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Authors

Moazzam Shahzad, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Muhammad Fareed Khalid, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Muhammad Kashif Amin, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Mohammad Ammad-Ud-Din, Division of Hematology and Oncology, H. Moffitt Cancer Center, University of South Florida, Tampa, FL
Usman Ilyas, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City
Ali H. Mushtaq, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Atif Butt, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Iqra Anwar, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Sibgha Gull Chaudhary, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Nausheen Ahmed, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Leyla Shune, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Anurag K. Singh, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Sunil H. Abhyankar, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Joseph P. McGuirk, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS
Muhammad Umair Mushtaq, Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KSFollow

Abstract

This systematic review aimed at evaluating the proportion of primary and secondary endpoints in hematopoietic stem cell transplant (HSCT) phase III randomized clinical trials (RCTs) and their trends over time and by study sponsorship status. Chi-square test and logistic regression analyses were performed using SPSS version 28. A total of 147 HSCT phase III RCTs from 2006-2021 that reported 197 primary and 600 secondary endpoints were included for the analysis. Overall survival (OS, 17%), progression-free survival (PFS, 15%), graft-versus-host disease (GVHD, 8%), event-free survival (EFS, 8%), and organ function (8%) were the most common primary endpoints. GVHD (12.3%, n=74), safety/toxicity/adverse events (11.8%, n=71), OS (11.5%, n=69), PFS (9.3%, n=56), and relapse rate (RR) (7.5%, n=45) were the most common secondary endpoints during 2006-2021. After 2013, an increase in the use of PFS (12% to 18%, p=0.196) as a primary endpoint was noted, while the use of OS as a primary endpoint declined from 20% to 13% (p=0.170). Among secondary endpoints, a statistically significant increase in the use of RR (5% to 10%, p=0.047) and NRM (3% to 6%, p=0.047) was observed. There was a significantly higher use of EFS (14% vs 4%, p=0.012) and ORR (11% vs 2%, p=0.003) as a primary endpoint in pharmaceutical-sponsored studies as compared to non-pharmaceutical-sponsored studies. As a secondary endpoint, the use of EFS (4% vs 1%, p=0.013) and ORR (4% vs 1%, p=0.028) was higher, whereas the use of organ systems/functions (1.5% vs 5.5%, p=0.022) and GVHD (6.5% vs 15%, p=0.002) was lower in pharmaceutical-sponsored studies as compared to non-pharmaceutical sponsored studies. GVHD-free relapse-free survival (GRFS) was reported as a primary endpoint in 2% of studies while only 5% of the studies reported Quality of life (QoL) as a secondary endpoint. We described commonly used endpoints in HSCT phase III RCTs and patterns in their use over time, by funding source, and study intervention category.

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Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.

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