID 36387650›Full record

ArticleJournal of family medicine and primary care2022

Clinical spectrum and treatment response in patient of chronic myeloid leukemia in correlation with ABO blood group.

Mukti P Meher, Saumya Gupta, Arun Kumar Singh, Prabhat Kumar, Sandeep Kumar, Amar Kumar Amrit, Disha Arora, Anju Bharti, Sandip Kumar, Lalit Prashant Meena

Open access · goldAbstract read
In one paragraph

Article in Journal of family medicine and primary care, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
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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

10 authors at 2 institutions in 1 country.

Mukti P MeherDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Saumya GuptaDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Arun Kumar SinghDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Prabhat KumarDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Sandeep KumarDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Amar Kumar AmritDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Disha AroraDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Anju BhartiDepartment of Pathology, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Sandip KumarDepartment of Pathology, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Lalit Prashant MeenaDepartment of General Medicine, Institute of Medical Sciences Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Banaras Hindu University · INInstitute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Several studies have been conducted to evaluate and investigate the molecular mechanisms underlying alterations in ABO blood group antigens in oncogenesis. We observed that no study has been reported yet that correlate cytological, molecular and haematological responses of Imatinib therapy in chronic myeloid leukemia (CML) patients with different types of blood groups. Objective: To determine the distribution of CML in the ABO blood group, clinical spectrum of CML in different blood groups, and treatment response of CML patients in correlation with ABO and Rh blood groups. Material and Methods: All the patients included in the study were diagnosed on the basis of clinical features, peripheral smears and bone marrow aspiration findings. Real-time reverse transcriptase polymerase chain reaction (PCR) and cytogenetic analysis were done in all patients at the time of initiation of therapy. Blood grouping and Rh typing of each patient were done at the initiation of therapy. Results: Out of 100 included patients, 58 were male and 42 were female patients. It was observed that 45 (45%) patients were having a B+ blood group; 33% patients were having O+ blood group, followed by A+ (10%), AB+ (8%), A- (2%), B- (1%) and AB- (1%). Around 43.64% study subjects with O + blood groups showed complete cytogenetic response, followed by B+ (41.82%), A+ (10.91), A- (1.82) and AB+ (1.82). An equal number of patients (40% each) with O+ and B+ blood groups, followed by A+ (20%) showed undetectable Abelson-breakpoint cluster region (BCR-ABL)/ratio (%). About 75% of patients showed complete haematological response (CHR) and 25% showed PHR. Patients with B+ and O+ blood groups (41.33%) showed a CHR. It was observed that a maximum number of patients were suffering from symptoms of an abdominal mass (37%), 43.24% of patients with B+ blood group showed an abdominal mass, followed by O+ (35.13%), A+ and AB+ (8.11% each), B - and AB- (2.70% each). Conclusion: This study revealed that study subjects with B+ and O+ blood groups showed better cytogenetic, molecular and haematological responses as compared with patients with other blood groups at 6 and 12 months of treatment with Imatinib.

Indexed as

ABO Blood groupCMLImatinib

Identifiers

PMID36387650
PMCPMC9648264
OpenAlexW4289210935

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.