Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL
David Cella , Toni K. Choueiri , Steven I. Blum , Flavia Ejzykowicz , Joel Wallace , Joshua Zhang , Burcin Simsek , Cristina Ivanescu , Robert J. Motzer
Background: In CheckMate 9ER, NIVO+CABO improved or maintained HRQoL vs SUN in previously untreated aRCC. We report an exploratory analysis of HRQoL in International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk-based subgroups treated with NIVO+CABO vs SUN in CheckMate 9ER (minimum follow-up, 36.5 mo). Methods: Subgroups were stratified by IMDC categories of favorable (F) risk (score = 0) or intermediate/poor (I/P) risk (score = 1–6) at randomization. HRQoL was evaluated using Functional Assessment of Cancer Therapy–Kidney Symptom Index (FKSI-19). Changes from baseline (BL) through wk 151 were analyzed using mixed-model repeated measures (MMRM). Bother due to treatment side effects (FKSI-19 item GP5) was assessed using a generalized estimating equations model (response dichotomized as minimal [“not at all” or “a little bit”] vs notable [“somewhat,”“quite a bit,” or “very much”]). Cox proportional hazards (CPH) modeling was used to evaluate time to confirmed deterioration (TTCD). Results: Differences in least square means (LSM) for FKSI-19 scores through wk 151 indicated HRQoL benefit in the NIVO+CABO arm over the SUN arm for I/P-risk patients (n = 505) but not for F-risk patients (n = 146). In the I/P-risk subgroup, longitudinal analysis of FKSI-19 total scores indicated that HRQoL improved through wk 151 in the NIVO+CABO arm but decreased from BL in the SUN arm. HRQoL declined from BL through wk 151 in F-risk patients in the NIVO+CABO and SUN arms. Patients were less likely to be bothered by side effects of NIVO+CABO vs SUN regardless of risk (I/P-risk odds ratio [OR], 0.50; 95% CI, 0.34–0.75; F-risk OR, 0.51; 95% CI, 0.28–0.91). TTCD analysis of FKSI-19 scores of the I/P-risk subgroup indicated that the NIVO+CABO arm had lower deterioration risk than the SUN arm. For the F-risk subgroup, risk based on FKSI-19 total scores was similar for both treatment arms. Conclusions: Compared with SUN, NIVO+CABO improved or maintained HRQoL in I/P-risk patients and had less side effect bother in all subgroups. There were no significant differences between treatment arms for F-risk patients. Clinical trial information: NCT03141177.
IMDC risk subgroup | FKSI-19 total or subscale | LSM differenceb(95% CI) | Hazard ratio for TTCD (95% CI) |
---|---|---|---|
I/P-risk (n = 505) | Total | 3.33 (1.96-4.70) | 0.58 (0.44-0.76) |
Disease-related symptoms (DRS) | 1.59 (1.01-2.18) | 0.55 (0.40-0.76) | |
DRS-physical (DRS-P) | 2.12 (1.27-2.96) | 0.51 (0.37-0.70) | |
Functional well-being (FWB) | 0.54 (0.09-0.98) | 0.58 (0.41-0.81) | |
F-risk (n = 146) | Total | -0.44 (-2.63 to 1.75) | 0.99 (0.64-1.54) |
DRS | 0.15 (-0.67 to 0.97) | 1.09 (0.66-1.82) | |
DRS-P | 0.04 (-1.21 to 1.30) | 0.78 (0.47-1.27) | |
FWB | -0.52 (-1.30 to 0.26) | 1.03 (0.61-1.73) |
aThrough wk 151. bPositive value favors NIVO+CABO over SUN; negative value indicates deterioration.
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