Evidence map›Paper›PMID 38111533›Full record

ArticleFrontiers in oncology2023

Immunomodulation of NK, NKT and B/T cell subtypes in relapsed/refractory multiple myeloma patients treated with pomalidomide along with velcade and dexamethasone and its association with improved progression-free survival.

Rao Prabhala, William E Pierceall, Mehmet Samur, Lakshmi B Potluri, Kevin Hong, Teresa Peluso, Srikanth Talluri, Angela Wang, Aishwarya Katiki, Sahan D Vangala and 13 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01734928 (A Phase 3, Multicenter, Randomized, Open-Label Study to Compare the Efficacy and Safety of Pomalidomide, Bortezomib and Low-Dose Dexamethasone Versus Bortezomib and Low-Dose Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 12% 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.

NCT01734928 phase3completednot on this map

A Phase 3, Multicenter, Randomized, Open-Label Study to Compare the Efficacy and Safety of Pomalidomide, Bortezomib and Low-Dose Dexamethasone Versus Bortezomib and Low-Dose Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma

TypeinterventionalSponsorCelgeneRan2013 to 2022Enrolled559ConditionsMultiple MyelomaArmsPomalidomide, Bortezomib, Dexamethasone
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
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

23 authors at 5 institutions in 2 countries.

Rao Prabhala *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
William E Pierceall *Bristol Myers Squibb, Summit, NJ, United States.
Mehmet Samur *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Lakshmi B Potluri *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Kevin HongBristol Myers Squibb, Summit, NJ, United States.
Teresa PelusoBristol Myers Squibb, Summit, NJ, United States.
Srikanth TalluriDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Angela WangDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Aishwarya KatikiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Sahan D VangalaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Michael BuonopaneDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Vaishnavi BadeDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Hannah SeahDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Arthur KrogmanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Sanika DerebailDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Mariateresa FulcinitiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Suzan B LazoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Paul RichardsonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Kenneth AndersonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Jill CorreInstitut Universitaire du Cancer de Toulouse-Oncopole, Toulouse, France.
Herve Avet-LoiseauInstitut Universitaire du Cancer de Toulouse-Oncopole, Toulouse, France.
Anjan ThakurtaBristol Myers Squibb, Summit, NJ, United States.
Nikhil MunshiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Dana-Farber Cancer Institute · USBristol-Myers Squibb (United States) · USHarvard University · USInstitut universitaire du cancer de Toulouse Oncopole · FRVA Boston Healthcare System · US

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C. · 2003 to 2023
$45.0M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
BLRD VA I01 BX001584NCI NIH HHS P01 CA155258NCI NIH HHS P50 CA100707
6 · The paper itself

Abstract

Background: Multiple Myeloma (MM) patients exhibit dysregulated immune system, which is further weakened by chemotherapeutic agents. While cereblon-modulating agents, such as pomalidomide and lenalidomide, have been found to improve the immune profile, the efficacy of their impact in combination with other treatments is yet unknown. Methods: We conducted an immune-profiling of a longitudinal cohort of 366 peripheral blood samples from the CC4047-MM-007 (OPTIMISMM, NCT01734928) study. This study followed relapsed/refractory Multiple Myeloma (RRMM) patients who were treated with Velcade + dexamethasone (Vd), or Vd with pomalidomide (PVd). 366 blood samples from 186 patients were evaluated using multi-color flow cytometry at 3 timepoints: screening, day 8 of cycle 1, and cycle 3. Results: Among NK and NKT cell populations, adding pomalidomide showed no inhibition in the frequency of NK cells. When expression of double positivity for activation markers like, p46/NKG2D, on NK cells was higher than the median, PVd treated patients showed significantly better (p=0.05) progression-free survival (PFS) (additional 15 months) than patients with lower than the median expression of p46/NKG2D on NK cells. PVd treated patients who expressed CD158a/b below the median at cycle 1 demonstrated a significantly better PFS (more than 18months). Among B cell subtypes, PVd treatment significantly increased the abundance of B1b cells (p<0.05) and decreased Bregs (p<0.05) at day 8 of both cycle 1 and cycle 3 when compared to screening samples. Of all the B cell-markers evaluated among paired samples, a higher expression of MZB cells at day 8 of cycle 1 has resulted in enhanced PFS in PVd treated patients. Within T cells, pomalidomide treatment did not decrease the frequency of CD8 T cells when compared with screening samples. The higher the surface expression of OX-40 on CD8 T cells and the lower the expression of PD-1 and CD25 on CD4 T cells by PVd treatment resulted in improved PFS. Conclusion: The prognostic significance for the number of immune markers is only seen in the PVd arm and none of these immune markers exhibit prognostic values in the Vd arm. This study demonstrates the importance of the immunomodulatory effects and the therapeutic benefit of adding pomalidomide to Vd treatment.

Indexed as

and T cellsB cellsmyelomaNK cellspomalidomide

Identifiers

PMID38111533
PMCPMC10726115
OpenAlexW4389309771

What OpenQuestion holds

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Registered trials

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.