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NCT04625907

FaR-RMS: An Overarching Study for Children and Adults With Frontline and Relapsed RhabdoMyoSarcoma

Datenbasis: WHO (Import vom 19.12.2024)
Geändert: 06.06.2024, 01:00
Krankheitskategorie:

Health conditions (Datenquelle: WHO)

Rhabdomyosarcoma

Interventions (Datenquelle: WHO)

Drug: Irinotecan;Drug: Actinomycin D;Drug: Doxorubicin;Drug: Ifosfamide;Drug: Vincristine;Drug: Vinorelbine;Drug: Cyclophosphamide;Drug: Temozolomide;Radiation: radiotherapy;Drug: Regorafenib

Inclusion/Exclusion Criteria (Datenquelle: WHO)

Gender: All
Maximum age: N/A
Minimum age: N/A

Inclusion Criteria for study entry - Mandatory at first point of study entry

1. Histologically confirmed diagnosis of RMS (except pleomorphic RMS)

2. Written informed consent from the patient and/or the parent/legal guardian

Phase 1b Dose Finding - IRIVA Inclusion

1. Entered in to the FaR-RMS study at diagnosis

2. Very High Risk disease

3. Age >12 months and =25 years

4. No prior treatment for RMS other than surgery

5. Medically fit to receive treatment

6. Adequate hepatic function:

1. Total bilirubin = 1.5 times upper limit of normal (ULN) for age, unless the
patient is known to have Gilbert's syndrome

2. ALT or AST < 2.5 X ULN for age

7. Absolute neutrophil count =1.0x 109/L

8. Platelets = 80 x 109/L

9. Adequate renal function: estimated or measured creatinine clearance =60 ml/min/1.73 m2

10. Documented negative pregnancy test for female patients of childbearing potential

11. Patient agrees to use contraception during therapy and for 12 months after last trial
treatment (females) or 6 months after last trial treatment (males), where patient is
sexually active

12. Written informed consent from the patient and/or the parent/legal guardian

Exclusion

1. Weight <10kg

2. Active > grade 2 diarrhoea

3. Prior allo- or autologous Stem Cell Transplant

4. Uncontrolled inter-current illness or active infection

5. Pre-existing medical condition precluding treatment

6. Urinary outflow obstruction that cannot be relieved prior to starting treatment

7. Active inflammation of the urinary bladder (cystitis)

8. Known hypersensitivity to any of the treatments or excipients

9. Second malignancy

10. Pregnant or breastfeeding women

Frontline chemotherapy randomisation Very High Risk - CT1a Inclusion

1. Entered in to the FaR-RMS study at diagnosis

2. Very High Risk disease

3. Age = 6 months

4. Available for randomisation =60 days after diagnostic biopsy/surgery

5. No prior treatment for RMS other than surgery

6. Medically fit to receive treatment

7. Adequate hepatic function :

a. Total bilirubin = 1.5 times upper limit of normal (ULN) for age, unless the patient
is known to have Gilbert's syndrome

8. Absolute neutrophil count =1.0x 109/L (except in patients with documented bone marrow
disease)

9. Platelets = 80 x 109/L (except in patients with documented bone marrow disease)

10. Fractional Shortening = 28%

11. Documented negative pregnancy test for female patients of childbearing potential

12. Patient agrees to use contraception during therapy and for 12 months after last trial
treatment (females) or 6 months after last trial treatment (males), where patient is
sexually active

13. Written informed consent from the patient and/or the parent/legal guardian

Exclusion

1. Active > grade 2 diarrhoea

2. Prior allo- or autologous Stem Cell Transplant

3. Uncontrolled inter-current illness or active infection

4. Pre-existing medical condition precluding treatment

5. Urinary outflow obstruction that cannot be relieved prior to starting treatment

6. Active inflammation of the urinary bladder (cystitis)

7. Known hypersensitivity to any of the treatments or excipients

8. Second malignancy

9. Pregnant or breastfeeding women

Frontline chemotherapy randomisation High Risk - CT1b Inclusion

1. Entered in to the FaR-RMS study at diagnosis

2. High Risk disease

3. Age = 6 months

4. Available for randomisation =60 days after diagnostic biopsy/surgery

5. No prior treatment for RMS other than surgery

6. Medically fit to receive treatment

7. Adequate hepatic function :

a. Total bilirubin = 1.5 times upper limit of normal (ULN) for age, except if the
patient is known to have Gilbert's syndrome

8. Absolute neutrophil count =1.0x 109/L

9. Platelets = 80 x 109/L

10. Documented negative pregnancy test for female patients of childbearing potential

11. Patient agrees to use contraception during therapy and for 12 months after last trial
treatment (females) or 6 months after last trial treatment (males), where patient is
sexually active

12. Written informed consent from the patient and/or the parent/legal guardian

Exclusion

1. Active > grade 2 diarrhoea

2. Prior allo- or autologous Stem Cell Transplant

3. Uncontrolled inter-current illness or active infection

4. Pre-existing medical condition precluding treatment

5. Urinary outflow obstruction that cannot be relieved prior to starting treatment

6. Active inflammation of the urinary bladder (cystitis)

7. Known hypersensitivity to any of the treatments or excipients

8. Second malignancy

9. Pregnant or breastfeeding women

Frontline Radiotherapy Note: eligible patients may enter multiple radiotherapy
randomisations.

