Rosuvastatin in the Treatment of Rectal Cancer

Rectal Cancer Clinical Trial

Official title:

Phase 2 Trial of Rosuvastatin (Crestor®) Combined With Standard Chemoradiation Therapy in the Treatment of High-Risk Locally Advanced Rectal Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02569645
• Other study ID #: OZM-064
• Status: Completed
• Phase: Phase 2
• Start date: November 2015
• Est. completion date: September 24, 2021

Study information

• Verified date: July 2022
• Source: AHS Cancer Control Alberta
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate whether the addition of Rosuvastatin to standard chemoradiation therapy for the treatment of locally advanced rectal cancer may improve the pathological response rate and survival compared to standard chemoradiation therapy alone.

Description:

The standard treatment of locally advanced rectal cancer involves neoadjuvant chemoradiation therapy (CRT) followed by surgery and further adjuvant chemotherapy. The pathologic complete responses associated with neoadjuvant CRT are 10-20%. The prognosis of patients undergoing neoadjuvant CRT is associated to the extent of post-treatment tumour regression, the final primary tumour stage and presence of involved lymph nodes in the surgical specimen. This data suggests that treatments that enhance the pathological response may result in improvements in survival. Overwhelming preclinical and clinical evidence suggests that statins demonstrate anticancer properties and sensitize cancer tissues and protects normal tissues to the effects of radiation. Hence, the investigators hypothesize that the addition of rosuvastatin to standard CRT for the treatment of locally advanced rectal cancer may improve the pathological response rate. This protocol describes an open-label single-arm phase 2 study designed to test this hypothesis. Moreover, this study will also identify genetic, serological, and pathological biomarkers that may be both prognostic and predictive of response and toxicity to treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: September 24, 2021
• Est. primary completion date: September 24, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Clinical stage 2-3 rectal adenocarcinoma, cT3/4N0/M0 or Tx N1-2/M0, within 5 cm of anal verge or less than 12cm from anal verge and threatened circumferential resection margin (=3mm). Patients must have histological confirmation of rectal adenocarcinoma prior to registration.

2. Patients must be 18 years or older.

3. Able to swallow oral medication.

4. Previous surgery, not for primary treatment of current rectal cancer, is permitted provided that wound healing has occurred and at least 14 days have elapsed prior to registration if surgery was major.

5. ECOG 2 or less.

6. Laboratory Requirements (must be done within 7 days prior to registration):

a. Hematology: i. Hemoglobin =90 g/L ii. Granulocytes (AGC) = 1.5 x 109/L iii. Platelets = 100 x 109/L b. Chemistry: i. Bilirubin =1.5 x UNL ii. ALT or AST = 1.5 x UNL iii. Proteinuria = grade 1 iv. Thyroid function within normal limits (TSH or free T4 within normal limits after correction) v. CPKs = ULN, vi. Urinary myoglobin within normal limits Note: If serum creatinine is abnormal, a creatinine clearance should be calculated and be = 60 ml/min.

7. Women must be post-menopausal, surgically sterile or use two reliable forms of contraception if of child-bearing potential. Women of childbearing potential must have a urine pregnancy test taken and proven negative within 7 days prior to registration. Men must be surgically sterile or use an effective barrier method of contraception if sexually active with a woman of child-bearing potential. Acceptable methods of contraception are condoms with contraceptive foam, oral, implantable or injectable contraceptives, contraceptive patch, intrauterine device, diaphragm with spermicidal gel, or a sexual partner who is surgically sterilized or post-menopausal. For both male and female patients, effective methods of contraception must be used throughout the study and for three months following the last dose.

8. Patient consent must be obtained according to local Institutional and/or University Human Experimentation Committee requirements. It will be the responsibility of the local participating investigators to obtain the necessary local clearance. The patient must sign the consent form prior to registration. The consent form for this study must contain a statement, which gives permission for the sponsor and monitoring agencies to review patient records.

9. Patients must be accessible for treatment and follow-up. Patients registered on this trial must be treated and followed at the participating centre. This implies there must be reasonable geographical limits (for example: 1 1/2 hours driving distance) placed on patients being considered for this trial. Investigators must assure themselves the patients registered on this trial will be available for complete documentation of the treatment, adverse events, and follow-up.

Exclusion Criteria:

1. Patients of Asian ethnicity (having Filipino, Chinese, Japanese, Korean, Vietnamese, or South Asian origin) will be excluded due to increased risk of toxicity.

2. Previous and concurrent, experimental, chemotherapy, or radiotherapy treatment for primary rectal carcinoma.

3. Statin exposure in the last 5 years.

4. Known evidence of distant metastatic disease on staging investigation, including a CT of the chest, abdomen, and pelvis performed within 6 weeks prior to registration.

5. Known history of previous malignancy, except adequately treated non-melanoma skin cancer or other solid tumour treated curatively with no evidence of disease for >5 years.

6. Patients with malabsorption syndrome, ulcerative colitis, inflammatory bowel disease, resection of the stomach or small bowel, or other disease significantly affecting gastrointestinal (GI) function.

7. Patients with a known history of documented upper GI bleeding or upper GI ulcerative disease.

8. Patients with hyperlipidemia with clinical indication for statin therapy or other prescribed medication (determination of acceptable fasting lipid values should be in accordance with current dyslipidemia management guidelines).

