HERACLES: Evaluation of Trastuzumab in Combination With Lapatinib or Pertuzumab in Combination With Trastuzumab-Emtansine to Treat Patients With HER2-positive Metastatic Colorectal Cancer

Sponsor

Fondazione del Piemonte per l'Oncologia (Other)

Overall Status

Unknown status

CT.gov ID

NCT03225937

Collaborator

(none)

Enrollment

Locations

Arms

Duration (Months)

7.7

Patients Per Site

0.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Metastatic Colorectal Cancer	Drug: Trastuzumab, Lapatinib Drug: Pertuzumab, trastuzumab-emtansine	Phase 2

Detailed Description

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.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

54 participants

Allocation:

Non-Randomized

Intervention Model:

Sequential Assignment

Intervention Model Description:

two sequential cohorts: cohort A (lapatinib + trastuzumab); cohort B (pertuzumab + trastuzumab-emtansine).two sequential cohorts: cohort A (lapatinib + trastuzumab); cohort B (pertuzumab + trastuzumab-emtansine).

Masking:

None (Open Label)

Primary Purpose:

Treatment

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

Study Start Date :

Aug 1, 2012

Anticipated Primary Completion Date :

Dec 1, 2018

Anticipated Study Completion Date :

Jun 1, 2019

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Cohort A Trastuzumab and lapatinib	Drug: Trastuzumab, Lapatinib Patients enrolled in Cohort A will receive lapatinib 1000 mg daily per os + trastuzumab 4 mg/kg iv load, followed by 2 mg/kg iv weekly. Patients will receive study medication until disease progression, unacceptable toxicity, withdrawal of consent or death, whichever come first.
Experimental: Cohort B Pertuzumab and Trastuzumab-emtansine	Drug: Pertuzumab, trastuzumab-emtansine Patients enrolled in Cohort B will receive pertuzumab 840 mg iv load, followed by 420 mg iv Q3weeks + trastuzumab-emtansine 3.6 mg/kg iv on day 1 of each subsequent 3 week cycle. Patients will receive study medication until disease progression, unacceptable toxicity, withdrawal of consent or death, whichever come first.

Arm

Intervention/Treatment

Experimental: Cohort A

Trastuzumab and lapatinib

Drug: Trastuzumab, Lapatinib

Patients enrolled in Cohort A will receive lapatinib 1000 mg daily per os + trastuzumab 4 mg/kg iv load, followed by 2 mg/kg iv weekly. Patients will receive study medication until disease progression, unacceptable toxicity, withdrawal of consent or death, whichever come first.

Experimental: Cohort B

Pertuzumab and Trastuzumab-emtansine

Drug: Pertuzumab, trastuzumab-emtansine

Patients enrolled in Cohort B will receive pertuzumab 840 mg iv load, followed by 420 mg iv Q3weeks + trastuzumab-emtansine 3.6 mg/kg iv on day 1 of each subsequent 3 week cycle. Patients will receive study medication until disease progression, unacceptable toxicity, withdrawal of consent or death, whichever come first.

Outcome Measures

Primary Outcome Measures

Objective Response Rate according to RECIST 1.1 criteria [Time Frame: every 8 weeks (cohort A) or every 9 weeks (cohort B) from date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]

Secondary Outcome Measures

Description of the frequency and severity of Adverse Events based on the NCI -CTCAE V4.0 [Time Frame: weekly (cohort A) or every 21 days (cohort B) from date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Progression Free Survival [Time Frame: every 8 weeks (cohort A) or every 9 weeks (cohort B) from date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion criteria COHORT A

Histological/confirmed adenocarcinoma of the colon or rectum with metastatic disease not amenable to salvage surgery.
Pathology mandatory requirements: the original tumour specimen must be KRAS WT and SISH/FISH positive or IHC 3+ positive in more than 50% cells. Note: for immunohistochemistry a positive staining (3+) is defined as an intense membrane staining which can be circumferential, basolateral, or lateral of the tumor cells. the original paraffin block or a minimum of 15 polarized unstained slides from the original paraffin block must be made available to the Pathology Core within 15 days from registration.
Age ≥18
ECOG PS 0-1
Measurable disease as defined by RECIST 1.1 criteria.
Progression (PD) while on, or within 6 months from therapy with approved standard drugs.
Unless otherwise contraindicated patients should have received and failed the following previous therapies for mCRC: fluoropyrimidines, oxaliplatin, irinotecan, cetuximab or panitumumab containing regimens. Bevacizumab is allowed
Adequate haematological function as defined by: ANC > 1.5 x 109/L, platelet count >100 x 109/L, haemoglobin > 10 g/dL
Adequate renal function, as defined by: creatinine < 1.5 x UNL
Adequate hepatobiliary function, as defined by the following baseline liver function tests: total serum bilirubin <1.5 upper normal limit (UNL); alanine aminotransferase (ALT), aspartate aminotransferase (AST) < 2.5xUNL; alkaline phosphatase (AP) < 2.5xUNL, if total alkaline phosphatase (AP) > 2.5xUNL, alkaline phosphatase liver fraction must be < 2.5xUNL
Adequate contraception for all fertile patients
Negative pregnancy test

Exclusion criteria COHORT A

Subjects meeting any of the following criteria must not be enrolled in the study:

