Evaluating early intervention in smoldering myeloma clinical trials: a systematic review

Author:

Kakkilaya Apoorva1,Trando Aaron2,Cliff Edward R Scheffer3ORCID,Mian Hira4,Al Hadidi Samer5ORCID,Aziz Muhammad6,Goodman Aaron M7,Jeong Ah-Reum7,Smith Wade L8,Kelkar Amar H9,Russler-Germain David A10,Mehra Nikita11,Chakraborty Rajshekhar12ORCID,Gertz Morie A13,Mohyuddin Ghulam Rehman14ORCID

Affiliation:

1. John Sealy School of Medicine, University of Texas Medical Branch , Galveston, TX , United States

2. School of Medicine, University of California San Diego , La Jolla, CA , United States

3. Program on Regulation, Therapeutics and Law, Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women’s Hospital, Harvard Medical School , Boston, MA , United States

4. Division of Hematology, McMaster University , Hamilton , Canada

5. Myeloma Center, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences , Little Rock, AR , United States

6. Division of Gastroenterology and Hepatology, University of Toledo , Toledo, OH , United States

7. Division of Blood and Marrow Transplantation, University of California San Diego , La Jolla, CA , United States

8. Mulford Health Science Library, University of Toledo , Toledo, OH , United States

9. Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School , Boston, MA , United States

10. Division of Oncology, Washington University School of Medicine , St. Louis, MO , United States

11. Department of Medical Oncology, Cancer Institute (WIA) , Chennai , India

12. Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center , New York, NY , United States

13. Division of Hematology, Mayo Clinic , Rochester, MN , United States

14. Division of Hematology, Huntsman Cancer Institute, University of Utah , Salt Lake City, UT , United States

Abstract

Abstract Background Smoldering multiple myeloma (SMM), an asymptomatic precursor of multiple myeloma (MM), carries a variable risk of progression to MM. There is little consensus on the efficacy or optimal timing of treatment in SMM. We systematically reviewed the landscape of all clinical trials in SMM. We compared the efficacy of treatment regimens studied in SMM to results from these regimens when used in newly diagnosed multiple myeloma (NDMM), to determine whether the data suggest deeper responses in SMM versus NDMM. Methods All prospective interventional clinical trials for SMM, including published studies, meeting abstracts, and unpublished trials listed on ClinicalTrials.gov up to April 1, 2023, were identified. Trial-related variables were captured, including treatment strategy and efficacy results. Relevant clinical endpoints were defined as overall survival (OS) and quality of life. Results Among 45 SMM trials identified, 38 (84.4%) assessed active myeloma drugs, while 7 (15.6%) studied bone-modifying agents alone. Of 18 randomized trials in SMM, only one (5.6%) had a primary endpoint of OS; the most common primary endpoint was progression-free survival (n = 7, 38.9%). Among 32 SMM trials with available results, 9 (28.1%) met their prespecified primary endpoint, of which 5 were single-arm studies. Six treatment regimens were tested in both SMM and NDMM; 5 regimens yielded a lower rate of very good partial response rate or better (≥VGPR) in SMM compared to the corresponding NDMM trial (32% vs 63%, 43% vs 53%, 40% vs 63%, 86% vs 89%, 92% vs 95%, and 94% vs 87%, respectively). Conclusion In this systematic review of all prospective interventional clinical trials in SMM, we found significant variability in trial design, including randomization status, primary endpoints, and types of intervention used. Despite the statistical limitations, comparison of treatment regimens revealed no compelling evidence that the treatment is more effective when introduced early in SMM compared to NDMM.

Publisher

Oxford University Press (OUP)

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