Study of Durvalumab (MEDI4736) After Chemo-Radiation for Microsatellite Stable Stage II-IV Rectal Cancer

Rectal Cancer Clinical Trial

Official title:

A Phase II Study to Assess the Activity of PD-L1 Inhibition With Durvalumab (MEDI4736) After Chemo-Radiotherapy in Patients With Stage II-IV Microsatellite Stable (MSS) Rectal Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03102047
• Other study ID #: NSABP FR-2
• Secondary ID: ESR-15-11477
• Status: Completed
• Phase: Phase 2
• Start date: May 14, 2018
• Est. completion date: December 30, 2021

Study information

• Verified date: April 2022
• Source: NSABP Foundation Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is being done to look at the safety and response to the investigational drug durvalumab (MEDI4736) following chemo-radiation therapy for patients with MSS stage II to IV rectal cancer. Durvalumab recognizes specific proteins on the surface of cancer cells and triggers the immune system to destroy the cancer cells. The chemoRT portion of the treatment will be completed just before the course of durvalumab is initiated.

In order to learn more about certain characteristics of rectal cancer tumors, this study includes special research tests using samples from diagnostic tumors, a tissue sample from tumors removed during surgery, fresh tumor samples from an area where the cancer has recurred, and blood samples.

Description:

The FR-2 study is designed as a phase II, open label, single arm study in patients with microsatellite stable (MSS) stages II-IV rectal cancer, to assess the activity of PD-L1 inhibition with durvalumab (MEDI4736) monotherapy after standard chemo-radiotherapy (chemoRT). The study's primary aim is to determine the safety and efficacy of durvalumab immediately following chemoRT in patients undergoing subsequent surgery with stage II-IV rectal cancer.

One dose of durvalumab will be given every 2 weeks for four total doses beginning within 3-7 days of completing chemoRT. Surgery for all patients must occur within 8-12 weeks of the final dose of RT. Adjuvant chemotherapy after surgical recovery is at the discretion of the treating physician.

During a safety run-in, the first 6 patients will be closely followed for 30 days after last dose of durvalumab without further accrual of patients. Patients will receive durvalumab (750mg IV infusion once every 2 weeks) for 4 total doses. No other concurrent anti-neoplastic medications or treatments aside from standard supportive care will be allowed during the durvalumab treatment phase.

The safety run-in portion of the study will proceed to full enrollment at the proposed study therapy dose, (750 mg IV infusion every 2 weeks), if one or less dose-limiting toxicity (DLT) or significant safety concern attributable to durvalumab is identified during the observation period of the first 6 patients. If there are two or more DLTs, accrual to the study will stop with reassessment of the protocol.

A total of 44 patients will be enrolled in this study for a sample size of 41 surgically evaluable patients.

Required tissue and blood samples will be collected at specific time points and submitted for correlative science studies. Optional tumor and blood samples will be collected from consenting patients upon disease recurrence or progression.

Given the increasing use of non-operative therapy for patients with rectal cancer who achieve a complete clinical response and in order to maximize the inclusion of patients participating in this trial, the primary endpoint was changed from NAR score to modified NAR score (mNAR). The mNAR score substitutes values from clinical staging for the pathologic T-Stage and N-Stage for those patients who don't go to surgery because of a complete clinical response and consequently have no pathology. Additionally, because of enrollment challenges related to COVID-19 pandemic and the exploratory nature of including stage IV patients, the stage IV analysis was moved to exploratory and reducing the number of patients needing to be enrolled in the study to approximately 44.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: December 30, 2021
• Est. primary completion date: February 22, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• The ECOG performance status must be 0 or 1

• Patients with biopsy-proven adenocarcinoma, stage II- IV rectal cancer.

• The tumor must have been determined to be mismatch repair proficient or microsatellite stable through CLIA approved testing (Immunohistochemistry [IHC], polymerase chain reaction [PCR], or Next-Generation Sequencing [NGS] assays).

• Patients must be candidates for planned surgical resection of their primary rectal cancer 8 - 12 weeks after completion of neoadjuvant chemoRT, even if stage IV.

• Planned neoadjuvant chemoRT treatment must conform to NCCN guidelines.

• Baseline staging prior to chemoRT initiation must be obtained. If stage IV, there must be documentation by PET/CT scan, CT scan, or MRI, that the patient has evidence of measurable distant disease per RECIST 1.1. Note: Patients with stage IV disease should have limited but measurable metastatic disease (one or two organs involved e.g., liver and lung) and primary tumor deemed resectable.

• Blood counts performed within 4 weeks prior to study entry must meet the following criteria:

• ANC must be greater than or equal to 1500/mm3

• Platelet count must be greater than or equal to 75,000/mm3; and

• Hemoglobin must be greater than or equal to 9 g/dL.