Radiotherapy Inclusion - for all radiotherapy randomisations

1. Entered in to the FaR-RMS study (at diagnosis or prior to radiotherapy randomisation)

2. Very High Risk, High Risk and Standard Risk disease

3. = 2 years of age

4. Receiving frontline induction treatment as part of the FaR-RMS trial or with a
IVA/IVADo based chemotherapy regimen patients for whom. Note that patients for whom
ifosfamide has been replaced with cyclophosphamide will be eligible

5. Patient assessed as medically fit to receive the radiotherapy

6. Documented negative pregnancy test for female patients of childbearing potential

7. Patient agrees to use contraception during therapy and for 12 months after last trial
treatment (females) or 6 months after last trial treatment (males), where patient is
sexually active

8. Written informed consent from the patient and/or the parent/legal guardian

Radiotherapy Exclusion - for all radiotherapy randomisations

1. Prior allo- or autologous Stem Cell Transplant

2. Second malignancy

3. Pregnant or breastfeeding women

4. Receiving radiotherapy as brachytherapy

RT1a Specific Inclusion

1. Primary tumour deemed resectable (predicted R0/ R1 resection feasible) after 3 cycles
of induction chemotherapy (6 cycles for metastatic disease)

2. Adjuvant radiotherapy required in addition to surgical resection (local

Weitere Angaben zur Studie im WHO-Primärregister

https://clinicaltrials.gov/ct2/show/NCT04625907

Weitere Angaben zur Studie aus der Datenbank der WHO (ICTRP)

https://trialsearch.who.int/Trial2.aspx?TrialID=NCT04625907
Weitere Informationen zur Studie

Datum der Studienregistrierung

22.11.2019

Rekrutierungsstatus

Recruiting

Wissenschaftlicher Titel (Datenquelle: WHO)

FaR-RMS: An Overarching Study for Children and Adults With Frontline and Relapsed RhabdoMyoSarcoma

Studientyp (Datenquelle: WHO)

Interventional

Design der Studie (Datenquelle: WHO)

Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).

Phase (Datenquelle: WHO)

Phase 1/Phase 2

Primäre Endpunkte (Datenquelle: WHO)

Event Free Survival (RT2);Event Free Survival (CT1A);Event Free Survival (CT1B);Event Free Survival (CT2A);Event Free Survival (CT2B);Event Free Survival (CT3);Local Failure Free Survival (RT1A and RT1B);Local Failure Free Survival (RT1C)

Sekundäre Endpunkte (Datenquelle: WHO)

Recommended Phase II Dose (Phase 1b);Maximum Tolerated Dose (Phase 1b);Toxicity (All chemotherapy randomisations);Dose Limiting Toxicity (Phase 1b);Response (Phase 1b, CT1A, CT1B);Tolerability (CT3);Overall Survival (CT1A);Overall Survival (CT1B);Overall Survival (CT2A);Overall Survival (CT2B);Overall Survival (RT1A and RT1B);Overall Survival (RT1C);Overall Survival (RT2);Overall Survival (CT3);Overall Survival (all patients);Acute wound complications and post-operative complications (RT1A and RT1B);Acute post-radiotherapy complications (All radiotherapy randomisations);Late complications (RT1A, RT1B. RT1C);Loco-regional failure-free survival (All radiotherapy randomisations);Health related quality of life (RT1A and RT2) self-reported questionnaire completed by patient;Health related quality of life (RT1A and RT2) self-reported questionnaire completed by the patient;Health related quality of life (CT3) self-reported questionnaire completed by the patient;Acceptability and Palatability of Regorafenib (CT3);PET Response (if participating in PET Sub-study);Event Free Survival (all patients);Event Free Survival (if participating in PET Sub-study);Local Failure Free Survival (if participating in PET Sub-study)

Kontakt für Auskünfte (Datenquelle: WHO)

Please refer to primary and secondary sponsors

Ergebnisse der Studie (Datenquelle: WHO)

Zusammenfassung der Ergebnisse

noch keine Angaben verfügbar

Link zu den Ergebnissen im Primärregister

noch keine Angaben verfügbar

Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten

noch keine Angaben verfügbar

Studiendurchführungsorte

Durchführungsländer (Datenquelle: WHO)

Australia, Austria, Belgium, Czechia, Denmark, France, Greece, Ireland, Israel, Italy, Netherlands, New Zealand, Norway, Portugal, Slovakia, Slovenia, Spain, Sweden, Switzerland, United Kingdom

Kontakt für weitere Auskünfte zur Studie

Kontakt für allgemeine Auskünfte (Datenquelle: WHO)

Meriel Jenney;Bridget Shaw
Chief Investigator
0121 414 2996
farrms@trials.bham.ac.uk

Kontakt für wissenschaftliche Auskünfte (Datenquelle: WHO)

Meriel Jenney;Bridget Shaw
Chief Investigator
0121 414 2996
farrms@trials.bham.ac.uk

Weitere Studienidentifikationsnummern

Secondary ID (Datenquelle: WHO)

2018-000515-24
45535982
RG_17-247
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