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Treatment Protocol for Non-Metastatic Unilateral Retinoblastoma (RbGALOP2)

Primary Purpose

Unilateral Retinoblastoma

Status
Recruiting
Phase
Phase 3
Locations
Argentina
Study Type
Interventional
Intervention
Combination Chemotherapy plus Intrathecal Topotecan
Higher Dose Combination Chemotherapy plus Intrathecal Topotecan
Higher Dose Combination Chemotherapy plus Intrathecal Topotecan and Orbital Radiotherapy
No Adjuvant Therapy
Sponsored by
Hospital JP Garrahan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Unilateral Retinoblastoma

Eligibility Criteria

undefined - 6 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histological diagnosis of retinoblastoma confirmed at participating institutions
  • Ophthalmological diagnosis of unilateral retinoblastoma in patients undergoing conservative therapy.
  • No prior therapy for retinoblastoma
  • Lansky Performance Scale greater or equal to 50
  • Normal organ function in those patients assigned for chemotherapy
  • Signed informed consent

Exclusion Criteria:

  • Patients with unilateral retinoblastoma and germline mutations of the Rb1 gene or family history for retinoblastoma

Sites / Locations

  • Hospital JP GarrahanRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Low Risk Patients

Higher Risk Patients

Stage II Patients

Patients with buphthalmus

Arm Description

Patients with IRSS stage I, pT1, pT2 and pT3 stage will not receive adjuvant therapy

Patients with IRSS stage I, pT3b, pT3c, pT3d will receive 6 cycles of adjuvant chemotherapy plus 6 doses of intrathecal topotecan

Patients with Stage II (pT4) will receive 6 cycles of adjuvant chemotherapy plus 6 doses of intrathecal topotecan and orbital radiotherapy

Patients with buphthalmus (cT3c, cT3e) will receive 2 cycles of neo-adjuvant chemotherapy plus 6 doses of intrathecal topotecan followed by secondary enucleation and 6 cycles of adjuvant chemotherapy.

Outcomes

Primary Outcome Measures

Rate of extraocular relapses
Number of participants experiencing extraocular relapse
Evaluation of number of patients experiencing acute, chronic and fatal toxicities
Number of participants experiencing treatment-related adverse effects and mortality as measured by CTCAE v4.0

Secondary Outcome Measures

Full Information

First Posted
March 12, 2018
Last Updated
August 5, 2019
Sponsor
Hospital JP Garrahan
Collaborators
Hospital San Juan de Dios, Santiago, Hospital Pereyra Rossell, Montevideo, National Cancer Institute Rio de Janeiro, Hospital Sant Joan de Deu
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1. Study Identification

Unique Protocol Identification Number
NCT03475121
Brief Title
Treatment Protocol for Non-Metastatic Unilateral Retinoblastoma
Acronym
RbGALOP2
Official Title
GALOP II Protocol for the Treatment of Unilateral Retinoblastoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital JP Garrahan
Collaborators
Hospital San Juan de Dios, Santiago, Hospital Pereyra Rossell, Montevideo, National Cancer Institute Rio de Janeiro, Hospital Sant Joan de Deu

