Evidence map›Paper›PMID 35468618›Full record

ArticleBlood advances2023

Phase 1 study of CART-ddBCMA for the treatment of subjects with relapsed and refractory multiple myeloma.

Matthew J Frigault, Michael R Bishop, Jacalyn Rosenblatt, Elizabeth K O'Donnell, Noopur Raje, Daniella Cook, Andrew J Yee, Emma Logan, David E Avigan, Andrzej Jakubowiak and 8 more

Registry-linked trialAbstract readClinical Trial, Phase I
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04155749 (Master Protocol for the Phase 1 Study of Cell Therapies for the Treatment of Patients With Relapsed Refractory Multiple Myeloma, Including Long-term Safety Follow-up), which is not on this map. Cited by 58 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 5 pooled it
–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.

NCT04155749 phase1active not recruitingnot on this map

Master Protocol for the Phase 1 Study of Cell Therapies for the Treatment of Patients With Relapsed Refractory Multiple Myeloma, Including Long-term Safety Follow-up

TypeinterventionalSponsorKite, A Gilead CompanyRan2019 to 2027Enrolled40ConditionsRelapsed and Refractory Multiple MyelomaArmsanitocabtagene-autoleucel
3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 5 syntheses or guidelines pooled it.

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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

18 authors.

Matthew J FrigaultMassachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0002-6774-5694
Michael R BishopDavid and Etta Jonas Center for Cellular Therapy, University of Chicago, Chicago, IL.
Jacalyn RosenblattBeth Israel Deaconess Medical Center, Boston, MA.
Elizabeth K O'DonnellMassachusetts General Hospital Cancer Center, Boston, MA.
Noopur RajeMassachusetts General Hospital Cancer Center, Boston, MA.
Daniella CookMassachusetts General Hospital Cancer Center, Boston, MA.
Andrew J YeeMassachusetts General Hospital Cancer Center, Boston, MA.
Emma LoganBeth Israel Deaconess Medical Center, Boston, MA.
David E AviganBeth Israel Deaconess Medical Center, Boston, MA.
Andrzej JakubowiakDavid and Etta Jonas Center for Cellular Therapy, University of Chicago, Chicago, IL.
Kit ShawDana Farber Cancer Institute, Cell Manipulation Core Facility, Brookline, MA.ORCID 0000-0002-1293-8050
Heather DaleyDana Farber Cancer Institute, Cell Manipulation Core Facility, Brookline, MA.
Sarah NikiforowDana Farber Cancer Institute, Cell Manipulation Core Facility, Brookline, MA.
Faith GriffinArcellx, Inc., Gaithersburg, MD.
Christine CornwellArcellx, Inc., Gaithersburg, MD.
Angela ShenArcellx, Inc., Gaithersburg, MD.
Christopher HeeryArcellx, Inc., Gaithersburg, MD.
Marcela V MausMassachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0002-7578-0393

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relapsed and refractory multiple myeloma (RRMM) is a plasma cell neoplasm defined by progressively refractory disease necessitating chronic and increasingly intensive therapy. Despite recent advances, limited treatment options exist for RRMM. This single-arm, open label phase 1 study aimed to evaluate the safety of novel B-cell maturation antigen (BCMA)-targeting chimeric antigen receptor (CAR) T construct that leverages a completely synthetic antigen-binding domain (CART-ddBCMA), which was specifically engineered to reduce immunogenicity and improve CAR cell surface stability. Thirteen patients ≥18 years with RRMM who received at least 3 prior regimens of systemic therapy were enrolled in the study. Patients received a single dose of 100 × 106 CART-ddBCMA (DL1) or 300 × 106 CART-ddBCMA (DL2) following standard lymphodepleting chemotherapy. The primary endpoints of the study were to evaluate the incidence of treatment emergent adverse events, including dose-limiting toxicities, and establish a recommended phase 2 dose. Results showed that CART-ddBCMA was well tolerated and demonstrated a favorable toxicity profile. Only 1 case of grade ≥3 cytokine release syndrome and 1 case of immune effector cell-associated neurotoxicity were reported; both were at DL2 and were manageable with standard treatment. No atypical neurological toxicities and Parkinson disease-like movement disorders were observed. The maximum tolerated dose was not reached. All infused patients responded to CART-ddBCMA, and 9/12 (75%) patients achieved complete response/stringent complete response. Responses deepened over time, and at the time of last data-cut (median follow-up 56 weeks), 8/9 (89%) evaluable patients achieved minimal residual disease negativity. In conclusion, the findings demonstrate the safety of CART-ddBCMA cells and document durable responses to CART-ddBCMA in patients with RRMM. This trial was registered at www.clinicaltrials.gov as #NCT04155749.

Indexed as

Multiple MyelomaNeurotoxicity SyndromesReceptors, Chimeric AntigenHumansLymphocytescell-associated neurotoxicityReceptors, Chimeric Antigen

Identifiers

PMID35468618
PMCPMC9989524

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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.