Radiotherapy ≤ 4 weeks prior to enrolment.
Other chemotherapy or biological therapy treatment ≤ 4 weeks prior to enrolment.
Symptomatic brain metastases.
Active infection.
Gastro-intestinal abnormalities, inability to take oral medication, any condition affecting absorption.
Impaired cardiac function including any of the following: uncontrolled hypertension (systolic >150 mmHg and/or diastolic > 100 mmHg) or clinically significant (i.e. active) cardiovascular disease: cerebrovascular accident/stroke or myocardial infarction within 6 months prior to first study medication; unstable angina; chronic heart failure (CHF) of New York Heart Association (NYHA) Grade II or higher (See Appendix 4); or serious cardiac arrhythmia requiring medication, baseline Left Ventricular Ejection Fraction (LVEF) ≤ 55% measured by echocardiography (ECHO).
Major surgery in the two weeks prior to entering the clinical trial.
Concurrent treatment with any other anti-cancer therapy.
History of another neoplastic disease (except basal cell carcinoma of the skin or uterine cervix carcinoma in situ adequately treated), unless in remission for ≥ 5 years.
Patient unable to comply with the study protocol owing to psychological, social or geographical reasons.
Pregnant and lactating women.
Patients with history of hypersensitivity to either IP or excipients.
Men and women of childbearing potential who are not using an effective method of contraception.
Participation in another clinical trial or treatment with any investigational product within 4 weeks prior to inclusion in this study.
Subjects who have current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment).
Patient with unresolved hypokalaemia, hypomagnesemia or hypocalcaemia

Inclusion criteria COHORT B

Histological/confirmed adenocarcinoma of the colon or rectum with metastatic disease not amenable to salvage surgery.
The original tumour specimen must be RAS (KRAS exons 2 3 4; NRAS exons 2 3 4) wild type and SISH/FISH positive or IHC 2+/3+ positive in more than 50% cells.
Age ≥18.
ECOG PS 0-1.
Measurable disease as defined by RECIST 1.1 criteria.
Progression (PD) while on, or within 6 months from therapy with approved standard drugs.
Unless otherwise contraindicated, patients must have received and failed fluoropyrimidines, oxaliplatin, irinotecan -containing regimens as previous therapies for metastatic disease.
Patients having failed only one line of chemotherapy for their metastatic diseases are eligible if they have received:
FOLFOXIRI;
FOLFIRI after progression to adjuvant FOLFOX, occurred on treatment or within 6 months after treatment completion.
Treatments with bevacizumab, aflibercept or regorafenib and cetuximab or panitumumab are allowed.
Adequate hematological function as defined by: ANC <= 1.5 x 109/L, platelet count

=100 x 109/L, haemoglobin >= 10 g/dL

Adequate renal function, as defined by: creatinine <= 1.5 x UNL
Adequate hepato-biliary function, as defined by the following baseline liver function tests:
total serum bilirubin <=1.5 upper normal limit (UNL)
alanine aminotransferase (ALT), aspartate aminotransferase (AST) < 2.5xUNL
alkaline phosphatase (AP) <= 2.5xUNL; if total alkaline phosphatase (AP) > 2.5xUNL, alkaline phosphatase liver fraction must be <= 2.5xUNL
Adequate contraception for all fertile patients
Negative pregnancy test

Exclusion criteria COHORT B

Radiotherapy <= 4 weeks prior to enrolment.
Other chemotherapy or biological therapy treatment ≤ 4 weeks prior to enrolment.
Symptomatic brain metastases.
Active infection.
Gastro-intestinal abnormalities, inability to take oral medication, any condition affecting absorption.
Impaired cardiac function including any of the following: uncontrolled hypertension (systolic >150 mmHg and/or diastolic > 100 mmHg) or clinically significant (ie active) cardiovascular disease: cerebrovascular accident/stroke or myocardial infarction within 6 months prior to first study medication; unstable angina; chronic heart failure (CHF) of New York Heart Association (NYHA) Grade II or higher (See Appendix 4); or serious cardiac arrhythmia requiring medication, baseline Left Ventricular Ejection Fraction (LVEF) ≤ 55% measured by echocardiography (ECHO).
Major surgery in the two weeks prior to entering the clinical trial.
Concurrent treatment with any other anti-cancer therapy.
History of another neoplastic disease (except basal cell carcinoma of the skin or uterine cervix carcinoma in situ adequately treated), unless in remission for ≥ 5 years
Patient unable to comply with the study protocol owing to psychological, social or geographical reasons.
Pregnant and lactating women.
Patients with history of hypersensitivity to either IP or excipients.
Men and women of childbearing potential who are not using an effective method of contraception.
Participation in another clinical trial or treatment with any investigational product within 4 weeks prior to inclusion in this study.
Subjects who have current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment).
Patient with unresolved hypokalaemia, hypomagnesemia or hypocalcaemia.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Fondazione del Piemonte per l'Oncologia - IRCCS	Candiolo	Please Select	Italy	10060
2	AOU Policlinico S. Orsola Malpighi	Bologna		Italy
3	Grande Ospedale Metropolitano Niguarda	Milano		Italy	20162
4	Seconda Università di Napoli	Napoli		Italy
5	Istituto Oncologico Veneto - IRCCS	Padova		Italy
6	Campus Biomedico	Roma		Italy
7	AOU Città della Salute e della Scienza di Torino	Torino		Italy