CAPOX, Bevacizumab and Trastuzumab for Patients With HER2-Positive Metastatic Esophagogastric Cancer

Gastric Cancer Clinical Trial

Official title:

Phase II Trial of CAPOX, Bevacizumab and Trastuzumab for Patients With HER2-Positive Metastatic Esophagogastric Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01191697
• Other study ID #: 09-457
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: February 2011
• Est. completion date: July 2024

Study information

• Verified date: August 2023
• Source: Dana-Farber Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the safety and effectiveness of a combination of chemotherapy, capecitabine and oxaliplatin, plus the antibodies bevacizumab and trastuzumab. Trastuzumab (also called Herceptin) is an antibody that attacks HER2 protein in tumor cells. Bevacizumab (also called Avastin) works by slowing or stopping the growth of cells in cancer tumors by decreasing the blood supply of the tumors. If blood supply is decreased, oxygen and nutrients that are needed for tumor growth are decreased. The chemotherapy used in this trial is called CAPOX, which is an abbreviation of capecitabine and oxaliplatin.

Description:

• We recommend that the participants have a vascular access device, more commonly known as a PORT, inserted prior to starting chemotherapy. A port is a small device that is inserted under the skin (usually near the collar bone) by a minor surgical procedure and is then connected to one of the large veins inside the chest. The port will be used to give the intravenous medications.

• During the first cycle, the participant will receive trastuzumab intravenously on Day 1. Cycle 2 will then start one week later. On this day, bevacizumab will be given intravenously first followed by trastuzumab and then oxaliplatin. The participant will then start taking capecitabine tablets orally twice a day for 14 days. Each treatment cycle is 21 days long.

• Participants will have the following tests and procedures at specific time points during study treatment; physical exam, blood tests, CT scan, MUGA scan or echocardiogram, and urine test.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 37
• Est. completion date: July 2024
• Est. primary completion date: December 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Confirmed HER2-positive esophageal, GE junction or gastric adenocarcinoma that is metastatic or unresectable.

• All patients must have available tumor sample (either paraffin block or 15 freshly cut, unstained slides) prior to study entry.

Part II: Patient must have primary esophagogastric tumor in place or other tumor that is accessible for mandatory biopsy.

• Measurable disease, defined in RECIST 1.1

• 18 years of age or older

• Life expectancy of greater than 12 weeks

• ECOG performance status of 0 or 1

• Organ and marrow function as outlined in the protocol

• Women of child-bearing potential and men must agree to use adequate contraception during study participation and for 30 days from the date of the last study drug administration.

• Part II only: Participant agrees to undergo mandatory pre and post loading dose of trastuzumab biopsy for correlative science.

Exclusion Criteria:

• Prior therapy with any of the following; capecitabine, oxaliplatin, bevacizumab or trastuzumab is not allowed. May have received and completed adjuvant therapy at least 6 months prior to study entry or one prior therapy for metastatic disease as long as it did not include any of the above agents.

• Chemotherapy or radiotherapy to greater then 25% of bone marrow within 4 weeks prior to entering the study.

• Palliative radiation therapy to isolated bone metastasis within 2 weeks of initiating therapy.

• Major surgery, open biopsy, significant traumatic injury within 4 weeks prior to study entry,.

• Minor surgery, including placement of vascular access device within 7 days prior to the first dose of bevacizumab.

• Residual toxicity from prior chemotherapy and/or radiation therapy of Grade 2 or greater.

• Participants may not be receiving any concurrent investigational agents

• Active brain or other CNS metastasis by history or clinical examination.

• History of allergic reactions attributed to compounds of similar chemical or biologic composition to capecitabine, bevacizumab or trastuzumab. No known allergy or hypersensitivity to Chinese hamster ovary, or any of the study agents. No known DPD deficiency.

• Warfarin is prohibited; anticoagulation using low molecular weight heparin is allowed.

• Uncontrolled, intercurrent illness

• Patients with a history of other malignancy are not eligible except for the following circumstances: disease-free for at least 3 years and are deemed to be at low risk for recurrence of that malignancy; cervical cancer in situ, basal cell or squamous cell carcinoma of the skin that was treated with curative intent within the past 5 years.

• Known HIV seropositivity, hepatitis C, acute or chronic hepatitis B or other serious active infection

• LVEF less than 50% as determined by MUGA scan or echocardiogram within 28 days prior to initiation of therapy

• Inadequately controlled hypertension

• History of prior hypertensive crisis or hypertensive encephalopathy

• History of any arterial thrombosis, CVA, TIA, MI or unstable angina in past 6 months.

• Evidence of bleeding diathesis or coagulopathy

• Serious, unhealed wounds, bone fractures or skin ulcers

• Pregnant or breast feeding

• Greater than grade 1 peripheral neuropathy at baseline

• Lack of physical integrity of the upper gastrointestinal tract or malabsorption syndrome.

Related Conditions & MeSH terms

• Esophageal Cancer
• Gastric Cancer

Intervention

Drug:
• bevacizumab
Given intravenously on day 1 of each cycle beginning cycle 2
• trastuzumab
Given intravenously on day 1 of each treatment cycle
• oxaliplatin
Given intravenously on day one of each cycle beginning cycle 2
• capecitabine
Taken orally on days 1-14 of each cycle beginning cycle 2

Locations

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

Sponsors (4)

Lead Sponsor	Collaborator
Dana-Farber Cancer Institute	Brigham and Women's Hospital, Genentech, Inc., Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

References & Publications (25)

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* Note: There are 25 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective Response Rate (ORR)	ORR was defined as the percentage of participants achieving complete response (CR) or partial response (PR) on treatment based on RECIST 1.1 criteria. Per RECIST 1.1 for target lesions: CR is complete disappearance of all target lesions and PR is at least a 30% decrease in the sum of longest diameter (LD) of target lesions, taking as reference baseline sum LD. PR or better overall response assumes at a minimum incomplete response/stable disease (SD) for the evaluation of non-target lesions and absence of new lesions.	Patients received a median of 19 cycles of therapy (Interquartile range (IQR): 8 - 34.5 cycles). Median duration of follow-up of 23.2 months (IQR: 11.0 - 46.9 months ).
Secondary	Median Overall Survival	Overall survival based on the Kaplan-Meier method is defined as the time from randomization to death. Participants alive are censored at the last date of contact (including lost-to-follow-up) or at the date of withdrawal of consent, if relevant.	23.2 months (IQR: 11.0 - 46.9 months ).
Secondary	Median Duration of Response (DOR)	DOR is defined as the time from date of first documented confirmed objective response to date of first documented progressive disease (PD). Per RECIST 1.1 for target lesions: PD is at least a 20% increase in sum LD, taking as reference the smallest sum on study with at least 5 mm absolute increase. For non-target lesions, progression-free means no new lesions or unequivocal progression on existing non-target lesions or not evaluated.	23.2 months (IQR: 11.0 - 46.9 months ).
Secondary	Median Progression Free Survival (PFS)	PFS is defined as the duration of time from study entry to documented disease progression (PD) requiring removal from the study or death. Participants alive without PD were censored at the earliest of the date of the last disease evaluation or start of new anticancer therapy. Per RECIST 1.1 for target lesions: PD is at least a 20% increase in sum LD, taking as reference the smallest sum on study with at least 5 mm absolute increase. For non-target lesions, progression-free means no new lesions or unequivocal progression on existing non-target lesions or not evaluated.	Patients received a median of 19 cycles of therapy (Interquartile range (IQR): 8 - 34.5 cycles). Median duration of follow up of 23.2 months (IQR: 11.0 - 46.9 months ).