Treatment and Natural History Study of Lymphomatoid Granulomatosis

PHASE2CompletedINTERVENTIONAL
Enrollment

94

Participants

Timeline

Start Date

May 5, 1995

Primary Completion Date

January 17, 2025

Study Completion Date

January 17, 2025

Conditions
Lymphomatoid GranulomatosisGranulomatosis, LymphomatoidNon-Hodgkins LymphomaLymphoproliferative Disorder
Interventions
BIOLOGICAL

Interferon

For lymphomatoid granulomatosis (LYG) Grade 1 and 2: Interferon starting at 7.5 million Units subcutaneous (subQ) 3 times a week and increasing on the following schedule: 10 million U; 15 million U; 20 million U; 25 million U; and increased in 5 million U increments, as tolerated. Patients continue taking interferon for 1 year beyond complete remission (CR).

DRUG

Rituxan and EPOCH

For lymphomatoid granulomatosis (LYG) Grade 3: EPOCH-R (etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, rituximab) every 3 weeks for 6 cycles.

PROCEDURE

Tumor biopsy

Baseline (optional).

PROCEDURE

Bone marrow biopsy

Baseline.

BIOLOGICAL

Bone marrow aspirate

Baseline.

PROCEDURE

Lumber puncture

Baseline.

DIAGNOSTIC_TEST

CT

Arm 1: At baseline, then every 4 weeks until on stable dose of interferon or a maximum of 6 monthly scans, then every 3 months while receiving interferon, and following completion of interferon. In surveillance, every 3 months for 1 year, every 4 months for 1 year, every 6 months for 1 year and yearly thereafter for 2 years. Arm 2: At baseline, following cycle 4, and following cycle 6 of etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (DA-EPOCH-R). In surveillance, every 3 months for 1 year, every 4 months for 1 year, every 6 months for 1 year and yearly thereafter for 2 years.

DIAGNOSTIC_TEST

Brain MRI

"Arm 1: At baseline, then every 4 weeks until on stable dose of interferon or a maximum of 6 monthly scans, then every 3 months while receiving interferon, and following completion of interferon. In surveillance, every 3 months for 1 year, every 4 months for 1 year, every 6 months for 1 year and yearly thereafter for 2 years (patients with central nervous system (CNS) disease only).~Arm 2: At baseline, following cycle 4, and following cycle 6 of etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (DA-EPOCH-R). In surveillance, every 3 months for 1 year, every 4 months for 1 year, every 6 months for 1 year and yearly thereafter for 2 years (patients with CNS disease only)."

DIAGNOSTIC_TEST

Echocardiogram

For participants receiving \> 450 mg/m\^2 doxorubicin.

DIAGNOSTIC_TEST

FDG-PET

Arm 1: Baseline and following completion of interferon. Arm 2: Baseline and following completion of etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (DA-EPOCH-R).

Trial Locations (1)

20892

National Institutes of Health Clinical Center, Bethesda

All Listed Sponsors
lead

National Cancer Institute (NCI)

NIH

NCT00001379 - Treatment and Natural History Study of Lymphomatoid Granulomatosis | Biotech Hunter | Biotech Hunter