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McMurray, Ryan

Mayo Clinic

Alliance Statistics and Data Center, Mayo Clinic, Rochester, Minnesota, USA.

Citations 1

Older-Patient-Specific Cancer Trials: A Pooled Analysis of 2,277 Patients (A151715)
Dao, Dyda , Jatoi, Aminah , Hurria, Arti , Muss, Hyman B. , Cohen, Harvey Jay, Citron, Marc L., Budman, Daniel R., Sedrak, Mina S. , Lafky, Jacqueline M., McMurray, Ryan, Le-Rademacher, Jennifer G , Zemla, Tyler , Freedman, Rachel A. , Shulman, Lawrence N. , McMurray, Ryan P. , Partridge, Ann H. , Carey, Lisa A. , Sedrak, Mina S. , Le‐Rademacher, Jennifer

The Oncologist | April 11, 2019 | Volume: 24 | Issue: 6 | Pages: e284-e291

10.1634/theoncologist.2018-0803 Get It

Abstract Background Less than 3% of older patients with cancer are enrolled in clinical trials. To reverse this underrepresentation, we compared older patients enrolled with older-patient-specific trials, defined as those designed for older patients with cancer, with those enrolled in age-unspecified trials. Materials and Methods We focused on individual patient data from those ≥65 years (younger patients excluded) and included all Alliance phase III adjuvant breast cancer trials from 1985–2012. Results Among 2,277 patients, 1,014 had been enrolled to older-patient-specific and 1,263 to age-unspecified trials. The median age (range) in the older-patient-specific trials was 72 (65–89) years compared with 68 (65–84) years in the cohort of older patients in age-unspecified trials; p < .0001. A greater percentage of patients 75 years or older had enrolled in older-patient-specific trials compared with the cohort of age-unspecified trials: 26% versus 6% (p < .0001). Median overall survival (OS) was 12.8 years (95% confidence interval [CI], 11.9–13.7) and 13.5 years (95% CI, 12.9–14.1) for older-patient-specific and age-unspecified trials, respectively. OS was comparable (hazard ratio [HR], 1.08; 95% CI, 0.92–1.28; p = .34; referent: age-unspecified trials), after adjusting for age, estrogen receptor status, tumor size, and lymph node status. Similar findings were reached for recurrence-free survival. A lower rate of grade 3–5 adverse events (hematologic and nonhematologic) was reported in older-patient-specific trials (43% vs. 58%; p < .0001). Sensitivity analysis with chemotherapy only trials and subset analysis, adjusted for performance score, yielded similar OS results. Conclusion Older-patient-specific trials appear to address this underrepresentation of older patients with ostensibly comparable outcomes. Clinical trial identification numbers. NCT00003088 (CALGB 9741); NCT00024102 (CALGB 49907); NCT00068601 (CALGB 40401); NCT00005970 (NCCTG N9831)