Pertuzumab and Cetuximab in Treating Patients With Previously Treated Locally Advanced or Metastatic Colorectal Cancer

Recurrent Rectal Cancer Clinical Trial

Official title:

A Phase I/II Trial of Pertuzumab in Combination With Cetuximab and Irinotecan in Previously Treated Metastatic Colorectal Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00551421
• Other study ID #: NCI-2009-00241
• Secondary ID: 07-070U01CA06249
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: October 30, 2007
• Last updated: March 11, 2015
• Start date: October 2007
• Est. completion date: June 2012

Study information

• Verified date: July 2014
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Monoclonal antibodies, such as pertuzumab and cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Giving pertuzumab together with cetuximab may kill more tumor cells. This phase I/II trial is studying the side effects and best dose of pertuzumab when given together with cetuximab and to see how well they work in treating patients with previously treated locally advanced or metastatic colorectal cancer

Description:

PRIMARY OBJECTIVES:

I. To determine the safety, tolerability, and recommended phase II dose of pertuzumab when administered in combination with cetuximab in patients with cetuximab-refractory locally advanced or metastatic colorectal cancer.

II. To evaluate the objective tumor response rate (RR) in patients treated with this regimen.

SECONDARY OBJECTIVES:

I. To evaluate the median progression-free survival (PFS) of patients treated with this regimen.

II. To evaluate the median overall survival (OS) of patients treated with this regimen.

III. To evaluate the RR, PFS, and OS in a subgroup of patients who are EGFR-positive by immunohistochemistry.

IV. To explore the relationship between skin rash and the efficacy outcomes of RR, PFS, and OS in these patients.

V. To explore the relationship between objective tumor response on positron emission tomography (PET) scan after course two and the efficacy outcomes of RR, PFS, and OS in these patients.

VI. To explore the relationship between a variety of laboratory correlates and the efficacy outcomes of RR, PFS, and OS in these patients.

OUTLINE: This is a multicenter, phase I dose-escalation study of pertuzumab followed by a phase II study.

PHASE I: Patients receive pertuzumab IV over 30-60 minutes on day 1. Patients also receive cetuximab IV over 60-120 minutes on days 2, 8, and 15 of course 1 and on days 1, 8, and 15 in all subsequent courses.

Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

PHASE II: Patients receive treatment as in phase I. Pertuzumab is administered at the recommended phase II dose (determined in phase I). Previously collected tumor tissue samples are analyzed for correlative studies. Samples are analyzed for KRAS mutations via polymerase chain reaction and pyrosequencing; EGFR expression via immunohistochemistry and fluorescent in situ hybridization (FISH); HER receptor and ligand gene expression; and circulating tumor cells. Additional blood samples are collected periodically to isolate circulating tumor cells and are analyzed via FISH analysis.

After completion of study treatment, patients are followed at 30 days and then periodically thereafter.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 17
• Est. completion date: June 2012
• Est. primary completion date: November 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with a history of colorectal cancer (CRC) treated by surgical resection and who develop radiological or clinical evidence of metastatic disease do not require separate histological or cytological confirmation of metastatic disease unless 1 of the following criteria are met:

• More than 5 years has elapsed between the primary surgery and the development of metastatic disease

• The primary cancer was stage I

• Patients must have representative tumor specimens in paraffin blocks or at least 15 unstained slides with an associated pathology report obtained at any time prior to study entry:

• Cytology specimens are not acceptable replacements

• Patients must have their tumor tissue screened for KRAS mutation status, and be found to have a KRAS wild-type tumor:

• No KRAS-mutated tumor

• Locally advanced or metastatic disease

• Not curable by surgery or amenable to radiotherapy with curative intent

• Must have received an cetuximab-containing regimen for at least 6 weeks for treatment of metastatic disease

• Documented progression of disease or intolerable toxicity during or within 3 months of receiving this regimen

• Patients who have received an cetuximab-containing regimen as adjuvant therapy for resected stage II or III CRC are eligible provided recurrent disease is documented < 6 months after completion of adjuvant treatment

• Must have received >= 1 prior chemotherapeutic regimen for treatment of metastatic disease with any of the following:

• Cetuximab

• Must have resolution of any skin rash related to prior treatment with cetuximab

• No prior cetuximab which required a dose reduction for toxicity

• 5-fluorouracil or capecitabine

• Irinotecan hydrochloride or oxaliplatin

• Measurable disease by CT scan or physical exam

• ECOG performance status (PS) 0-1 (Karnofsky PS 70-100%)

• Life expectancy > 12 weeks

• Absolute neutrophil count >= 1,500/mcL

• Platelet count >= 100,000/mcL

• Leukocytes >= 3,000/mcL

• Hemoglobin >= 9 g/dL (transfusion, erythropoietin, or other approved hematopoietic growth factors allowed)

• Total bilirubin =< 1.5 times upper limit of normal (ULN)

• AST and ALT =< 5 times ULN

• Creatinine normal OR Creatinine clearance >= 60 mL/min

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception prior to and during study therapy

• Cardiac left ventricular ejection fraction >= 50% OR >= lower limit of normal

• No evidence of left ventricular wall motion abnormalities as measured by ECHO or MUGA scan

• None of the following cardiac conditions:

• Uncontrolled high blood pressure

• Unstable angina

• Symptomatic congestive heart failure

• Congestive heart failure, cardiac dysfunction, or cardiomyopathy requiring medication treatment

