Metastatic Colorectal Cancer Clinical Trial
Official title:
Open-Label, Phase II Study of Trastuzumab in Combination With Lapatinib (Cohort A) or Pertuzumab in Combination With Trastuzumab-emtansine (Cohort B) in Patients With HER2-positive Metastatic Colorectal Cancer: the HERACLES (HER2 Amplification for Colo-rectaL Cancer Enhanced Stratification)Trial
This is a Phase II multi-center 2-sequential cohorts trial, designed to assess the objective
response rate of two anti HER2 combination in advanced disease CRC patients harbouring an
amplified HER2 tumor assessed according to HERACLES Diagnostic Criteria by FISH/SISH.
Cohort A: monoclonal antibody trastuzumab, used in combination with the small molecule
tyrosine kinase inhibitor lapatinib.
Cohort B, monoclonal antibody pertuzumab, used in combination with the antibody drug
conjugate trastuzumab-emtansine.
Please note that cohort A accrual has been closed and endpoint already reached.
Investigators identified HER2 amplification as a potential onco-driver and marker of de novo
resistance to anti-EGFR therapy in mCRC patients for which other known genetic alterations
conferring resistance to anti EGFR antibodies were excluded.
Exploiting direct transfer xenografts of mCRC surgical samples in mice (xenopatients),
investigators conducted a multi-arm study in HER2-amplified xenopatients showing that
combinations of the dual EGFR/HER2 inhibitor lapatinib and the anti-HER2 moAb trastuzumab
induced long-lasting tumor regressions, while monotherapy with lapatinib led to stabilization
and monotherapy with trastuzumab was ineffective. On these findings investigators designed
the HERACLES trial.
HERACLES is an open-label Phase II, 2-sequential cohorts trial, assessing the response rate
(ORR) of Trastuzumab combined Lapatinib (Cohort A) or Pertuzumab combined with
trastuzumab-emtansine (Cohort B), in metastatic colorectal patients harboring an amplified
HER2 tumors .
HER2 positivity is centrally established by immunohistochemistry (IHC) and Silver In Situ
Hybridization (SISH). To be HER2 eligible the original tumor, or the biopsied metastasis
(whichever is last available), must be IHC 3+ or 2+ in more than 50% of cells, confirmed by
SISH or FISH with a HER2:CEP17 ratio ≥ 2.0. For IHC a positive staining (3+) is defined as an
intense membrane staining which can be circumferential, basolateral, or lateral of the tumor
cells.
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