Evidence map›Paper›PMID 33184452›Full record

ArticleBone marrow transplantation2021

Allogeneic hematopoietic stem cell transplant in rare hematologic disorders: a single center experience from Pakistan.

Maryam Khan, Raheel Iftikhar, Tariq Ghafoor, Fayyaz Hussain, Qamar Un Nisa Chaudhry, Syed Kamran Mahmood, Nighat Shahbaz, Mehreen Ali Khan, Tariq Azam Khattak, Ghassan Umair Shamshad and 7 more

Abstract read
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Article in Bone marrow transplantation, 2021. 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
0.2field-weighted citation impact, top 50% 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, 5 citations in OpenAlex.

  1. Article
  2. Therapeutic Application of mRNA for Genetic Diseases.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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

17 authors at 6 institutions in 2 countries.

Maryam KhanArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Raheel IftikharArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan. drraheeliftikhar@gmail.com.ORCID http://orcid.org/0000-0001-8767-3491
Tariq GhafoorArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.ORCID http://orcid.org/0000-0003-1279-7160
Fayyaz HussainArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Qamar Un Nisa ChaudhryArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Syed Kamran MahmoodArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Nighat ShahbazArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Mehreen Ali KhanArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Tariq Azam KhattakArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Ghassan Umair ShamshadArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Jahanzeb RehmanArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Sundas AliRawalpindi Medical University, Rawalpindi, Pakistan.
Zunaira ShahPgy-1Weiss Memorial Hospital Chicago, Chicago, IL, USA.
Abdul RafaeDepartment of Internal Medicine, McLaren Flint Michigan State University, Chicago, IL, USA.ORCID http://orcid.org/0000-0003-4113-3304
Muhammad FarhanArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Faiz AnwerTausig Cancer Center, Cleveland Clinic, Cleveland, OH, USA.
Parvez AhmedQuaid-e-Azam International Hospital, Islamabad, Pakistan.
Armed Forces Institute of Pathology · PKCleveland Clinic · USMcLaren Regional Medical Center · USRawalpindi Medical University · PKShifa International Hospital · PKWeiss Memorial Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Management of rare hematological disorders pose unique diagnostic and therapeutic challenges due to unusual occurrence and limited treatment options. We retrospectively identified 45 patients receiving matched related donor transplant for rare hematological disorders from 2006 to 2019. Patients were divided into two groups (1) malignant and (2) non malignant. The malignant disorder group included four patients while the nonmalignant group included 41 patients divided into immune dysregulation (n = 23), bone marrow failure (n = 10), metabolic (n = 5), and bleeding diathesis (n = 3). Twenty-six (57.8%) patients received myeloablative conditioning (MAC) and 16 (35.6%) received reduced intensity conditioning (RIC), while 3 (6.6%) patients with severe combined immunodeficiency received stem cell infusion alone without conditioning. The cumulative incidence (CI) of grade II-IV acute GVHD (aGVHD) was 39.1% (n = 18) and chronic GVHD (cGVHD) 15.2% (n = 7). There was no primary graft failure while CI of secondary graft failure was 9%. Overall survival (OS) and disease-free survival (DFS) was 82.2% and 77.8% respectively. Group wise OS was 75% in the malignant group, 82.6% in the immune dysregulation group, 80% in patients with metabolic disorders and bone marrow failure, while 100% in patients with bleeding diathesis. This retrospective analysis shows that hematopoietic stem cell transplant can be a feasible treatment option for rare hematological disorders.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansPakistanRetrospective StudiesTransplantation Conditioning

Identifiers

PMID33184452
OpenAlexW3099946139

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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.