BrUOG 302:BYL719, Capecitabine and Radiation for Rectal Cancer: A Brown University Oncology Research Group Study

NCT02550743 | Terminated Phase 1 Results DMC

• 1 other identifier: BrUOG 302
• Study Type: interventional
• Target: 7
• Locations: 1 country
• Sites: 1

Brief Summary

The primary goal of this Brown University Oncology Research Group is to determine that a safe dose of BYL719 can be administered with capecitabine and radiation in patients with rectal cancer. Therefore, the threshold of success for this phase I study is to establish safety.

Conditions

Rectal Cancer

Keywords

Stage II; Stage III; Stage IV; metastatic

Outcome Measures

Primary Outcomes (1)

• Maximum Tolerated Dose of BYL719

  approximately 6 weeks

Secondary Outcomes (1)

• Pathologic Complete Response for Patients With Rectal Cancer

  Approximately 6-10 weeks post treatment

Study Arms (4)

Dose 1

EXPERIMENTAL

BYL719, capectabine and radiation Dose BYL719: 200mg/day

Drug: BYL719; Drug: Capecitabine; Radiation: Radiation

Dose 2

EXPERIMENTAL

BYL719, capectabine and radiation Dose BYL719: 250mg/day

Drug: BYL719; Drug: Capecitabine; Radiation: Radiation

Dose 3

EXPERIMENTAL

BYL719, capectabine and radiation Dose BYL719: 300mg/day

Drug: BYL719; Drug: Capecitabine; Radiation: Radiation

Dose -1

EXPERIMENTAL

BYL719, capectabine and radiation Dose BYL719: 150mg/day

Drug: BYL719; Drug: Capecitabine; Radiation: Radiation

Interventions

BYL719 DRUG

Dose -1; Dose 1; Dose 2; Dose 3

Capecitabine DRUG

Also known as: Xeloda

Dose -1; Dose 1; Dose 2; Dose 3

Radiation RADIATION

Dose -1; Dose 1; Dose 2; Dose 3

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients must have histologically proven adenocarcinoma of the rectum with no evidence of distant metastases.
• The tumor must be clinically Stage II (T3-4 N0) or stage III (N+). Stage of the tumor may be determined by CT scan, endorectal ultrasound or MRI. (For patients receiving chemotherapy prior to protocol chemoradiation, the initial clinical stage applies. CT/MRI/PET should be performed within 2 months of study entry to exclude disease progression.). For the MTD expansion phase only: patients who are stage IV, and in whom it is planned to administer capecitabine and radiation then have a resection of their rectal cancer, are also eligible.
• Measurable disease not required at baseline. Patient's without measurable disease may be enrolled as long as they clinically meet stage II or III criteria or for MTD expansion phase: also stage IV.
• Patients must not have received pelvic radiation for rectal cancer, or prior pelvic radiation for any other malignancy that would prevent the patient from receiving the required radiation treatments for this study. (Patients may receive neoadjuvant chemotherapy prior to study chemoradiation)
• Patients must not have an active concurrent invasive malignancy. Patients with prior malignancies, including invasive colon cancer, are eligible if they are deemed by their physician to be at low risk for recurrence. For example, patients with squamous or basal cell carcinoma of the skin, melanoma in situ, carcinoma of the cervix, or carcinoma in situ of the colon or rectum that have been effectively treated are eligible, even if these conditions were diagnosed within 3 years prior to registration.
• Patients must be \> 18 years of age,
• ECOG performance status 0-1
• Neutrophil Count \>1,000/µl, platelets \>100,000/µl, total bilirubin \< 1.5 x\< ULN ULN (except for patients with Gilbert's syndrome who may only be included if total bilirubin is \< 3xULN with direct bilirubin within normal range), ALT \<2.5xULN, AST \< 2.5xULN, creatinine \<1.5xULN, fasting plasma glucose \< 140 mg/dL and HbA1c \< 6.4% (both criteria have to be met), anemia \> 9.0g/dL.Potassium, Calcium and Magnesium (corrected for albumin) within normal range or \< grade 1 if determined not clinically significant by treating investigator. INR \< 1.5
• Patient is able to swallow and retain oral medication.
• Left ventricular ejection fraction within normal \>50%
• Signed informed consent and is able to comply with study and/or follow- up procedures.
• QTcF \<480 msec
• Patients history of diarrhea has been review and patient has been informed of potential study drug induced diarrhea and management. This must be documented by treating MD. See section 5 for baseline assessments of patient history of diarrhea.

