TY - JOUR
T1 - Racial and ethnic differences in clinical outcomes among patients with multiple myeloma treated with CAR T-cell therapy
AU - Peres, Lauren C.
AU - Oswald, Laura B.
AU - Dillard, Christen M.
AU - De Avila, Gabriel
AU - Nishihori, Taiga
AU - Blue, Brandon J.
AU - Freeman, Ciara L.
AU - Locke, Frederick L.
AU - Alsina, Melissa
AU - Puglianini, Omar Castaneda
AU - Shune, Leyla
AU - Sborov, Douglas W.
AU - Wagner, Charlotte
AU - Dima, Danai
AU - Hashmi, Hamza
AU - Davis, James A.
AU - Kocoglu, Mehmet H.
AU - Badros, Ashraf Z.
AU - Atrash, Shebli
AU - Simmons, Gary
AU - Kalariya, Nilesh
AU - Ferreri, Christopher
AU - Anderson, Larry D.
AU - Afrough, Aimaz
AU - Kaur, Gurbakhash
AU - Lin, Yi
AU - Liu, Lawrence
AU - Nadeem, Omar
AU - Voorhees, Peter
AU - Khouri, Jack
AU - McGuirk, Joseph
AU - Sidana, Surbhi
AU - Hansen, Doris K.
AU - Patel, Krina
N1 - Publisher Copyright:
© 2024 by The American Society of Hematology.
PY - 2024/1/9
Y1 - 2024/1/9
N2 - Idecabtagene vicleucel (ide-cel) was the first chimeric antigen receptor T-cell therapy to gain US Food and Drug Administration approval for patients with relapsed/refractory multiple myeloma (RRMM). The clinical outcomes of standard of care (SOC) ide-cel in racially and ethnically diverse populations have been understudied. This study pooled data from 207 patients with RRMM (28% patients of racial and ethnic minority groups) treated with SOC ide-cel across 11 institutions to examine racial and ethnic differences in the incidence of toxicities and adverse events, response to ide-cel, and survival. This study included 22 (11%) Hispanic, 36 (17%) non-Hispanic Black, and 149 (72%) non-Hispanic White patients with RRMM. Compared with Hispanic and non-Hispanic White patients, non- Hispanic Black patients had higher median levels of C-reactive protein (1.0, 0.8, and 3.5 mg/ dL, respectively; P = .02) and baseline ferritin (362.0 vs 307.0 vs 680.5, respectively; P = .08) and were more likely to develop cytokine release syndrome (77%, 85%, and 97%, respectively; P = .04). Although best overall response rate was lower among Hispanic patients (59%) than among non-Hispanic Black (86%) and White patients (86%; P = .01), there were no racial and ethnic differences in progression-free or overall survival. We provide, to our knowledge, the first and largest investigation of clinical outcomes of SOC idecel by race and ethnicity. Despite differences in safety and response to ide-cel, our findings encourage the use of ide-cel in all patients with RRMM. These findings should be confirmed in larger samples of diverse patients with RRMM, with longer follow-up time.
AB - Idecabtagene vicleucel (ide-cel) was the first chimeric antigen receptor T-cell therapy to gain US Food and Drug Administration approval for patients with relapsed/refractory multiple myeloma (RRMM). The clinical outcomes of standard of care (SOC) ide-cel in racially and ethnically diverse populations have been understudied. This study pooled data from 207 patients with RRMM (28% patients of racial and ethnic minority groups) treated with SOC ide-cel across 11 institutions to examine racial and ethnic differences in the incidence of toxicities and adverse events, response to ide-cel, and survival. This study included 22 (11%) Hispanic, 36 (17%) non-Hispanic Black, and 149 (72%) non-Hispanic White patients with RRMM. Compared with Hispanic and non-Hispanic White patients, non- Hispanic Black patients had higher median levels of C-reactive protein (1.0, 0.8, and 3.5 mg/ dL, respectively; P = .02) and baseline ferritin (362.0 vs 307.0 vs 680.5, respectively; P = .08) and were more likely to develop cytokine release syndrome (77%, 85%, and 97%, respectively; P = .04). Although best overall response rate was lower among Hispanic patients (59%) than among non-Hispanic Black (86%) and White patients (86%; P = .01), there were no racial and ethnic differences in progression-free or overall survival. We provide, to our knowledge, the first and largest investigation of clinical outcomes of SOC idecel by race and ethnicity. Despite differences in safety and response to ide-cel, our findings encourage the use of ide-cel in all patients with RRMM. These findings should be confirmed in larger samples of diverse patients with RRMM, with longer follow-up time.
UR - http://www.scopus.com/inward/record.url?scp=85182384157&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85182384157&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2023010894
DO - 10.1182/bloodadvances.2023010894
M3 - Article
C2 - 37855718
AN - SCOPUS:85182384157
SN - 2473-9529
VL - 8
SP - 251
EP - 259
JO - Blood Advances
JF - Blood Advances
IS - 1
ER -