MétaCan
Menu
Back to cohort
Record W4403568842 · doi:10.1016/j.htct.2024.09.865

LONG-TERM FOLLOW-UP FROM THE PHASE 1/2 MAJESTEC-1 TRIAL OF TECLISTAMAB IN PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA: SUBGROUP ANALYSIS BY LINES OF THERAPIES

2024· article· en· W4403568842 on OpenAlexaff
Luciano J. Costa, N. W. van de Donk, Laura Rosiñol, Rakesh Popat, Be semer, Joaquín Martínez‐López, D Trancucci, Tara Stephenson, Katherine Chastain, NJ Bahlis

Bibliographic record

VenueHematology Transfusion and Cell Therapy · 2024
Typearticle
Languageen
FieldMedicine
TopicMultiple Myeloma Research and Treatments
Canadian institutionsInstitute of Cancer ResearchUniversity of Calgary
Fundersnot available
KeywordsMedicineSubgroup analysisRefractory (planetary science)Multiple myelomaInternal medicineTerm (time)OncologyMeta-analysis

Abstract

fetched live from OpenAlex

Teclistamab is the first approved B-cell maturation antigen × CD3 bispecific antibody (BsAb) for the treatment of triple-class exposed (TCE) relapsed/refractory multiple myeloma (RRMM), with weight-based dosing and the longest study follow-up of any BsAb in MM. In the pivotal phase 1/2 MajesTEC-1 study (NCT03145181/NCT04557098), teclistamab demonstrated rapid, deep, and durable responses (overall response rate [ORR], 63.0%; complete response or better [≥CR] rate, 46.1%; median duration of response [mDOR], 24 mo) and a low rate of discontinuations due to adverse events (AEs; 4.8%). This subgroup analysis of MajesTEC-1 reports the overall safety and efficacy of RRMM patients (pts) who received 2-3 prior lines of therapy vs. pts with 4 or more prior lines of therapies, with extended follow-up of 30 months. Pts received the recommended phase 2 dose (RP2D) of teclistamab (1.5 mg/kg QW) and could switch to Q2W dosing if in partial response or better after ≥4 cycles of therapy (phase 1) or in ≥CR for ≥6 mo (phase 2). The primary endpoint was ORR (assessed per IMWG 2016 criteria). AEs were graded per CTCAE v4.03. CRS and ICANS were graded per ASTCT. Safety was reported in the overall population and efficacy was evaluated in pts who received 2-3 prior lines of therapy (≤3 LoT) vs. pts who received more than 3 prior lines of therapies (> 3 LoT). Of 165 pts who had received teclistamab as of Aug 2023, 26% (43/165) pts received ≤ 3 prior LoT and 74% (122/165) patients received > 3 prior LoT. Pts characteristics were similar between the groups, especially in terms of high-risk features. At 30.4 mo mFU, pts that received ≤3 prior LoT achieved an ORR of 74.4% with 60.5% of pts achieving ≥ CR [sCR 46.5% and CR 14%]. mPFS was 21.7 mo (95% CI, 13.8–NR), mDOR was 24.0 mo (95% CI, 14.0–NE) and median overall survival was not reached (95% CI, 18.3–NE). Pts who had > 3 prior LoT had an ORR of 59%, with 41% of pts achieving ≥CR [sCR 36.1% and CR 4.9%], mPFS was 9.7 mo (95% CI, 6.4–13.1), mDOR was 22.4 mo (95% CI, 14.9–NE) and median overall survival was 17.7 mo (95% CI, 12.2–29.7). In the overall population, hematologic AEs (any grade/grade 3/4) included neutropenia (72%/65%), anemia (55%/38%), thrombocytopenia (42%/23%), and lymphopenia (36%/35%). Infections occurred in 79% of pts (55% grade 3/4). Of grade 5 infections, 18/22 were due to COVID-19, reflecting study conduct during the COVID-19 pandemic. Onset of new grade ≥3 infections generally decreased over time, which aligned approximately with the median time of switch to Q2W dosing; other factors, such as increasing use of IVIG, may also contribute to this trend. AEs leading to dose reduction (n = 1) or discontinuation (n = 8; 5 due to infection) were infrequent. No new safety signals were reported. With the longest follow-up of any BsAb in MM, teclistamab continues to demonstrate deep and durable responses, especially in the subgroup of less heavily treated patients (≤3 prior LoT), which demonstrates even better PFS and complete response rates results than those patients in later lines of treatment (> 3 prior LOT). The safety profile of teclistamab remains consistent with that of BCMA-targeted bispecific therapies, with an important decrease in new onset of severe infections with time. This study was funded by Johnson & Johnson Innovative Medicine.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.311
Threshold uncertainty score0.515

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.016
GPT teacher head0.284
Teacher spread0.268 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations3
Published2024
Admission routes1
Has abstractyes

Explore more

Same venueHematology Transfusion and Cell TherapySame topicMultiple Myeloma Research and TreatmentsFrench-language works237,207