• Adequate hepatic function performed within 4 weeks prior to study entry must be met:

• Total bilirubin must be less than or equal to 1.5 x ULN (upper limit of normal) for the lab unless the patient has a bilirubin elevation greater than 1.5 x Upper limit of normal (ULN) to 3 x ULN due to Gilbert's disease or similar syndrome involving slow conjugation of bilirubin; and

• AST and ALT must be less than or equal to 2.5 x ULN for the lab with the following exception: for patients with documented liver metastases, AST and ALT must be less than or equal to 5 x ULN.

• Adequate renal function within 4 weeks of study entry, defined as serum creatinine less than or equal to 1.5 x ULN for the lab. (If creatinine is 1.0-1.5 x ULN, the creatinine clearance should be greater than 40 mL/min per Cockcroft-Gault formula (Cockcroft-Gault 1976), or by 24-hour urine collection for determination of creatinine clearance.)

• Patients with reproductive potential (male/female) must agree to use accepted and highly effective methods of contraception while receiving durvalumab, and for at least 3 months after the last dose of durvalumab.

Exclusion Criteria:

• Diagnosis of anal or small bowel carcinoma.

• Histopathology other than adenocarcinoma, e.g., sarcoma, lymphoma, carcinoid.

• Previous therapy with any PD1 or PD-L1 inhibitor (including durvalumab) for any malignancy.

• Completion of pelvic radiotherapy treatment for this current rectal cancer or any prior pelvic radiotherapy (e.g., prior prostate or cervical cancer therapy).

• Receipt of live attenuated vaccination within 30 days prior to study entry or within 30 days after receiving the last dose of durvalumab.

• Acute or chronic hepatitis B or hepatitis C.

• Known history of human immunodeficiency virus (HIV) or acquired immunodeficiency-related (AIDS) illnesses.

• History of brain metastases, uncontrolled spinal cord compression, carcinomatous meningitis, or new evidence of brain or leptomeningeal disease.

• Active infection or chronic infection requiring chronic suppressive antibiotics.

• History of allogeneic organ transplantation.

• Active or prior documented inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis).

• Active or prior history of autoimmune or inflammatory condition requiring ongoing immunosuppressive medications. This specifically includes use of immunosuppressive medication within 28 days before the first dose of durvalumab with the exceptions of intranasal corticosteroids or systemic corticosteroids at physiological doses, which do not exceed 10mg/day of prednisone or an equivalent corticosteroid.

• Any of the following cardiac conditions:

• Documented NYHA Class III or IV congestive heart failure

• Myocardial infarction within 6 months prior to study entry

• Unstable angina within 6 months prior to study entry

• Symptomatic arrhythmia

• Uncontrolled high blood pressure defined as systolic BP greater than or equal to 150 mmHg or diastolic BP greater than or equal to 100 mmHg with or without anti-hypertensive medication. Patients with initial BP elevations are eligible if initiation or adjustment of BP medication lowers pressure to meet entry criteria.

• Ongoing or active gastritis or peptic ulcer disease.

• Active bleeding diatheses which in the opinion of the treating physician poses a significantly increased operative risk.

• Known history of previous diagnosis of tuberculosis.

• History of hypersensitivity to durvalumab or any excipient.

• Known history of active pneumonia, pneumonitis, symptomatic interstitial lung disease, or definitive evidence of interstitial lung disease described on CT scan, MRI, or chest x-ray in asymptomatic patients; dyspnea at rest requiring current continuous oxygen therapy.

• Other malignancies unless the patient is considered to be disease-free and has completed therapy for the malignancy greater than or equal to 12 months prior to study entry. Patients with the following cancers are eligible if diagnosed and treated within the past 12 months: carcinoma in situ of the cervix, colorectal carcinoma in situ, melanoma in situ, and basal cell and squamous cell carcinoma of the skin.

• Psychiatric or addictive disorders or other conditions that, in the opinion of the investigator, would preclude the patient from meeting the study requirements, or interfere with interpretation of study results.

• Pregnancy or lactation at the time of study entry. (Note: Pregnancy testing should be performed within 14 days prior to study entry according to institutional standards for women of childbearing potential.)

• Use of any investigational agent within 4 weeks prior to study entry.

