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CompletedLast updated: 5 February 2024

SIOPEN LINES: This Phase III trial is managing the treatment (which may involve chemotherapy, radiotherapy and/or surgery) of people with low and intermediate risk patients with neuroblastomaEuropean Low and Intermediate Risk Neuroblastoma Protocol

Clinical summary

Summary

This trial groups together into a single protocol the treatment of all patients with "non high risk" neuroblastoma, with stratification into two groups: low risk and intermediate risk. Treatment may include chemotherapy, surgery and radiotherapy, or a combination of these treatments, depending on individual cases.

Conditions

This trial is treating patients with neuroblastoma.

Cancer

Brain and Spinal Cancers Brain and Spinal

Age

People0 - 18

Phase

III

Trial Acronym

SIOPEN LINES

More information

Trial Identifiers

Use the hyperlinks, where available to access additional clinical trial information.

Trial sponsor

Instituto de Investigacion Sanitaria La Fe

Scientific Title

European Low and Intermediate Risk Neuroblastoma Protocol

Eligibility

Inclusion

  1. LOW RISK STUDY

    Inclusion criteria for the whole low risk group:

    • informed consent and follow-up warranted; group assignment completed within 6 weeks from diagnosis; no prior chemotherapy or radiotherapy
    • Biopsy proven neuroblastoma
    • Tumour genomic profile obtained in a NRL according to guidelines
    • MYCN non-amplified

    Exclusion criteria for the whole low risk group:

    * Diagnosis of ganglioneuroma or ganglioneuroblastoma intermixed INRG Stage L2

    Inclusion criteria:

    *age ≤ 18 months

    Exclusion criteria:

    • any metastatic site
    • MYCN amplification
    • age > 18 months INRG Stage Ms

    Inclusion criteria:

    * age ≤ 12 months

    Exclusion criteria:

    • bone, pleura/lung and/or CNS metastasis
    • MYCN amplification
    • age > 12 months
  2. INTERMEDIATE RISK STUDY

    Inclusion criteria for the whole intermediate risk group:

    • informed consent and follow-up warranted; group assignment completed within 6 weeks from diagnosis; no prior chemotherapy or radiotherapy
    • Tumour material available for biological studies according to guidelines
    • Biopsy proven neuroblastoma confirmed in a National Reference Laboratory (NRL)

    Exclusion criteria for the whole intermediate risk group:

    * Diagnosis of ganglioneuroma or ganglioneuroblastoma intermixed

    INRG Stage L1 and INSS stage 1:

    Inclusion criteria:

    * MYCN amplified

    Exclusion criteria:

    • MYCN non-amplified
    • INSS stages 2, 3, 4, 4s

    INRG Stage L2:

    Inclusion criteria:

    • Histology: differentiating, poorly differentiated, undifferentiated neuroblastoma or ganglioneuroblastoma nodular
    • MYCN non-amplified
    • age >18 months

    Exclusion criteria:

    • neuroblastoma NOS
    • MYCN amplification.
    • age ≤ 18 months

    INRG Stage M:

    Inclusion criteria:

    • Any histology
    • MYCN non-amplified
    • age ≤ 12 months

    Exclusion criteria:

    • MYCN amplification
    • age > 12 months
  3. NEONATAL SUPRARENAL MASSES

Inclusion criteria:

  • Age less than or equal to 90 days when the suprarenal mass is discovered.
  • Suprarenal mass detected by ultrasound and/or MRI. The suprarenal mass may be cystic and/or solid, but IT CANNOT REACH THE MIDLINE AND should MEASURE ≤ 5 CM AT THE LARGEST DIAMETER.
  • No regional involvement: MRI scan does not show evidence of positive ipsi/contralateral lymph nodes or other spread outside the suprarenal gland.
  • No metastatic involvement.
  • Frozen plasma available.
  • Informed consent.
  • Availability to do the adequate follow-up

Exclusion criteria:

  • Age older than 90 days.
  • Suprarenal mass bigger than 5 cm.
  • Regional involvement.
  • Metastatic involvement.
  • Inability to undertake mandatory diagnostic studies (biological markers, US, MRI, MIBG).
  • Follow-up not guaranteed by parents/guardians.
Message

Clinical trials have complex eligibility criteria.

Ask your doctor if this trial could be right for you.

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