TABLE 5

Select Studies Reporting Survival in G3 NENs After Treatment with PRRT, 2016 and 2018

StudyTotal no. patients (N)N: Ki-67 or differentiationTumor primary sitePRRT type administeredPRRT dose reportedOutcome
Thapa et al. 2016 (33)503: Ki-67 > 20%2 panc, 1 rectal, or 2 unknown primary177Lu-DOTATATE (at least 3 cycles)5.55 GBq at 12- to 16-wk intervalsResponders: 2/3 G3, 1/2 poorly diff, 3/5 total
2: poorly diff
Nilica et al. 2016 (40)667: Ki-67 > 20%Panc, GI, lung, unknown90Y-DOTATOC first line; 177Lu-DOTATATE if <2 cm or retreatment (3–4 cycles)3.7 GBq 90Y. 7.4 GBq 177Lu at 10- to 14-wk intervalsNo specific comment
Cycles 2–4 included radiosensitizing chemo: 5FU or capecitabine, or capecitabine temozolomide in pancreatic
Zhang et al. 2018 (29)6969: Ki-67 ≥ 20%46 panc, 11 unknown, 6 small bowel, 3 stomach, 3 rectal177Lu (median number of cycles not mentioned)Median per cycle: 4.5 GBqMedian PFS of 9.6 mo, median OS of 19.9 mo
90Y (median number of cycles not mentioned)Median per cycle: 3.2 GBqKi-67 ≤ 55%, median PFS of 11 mo, OS of 22 mo
Ki-67 > 55%, median PFS of 4 mo, OS of 7 mo
At 3 mo: 34/69 with PR, 15/69 with stable disease, 20/69 with PD
Nicolini et al. 2018 (30)3328: Ki-67 ≥ 20%20 panc, 5 small bowel, 2 stomach, 1 large bowel177Lu (in 4–5 cycles)Median cumulative activity: 21.5 GBq at 6- to 8-wk intervalsOverall median PFS of 23 mo, median OS of 59.9 mo
5: Ki-67 of 15%–20%3 panc, 2 small bowelMedian PFS for Ki-67 ≤ 35% of 26.3 mo vs. 6.8 mo for Ki-67 > 35%
14: poorly diff2/33 patients with PR; 21/33 patients with stable disease
  • Panc = pancreatic; GI = gastrointestinal; diff = differentiated; PR = partial response; PD = progressive disease; In = indium; CI = confidence interval.