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Absolute Lymphocyte Count and Outcomes of Multiple Myeloma Patients Treated with Idecabtagene Vicleucel: The US Myeloma Immunotherapy Consortium Real- World Experience.
Khouri, Jack; Dima, Danai; Li, Hong; Hansen, Doris; Sidana, Surbhi; Shune, Leyla; Anwer, Faiz; Sborov, Douglas; Wagner, Charlotte; Kocoglu, Mehmet H; Atrash, Shebli; Voorhees, Peter; Peres, Lauren; Hovanky, Vanna; Simmons, Gary; Williams, Louis; Raza, Shahzad; Afrough, Aimaz; Anderson, Larry D; Ferreri, Christopher; Hashmi, Hamza; Davis, James; McGuirk, Joseph; Goldsmith, Scott; Borogovac, Azra; Lin, Yi; Midha, Shonali; Nadeem, Omar; Locke, Frederick L; Baz, Rachid; Hamilton, Betty; Alsina, Melissa; Sauter, Craig; Patel, Krina; Kaur, Gurbakhash.
Affiliation
  • Khouri J; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.
  • Dima D; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio. Electronic address: dimad@ccf.org.
  • Li H; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.
  • Hansen D; H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
  • Sidana S; Stanford University School of Medicine, Stanford, California.
  • Shune L; University of Kansas Medical Center, Kansas City, Kansas.
  • Anwer F; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.
  • Sborov D; University of Utah Huntsman Cancer Institute, Salt Lake City, Utah.
  • Wagner C; University of Utah Huntsman Cancer Institute, Salt Lake City, Utah.
  • Kocoglu MH; University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, Maryland.
  • Atrash S; Levine Cancer Institute, Charlotte, North Carolina.
  • Voorhees P; Levine Cancer Institute, Charlotte, North Carolina.
  • Peres L; H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
  • Hovanky V; Stanford University School of Medicine, Stanford, California.
  • Simmons G; Virginia Commonwealth University Massey Cancer Center, Richmond, Virginia.
  • Williams L; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.
  • Raza S; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.
  • Afrough A; UT Southwestern Harold C. Simmons Comprehensive Cancer Center, Dallas, Texas.
  • Anderson LD; UT Southwestern Harold C. Simmons Comprehensive Cancer Center, Dallas, Texas.
  • Ferreri C; The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Hashmi H; Medical University of South Carolina, Charleston, South Carolina.
  • Davis J; Medical University of South Carolina, Charleston, South Carolina.
  • McGuirk J; University of Kansas Medical Center, Kansas City, Kansas.
  • Goldsmith S; City of Hope Cancer Center, Duarte, California.
  • Borogovac A; City of Hope Cancer Center, Duarte, California.
  • Lin Y; Mayo Clinic Cancer Center, Rochester, Minnesota.
  • Midha S; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Nadeem O; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Locke FL; H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
  • Baz R; H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
  • Hamilton B; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.
  • Alsina M; H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
  • Sauter C; Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.
  • Patel K; The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Kaur G; UT Southwestern Harold C. Simmons Comprehensive Cancer Center, Dallas, Texas.
Article in En | MEDLINE | ID: mdl-38834151
ABSTRACT
Idecabtagene vicleucel (ide-cel) has shown impressive efficacy in relapsed/refractory multiple myeloma (RRMM). This study aimed to investigate the impact of absolute lymphocyte count (ALC) on the survival outcomes of RRMM patients treated with standard of care (SOC) ide-cel. Data were collected retrospectively from 11 institutions in the U.S. Impact of ALC parameters including pre-apheresis (pre-A), pre-lymphodepletion (pre-LD), absolute and percent difference from pre-A to pre-LD on clinical outcomes after ide-cel were examined using survival analysis. A new ALC profile was created based on univariate analysis that comprises 3 groups normal (≥1 × 109/L) pre-LD ALC (LDN), low (<1 × 109/L) pre-LD ALC (LDL) + percent reduction <37.5 (%RL), and LDL ALC + percent reduction ≥37.5 (%RH). A total of 214 SOC ide-cel recipients were included in this analysis. The median patient age was 64 years (interquartile range [IQR], 57 to 69 years), median number of prior therapies was 6 (IQR, 5 to 9), and median duration of follow-up was 5.4 months (IQR, 2.1 to 8.3 months). Most patients had both low pre-A ALC (75.3%) and pre-LD ALC (77.2%), and the reduction from pre-A to pre-LD (median, .65 to .55 × 109/L) was statistically significant. Univariate analysis showed that the LDL + %RH group had significantly worse progression-free survival (PFS) and overall survival (OS) compared to the LDL + %RL and LDN ALC groups (6-month PFS 40% versus 67.6% and 60.9%; 6-month OS 69.5% versus 87% and 94.3%). In multivariable analysis, after adjusting for age, performance status, cytogenetic risk, use of bridging therapy, and extramedullary disease, PFS did not maintain its statistical significance; however, OS remained significantly worse for LDL + %RH group compared to the LDN ALC group (hazard ratio [HR], 4.3; 95% confidence interval [CI], 1.1 to 17), but the difference between the LDL + %RH versus %RL groups was not statistically significant (HR, 1.7; 95% CI, .8 to 4.0). Our findings indicate that low pre-LD ALC with high %R from pre-A to pre-LD was associated with inferior survival outcomes, particularly OS, in patients who received SOC ide-cel.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Transplant Cell Ther Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Transplant Cell Ther Year: 2024 Type: Article