Does enrolment in clinical trials improve survival in patients with multiple myeloma?

06 Dec 2021
Does enrolment in clinical trials improve survival in patients with multiple myeloma?

Enrolment in clinical trials does not seem to increase survival among patients with multiple myeloma, a recent study has found.

“Patients enrolled in clinical trials underwent more lines of therapy, suggesting they may have had more treatment-resistant cancers,” the authors said. “A small survival benefit in this cohort may be obscured by the lack of difference in survival between trial and nontrial patients.”

A total of 1,285 patients receiving care for multiple myeloma at a National Cancer Institute-designated cancer centre from 2012 to 2018 were identified. Of these, 1,065 (83 percent) were nontrial and 220 (17 percent) were trial participants.

The authors used time-to-event analysis to adjust for baseline characteristics and account for clinical trial enrolment as a time-varying covariate. They also analysed propensity-matched cohort of trial and nontrial patients to reduce potential bias in observational data.

Compared with nontrial patients, trial participants were younger (mean age, 60 vs 63 years; p<0.001), underwent more lines of therapy (treatment lines ≥6, 39 percent vs 17 percent; p<0.001), and had more comorbidities.

Survival did not differ significantly between trial and nontrial participants (hazard ratio [HR], 1.34, 95 percent confidence interval [CI], 0.90–1.99) or between propensity-matched trial and nontrial participants (205 in each cohort; HR, 1.36, 95 percent CI, 0.83–2.23) after controlling for baseline characteristics and clinical trial enrolment as a time-varying covariate.

Results from overall analyses were consistent with those from subgroup analyses by lines of therapy.

Survival also did not significantly differ by race/ethnicity (logrank p=0.09). However, nontrial Black/Hispanic patients had a significantly higher risk of death than their White counterparts (HR, 1.76, 95 percent CI, 1.01–3.08).

Am J Clin Oncol 2021;44:603-612