You may not qualify if:

• Patient has a known hypersensitivity to any of the excipients of BYL719 (alpelisib)
• Suspected or confirmed metastatic disease including CNS involvement. For stage IV patients: CNS involvement.
• Patient with clinically manifest diabetes mellitus, or documented steroid induced diabetes mellitus
• Patient with impaired gastrointestinal (GI) function or GI disease that may significantly alter the absorption of oral BYL719 (e.g. ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection). Patients with colostomies are allowed unless colostomy is for one of the precluded reason above.
• Patient who has not recovered to grade 1 or better (except alopecia) from related side effects of any prior antineoplastic therapy
• Patient who has had systemic therapy within 4 weeks of starting study treatment (6 weeks for nitrosoureas or mitomycin C)
• Patient who has undergone major surgery ≤ 4 weeks prior to starting study treatment or in the investigators opinion who has not recovered from side effects of such procedure
• Patient has any of the following cardiac abnormalities: A. symptomatic Congestive heart failure i. history of documented congestive heart failure (New York Heart Association functional classification III-IV), documented cardiomyopathy ii. Left Ventricular Ejection Fraction (LVEF) \<50% as determined by Multiple Gated acquisition (MUGA) scan or echocardiogram (ECHO) B. myocardial infarction \< 6 months prior to enrollment C. unstable angina pectoris D. serious uncontrolled cardiac arrhythmia E. symptomatic pericarditis F. QTcF \> 480 msec on the screening ECG (using the QTcF formula)
• Patient who is currently receiving medication with a known risk of prolonging the QT interval or inducing Torsades de Pointes (TdP) and the treatment cannot either be discontinued or switched to a different medication prior to starting study drug treatment. To be documented and submitted to BrUOG with registration. Please refer to appendices F and G.
• Patient who has participated in a prior investigational cancer treatment study within 30 days prior to enrollment. This refers to treatment not follow-up.
• Patient is currently receiving warfarin or other coumarin derived anti-coagulant, for treatment, prophylaxis or otherwise. Therapy with heparin, low molecular weight heparin (LMWH), or fondaparinux is allowed. To be documented and submitted to BrUOG with registration. Eliquis is allowed.
• Patient is currently receiving treatment with drugs known to be strong inhibitors or inducers of isoenzyme CYP3A. The patient must have discontinued strong inducers for at least one week and must have discontinued strong inhibitors before the start of treatment. Switching to a different medication prior to registration is allowed; (Refer to Section Concomitant Medication, Appendix F and G).
• Patient with known positive serology for human immunodeficiency virus (HIV)
• Patient with any other condition that would, in the Investigator's judgment, preclude patient's participation in the clinical study due to safety concerns or compliance with clinical study procedures, e.g. infection/inflammation, intestinal obstruction, unable to swallow oral medication, social/psychological complications, chronic active hepatitis, severe hepatic impairment etc
• Patients who have other concurrent severe and/or uncontrolled medical conditions that would, in the Treating Physician's judgment, contraindicate patient participation in the individual patient program (eg. active or uncontrolled severe infection, chronic active hepatitis, immuno-compromised, acute or chronic pancreatitis, uncontrolled high blood pressure, interstitial lung disease, etc.)

Sponsors & Collaborators

• howard safran: lead
• Brown University: collaborator
• Lifespan: collaborator
• Novartis Pharmaceuticals Corporation (Financial supporter): collaborator

Study Sites (1)

Rhode Island Hospital and The Miriam Hospital

Providence, Rhode Island, 02903, United States

Location

MeSH Terms

Conditions

Rectal Neoplasms; Neoplasm Metastasis

Interventions

Alpelisib; Capecitabine; Radiation

Condition Hierarchy (Ancestors)

Colorectal Neoplasms; Intestinal Neoplasms; Gastrointestinal Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Intestinal Diseases; Rectal Diseases; Neoplastic Processes; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Deoxycytidine; Cytidine; Pyrimidine Nucleosides; Pyrimidines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Fluorouracil; Uracil; Pyrimidinones; Deoxyribonucleosides; Nucleosides; Nucleic Acids, Nucleotides, and Nucleosides; Physical Phenomena

Results Point of Contact

• Title: Howard Safran, MD, Principal Investigator
• Organization: Brown University Oncology Research Group (BrUOG)

kayla_rosati@brown.edu

14018633000

Study Officials

• Howard Safran, MD

  BrUOG Study Chair

  STUDY CHAIR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SEQUENTIAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Principal Investigator

Model Details: This is a phase I dose escalation study adding BYL719 to standard capecitabine and radiation.

Study Record Dates

• First Submitted: September 11, 2015
• First Posted: September 15, 2015
• Study Start: June 3, 2016
• Primary Completion: November 16, 2018
• Study Completion: November 16, 2018
• Last Updated: March 12, 2021
• Results First Posted: March 12, 2021

Record last verified: 2021-03

Locations

US (1)