Midostaurin (PKC412) for Locally Advanced Rectal Cancer

Mass General Brigham

Status and phase: Completed; Phase 1

Conditions: Adenocarcinoma of the Rectum

Treatments: Drug: Midostaurin

Study type: Interventional

Funder types: Other

Identifiers

NCT01282502

10-457

Details and patient eligibility

About

This study combines midostaurin (PKC412) with radiation and a standard chemotherapy drug call 5-Fluorouracil (5-FU) for subjects with advanced rectal cancer. Midostaurin is a type of kinase inhibitor which works by blocking proteins associated with cancer cell growth. Previous studies also suggest that midostaurin may help increase the effectiveness of radiation therapy. In this research we are looking for the highest dose of midostaurin that can be given safely in combination with standard chemoradiation.

Full description

Midostaurin capsules will be taken by mouth for 8 weeks. For the first 2 weeks midostaurin will be taken alone (no chemoradiation). After 2 weeks standard chemoradiation will be added to the midostaurin regimen. Subjects receive midostaurin and chemoradiation for an additional 6 weeks. Physical exams will be done weekly. Blood samples will be taken and an optional tumor biopsy will be performed in week 2.

4-5 weeks after completing chemoradiation and midostaurin subjects will undergo surgery as standard of care. Tumor tissue from the surgery will be used for research purposes. A Ct scan of chest, abdomen, and pelvis will be performed.

After completion of surgery, subjects will have an end of study visit with physical exam, blood tests. CT scans of chest, abdomen, and pelvis will be performed yearly for 5 years.

Enrollment: 19 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adenocarcinoma of the rectum
• T3/4 or N+ disease
• Life expectancy > 3 months
• Normal organ and marrow function

Exclusion criteria

• Metastatic disease
• Pregnant or breastfeeding
• Prior radiotherapy
• Receiving other investigational agents
• History of inflammatory bowel disease
• Active scleroderma or CREST syndrome
• Uncontrolled intercurrent illness
• History of a different malignancy unless disease free for at least 5 years
• HIV or active viral hepatitis
• Impaired cardiac function

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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19 participants in 1 patient group

Midostaurin with chemoradiation

Experimental group

Treatment:

Drug: Midostaurin