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This protocol provides guidelines for the management of non-metastatic unilateral retinoblastoma and introduces an innovative adjuvant therapy for higher risk patients based upon the results of the Grupo de America Latina de Oncologia Pediatrica (GALOP) I study. Conservative therapy will be not protocolized.
Detailed Description
Patients with non-metastatic retinoblastoma undergoing enucleation will be staged using the American Joint Committee on Cancer (AJCC), version 8, Tumor, Node, Metastasis (TNM)- H system and the International Retinoblastoma Staging System (IRSS). IRSS stage I patients recognized as higher risk will be assigned for adjuvant therapy. Those with standard risk will not receive adjuvant therapy after enucleation. Higher risk patients are defined as those with pathological retrolaminar optic nerve invasion and-or any degree of scleral invasion (pT3b, pT3c, pT3d). Based on the results of the GALOP I protocol, they will receive a reduced dose adjuvant chemotherapy regimen with 3 cycles of alternating cyclophosphamide, vincristine and idarubicin alternating with another 3 cycles of carboplatin and etoposide. Six doses of intrathecal topotecan will be given. Patients presenting with severe buphthalmia (cT3c-cT3e) will receive neo-adjuvant therapy with the same intensive regimen but including a higher dose of carboplatin as per GALOP I protocol plus intrathecal topotecan and secondary enucleation followed by adjuvant chemotherapy for a total of 8 cycles. Stage II patients (pT4) will receive the same adjuvant regimen plus orbital radiotherapy (45 cGy).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unilateral Retinoblastoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low Risk Patients
Arm Type
Experimental
Arm Description
Patients with IRSS stage I, pT1, pT2 and pT3 stage will not receive adjuvant therapy
Arm Title
Higher Risk Patients
Arm Type
Experimental
Arm Description
Patients with IRSS stage I, pT3b, pT3c, pT3d will receive 6 cycles of adjuvant chemotherapy plus 6 doses of intrathecal topotecan
Arm Title
Stage II Patients
Arm Type
Experimental
Arm Description
Patients with Stage II (pT4) will receive 6 cycles of adjuvant chemotherapy plus 6 doses of intrathecal topotecan and orbital radiotherapy
Arm Title
Patients with buphthalmus
Arm Type
Experimental
Arm Description
Patients with buphthalmus (cT3c, cT3e) will receive 2 cycles of neo-adjuvant chemotherapy plus 6 doses of intrathecal topotecan followed by secondary enucleation and 6 cycles of adjuvant chemotherapy.
Intervention Type
Combination Product
Intervention Name(s)
Combination Chemotherapy plus Intrathecal Topotecan
Intervention Description
Adjuvant chemotherapy with a reduced dose (compared to GALOP I protocol) of carboplatin
Intervention Type
Combination Product
Intervention Name(s)
Higher Dose Combination Chemotherapy plus Intrathecal Topotecan
Intervention Description
GALOP I-based systemic adjuvant therapy plus intrathecal topotecan
Intervention Type
Combination Product
Intervention Name(s)
Higher Dose Combination Chemotherapy plus Intrathecal Topotecan and Orbital Radiotherapy
Intervention Description
GALOP I-based systemic adjuvant therapy plus intrathecal topotecan and orbital radiotherapy (45 Gy) up to chiasm
Intervention Type
Other
Intervention Name(s)
No Adjuvant Therapy
Intervention Description
Patients will not receive any adjuvant therapy after enucleation of the affected eye.
Primary Outcome Measure Information:
Title
Rate of extraocular relapses
Description
Number of participants experiencing extraocular relapse
Time Frame
3 years
Title
Evaluation of number of patients experiencing acute, chronic and fatal toxicities
Description
Number of participants experiencing treatment-related adverse effects and mortality as measured by CTCAE v4.0
Time Frame
5 years

10. Eligibility

Sex
All
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histological diagnosis of retinoblastoma confirmed at participating institutions Ophthalmological diagnosis of unilateral retinoblastoma in patients undergoing conservative therapy. No prior therapy for retinoblastoma Lansky Performance Scale greater or equal to 50 Normal organ function in those patients assigned for chemotherapy Signed informed consent Exclusion Criteria: Patients with unilateral retinoblastoma and germline mutations of the Rb1 gene or family history for retinoblastoma
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guillermo L Chantada, MD, PhD
Phone
5411-4122-6000
Email
gchantada@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Claudia Sampor
Phone
5411-4122-6000
Email
claudiasampor@hotmail.com
Facility Information:
Facility Name
Hospital JP Garrahan
City
Buenos Aires
State/Province
CF
ZIP/Postal Code
C1245AAL
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carolina Cernadas, MD
Phone
541141226335
Email
coordinacioninvestigacion@garrahan.gov.ar
First Name & Middle Initial & Last Name & Degree
Guillermo Chantada, MD, PhD
Phone
541141226000
Email
gchantada@yahoo.com
First Name & Middle Initial & Last Name & Degree
Claudia Sampor, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Treatment Protocol for Non-Metastatic Unilateral Retinoblastoma

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