Alternating Systemic Chemotherapy and Intra-Arterial Melphalan (IAM) Chemotherapy in Children With Intra-Ocular Retinoblastoma

NCT ID: NCT02116959

Last Updated: 2020-04-16

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-07-23
• Study Completion Date: 2019-05-25

Brief Summary

The purpose of this study is to test the safety of the treatment combination of alternating standard chemotherapy and another (melphalan) chemotherapy at different interval schedules. Researchers want to find out what effects, good and/or bad, the treatment combination has on the patients and their retinoblastoma.

Conditions

Advanced Intra-Ocular Retinoblastoma; Retinoblastoma

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cohort 1

Patients will receive alternating treatments beginning with systemic chemotherapy then followed by intra-arterial (IA) therapy.

Bilateral retinoblastoma patients will be in Cohort 1.

For bilateral Bilateral retinoblastoma patients where one eye is stage A or B and the other eye is C, D, or E, only the higher stage eye (C, D, E) will be treated with IA chemotherapy unless the stage A or B eye is not amenable or has failed local therapy.

Group Type: EXPERIMENTAL

Melphalan

Intervention Type: DRUG

Carboplatin

Intervention Type: DRUG

Etoposide

Intervention Type: DRUG

Vincristine

Intervention Type: DRUG

Cohort 2

Patients will receive only intra-arterial (IA) therapy for more limited disease.

Group Type: EXPERIMENTAL

Melphalan

Intervention Type: DRUG

Carboplatin

Intervention Type: DRUG

Etoposide

Intervention Type: DRUG

Vincristine

Intervention Type: DRUG

Interventions

Melphalan

Intervention Type: DRUG

Carboplatin

Intervention Type: DRUG

Etoposide

Intervention Type: DRUG

Vincristine

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Age greater than or equal to 3 months up to 18 years.
• Intraocular retinoblastoma not previously treated with systemic chemotherapy, radiation therapy, or IA therapy. Local retinal therapy such as laser photocoagulation and cryotherapy will be permitted.
• Unilateral or bilateral retinoblastoma (RB) patients are eligible
• Patients will be registered on study based on the local exam under anesthesia (EUA) done for diagnostic purposes prior to study entry. The EUA done at study entry should be done within 14 days prior to study entry
• Patients may have had enucleation of one eye, as long as the remaining eye meets the eligibility criteria
• Involved eye(s) must meet the definition for International Classification of Retinoblastoma
• For unilateral retinoblastoma (see Appendix 1 for International Classification of Retinoblastoma):

1. Group A eye that has failed local therapy

2. Group B eye that has failed local therapy

3. Group C eye that has failed local therapy

4. Group D eye

5. Group E eye that is not buphthalmic, is not planned for enucleation after first cycle of chemotherapy, and is in a child less than 1 year of age

• For bilateral retinoblastoma (see Appendix 1 for International Classification of Retinoblastoma):

1. Group A and Group A eyes that have failed local therapy

2. Group A and Group B eyes that have failed local therapy

3. Group A and Group C eyes

4. Group A and Group D eyes

5. Group A and Group E eyes in which the Group E eye is not planned for enucleation after first cycle of chemotherapy

6. Group B and Group B eyes that have failed local therapy

7. Group B and Group C eyes

8. Group B and Group D eyes

9. Group B and Group E eyes in which the Group E eye is not planned for enucleation after first cycle of chemotherapy

10. Group C and Group C eyes

11. Group C and Group D eyes

12. Group C and Group E eyes even if early enucleation is planned for the Group E eye.

13. Group D and Group D eyes

14. Group D and Group E eyes even if early enucleation is planned for the Group E eye.

15. Group E and Group E eyes if at least one eye is not planned for enucleation.

• Adequate Renal Function defined as: creatinine clearance or radioisotope Glomerular filtration rate (GFR) ³ 70 milliliter (mL)/min/1.73 m2 OR a serum creatinine based on age and gender derived from the Schwartz formula for estimating GFR (Schwartz et al. J. Peds, 106:522, 1985) utilizing child length and stature data published by the Center for Disease Control (CDC).
• Adequate hematological function defined as:

1. Absolute Neutrophil Count > 1000/microliter

2. Platelet Count > 100,000/microliter

• Adequate liver function defined as total bilirubin should be less than or equal to 1.5 x upper limit of normal (ULN) for age and serum glutamic-oxaloacetic transaminase (SGOT) / aspartate aminotransferase (AST) and serum glutamic-pyruvic transaminase (SGPT)

/ alanine aminotransferase (ALT) < 5 x upper limit of normal (ULN) for age

• Adequate coagulation system as defined as an international normalized ratio (INR) of less than 1.4 and a partial thromboplastin time (PTT) of less than 34
• Women and men of child-bearing potential must agree to use adequate contraception such as hormonal or barrier method of birth control or abstinence prior to study entry and for the duration of study participation. Should the subject or the subject's partner become pregnant or suspect pregnancy while on protocol therapy, the treating physician must be informed immediately.

• Eyes with tumors that are amenable to local therapy with laser or cryotherapy without threat to vision
• Any technical factor that would prohibit use of catheterization of the ophthalmic artery (e.g., small for age infant, untreatable allergy to contrast).
• Abnormal cerebral vasculature noted on MR angiography that would increase the risk of the procedure, including but not limited to an incomplete Circle of Willis. Other abnormalities that are less severe than an incomplete Circle of Willis will be reviewed by the study chair in consultation with a neuro-interventional radiologist.
• Any serious ongoing condition, such as an untreated infection or organ dysfunction.
• Patients receiving any medications or substances that are inhibitors or inducers of CYP450 enzyme(s) are ineligible.
• Pregnant women are excluded from this study due to potential for teratogenic or abortifacient effects of therapy. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother breastfeeding should be discontinued upon start of protocol therapy.

Exclusion Criteria

• Any evidence of extraocular retinoblastoma clinically or by magnetic resonance imaging (MRI) of brain and orbits with and without gadolinium. MRI may be done within 21 days prior to study entry.

1. Evidence of systemic metastases on bilateral bone marrow, lumbar puncture, bone scan (or Fluorodeoxyglucose (FDG) Positron Emission Tomography (PET) scan), and/or any other additional tests done at study entry.

• Minimum Eligible Age: 3 Months
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of California, San Francisco

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Anuradha Banerjee, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Locations

University of California, San Francisco

San Francisco, California, United States

Countries

United States

Other Identifiers

NCI-2015-01749

Identifier Type: REGISTRY

Identifier Source: secondary_id

13087

Identifier Type: -

Identifier Source: org_study_id