Table 2.

Survival estimates

Total trial cohort (n = 39)Low risk (n = 16)High risk (n = 23)
No. of events1 y2 yNo. of events1 y2 yNo. of events1 y2 y
PFS 18 63% (50-81) 58% (44-76) 75% (57-100) 69% (49-96) 63% (45-87) 63% (45-87) 
PFS post-IR 15 71% (57-87) 65% (52-82) — — 
EFS 19 61% (47-78) 55% (41-74) 69% (49-96) 63% (43-91) 10 58% (40-83) 58% (40-83) 
OS 10 81% (70-95) 76% (63-91) 88% (73-100) 88% (73-100) 72% (55-94) 67% (50-90) 
Total trial cohort (n = 39)Low risk (n = 16)High risk (n = 23)
No. of events1 y2 yNo. of events1 y2 yNo. of events1 y2 y
PFS 18 63% (50-81) 58% (44-76) 75% (57-100) 69% (49-96) 63% (45-87) 63% (45-87) 
PFS post-IR 15 71% (57-87) 65% (52-82) — — 
EFS 19 61% (47-78) 55% (41-74) 69% (49-96) 63% (43-91) 10 58% (40-83) 58% (40-83) 
OS 10 81% (70-95) 76% (63-91) 88% (73-100) 88% (73-100) 72% (55-94) 67% (50-90) 

Data are survival estimate (95% CI).

Risk stratified survival times are calculated from the date of interim assessment.

or Create an Account

Close Modal
Close Modal