Concordance between blinded independent central review committee and physician-assessed responses: Analyses based on a real-world external control arm in relapsed/refractory multiple myeloma using International Myeloma Working Group data.

B Brian G. Durie (Cedars-Sinai Medical Center, Los Angeles, CA) L Laura Rosiñol (Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona) K Katja C. Weisel S Sundar Jagannath (Icahn School of Medicine at Mount Sinai, New York) M Muhaimen Siddiqui (EVERSANA, Burlington, ON, Canada) N Nicolle Bonar (EVERSANA, Toronto, ON, Canada) M Mostafa Shokoohi (3EVERSANA Life Sciences, Burlington, Canada) M Michael West (EVERSANA, Burlington, ON, Canada) P Paul Spin (EVERSANA, Burlington, ON, Canada) C Christian Hampp (3Regeneron Pharmaceuticals, Inc., Tarrytown, United States) J James Harnett (Regeneron Pharmaceuticals, Inc., Tarrytown, NY) O Olivier Humblet (3Regeneron Pharmaceuticals, Inc., Tarrytown, United States) J Jeannette Green (Regeneron Pharmaceuticals, Inc., Tarrytown, NY) A Alexander Breskin (Regeneron Pharmaceuticals, Inc., Tarrytown, NY) G Glenn Scott Kroog (Regeneron Pharmaceuticals, Inc., Tarrytown, NY) Q Qiufei Ma (3Regeneron Pharmaceuticals, Inc., Tarrytown, United States) S Shaji Kumar

Abstract

e19521 Background: Blindedindependent central review (BICR) committees are often established for oncology trials to assessbestoverall response (BOR), while real-world (RW) studies typically rely on physician-assessed responses. To emulate clinical trial rigor, a BICR committee was implemented in the R5458-ONC-21101 RW data-derived external control arm study (NCT05673967) to evaluate BOR using International Myeloma Working Group (IMWG) criteria. A pre-specified concordance analysis compared BOR assessments between the BICR committee and treating site physicians. Methods: RW data were obtained from chart reviews at 15 participating International Myeloma Foundation IMWG sites. The BICR committee, comprised of three multiple myeloma experts, evaluated BOR through consensus voting. Per protocol, the committee reviewed case report forms consisting of data on serum and urine myeloma protein and free light chain levels; and, where available, bone marrow plasma cell percentage, presence of plasmacytomas, and bone lesion changes. Concordance between BICR- and physician-assessed BOR was evaluated for objective response rate defined as ≥partial response (PR), ≥very good partial response (VGPR), ≥complete response (CR), and stringent complete response (sCR), with non-evaluable responses excluded from the analysis. Cohen’s kappa (κ) was used to measure agreement, with values >0.6 indicating strong concordance. 1 Results: Of 279 evaluable lines of therapy from 203 patients (Table), the BOR of ≥PR was 45.2% by BICR assessment and 42.3% by treating physicians (κ=0.622). Concordance improved for BOR of ≥VGPR (22.2% by BICR vs 24.7% by treating physicians; κ=0.731) but was low for BOR of ≥CR (3.9% vs. 10.8%; κ=0.508) and sCR (1.1% vs. 4.7%; κ=0.364). Conclusions: BICR- and physician-assessed responses showed strong concordance for BOR of ≥PR and ≥VGPR. However, as expected, lower concordance for ≥CR and sCR was observed, as evaluation of CR per IMWG criteria requires a bone marrow biopsy, which is rarely performed in clinical practice. While the reliability of CR and sCR in RW data is less certain, these results suggest that BOR of ≥VGPR or ≥PR may be reliably ascertained in academic settings based on treating physician evaluations. 1. Landis JR, Koch GG. Biometrics 1977;33(1):159–74. Clinical trial information: NCT05673967 . Agreement of BICR- and physician-assessed responses. BICR assessed Physician assessed Observed agreement, % Cohen’s kappa* Number of evaluable lines of therapy 279 279 - - ≥PR, n (%) 126 (45.2) 118 (42.3) 81.4 0.622 ≥VGPR, n (%) 62 (22.2) 69 (24.7) 90.3 0.731 ≥CR, n (%) 11 (3.9) 30 (10.8) 93.2 0.508 sCR, n (%) 3 (1.1) 13 (4.7) 96.4 0.364 *A kappa value >0.6 indicates strong concordance. 1

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (17)

B

Brian G. Durie

Cedars-Sinai Medical Center, Los Angeles, CA

L

Laura Rosiñol

Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona

K

Katja C. Weisel

S

Sundar Jagannath

Icahn School of Medicine at Mount Sinai, New York

M

Muhaimen Siddiqui

EVERSANA, Burlington, ON, Canada

N

Nicolle Bonar

EVERSANA, Toronto, ON, Canada

M

Mostafa Shokoohi

3EVERSANA Life Sciences, Burlington, Canada

M

Michael West

EVERSANA, Burlington, ON, Canada

P

Paul Spin

EVERSANA, Burlington, ON, Canada

C

Christian Hampp

3Regeneron Pharmaceuticals, Inc., Tarrytown, United States

J

James Harnett

Regeneron Pharmaceuticals, Inc., Tarrytown, NY

O

Olivier Humblet

3Regeneron Pharmaceuticals, Inc., Tarrytown, United States

J

Jeannette Green

Regeneron Pharmaceuticals, Inc., Tarrytown, NY

A

Alexander Breskin

Regeneron Pharmaceuticals, Inc., Tarrytown, NY

G

Glenn Scott Kroog

Regeneron Pharmaceuticals, Inc., Tarrytown, NY

Q

Qiufei Ma

3Regeneron Pharmaceuticals, Inc., Tarrytown, United States

S

Shaji Kumar