Evidence map›Paper›PMID 41827675›Full record

ArticleCancers2026

A Real-World Analysis of the Safety and Efficacy of Teclistamab for Patients with Relapsed/Refractory Multiple Myeloma and Baseline Renal Impairment-USMIRC Group.

Maha Hameed, Alma Habib, Abdullah Mohammad Khan, Mehak Masood Laharwal, Prerna Mewawalla, Marshall McKenna, Yun Kyuong Ryu Tiger, Mansi Shah, Hira Shaikh, Christopher Strouse and 9 more

Abstract read
In one paragraph

Article in Cancers, 2026. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

19 authors.

Maha HameedInternal Medicine, Florida State University, Sarasota, FL 34239, USA.ORCID 0000-0001-8066-4584
Alma HabibDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Abdullah Mohammad KhanDivision of Hematology, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0003-2166-2583
Mehak Masood LaharwalDivision of Hematology and Cellular Therapy, Allegheny Health Network Cancer Institute, Pittsburgh, PA 15224, USA.
Prerna MewawallaDivision of Hematology and Cellular Therapy, Allegheny Health Network Cancer Institute, Pittsburgh, PA 15224, USA.
Marshall McKennaRutgers Cancer Institute, New Brunswick, NJ 08901, USA.
Yun Kyuong Ryu TigerRutgers Cancer Institute, New Brunswick, NJ 08901, USA.
Mansi ShahRutgers Cancer Institute, New Brunswick, NJ 08901, USA.
Hira ShaikhDivision of Hematology, Oncology, and Blood & Marrow Transplantation, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0001-5604-4166
Christopher StrouseDivision of Hematology, Oncology, and Blood & Marrow Transplantation, University of Iowa, Iowa City, IA 52242, USA.
Kimberly GreenDivision of Hematology-Oncology, Medical University of South Carolina, Charleston, SC 29425, USA.
Jordan SnyderDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Zahra MahmoudjafariDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.ORCID 0000-0002-3168-2521
Muhammad Umair MushtaqDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Nausheen AhmedDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Al-Ola AbdallahDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.ORCID 0000-0002-6603-185X
Shebli AtrashLevine Cancer Institute, Atrium Health Wake Forest University School of Medicine, Charlotte, NC 28204, USA.ORCID 0000-0003-4547-7534
Barry PaulLevine Cancer Institute, Atrium Health Wake Forest University School of Medicine, Charlotte, NC 28204, USA.ORCID 0000-0003-2702-8225
Reed FriendLevine Cancer Institute, Atrium Health Wake Forest University School of Medicine, Charlotte, NC 28204, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple myeloma (MM) is a hematologic malignancy characterized by the clonal proliferation of plasma cells and a rapidly evolving treatment landscape. Bispecific antibodies targeting B-cell maturation antigens (BCMA) have emerged as promising therapeutic options for relapsed and/or refractory multiple myeloma (RRMM).

methodsThis retrospective study evaluated the efficacy and safety of teclistamab, a BCMA-directed bispecific antibody, in patients with RRMM with renal impairment (RI) at baseline compared to those without. Conducted across seven academic centers, the study included 195 patients with RRMM, of whom 34 had baseline RI.

resultsPerformance status, previous lines of treatment, and prior BCMA exposure were identified as significant predictors of progression-free survival. Notably, patients with RI demonstrated overall response rates and toxicity profiles comparable to those without RI, although they required more packed red blood cell transfusions. No statistically significant differences were observed in adverse events, including cytokine release syndrome and infections.

conclusionsOverall, the findings support the efficacy and safety of teclistamab in patients with RRMM and RI, highlighting the need for prospective clinical trials to optimize the treatment strategies for this population.

Indexed as

cytokine release syndromeefficacyrenal impairmentteclistamabtoxicity

Identifiers

PMID41827675
PMCPMC12984311

What OpenQuestion holds

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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.