9. Patients with inadequately treated hypothyroidism, as determined by the investigator.

10. Patients with a known history of myopathy or rhabdomyolysis.

11. Patients who have experienced untreated and/or uncontrolled cardiovascular conditions and/or have symptomatic cardiac dysfunction.

12. Deemed by the physician to be at low risk for recurrence.

13. No other non-malignant systemic disease that would preclude rosuvastatin administration or prolonged follow-up.

14. Concurrent chronic use of NSAIDs.

15. Concurrent chronic drug therapy with cyclosporine, colchicine, coumarin anticoagulants, amiodarone, gemfibrozil, other lipid-lowering therapies (e.g., fibrates or niacin), lopinavir/ritonavir, azole antifungals, and macrolide antibiotics.

16. Known personal or family history of hereditary neuromuscular disorders.

17. Known previous history of muscular toxicity with another HMG-CoA reductase inhibitor.

18. Known history of alcohol abuse.

19. Any known condition that could affect absorption of study oral drugs (capecitabine and rosuvastatin).

20. Known contraindication to statin.

21. Pregnant or nursing.

22. Patients with symptomatic inflammatory bowel disease.

23. Patients with uncontrolled hypothyroidism.

24. Patients with chronic liver or disease.

25. Patients with unexplained elevated serum transaminases exceeding 3x ULN.

26. Patients known to be suffering from infection with HIV, Tuberculosis, Hepatitis C or Hepatitis B.

Related Conditions & MeSH terms

• Rectal Cancer
• Rectal Neoplasms

Intervention

Drug:
• Rosuvastatin
40 mg rosuvastatin orally once per day with or without food, swallowed whole (not chewed, crushed or divided) starting 2 weeks prior to the initiation of radiation therapy and stopped at 4 weeks after the completion of radiation. Total duration of Rosuvastatin is 11 weeks if 25 fractions of radiotherapy are given, or 12 weeks if 30 fractions of radiotherapy are given.

Locations

Country	Name	City	State
Canada	Tom Baker Cancer Centre	Calgary	Alberta

Sponsors (2)

Lead Sponsor	Collaborator
AHS Cancer Control Alberta	Ozmosis Research Inc.

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To determine the pathological complete response rate in patients with high-risk locally advanced rectal cancer treated with standard neo-adjuvant chemotherapy and radiation in combination with rosuvastatin.	The rate of post-surgical specimens that demonstrate absence of any residual invasive disease or Grade 4 (complete) histological regression using the Dworak classification.	Up to 3 years
Secondary	To determine the Ro resection rate	The rate that the surgical margins are negative of any invasive disease.	Up to 3 years
Secondary	To determine the pathological near-complete or complete tumour response rate	Grade 3 (near-complete) or 4 (complete) histological regression using the Dworak classification.	Up to 3 years
Secondary	To determine the sphincter preservation rate	The proportion of patients that undergo a sphincter preservation surgery versus abdominoperineal resection.	Up to 3 years
Secondary	To determine the down staging rate	Proportion of patients that have a down staging of the primary tumour and/or lymph nodes; i.e. comparison between cT/N and ypT/N	Up to 3 years
Secondary	To determine 3-year disease free survival	The proportion of patients alive with no clinical, radiological, or pathological evidence of rectal cancer recurrence at 3 years, starting at the time treatment was initiated. This definition includes, recurrence or relapse of rectal cancers, second primary cancer or death as events	Up to 3 years
Secondary	To determine 3-year overall survival	The proportion of patients alive at 3 years, starting at the time treatment was initiated.	Up to 3 years
Secondary	To determine the neoadjuvant rectal cancer (NAR) score	A surrogate endpoint of overall survival following neoadjuvant rectal cancer therapy.	Up to 3 years
Secondary	Number of participants with treatment-related adverse events as assessed by CTCAE v4.0.		Up to 3 years
Secondary	To identify the genetic biomarkers that may be both prognostic and predictive of response and toxicity to treatment.	BRAF and KRAS genetic testing. Direct exon sequencing.	up to 3 years
Secondary	To identify serological biomarkers that may be both prognostic and predictive of response and toxicity to treatment.	Changes in the levels of HMG CoA reductase pathway metabolites (Mevalonate, Ubiquinone) will also be performed using pre- and post-treatment serological markers.	up to 3 years
Secondary	To identify pathological biomarkers that may be both prognostic and predictive of response and toxicity to treatment.	IHC using pre- and post FFPE tumour tissue samples. (Ki67, phopsorylated AKT, HMG CoA reductase, GGPS1 and ApopTag, p21, p27 and rhoA)	up to 3 years
Secondary	Tmax will be collected as pharmacokinetic data		up to 3 years
Secondary	Cmax will be collected as pharmacokinetic data		up to 3 years
Secondary	T1/2 will be collected as pharmacokinetic data		up to 3 years
Secondary	Dose normalized Cmax will be collected as pharmacokinetic data		up to 3 years
Secondary	Area under the curve (AUC) will be collected as pharmacokinetic data		up to 3 years
Secondary	Dose normalized AUC will be collected as pharmacokinetic data		up to 3 years