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. 2023 Aug 30;15(17):4330.
doi: 10.3390/cancers15174330.

Combined Nivolumab and Ipilimumab in Octogenarian and Nonagenarian Melanoma Patients

Affiliations

Combined Nivolumab and Ipilimumab in Octogenarian and Nonagenarian Melanoma Patients

Constance Reichert et al. Cancers (Basel). .

Abstract

Data regarding elderly melanoma patients treated with anti-PD-1 or anti-CTLA-4 antibodies are in favor of tolerability outcomes that are similar to those of younger counterparts. However, there are very few studies focusing on elderly patients receiving nivolumab combined with ipilimumab (NIVO + IPI). Here, we ask what are the current prescribing patterns of NIVO + IPI in the very elderly population and analyze the tolerance profile. This French multicenter retrospective study was conducted on 60 melanoma patients aged 80 years and older treated with NIVO + IPI between January 2011 and June 2022. The mean age at first NIVO + IPI administration was 83.7 years (range: 79.3-93.3 years). Fifty-five patients (92%) were in good general condition and lived at home. Two dosing regimens were used: NIVO 1 mg/kg + IPI 3 mg/kg Q3W (NIVO1 + IPI3) in 27 patients (45%) and NIVO 3 mg/kg + IPI 1 mg/kg Q3W (NIVO3 + IPI1) in 33 patients (55%). NIVO + IPI was a first-line treatment in 39 patients (65%). The global prevalence of immune-related adverse events was 63% (38/60), with 27% (16/60) being of grade 3 or higher. Grade ≥ 3 adverse events were less frequent in patients treated with NIVO3 + IPI1 compared with those treated with NIVO1 + IPI3 (12% versus 44%, p = 0.04). In conclusion, the prescribing patterns of NIVO + IPI in very elderly patients are heterogeneous in terms of the dosing regimen and line of treatment. The safety profile of NIVO + IPI is reassuring; whether or not the low-dose regimen NIVO3 + IPI1 should be preferred over NIVO1 + IPI3 in patients aged 80 years or older remains an open question.

Keywords: anti-CTLA-4; anti-PD-1; elderly; immune checkpoint inhibitors; melanoma; nonagenarian; octogenarian.

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Conflict of interest statement

E.M., C.L., L.M., C.N., E.F.B., and F.B.-P. received financial support from BMS, MSD, Pierre Fabre, and Novartis outside the submitted work. C.B. received financial support from BMS and MSD outside the submitted work. B.B. received financial support from BMS, MSD and Pierre Fabre outside the submitted work. N.M. received financial support from BMS, MSD, Novartis, Sanofi outside the submitted work. The other authors declare no conflict of interest.

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