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. Author manuscript; available in PMC: 2021 Aug 1.
Published in final edited form as: Clin Genitourin Cancer. 2020 Mar 14;18(4):252–257.e2. doi: 10.1016/j.clgc.2020.03.003

Table 1.

Treatment exposure

P# Prior treatment
(line)
Time on
prior
therapy
(months)
Line of
LEN + EVE
treatment
Discontinued
LEN + EVE
treatment
Reason for
discontinuation
Time on
therapy
(months)
Follow-up
(months)
Prior TKI
1 Sunitinib (1) 0.8 2nd Yes PD 15c 17
3 Pazopaniba (1) 1.5 Start new
Cabozantinibb (2) 0.5 3rd Yes anticancer
regimen
7d 9
Prior ICI
4 Ipilimumab + nivolumab (1) 1 2nd Yes AE 8 9
5 Ipilimumab + nivolumab (1) 2 2nd No NA 6+ 11+
7 Ipilimumab + nivolumabb (1) 1 2nd Yes AE 7 9+
Prior TKI and ICI
2 Sunitinib (1) 2
Nivolumab + lenvatinib (2) 3 3rd Yes PD 8 11
6 Cabozantinibb (1) 1.5
Ipilimumab + nivolumab (2) 1.5 3rd Yes PD 3 4
a

Patient had mixed response.

b

Discontinued because of toxicity rather than disease progression.

c

Treatment was discontinued for 5 days due to toxicity, then resumed due to progression of brain metastasis.

d

Treatment was discontinued for 5 weeks because of the approval of nivolumab plus ipilimumab combination in mRCC but was later resumed due to progression of skin lesions on the ICI combination.

AE, adverse event; EVE, everolimus; ICI, immune checkpoint inhibitor; LEN, lenvatinib; NA, not applicable: P, patient; PD, progressive disease; TKI, tyrosine kinase inhibitor.