Evidence map›Paper›PMID 38566804›Full record

ArticleHemaSphere2024

Circulating tumor plasma cells and peripheral blood measurable residual disease assessment in multiple myeloma patients not planned for upfront transplant.

Prashant R Tembhare, Harshini Sriram, Twinkle Khanka, Sanghamitra Gawai, Bhausaheb Bagal, Sitaram G Ghogale, Nilesh Deshpande, Karishma Girase, Jagruti Patil, Syed Khaizer Hasan and 15 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Measurable Residual Disease.Methods in molecular biology (Clifton, N.J.) · 2027
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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

25 authors at 2 institutions in 1 country.

Prashant R TembhareDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.ORCID 0000-0002-9030-0415
Harshini SriramDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Twinkle KhankaDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Sanghamitra GawaiDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Bhausaheb BagalDepartment of Medical Oncology, Tata Memorial Centre HBNI University Mumbai Maharashtra India.
Sitaram G GhogaleDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Nilesh DeshpandeDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Karishma GiraseDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Jagruti PatilDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Syed Khaizer HasanHasan Laboratory, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Dhanalaxmi ShettyDepartment of Cancer Cytogenetics, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Kinjalka GhoshDepartment of Biochemistry, Tata Memorial Centre HBNI University Mumbai Maharashtra India.
Gaurav ChatterjeeDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Sweta RajpalDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Nikhil V PatkarDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Hasmukh JainDepartment of Medical Oncology, Tata Memorial Centre HBNI University Mumbai Maharashtra India.
Sachin PunatarBone Marrow Transplant Unit, Department of Medical Oncology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Anant GokarnBone Marrow Transplant Unit, Department of Medical Oncology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Lingaraj NayakBone Marrow Transplant Unit, Department of Medical Oncology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Sumeet MirghBone Marrow Transplant Unit, Department of Medical Oncology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Nishant JindalBone Marrow Transplant Unit, Department of Medical Oncology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Manju SengarDepartment of Medical Oncology, Tata Memorial Centre HBNI University Mumbai Maharashtra India.
Navin KhattryBone Marrow Transplant Unit, Department of Medical Oncology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Papagudi G SubramanianDepartment of Hematopathology, ACTREC, Tata Memorial Centre HBNI University Navi Mumbai Maharashtra India.
Sumeet GujralDepartment of Pathology, Tata Memorial Hospital, Tata Memorial Centre HBNI University Mumbai Maharashtra India.
Homi Bhabha National Institute · INTata Memorial Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor plasma cells (CTPCs) provide a noninvasive alternative for measuring tumor burden in newly diagnosed multiple myeloma (NDMM). Moreover, measurable residual disease (MRD) assessment in peripheral blood (PBMRD) can provide an ideal alternative to bone marrow MRD, which is limited by its painful nature and technical challenges. However, the clinical significance of PBMRD in NDMM still remains uncertain. Additionally, data on CTPC in NDMM patients not treated with transplant are scarce. We prospectively studied CTPC and PBMRD in 141 NDMM patients using highly sensitive multicolor flow cytometry (HS-MFC). PBMRD was monitored at the end of three cycles (PBMRD1) and six cycles (PBMRD2) of chemotherapy in patients with detectable baseline CTPC. Patients received bortezomib-based triplet therapy and were not planned for an upfront transplant. Among baseline risk factors, CTPC ≥ 0.01% was independently associated with poor progression-free survival (PFS) (hazard ratio [HR] = 2.77;

Identifiers

PMID38566804
PMCPMC10983024
OpenAlexW4393388193

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.