Olaparib for Pediatric Cancer

No longer recruiting at 32 trial locations
AC
Overseen ByAstraZeneca Clinical Study Information Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 2 JurisdictionsThis treatment is already approved in other countries

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to determine if olaparib is safe and tolerable for children and teens with solid tumors that have returned or resist treatment. Researchers are testing olaparib, an experimental medication, in different age groups to evaluate its performance. Eligible participants have a solid tumor or primary central nervous system tumor with a specific genetic issue (HRR deficiency) and have exhausted standard treatment options. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.

Do I have to stop taking my current medications for the trial?

The trial requires that you do not use strong or moderate CYP3A inhibitors or inducers while participating. If you are taking these, you may need to stop. The protocol does not specify other medications, but you should discuss with the trial team.

Is there any evidence suggesting that olaparib is likely to be safe for children and adolescents?

Research has shown that olaparib has been promising in earlier studies with children. In these studies, most children tolerated the medication well. Some children with specific DNA issues in their tumors even responded positively. However, possible serious side effects should be noted. These can include bone marrow problems, such as Myelodysplastic Syndrome (MDS) or Acute Myeloid Leukemia (AML), which affect blood cell production. Although olaparib is approved for adults with certain cancers, its safety and effectiveness in children remain under investigation. While some evidence suggests children can tolerate it, further research is needed to confirm its safety for them.12345

Why do researchers think this study treatment might be promising?

Olaparib is unique because it targets cancer by inhibiting PARP, an enzyme involved in DNA repair. Unlike traditional chemotherapy, which attacks rapidly dividing cells indiscriminately, olaparib specifically targets cancer cells with defective DNA repair mechanisms. This precision reduces damage to healthy cells, potentially leading to fewer side effects. Additionally, olaparib's oral administration offers convenience compared to intravenous options, making it a more appealing choice for pediatric patients and their caregivers. Researchers are excited about this targeted approach as it represents a shift towards more personalized and less toxic cancer therapies.

What evidence suggests that olaparib might be an effective treatment for pediatric cancer?

Research has shown that olaparib might help treat solid tumors in children. In a previous study, olaparib was generally well tolerated and helped shrink tumors in 2 out of 15 patients, indicating possible benefits. Early results suggest the drug can reduce DNA damage in about half of the patients. While olaparib already treats other cancers like ovarian cancer, its success there offers hope for treating children's cancers. This trial will evaluate olaparib in different pediatric age groups, targeting specific gene changes that allow cancer cells to repair themselves, potentially stopping tumor growth.26789

Who Is on the Research Team?

MT

Milenkova Tsveta

Principal Investigator

AstraZeneca

Are You a Good Fit for This Trial?

This trial is for children and adolescents aged 6 months to under 18 with solid tumors that have relapsed or are resistant to treatment. They must be able to swallow tablets, have a tumor sample available for testing, and meet specific genetic criteria indicating a deficiency in HRR (a DNA repair process). Patients who've had certain recent treatments or those with blood disorders like MDS/AML can't participate.

Inclusion Criteria

My cancer has returned or is not responding to treatment, and it lacks certain repair genes.
For dose finding phase only: recruitment will be open to all patients with HRR deficiency, based on a local test. For the signal identification phase: recruitment will be open only to patients with documented evidence of a deleterious or suspected deleterious germline or tumour HRR gene mutation that meets the AZ HRR rules
I can provide a tumor sample and, if I'm over 2, a blood sample for testing.
See 4 more

Exclusion Criteria

I am not taking any strong or moderate drugs that affect enzyme CYP3A.
I have been treated with a PARP inhibitor like olaparib before.
I haven't had cancer radiotherapy (except for comfort care) or any approved cancer drugs in the last 30 days.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive olaparib monotherapy with a single dose on Day 1, followed by continuous dosing from Day 2 onwards

28 days
Daily dosing with specific PK sampling on Day 8 and Day 28

Follow-up

Participants are monitored for safety and effectiveness after treatment

30 days

Signal Identification

Secondary analysis of response in patients with HRR gene mutations

Up to 64 months

What Are the Treatments Tested in This Trial?

