Rituximab, Combination Chemotherapy, and Yttrium Y 90 Ibritumomab Tiuxetan in Treating Patients With Relapsed Follicular Non-Hodgkin Lymphoma

Lymphoma Clinical Trial

Official title:

Short Chemo Radiotherapy in Follicular Lymphoma Trial of 90Y Ibritumomab Tiuxetan (ZevalinTM) as Therapy for First and Second Relapse in Follicular Lymphoma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00637832
• Other study ID #: CDR0000588042
• Secondary ID: USCTU-SCHRIFT-06
• Status: Terminated
• Phase: Phase 2
• Start date: April 1, 2008
• Est. completion date: January 6, 2015

Study information

• Verified date: December 2021
• Source: University of Southampton
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Radiolabeled monoclonal antibodies, such as yttrium Y 90 ibritumomab tiuxetan, can find cancer cells and carry cancer-killing substances to them without harming normal cells. Giving rituximab together with combination chemotherapy and yttrium Y 90 ibritumomab tiuxetan may kill more cancer cells.

PURPOSE: This phase II trial is studying how well giving rituximab together with combination chemotherapy and yttrium Y 90 ibritumomab tiuxetan works in treating patients with relapsed follicular non-Hodgkin lymphoma.

Description:

OBJECTIVES:

Primary

• To evaluate the response rates in patients with relapsed follicular non-Hodgkin lymphoma treated with short-duration rituximab and combination chemotherapy (R-chemo) followed by rituximab and yttrium Y 90 ibritumomab tiuxetan.

Secondary

• To evaluate the duration of response in patients treated with this regimen.

• To evaluate the quality of response in order to determine the conversion rate from partial response to complete response in patients treated with this regimen.

• To evaluate the toxicity of yttrium Y 90 ibritumomab tiuxetan when administered after 3 courses of R-chemo.

OUTLINE: This is a multicenter study.

• Chemoimmunotherapy (R-CHOP or R-CVP): Patients receive R-CHOP comprising rituximab IV, cyclophosphamide IV, doxorubicin hydrochloride IV, and vincristine IV on day 1 and oral prednisolone on days 1-5. Alternatively, patients who have already been exposed to prior tolerance doses of anthracyclines receive R-CVP comprising rituximab IV, cyclophosphamide IV, and vincristine IV on day 1 and oral prednisolone on days 1-5. Treatment repeats every 3 weeks for up to 3 courses.

Patients with objective evidence of response on CT scan or those with < 25% bone marrow involvement and no signs of bone marrow hypocellularity (< 15%) on bone marrow biopsy proceed to radioimmunotherapy.

• Radioimmunotherapy: Four to 6 weeks after completion of R-CHOP or R-CVP, patients receive rituximab IV followed no more than 4 hours later by yttrium Y 90 ibritumomab tiuxetan IV over 10 minutes.

After completion of study therapy, patients are followed periodically for up to 5 years.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 1
• Est. completion date: January 6, 2015
• Est. primary completion date: January 6, 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 120 Years

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed grade 1, 2, or 3 follicular non-Hodgkin lymphoma

• Stage II, III, or IV disease (according to the Ann Arbor staging system)

• CD20-positive disease

• Initial disease bulk = 10 cm

• In first or second relapse after prior treatment with a rituximab-containing chemotherapy regimen (R-chemo) or chemotherapy alone

• Relapse must have occurred = 6 months after completion of R-chemo

• Relapse that occurred < 6 months after completion of chemotherapy alone allowed

• Has at least one of the following symptoms requiring initiation of treatment:

• Nodal mass > 5 cm in its greater diameter

• B symptoms

• Elevated serum lactate dehydrogenase (LDH) or ß2-microglobulin

• Involvement of = 3 nodal sites (each with a diameter > 3 cm)

• Symptomatic splenic enlargement

• Compressive syndrome

• No primary refractory disease

• No large pleural or peritoneal effusions

• No CNS disease

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2

• Life expectancy = 6 months

• Absolute granulocyte count = 1,500/mm³

• Platelet count = 1,000/mm³

• Serum creatinine < 1.5 times upper limit of normal (ULN)

• Total bilirubin < 1.5 times ULN

• AST < 5 times ULN

• No active obstructive hydronephrosis

• No evidence of active infection requiring IV antibiotics

• No advanced heart disease or other serious illness that would preclude study evaluation

• No known HIV infection

• No human anti-mouse antibody (HAMA) reactivity

• No known hypersensitivity to murine antibodies or proteins

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during and for 12 months after completion of study treatment

• No other prior malignancy, except for adequately treated skin cancer, cervical cancer in situ, or other cancer for which the patient has been disease-free for 5 years

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• At least 4 weeks since prior investigational drugs and recovered

• No prior radioimmunotherapy

Related Conditions & MeSH terms

• Lymphoma
• Lymphoma, Follicular

Intervention

Biological:
• rituximab

Drug:
• cyclophosphamide

• doxorubicin hydrochloride

• prednisolone

• vincristine sulfate

Radiation:
• yttrium Y 90 ibritumomab tiuxetan

Locations

Country	Name	City	State
United Kingdom	Saint Bartholomew's Hospital	London
United Kingdom	Christie Hospital	Manchester	England
United Kingdom	Mount Vernon Cancer Centre at Mount Vernon Hospital	Northwood	England
United Kingdom	Dorset Cancer Centre	Poole Dorset	England
United Kingdom	Southampton General Hospital	Southampton	England

Sponsors (1)

Lead Sponsor	Collaborator
University of Southampton

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall response rate, including combined complete response and partial response
Secondary	Time to disease progression
Secondary	Time to next treatment
Secondary	Response duration in patients with responding disease
Secondary	Safety