Evidence map›Paper›PMID 42440648›Full record

ArticleCureus2026

Non-cryopreserved Autologous Peripheral Blood Stem Cell Transplantation for Lymphoma in a Resource-Limited Setting: Feasibility, Engraftment Kinetics, and Early Outcomes From Kashmir, India.

Mohmad Hussain Mir, Suhail Ahmad Wani, Sheikh Muzamil Manzoor, Ajas Ibrahim, Farhana Siraj, Nisar Ahmad Syed, Faisal R Guru, Zeeza H Shah, Jaskaran Singh Sarao, Abrar Rasool and 11 more

Abstract read
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Mohmad Hussain MirDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Suhail Ahmad WaniDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Sheikh Muzamil ManzoorDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Ajas IbrahimDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Farhana SirajDepartment of Internal Medicine, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Nisar Ahmad SyedDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Faisal R GuruDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Zeeza H ShahDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Jaskaran Singh SaraoDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Abrar RasoolDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Afshan AttaDepartment of Hematopathology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Malik T RasoolDepartment of Radiation Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Mushtaq Ahmad SofiDepartment of Radiation Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Rubiya RyhanDepartment of Blood Transfusion and Immunohematology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Mohd Zubair QureshiDepartment of Blood Transfusion and Immunohematology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Sumyra Khurshid QadriDepartment of Pathology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Sunil K RegmiDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Ulfat AraDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Shashwat LohiaDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Aamir Sultan LoneDepartment of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.
Nazir Ahmad DarDepartment of Radiation Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background  Autologous stem cell transplantation (ASCT) is a standard consolidation strategy for selected patients with relapsed or high-risk lymphoma, but access remains limited in many low- and middle-income regions because of the cost and infrastructure required for stem cell cryopreservation. Non-cryopreserved ASCT using fresh peripheral blood stem cells stored at 4°C may provide a practical alternative. Methods  We retrospectively analyzed 11 consecutive patients with lymphoma who underwent non-cryopreserved ASCT at the Department of Medical Oncology, Sher-i-Kashmir Institute of Medical Sciences (SKIMS), Srinagar. Peripheral blood stem cells were mobilized with granulocyte colony-stimulating factor (G-CSF) alone or G-CSF plus plerixafor, stored at 4°C, and infused after institutional modified BEAM conditioning. Primary endpoints were feasibility, CD34+ cell collection, neutrophil and platelet engraftment, early toxicities, and day +100 survival. Results  The median age was 41 years (range, 22-58), and 9 patients (81.8%) were male. Diagnoses included classical Hodgkin lymphoma in 4 patients (36.4%) and non-Hodgkin lymphoma in 7 patients (63.6%). Stage III-IV disease was present in 8 patients (72.7%), and 9 patients (81.8%) were in complete remission before transplant. G-CSF plus plerixafor was used in 9 patients (81.8%). The median CD34+ cell dose collected was 5.5 × 10^6/kg (range, 3.6-13.5), with a median of 2 apheresis sessions (range, 1-2). All grafts were stored for 6 days at 4°C. Median neutrophil and platelet engraftment occurred on day 11 (range, 10-13) and day 12 (range, 10-18), respectively. Febrile neutropenia occurred in 10 patients (90.9%); grade 3-4 mucositis occurred in 6 patients (54.5%). Day +30 survival was 100%, and day +100 survival was 90.9%, with one transplant-related death. Conclusion Non-cryopreserved ASCT for lymphoma was feasible at SKIMS Srinagar, with adequate CD34+ cell collection, rapid engraftment, and acceptable early survival. Larger prospective studies with standardized graft-quality monitoring, longer follow-up, and cost-effectiveness analysis are needed.

Indexed as

autologious stem cell transplantengraftmentkashmirlymphomamodified beamnon-cryopreserved stem cellsperipheral blood stem cellsresource-limited setting

Identifiers

PMID42440648
PMCPMC13333545

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