A Pilot Study of Neoadjuvant Therapy With Gemcitabine and Cisplatin in Patients With Resectable or Unresectable Intrahepatic Cholangiocarcinoma

Unresectable Intrahepatic Cholangiocarcinoma Clinical Trial

Official title:

A Pilot Study of Neoadjuvant Therapy With Gemcitabine and Cisplatin in Patients With Resectable or Unresectable Intrahepatic Cholangiocarcinoma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02256982
• Other study ID #: 14-275
• Status: Terminated
• Phase: N/A
• First received: September 25, 2014
• Last updated: April 11, 2016
• Start date: October 2014
• Est. completion date: March 2016

Study information

• Verified date: April 2016
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This research study is evaluating the use of radiation therapy in combination with chemotherapy as a possible treatment for intrahepatic cholangiocarcinoma, a rare form of gastrointestinal cancer.

Description:

This study is to assess the possibility of using radiation therapy to treat intrahepatic cholangiocarcinoma. Radiation therapy is used for many other types of malignancies, but its use for the treatment of this form of gastrointestinal cancer has been limited. This treatment is still being studied as research doctors are trying to find out more about its use in the treatment of your form of gastrointestinal cancer. Short course photon radiation and short course proton beam radiation therapies are FDA (U.S. Food and Drug Administration) approved radiation delivery systems. This study will also test the safety of neoadjuvant chemotherapy versus adjuvant chemotherapy. Neoadjuvant therapy is treatment given as a first step to shrink a tumor before the main treatment, which is usually surgery, is given. Adjuvant therapy is additional cancer treatment given after the primary treatment to lower the risk that the cancer will come back.

The current standard of care for patients with intrahepatic cholangiocarcinoma is to offer surgical resection to all patients who have resectable disease and are able to tolerate a major surgical intervention.

The study interventions involved this trial may include one or more of the following:

• Chemotherapy (Gemcitabine and Cisplatin)

• Surgical Resection and Lymphadenectomy

• Radiation Therapy

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Participants must meet the following criteria on screening examination to be eligible to participate in the study:

• Participants must have histologically confirmed Intrahepatic Cholangiocarcinoma (IHC) without evidence of extrahepatic metastasis.

• Participants must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as = 20 mm with conventional techniques or as =10 mm with spiral CT scan.

• Participants with resectable disease must have a single tumor (with no satellite lesions) with a total diameter or longest dimension of = 20cm. Patients with unresectable disease must have a total tumor diameter of <20cm and = 3 lesions. Satellite lesions defined as lesions = 2cm from the dominant lesion are permitted for participants with unresectable disease

• Patients are not allowed to receive prior surgery or chemotherapy for the IHC.

• Patients with age =18 will be included in the study.

• Expected survival must be three months or greater.

• ECOG performance status = 2 (Karnofsky = 70%, see Appendix A).

• Participants must have normal organ and marrow function as defined below:

• Absolute neutrophil count = 1,500/mcL

• Platelets = 100,000/mcL

• Total bilirubin = 2.5 mg/dl

• AST (SGOT)/ALT (SGPT) = 5.0 X institutional upper limit of normal

• Creatinine within normal institutional limits or creatinine clearance = 60 mL/min/1.73 m2 for subjects with creatinine levels above institutional normal .

• No other known active secondary primary malignancy.

• If patient has underlying cirrhosis, only Child-Pugh classification Group A patients may be included in the resectable cohort of this study. For patients with unresectable disease, Child-Pugh classification Groups A and B are allowed. Clinical assessment of ascites and encephalopathy is required. Child-Pugh classification must be determined for all study participants at the time of eligibility analysis. Note albumin and PT/INR are required for Child-Pugh classification; these labs should be drawn with the other labs required for eligibility analysis.

Table 1: Child-Pugh classification of liver function

• Score 1 2 3

• Ascites Absent Slight to moderate Severe

• Encephalopathy Absent Slight to moderate Severe

• Serum albumin >3.5 g/dl 3-3.5 g/dl <3 g/dl

• Serum bilirubin <2 mg/dl 2-3 mg/dl >3 mg/dl

• Prolongation of prothrombin time <4 seconds 4-6 seconds >6 seconds

• Score of 5 to 6 corresponds to Child-Pugh class A

• Score of 7 to 11 corresponds to Child-Pugh class B

• Score of 12 to 15 corresponds to Child-Pugh class

• The effects of gemcitabine+cisplatin on the developing human fetus are unknown. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study treatment. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately. Female patients of child bearing potential must indicate to their physician that they are not pregnant at the time of enrollment or have a negative serum pregnancy test.

• Ability to understand and the willingness to sign a written informed consent document.

• Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

• Participants who exhibit any of the following conditions at screening will not be eligible for admission into the study.

• Participants who have had chemotherapy or radiotherapy for intrahepatic cholangiocarcinoma.

• Participants receiving any other anti-cancer or investigational agents.

• History of allergic reactions attributed to compounds of similar chemical or biologic composition to gemcitabine or cisplatin.

• Women who are pregnant or lactating.

• Participants with evidence of non-hepatic metastatic disease.

• Local conditions or systemic illnesses which would reduce the local tolerance to radiation treatment, such as serious local injuries, active collagen vascular disease, etc.

• Participants with a serious medical illness which may limit expected survival to less than 3 months.

• Participants with serious psychiatric illness or social situations which would limit adherence to study requirements.

• Participants receiving any medications or substances that are strong inhibitors or inducers of CYP3A4 are ineligible.

• Because no dosing or adverse event data are currently available on the use of gemcitabine+cisplatin in participants <18 years of age, children are excluded from this study.

• Patients who require anticoagulation should receive low-molecular weight or standard heparin and not warfarin.

• Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

• Pregnant women are excluded from this study because gemcitabine is a class D agent with the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk of adverse events in nursing infants secondary to treatment of the mother with gemcitabine, breastfeeding should be discontinued if the mother is treated with gemcitabine. These potential risks may also apply to other agents used in this study.

• Individuals with a history of a different malignancy are ineligible except for the following circumstances. Individuals with a history of other malignancies are eligible if they have been disease-free for at least 5 years and are deemed by the investigator to be at low risk for recurrence of that malignancy. Individuals with the following cancers are eligible if diagnosed and treated within the past 5 years: cervical cancer in situ, DCIS, stage I prostate cancer, and basal cell or squamous cell carcinoma of the skin.

• HIV-positive individuals on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with gemcitabine+cisplatin. In addition, these individuals are at increased risk of lethal infections when treated with marrow-suppressive therapy. Appropriate studies will be undertaken in participants receiving combination antiretroviral therapy when indicated. HIV-positive individuals on HAART will be considered eligible of they have demonstrated good compliance and have a CD4 count > 500.

• Prior liver directed radiation.

• Patients with peripheral neuropathy = grade 2.

Study Design

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

Related Conditions & MeSH terms

• Cholangiocarcinoma
• Liver Neoplasms
• Resectable Intrahepatic Cholangiocarcinoma
• Unresectable Intrahepatic Cholangiocarcinoma

Intervention

Drug:
• Gemcitabine

• Cisplatin

Procedure:
• Surgery
Surgical Resection and Lymphadenectomy

Radiation:
• Radiation
Radiation Therapy

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants Post Operative/Radiation Therapy Complications	Out of the 3 participants enrolled, the patient in cohort 1 proceeded to surgery and 1 of the 2 patients in cohort 2 proceeded to RT. The other patient in cohort 2 developed disease progression and was removed from protocol.	90 Days	Yes