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. 2024 Mar 20;10:23. doi: 10.1038/s41523-024-00627-5

Table 2.

Clinical drug trial with documentation on ILC available

SETTING TRIAL DRUG PATIENT POPULATION % ILC INCLUDED SUB-ANALYSIS CENTRAL PATHOLOGY
Neoadjuvant SAFIA59 palbociclib (CDK4/6i) HR+HER2− 12.0 No No
IMpassion03133,a atezolizumab (ICI) TNBC 2.0 No No
GeparQuinto Lapatinib36 lapatinib (TKI) HR− HER2+ or HR+HER2+ if cN+ 2.8 Yes No
EPHOS B60 lapatinib (TKI) HER2+ 4.0 No No
GeparQuinto Everolimus35 everolimus (mTORi) HR− HER2+ or HR+HER2+ if cN+ 10.8 Yes No
Adjuvant MAINtenance Afinitor61 everolimus (mTORi) HR+HER2− 16.3 No No
Metastatic PALOMA 223,b] palbociclib (CDK4/6i) HR+HER2− 14.7 No No
PALOMA 424,b] palbociclib (CDK4/6i) HR+HER2− 3.8 No No
NCT0028165834,a] lapatinib (TKI) HER2+ 4.7 No No
DETECT III62 lapatinib (TKI) HER2− with HER2+ CTCs 9.8 No No
BELLE-238 buparlisib (PI3Ki) HR+HER2− 13.0 No No
INPRES63 everolimus (mTORi) HR+HER2− 26.0 Yes No
IMPROVE37 everolimus (mTORi) HR+HER2− 24.7 No No

cN clinical nodal status, CTCs circulating tumor cells, HR hormone receptor, TNBC triple negative breast cancer.

aExclusion of non-measurable disease.

bExclusion of non-measurable disease with the exception of bone-only disease.