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A prospective, non-randomised study of chemotherapy and radiotherapy for osteolymphoma (OL)

Trans Tasman Radiation Oncology Group (TROG) 99.04 - A prospective, non-randomised study of chemotherapy (cyclophosphamide, doxorubicin, vincristine, prednisolone) and radiotherapy for osteolymphoma (OL) to determine the outcome of optimal treatment on low grade follicular lymphoma progression.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12607000111471
Acronym
TROG 99.04
Enrollment
32
Registered
2003-12-22
Start date
2000-09-15
Completion date
2007-02-28
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Osteolymphoma is a cancer of the bone marrow that responds well to radiation therapy and chemotherapy but may come back in other parts of the body. This trial will determine the results of combining radiation therapy and chemotherapy in a standardised way.

Interventions

Chemotherapy Given Intravenously on days 1, 22, 43: - Cyclophosphamide 750 mg per metre squared - Doxorubicin 50 mg per metre squared - Vincristine 1.4mg per metre squared Prednisolone 50 mg per metre squared. Given orally for five days on each of these occassions. ie days 1-5, 22-27 etc. A total of three 21 day cycles of chemotherapy should be administered. Radiotherapy should be given 3 weeks after the last cycle of chemotherapy (day 64). Fractions should be given daily - 9-10 times per

Chemotherapy Given Intravenously on days 1, 22, 43: - Cyclophosphamide 750 mg per metre squared - Doxorubicin 50 mg per metre squared - Vincristine 1.4mg per metre squared Prednisolone 50 mg per metre squared. Given orally for five days on each of these occassions. ie days 1-5, 22-27 etc. A total of three 21 day cycles of chemotherapy should be administered. Radiotherapy should be given 3 weeks after the last cycle of chemotherapy (day 64). Fractions should be given daily - 9-10 times per fortnight. Phase I (large volume): 36Gy in 20 fractions and Phase II (small volume): 9 GY in 5 fractions to the boost volume (area of tumour that requires a boost of radiotherapy). Total dose 45 Gy in 25 fractions. Phase I and II are given over the course of one fortnight.

Sponsors

David Christie
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
17 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Histologically confirmed non-Hodgkin’s lymphoma in a bony site - Limited extraosseous disease - Ann Arbor stage IE Age >17- ECOG performance status >3 - Expected survival > 6 months - Written informed consent

Exclusion criteria

Previous radiotherapy or chemotherapy- Previous malignancy - Medically unfit to undergo treatment

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026