Interventions

  • Olaparib
Trial Overview The study tests the safety and tolerability of Olaparib, a medication targeting cancer cells' DNA repair mechanisms. It's given to young patients with solid tumors. The trial has two phases: dose finding for all eligible patients and signal identification specifically for those with confirmed HRR gene mutations.
How Is the Trial Designed?
4Treatment groups
Experimental Treatment
Group I: Signal identificationExperimental Treatment1 Intervention
Group II: Cohort C: ≥6 months to <6 yearsExperimental Treatment1 Intervention
Group III: Cohort B: ≥3 to <12 yearsExperimental Treatment1 Intervention
Group IV: Cohort A: ≥12 to <18 yearsExperimental Treatment1 Intervention

Olaparib is already approved in European Union, United States for the following indications:

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Approved in European Union as Lynparza for:
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Approved in United States as Lynparza for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

AstraZeneca

Lead Sponsor

Trials
4,491
Recruited
290,540,000+

Sir Pascal Soriot

AstraZeneca

Chief Executive Officer since 2012

Veterinary Medicine from École nationale vétérinaire d'Alfort, MBA from HEC Paris

Dr. Cristian Massacesi

AstraZeneca

Chief Medical Officer since 2021

MD from Marche Polytechnic University, Oncology training at Royal Marsden Hospital, Kaplan Comprehensive Cancer Center, and European Institute of Oncology

Pascal Soriot

AstraZeneca

Chief Executive Officer since 2012

Veterinary Medicine from École nationale vétérinaire d'Alfort, MBA from HEC Paris

Cristian Massacesi

AstraZeneca

Chief Medical Officer since 2021

MD from Marche Polytechnic University, Medical Oncology training at Royal Marsden Hospital, Kaplan Comprehensive Cancer Center, and European Institute of Oncology

Published Research Related to This Trial

Olaparib is an effective treatment for patients with platinum-sensitive, relapsed BRCA-mutated high-grade serous ovarian cancer, showing significant improvement in progression-free survival compared to placebo in a study of 265 patients.
The treatment is generally well tolerated, with most side effects being mild to moderate, although fatigue, anemia, and neutropenia were noted as more severe adverse events.
Olaparib: a review of its use as maintenance therapy in patients with ovarian cancer.Frampton, JE.[2016]
Olaparib is a powerful inhibitor of PARP-1 and PARP-2, showing effectiveness in treating ovarian cancer, particularly in patients with germline BRCA mutations.
Phase III trials are currently evaluating olaparib's efficacy as a maintenance therapy after initial treatment in patients with BRCA mutations, highlighting its potential role in long-term cancer management.
Olaparib: an oral PARP-1 and PARP-2 inhibitor with promising activity in ovarian cancer.Gunderson, CC., Moore, KN.[2016]
Olaparib (Lynparza) is approved for treating adult patients with high-risk early breast cancer that has a germline BRCA mutation, following chemotherapy treatment.
This approval highlights Olaparib's role as an adjuvant therapy, which means it is used after initial treatments to help prevent cancer recurrence.
New Adjuvant Treatment for High-Risk Early Breast Cancer.Aschenbrenner, DS.[2022]

Citations

1.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/35593736/
First phase 1 clinical study of olaparib in pediatric patients ...Olaparib was well tolerated, achieving objective response in 2/15 patients. The DNA damage response was attenuated in nearly one-half of ...
First phase 1 clinical study of olaparib in pediatric patients with ...The results of these previous studies indicate that olaparib may be effective for the treatment of pediatric solid tumors.
LYNPARZA® (olaparib): 10 Years Dedicated to ... - OncLiveAt the 7-year interim overall survival analysis, ~67% of patients were alive with LYNPARZA and ~46.5% were alive with placebo (HR=0.55, 95% CI: ...
arm H of the NCI-COG Pediatric MATCH trial - Oxford AcademicSix patients enrolled and received the olaparib starting dose of 135 mg/m2/dose. Two participants were fully evaluable; 4 were inevaluable ...
Olaparib for Pediatric Cancer · Info for ParticipantsThere is no direct data provided on its effectiveness for pediatric cancer. However, its success in treating other cancers, such as ovarian cancer, where it has ...
6.lynparzahcp.comlynparzahcp.com/
LYNPARZA® (olaparib) PARP Inhibitor | HCP sitePediatric Use: The safety and efficacy of LYNPARZA have not been established in pediatric patients. ... There are no data in patients with severe hepatic ...
7.lynparza.comlynparza.com/
LYNPARZA® (olaparib) - Official Patient WebsiteLYNPARZA may cause serious side effects, including: Bone marrow problems called Myelodysplastic Syndrome (MDS) or Acute Myeloid Leukemia (AML). Some people who ...
Olaparib Plus Ceralasertib May Benefit Pediatric Cancer ...“This is the first proof of principle that the combination is well tolerated and can lead to clinically relevant responses in pediatric cancers.
Safety & Tolerability in the OlympiA Trial 1Pediatric Use: The safety and efficacy of LYNPARZA have not been established in pediatric patients. ... olaparib in germline BRCA1/2 mutation-associated breast ...
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