OnCo
trialsTrialNegative

XPORT-EC-042 / ENGOT-EN20 / GOG-3083

A promising subgroup finding from an earlier trial did not hold up: selinexor maintenance missed its main goal in TP53-normal endometrial cancer.

The primary PFS endpoint was not met (topline 30 July 2026). A trend favoured selinexor in the modified intent-to-treat population (median PFS 12.75 vs 7.43 months), consistent with the SIENDO exploratory subgroup that motivated the trial, but not statistically significant. Karyopharm cut its endometrial investment. A lesson in the limits of post-hoc biomarker subgroups.

Setting
TP53-wild-type advanced or recurrent endometrial cancer after response to platinum: maintenance selinexor vs placebo
Phase
Phase 3
Sponsor
Karyopharm
Registry
Headline result
Primary PFS endpoint not met; mPFS 12.75 vs 7.43 months (mITT) not significant.
Reported
2026

Outcomes

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In plain words
What these results mean for people, not percentages
Progression-free survival (mITT)primarysurrogate endpoint
  • Median 12.8 vs 7.4 months with Selinexor compared with Placebo; about 5.3 months longer for half the group.
  • A median is a midpoint: half the people did better than this and half did worse, so it is not a prediction for any one person.
  • The p-value (not significant) means the difference could plausibly be due to chance.
  • This is a surrogate endpoint: it measures the cancer being controlled or absent on scans and tests, which often, but not always, translates into living longer.
  • These results apply to the people the trial enrolled: TP53-wild-type advanced or recurrent endometrial cancer after response to platinum: maintenance selinexor vs placebo. People in a different situation may not see the same effect.
  • The trial selected people by a biomarker (TP53); the result should not be assumed for people whose cancer does not have it.

Numbers are from the trial as recorded here; see the source links in the table below. This is orientation, not medical advice: ask your team how closely the trial population matches you.

Progression-free survival (mITT)primary
· p = not significant
Selinexor
12.75 mo
Placebo
7.43 mo

Not statistically significant

Source
EndpointArmnValueHR (95% CI)pSource
Progression-free survival (mITT)primarySelinexor12.75 monthsnot significantlink
Placebo7.43 months

Connected

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