• Myocardial infarction within the past 6 months

• Serious uncontrolled cardiac arrhythmia

• New York Heart Association class III or IV heart disease

• No active or uncontrolled infection

• No predisposing colonic or small bowel disorders in which the symptoms are uncontrolled as indicated by baseline pattern of > 3 loose stools/day (in patients without a colostomy or ileostomy)

• Patients with a colostomy or ileostomy may be eligible at investigator discretion

• No psychiatric illness/social situation that would limit compliance with study requirements

• No other prior or concurrent malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ carcinoma of the cervix, lobular carcinoma in situ in one breast, or other cancer from which the patient has been disease-free for at least 5 years

• No other medical or psychiatric disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the study results or render the patient at high risk for treatment complications

• No history of allergic reactions, hypersensitivity, or intolerance to cetuximab, and/or compounds of similar chemical or biologic composition to pertuzumab or cetuximab (i.e., other monoclonal antibodies such as bevacizumab) that led to discontinuation of the drug

• Patients able to tolerate subsequent infusions after a reaction are eligible

• At least 4 weeks since prior major surgery (e.g., laparotomy) and recovered (Insertion of a vascular access device is not considered major or minor surgery)

• At least 2 weeks since prior minor surgery and recovered (Insertion of a vascular access device is not considered major or minor surgery)

• At least 4 weeks since prior major radiotherapy (e.g., chest or bone palliative radiotherapy)

• At least 4 weeks since prior bevacizumab

• More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin C) and recovered

• No prior agents directed against EGFR and/or HER2

• No more than one prior treatment regimen for metastatic disease; Prior chemotherapy in the adjuvant setting following resection of stage II or III disease allowed provided the regimen did not contain irinotecan hydrochloride and/or an agent directed against EGFR and/or HER2

• No prior doxorubicin or liposomal doxorubicin at doses > 360 mg/m^2; epirubicin at doses > 720 mg/m^2; mitoxantrone at doses > 120 mg/m^2; or idarubicin at doses > 90 mg/m^2

• No prior radiotherapy to > 15% of the bone marrow

• No prior standard adjuvant chemoradiotherapy for rectal cancer

• No phenytoin, phenobarbital, carbamazepine, or any other enzyme-inducing anti-convulsant drugs (EIACDs) for at least 7 days before, during, and for 7 days after the final dose of irinotecan hydrochloride

• Concurrent gabapentin or other non-EIACDs are allowed

• No St. John's wort for at least 14 days before, during, and for 7 days after the final dose of irinotecan hydrochloride

• No concurrent corticosteroids, except for stable doses of prednisone (< 20 mg/day or equivalent), topical or inhaled corticosteroids, or corticosteroids for reasons unrelated to treatment of colorectal cancer

• No concurrent combination antiretroviral therapy for HIV-positive patients

• No concurrent filgrastim (G-CSF) or sargramostim (GM-CSF) for any of the following reasons:

• To avoid dose reductions or delays

• Prophylactic treatment

• Treatment of febrile neutropenia

• No other concurrent HER family-targeted therapy

• No concurrent rifampin

• No concurrent herbal remedies unless initiated prior to study entry

• No other concurrent investigational agents

• No other concurrent anticancer therapy, including cytotoxic chemotherapy, radiotherapy, immunotherapy, hormonal therapy, or biological anticancer therapy

• Histologically or cytologically confirmed adenocarcinoma of the colon or rectum

• Site of the primary lesion must be or have been confirmed endoscopically, radiologically, or surgically to be or have been in the large bowel

• No known brain metastases

• No concurrent fluconazole

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Adenocarcinoma
• Adenocarcinoma of the Colon
• Adenocarcinoma of the Rectum
• Colorectal Neoplasms
• Rectal Neoplasms
• Recurrent Colon Cancer
• Recurrent Rectal Cancer
• Stage III Colon Cancer
• Stage III Rectal Cancer
• Stage IV Colon Cancer
• Stage IV Rectal Cancer

Intervention

Biological:
• pertuzumab
Given IV
• cetuximab
Given IV

Drug:
• irinotecan hydrochloride
Given IV

Other:
• immunohistochemistry staining method
Correlative study
• fluorescence in situ hybridization
Correlative study
• gene expression analysis
Correlative study
• mutation analysis
Correlative study
• polymerase chain reaction
Correlative study
• laboratory biomarker analysis
Correlative study

Locations

Country	Name	City	State
United States	Dana-Farber Cancer Institute	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Recommended Phase II Dose of Pertuzumab When Administered in Combination With Cetuximab (Phase I)	The regimen was deemed intolerable so there was no recommended phase II dose.	28 days	Yes
Primary	Objective Tumor Response Rate Defined as the Proportion of Patients With a Best Overall Response of CR or PR, Per RECIST Criteria (Phase II)	Objective tumor response rate defined as the proportion of patients with a best overall response of CR or PR, per RECIST criteria (Phase II).	Best tumor response from time period of start of study treatment to study discontinuation.	No
Secondary	Progression-free Survival	The duration of time from start of study treatment to time of objective disease progression or death.	The duration of time from start of study treatment to time of objective disease progression or death.	No
Secondary	Overall Survival	The duration of time from start of study treatment to death from any cause.	The duration of time from start of study treatment to death from any cause.	No