Aflac ST0901 CHOANOME - Sirolimus in Solid Tumors

Renal Cell Carcinoma Clinical Trial

— Aflac ST0901  

Official title:

Sirolimus in Combination With Metronomic Therapy in Children With Recurrent and Refractory Solid Tumors: A Phase I Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01331135
• Other study ID #: IRB00047016
• Secondary ID: Aflac ST0901 CHO
• Status: Completed
• Phase: Phase 1
• Start date: April 2011
• Est. completion date: August 9, 2017

Study information

• Verified date: May 2020
• Source: Emory University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The best treatment for recurrent cancers or those that do not respond to therapies is not known. Typically, patients with these cancers receive a combination of cancer drugs (chemotherapy), surgery, or radiation therapy. These treatments can prolong their life but may not offer a long-term cure.

This study proposes using a drug called Sirolimus in combination with common chemotherapy drugs to treat patients with recurrent and refractory solid tumors. Sirolimus has been found to inhibit cell growth and to have anti-tumor activity in pediatric solid tumors in previous studies and, therefore, has the potential to increase the effectiveness of the chemotherapy drugs when given together.

This study wil investigate the highest dose of Sirolimus that can be given orally with other oral chemotherapy drugs. Cohorts of 2 subjects will be started at the minimum dose. The dose will be increased in the next 2 subjects as long as there were no major reactions in the previous groups. This study will also seek to learn more about the side effects of sirolimus when used in this combination and what effects the drug has on the white cells and the immune system. Successful use of this drug will impact the cancer population greatly by providing an increased chance of survival to those with resistant or recurrent cancers.

Description:

Sirolimus, is a potent immunosuppressive drug that is approved for use in prevention against allograft rejection following solid organ transplant. It has anti-tumor effects mainly by blocking signals which drive cells from G1 to S phase during cell cycle through inhibition of mTOR, thus inhibiting cell growth. Sirolimus, as well as other mTOR inhibitors, has shown anti-tumor activity in pediatric solid tumor xenografts. Children with relapsed and/or refractory solid tumors are in need of novel therapeutic approaches. One option for these patients is the use of prolonged exposure to low dose antiangiogenic chemotherapy, with agents such as etoposide and cyclophosphamide. In this phase I trial the feasibility and optimal dosing for daily sirolimus, in combination with daily celecoxib, and low dose etoposide alternating with cyclophosphamide, will be determined in children with relapsed and refractory solid tumors. p70S6 kinase inhibition will be used as a surrogate for mTOR inhibition. The potential immunosuppressive effect of sirolimus administered on this schedule will be assessed by serial lymphocyte subsets and assessment of memory T cell number.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: August 9, 2017
• Est. primary completion date: August 9, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 30 Years

Eligibility

Inclusion Criteria:

• must be <=30 years of age at time of study enrollment

• histologic verification of malignancy at original diagnosis or relapsis except in patients with intrinsic brain stem tumors, optic pathway gliomas or patients wtih pineal tumors and evaluations of serum or CSF alpha-fetoprotein or beta-HCG

• measurable or evaluable disease

• disease state must be one for which there is no known curative therapy

• Performance level >=50%

• Patients must have fully recovered from acute toxic effects of all prior chemotherapy, immunotherapy or radiotherapy

• no evidence of acute graft vs. host disease and >=3 months since transplant

• organ function as defined in eligibility section of protocol

Exclusion Criteria:

• patients cannot be pregnant or breast-feeding

• patients must agree to use of an effective contraceptive method

• no growth factors that support platelet or white cell number or function for at least 7 days prior to enrollment

• patients receiving corticosteroids who have not been on a stable or decreasing dose of corticosteroid for the prior 7 days are not eligible

• patients receiving any other investigational drugs

• patients receiving any other anti-cancer drugs

• patients who have an uncontrolled infection

Related Conditions & MeSH terms

• Astrocytoma
• Atypical Teratoid/Rhabdoid Tumor
• Clear Cell Sarcoma
• Ependymoma
• Ewing's Sarcoma
• Germ Cell Tumor
• Glioma
• Hepatoblastoma
• Medulloblastoma
• Neoplasms
• Neuroblastoma
• Osteosarcoma
• Renal Cell Carcinoma
• Retinoblastoma
• Rhabdoid Tumor
• Rhabdomyosarcoma
• Sarcoma
• Sarcoma, Clear Cell
• Sarcoma, Ewing
• Wilms Tumor

Intervention

Drug:
• sirolimus
daily administration of sirolimus in oral form starting at a dose of 1 mg/m2 and increasing to a possible 3 mg/m2.

Locations

Country	Name	City	State
United States	Children's Healthcare of Atlanta	Atlanta	Georgia

Sponsors (2)

Lead Sponsor	Collaborator
Emory University	Children's Healthcare of Atlanta

Country where clinical trial is conducted

United States, 

References & Publications (1)

Qayed M, Cash T, Tighiouart M, MacDonald TJ, Goldsmith KC, Tanos R, Kean L, Watkins B, Suessmuth Y, Wetmore C, Katzenstein HM. A phase I study of sirolimus in combination with metronomic therapy (CHOAnome) in children with recurrent or refractory solid an — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum tolerated dose (MTD)	estimate the maximum tolerated dose (MTD) and recommended Phase II dose of sirolimus administered orally once daily for 42 days in combination with metronomic chemotherapy in children with recurrent or refractory solid tumors.	2 years after treatment starts
Secondary	define and describe toxicities of sirolimus	To define and describe the toxicities of sirolimus administered in combination with metronomic chemotherapy administered according to this schedule.	2 years post treatment
Secondary	anti-tumor activity of sirolimus	To assess the antitumor activity of sirolimus administered in combination with metronomic chemotherapy to children with recurrent and refractory solid tumors within the confines of a Phase I study.	2 years post treatment
Secondary	evaluate correlation of p70S6 kinase activity	To evaluate the correlation of p70S6 kinase activity inhibition with tumor response.	2 years post treatment
Secondary	evaluate risk of infection	To evaluate the effect of this combination therapy on lymphocyte subsets and memory T-cells, and to correlate that with risk of infection.	2 years post treatment

External Links

•   Clinical trials website for Children's Healthcare of Atlanta