CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 13 enrolled
Drug / intervention
Topotecan +7 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02786719
NCT02786719N/ACompleted

A Safety Pilot Study of High Risk Induction Chemotherapy for Neuroblastoma Without Prophylactic Administration of Myeloid Growth Factors

Baylor College of Medicine·interventional·Posted Jun 1, 2016·Updated Mar 12, 2020

In Brief

A clinical study evaluating Topotecan, Cyclophosphamide, and 5 other interventions for Neuroblastoma. Completed, enrolled 13 participants across 2 sites.

Detailed Summary

Patients will be asked to participate in this study because patients have been diagnosed with high-risk neuroblastoma, a common childhood cancer which has aggressive features. If left untreated, high-risk neuroblastoma is fatal. Children with high-risk neuroblastoma often respond to current available treatments, but there is a high risk that the cancer will return. This study will test the safety of giving standard induction treatment for high-risk neuroblastoma without one of the drugs commonly used to prevent side effects. Current treatment for high-risk neuroblastoma includes anti-cancer drugs (chemotherapy), surgery, radiation therapy and high-dose chemotherapy with hematopoietic stem cell rescue. Treatment takes about one year to complete and occurs in 3 phases: induction, consolidation, and maintenance. This study is limited to the induction phase of treatment. Induction therapy includes six chemotherapy drugs given in different combinations every 3 weeks for a total of 6 courses. For the past decade, induction chemotherapy has been followed by a drug called granulocyte colony stimulating factor (G-CSF, filgrastim, peg-filgrastim, Neupogen, or Neulasta) to prevent side effects from the chemotherapy. G-CSF is routinely given to patients with high risk neuroblastoma after chemotherapy to stimulate white blood cell production and shorten the time period when the absolute neutrophil count (ANC), a type of white blood cell, is low after chemotherapy. G-CSF is known to shorten the period of low ANC by approximately 3 days. When the ANC is lowest, a patient is most at risk of getting a bacterial infection. Recent lab experiments in mice have shown that neuroblastoma tumor cells may respond to G-CSF by growing faster and metastasizing (spreading to other parts of the body). There have been no clinical trials comparing the survival of children with high risk neuroblastoma with or without G-CSF. This clinical trial is the first step towards giving induction chemotherapy with less G-CSF. The goal of this study is to determine if it is safe to give induction chemotherapy to children with neuroblastoma without giving G-CSF routinely.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNeuroblastoma
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJun 1, 2016
Enrollment StartJun 1, 2016
Primary CompletionFeb 5, 2019
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 10.1 years ago

Interventions

Topotecandrug

CYCLE 1+2 (given by intravenous catheter daily for 5 days)

Cyclophosphamidedrug

CYCLE 1+2 (given by intravenous catheter daily for 5 days)

Cisplatindrug

Cycle 3+5 (given daily x 4 days)

Etoposidedrug

Cycle 3+5 (given daily for 3 days)

Vincristinedrug

Cycle 4+6 (given daily for 3 days)

Cyclophosphamidedrug

Cycle 4+6 (given daily for 2 days)

Doxorubicindrug

Cycle 4+6 (given daily for 3 days)

Sargramostimdrug

Granulocyte macrophage colony stimulating factor (rhu GM-CSF, rGM-CSF, GM-CSF)