Neoadjuvant Accelerated Short Course Radiation Therapy With Proton Beam and Capecitabine for Resectable Pancreatic Cancer

NCT ID: NCT00438256

Last Updated: 2019-01-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-12-31
• Study Completion Date: 2017-12-31

Brief Summary

A standard treatment for pancreatic cancer is radiation therapy plus chemotherapy after surgery. Radiation therapy and chemotherapy are commonly given for up to six weeks. Previous research has suggested that giving the radiation and chemotherapy for a shorter amount of time (accelerated schedule) before surgery may be better tolerated. In this research study, different schedules of proton radiation therapy will be used. Each schedule will give about the same total dose of radiation. However, the total dose will be spread out over different time periods and different numbers of sessions. The purpose is to find the shortest schedule of radiation therapy that can be given without unacceptable side effects. Proton beam radiation is being used because of its unique ability to deposit its energy directly in the tumor, resulting in less radiation to normal tissue. A new type of PET scan is also being studied to see if it can help predict the response to pre-surgery treatment.

Detailed Description

• Not everyone who participates in this research study will receive the same schedule of radiation therapy. The schedule of radiation therapy will depend on the number of participants enrolled on the study and how well they have tolerated their radiation schedule. All patients will receive proton beam therapy.
• Here are the proposed schedules of radiation therapy. If at any point too many subjects experience too many unacceptable side effects, no subject will be enrolled to the next level. Dose Level 1: 10 radiation sessions given Monday-Friday for two weeks. Dose Level 2: 5 radiation sessions given Monday, Wednesday and Friday in Week 1 and Tuesday and Thursday in Week 2. Dose Level 3: 5 radiation sessions given Monday, Tuesday, Thursday and Friday in Week 1 and Monday in Week 2. Dose Level 4: 5 Radiation sessions given Monday through Friday in Week 1.
• In Dose Levels 2, 3 and 4, there are fewer radiation sessions, but the radiation dose given at each session is slightly higher than the dose given in each of the 10 sessions of Dose Level 1.
• Capecitabine will be given orally (pill form) starting on the first day of radiation therapy and will be taken for the two weeks that the participant receives radiation therapy.
• On days 1, 8 and 15 of each study cycle, the participant will be seen at the clinic for: physical examination, questions about side effects; and routine blood tests.
• After the last day of study treatment there will be up to a six-week rest period before surgery is performed.
• About three to six weeks after the participant has finished study treatment, the following procedures will be done: CT or MRI, physical examination; questions about side effects and blood tests.

Conditions

Pancreatic Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Group 1

10 Radiation Sessions over 2 weeks

Group Type: EXPERIMENTAL

Proton Beam Radiation

Intervention Type: PROCEDURE

Given over different schedules and duration

Capecitabine

Intervention Type: DRUG

Given orally starting on day one of radiation therapy for 2 weeks

Group 2

5 Radiation sessions: 3 in week 1 and 2 in week 2

Group Type: EXPERIMENTAL

Proton Beam Radiation

Intervention Type: PROCEDURE

Given over different schedules and duration

Capecitabine

Intervention Type: DRUG

Given orally starting on day one of radiation therapy for 2 weeks

Group 3

5 Radiation sessions: 4 in week 1 and 1 in week 2

Group Type: EXPERIMENTAL

Proton Beam Radiation

Intervention Type: PROCEDURE

Given over different schedules and duration

Capecitabine

Intervention Type: DRUG

Given orally starting on day one of radiation therapy for 2 weeks

Group 4

5 Radiation Sessions in one week

Group Type: EXPERIMENTAL

Proton Beam Radiation

Intervention Type: PROCEDURE

Given over different schedules and duration

Capecitabine

Intervention Type: DRUG

Given orally starting on day one of radiation therapy for 2 weeks

Interventions

Proton Beam Radiation

Given over different schedules and duration

Intervention Type: PROCEDURE

Capecitabine

Given orally starting on day one of radiation therapy for 2 weeks

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Cytologic of histologic proof of pancreatic ductal carcinoma
• No evidence of metastatic disease
• 18 years of age or older
• ECOG Performance Status of 0 or 1 - Lab values as outlined in the protocol

Exclusion Criteria

• Tumors in the body or tail of the pancreas
• Hepatic or peritoneal metastases detected by imaging or laparoscopy prior to chemoradiation
• Serious concomitant systemic disorders incompatible with the study, such as significant cardiac or pulmonary morbidity, ongoing infection as manifested by fever
• Pregnant or lactating women
• Life expectancy of < 3 months
• Serious, uncontrolled, concurrent infection (s)
• Prior chemotherapy or radiation for treatment of the patient's pancreatic tumor
• Clinically significant cardiac disease or myocardial infarction within the last 12 months
• Other serious uncontrolled medical condition that the investigator feels might compromise study participation
• Lack of physical integrity of the upper gastrointestinal tract or malabsorption syndrome
• Known, existing uncontrolled coagulopathy
• Any prior fluoropyrimidine therapy
• Prior unanticipated severe reaction to fluoropyrimidine therapy, or known hypersensitivity to a 5-fluorouracil or known DPD deficiency
• Participation in any investigational drug study within 4 weeks preceding the start of the study
• History of uncontrolled seizures, central nervous system disorders or psychiatric disability
• Major surgery, excluding laparoscopy, within 4 weeks of the start of study treatment, without complete recovery
• Patients on cimetidine

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Dana-Farber Cancer Institute

OTHER

Sponsor Role: collaborator

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Massachusetts General Hospital

OTHER

Sponsor Role: lead

Responsible Party

Theodore Sunki Hong

Attending Radiation Oncologist

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Theodore Hong, MD

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Massachusetts General Hospital

Boston, Massachusetts, United States

Countries

United States

References

Hong TS, Ryan DP, Borger DR, Blaszkowsky LS, Yeap BY, Ancukiewicz M, Deshpande V, Shinagare S, Wo JY, Boucher Y, Wadlow RC, Kwak EL, Allen JN, Clark JW, Zhu AX, Ferrone CR, Mamon HJ, Adams J, Winrich B, Grillo T, Jain RK, DeLaney TF, Fernandez-del Castillo C, Duda DG. A phase 1/2 and biomarker study of preoperative short course chemoradiation with proton beam therapy and capecitabine followed by early surgery for resectable pancreatic ductal adenocarcinoma. Int J Radiat Oncol Biol Phys. 2014 Jul 15;89(4):830-8. doi: 10.1016/j.ijrobp.2014.03.034. Epub 2014 May 24.

Reference Type: DERIVED

PMID: 24867540 (View on PubMed)

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

06-248

Identifier Type: -

Identifier Source: org_study_id