Evidence map›Paper›PMID 40296907›Full record

ReviewOncology research2025

A review on pathobiology of circulating tumour plasma cells: The sine qua non of poor prognosis in plasma cell neoplasms.

Pratibha Suku, Aishwarya Dash, Aravind Radhakrishnan, Pankaj Malhotra, Man Updesh Singh Sachdeva

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In one paragraph

Review in Oncology research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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.

2 · The registry

The trial behind it

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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

5 authors.

Pratibha SukuDepartment of Hematology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, P.O. Box 160012, India.
Aishwarya DashDepartment of Hematology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, P.O. Box 160012, India.
Aravind RadhakrishnanDepartment of Hematology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, P.O. Box 160012, India.
Pankaj MalhotraDepartment of Clinical Hematology and Medical Oncology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, P.O. Box 160012, India.
Man Updesh Singh SachdevaDepartment of Hematology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, P.O. Box 160012, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating plasma cells (CPCs) in patients of plasma cell neoplasm have been an area of intense research in recent decades. Circulating tumor plasma cells (CTPCs) might represent a sub-clone of tumor cells that have exited into peripheral blood as a result of the dynamic interactions between the bone marrow (BM) microenvironment and neoplastic plasma cells. Chemokine receptors like chemokine receptor 4 (CXCR4) and integrins are known to play a role in homing and migration of plasma cells (PCs). The hypoxic microenvironment in the BM niche also contributes to their circulation through various mechanisms. In addition, the CCL3-CCR1 axis probably competes with the retention signals from the CXCR4-α4β1 (VLA-4) interaction and actively promotes the exit of PCs from the BM. CTPCs, even in extremely low numbers, can be detected and quantified by high-sensitivity techniques like multi-color flow cytometry and next-generation sequencing. High load of CTPCs noted in patients of plasma cell neoplasm; monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), multiple myeloma (MM) is a strong predictor of shorter progression free survival (PFS) as well as overall survival (OS). In newly diagnosed patients of MM, a load of CTPCs correlates with the outcomes, i.e., OS and PFS. With more studies collaborating on the results of previous reports, assessment of the burden of CTPCs may become a complimentary approach for non-invasive risk stratification of MM patients and evaluating the response to therapy. Future research on larger cohorts and longer follow-ups may help to improve the existing staging system by incorporating the load of CTPCs as one of the prognostic indicators. Further studies based on isolation and genetic characterization of CTPCs may help in understanding the pathophysiology of the progression of the disease and may open avenues for newer treatment modalities. This review discusses the pathobiological aspects leading to circulation of neoplastic/tumor plasma cells in peripheral blood and provides a summary of research work done in last two decades on its prognostic importance in various plasma cells neoplasms.

Indexed as

Neoplasms, Plasma CellNeoplastic Cells, CirculatingPlasma CellsBiomarkers, TumorHumansPrognosisTumor MicroenvironmentBiomarkers, TumorCirculating Plasma Cells (CPCs)Circulating Tumor Plasma Cells (CTPCs)Flow cytometryMicroenvironmentMonoclonal gammopathyMultiple Myeloma (MM)

Identifiers

PMID40296907
PMCPMC12034004

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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.