Related Conditions & MeSH terms

• Rectal Cancer
• Rectal Neoplasms

Intervention

Drug:
• durvalumab
Within 3-7 days after completion of chemoradiation, patients will receive durvalumab (750 mg IV infusion) every 2 weeks for 4 doses on Day 1(Dose 1), Day 15 (Dose 2), Day 29 (Dose 3), and Day 43 (Dose 4)

Locations

Country	Name	City	State
United States	University of Michigan	Ann Arbor	Michigan
United States	University of Michigan Oncology	Ann Arbor	Michigan
United States	Strecker Cancer Center	Belpre	Ohio
United States	UPMC Hillman Cancer at Upper St Clair	Bethel Park	Pennsylvania
United States	Adena Regional Medical Center	Chillicothe	Ohio
United States	Columbus NCORP	Columbus	Ohio
United States	Doctors Hospital	Columbus	Ohio
United States	Grant Medical Center	Columbus	Ohio
United States	Cancer Care Specialists of Central Illinois	Decatur	Illinois
United States	Columbus Oncology and Hematology Associates, Inc.	Delaware	Ohio
United States	Delaware Health Center Grady Cancer Center	Delaware	Ohio
United States	Cancer Care Specialists of Central Illinois-Crossroads Cancer Center	Effingham	Illinois
United States	University of Florida	Gainesville	Florida
United States	UPMC Hillman Cancer Center at Mt. View	Greensburg	Pennsylvania
United States	Smilow Cancer Hospital Care Center at Guilford	Guilford	Connecticut
United States	AHN Cancer Institute at Jefferson	Jefferson Hills	Pennsylvania
United States	Marietta Memorial Hospital	Marietta	Ohio
United States	Marion General Hospital	Marion	Ohio
United States	The Mark H. Sangmeister Center	Marion	Ohio
United States	Forbes Regional Hospital	Monroeville	Pennsylvania
United States	UPMC Hillman Cancer Center at Monroeville	Monroeville	Pennsylvania
United States	West Virginia University	Morgantown	West Virginia
United States	West Virginia University Medicine	Morgantown	West Virginia
United States	Knox Community Hospital	Mount Vernon	Ohio
United States	Smilow Cancer Hospital Care Center at Yale	New Haven	Connecticut
United States	Yale University, Yale Cancer Center	New Haven	Connecticut
United States	Licking Memorial Hospital	Newark	Ohio
United States	Smilow Cancer Hospital Care Center at North Haven	North Haven	Connecticut
United States	Allegheny General Hospital	Pittsburgh	Pennsylvania
United States	UPCI Hillman/Shadyside	Pittsburgh	Pennsylvania
United States	UPMC Cancer Center at Passavant OHA	Pittsburgh	Pennsylvania
United States	UPMC Hillman Cancer Center	Pittsburgh	Pennsylvania
United States	UPMC Hillman Cancer Center at Passvant HOA	Pittsburgh	Pennsylvania
United States	Western Pennsylvania Hospital dba West Penn Hospital	Pittsburgh	Pennsylvania
United States	WPAON/Medical Center Clinic	Pittsburgh	Pennsylvania
United States	Southern Ohio Medical Center	Port Clinton	Ohio
United States	Cancer Care Specialists of Central Illinois-Swansea	Swansea	Illinois
United States	Smilow Cancer Hospital Care Center at Trumbull	Trumbull	Connecticut
United States	UPMC Hillman Cancer Center at Washington	Washington	Pennsylvania
United States	Smilow Cancer Hospital at Lawrence + Memorial Cancer Center	Waterford	Connecticut
United States	Wake Forest Baptist Comprehensive Cancer Center	Winston-Salem	North Carolina
United States	Wake Forest Medical Center	Winston-Salem	North Carolina
United States	Genesis Health Care Center	Zanesville	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
NSABP Foundation Inc

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Median modified Neoadjuvant Rectal (mNAR) Score	Compare Median modified Neoadjuvant Rectal (mNAR) Score to historic control using the Wilcoxon test	From the beginning of the study to time of surgical resection, assessed over an estimated 12 weeks
Secondary	Pathologic complete response rate to study therapy	Pathologic Complete response rate ( pCR) (ypT0 and ypN0) of primary rectal cancer and regional nodes determined by pathological examination	At the time of surgical resection
Secondary	Clinical complete response rate to study therapy	Clinical complete response rate cCR (ycT0) determined by the clinical absence of the primary tumor via digital rectal exam and proctoscopic exam	From one week prior to surgical resection up to time of surgical resection
Secondary	Rate of negative circumferential margin	Rate of negative circumferential margin in surgical resection specimens	At the time of surgical resection
Secondary	Sphincter function in patients with sphincter preserving surgery	Sphincter function as determined by number of adverse events related to bowel control	From the time of surgical resection to 30 days after surgery
Secondary	Severity of post-operative complications	Surgical complications that result in re-hospitalizations or death	From time of surgical resection to within 30 days post-operation
Secondary	Frequency of adverse events assessed by CTCAE 4.0	Frequency of adverse events categorized using the NCI Common Terminology Criteria for Adverse Events version 4.0	From beginning of study therapy to 90 days after last dose of study therapy