Phase II Study Of Roferon and Accutane For Patients With T-Cell Malignancies

Sponsor

M.D. Anderson Cancer Center (Other)

Overall Status

Completed

CT.gov ID

NCT00038376

Collaborator

(none)

Enrollment

Location

Arm

181.7

Actual Duration (Months)

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the response rate of patients with T-cell malignancies to combination therapy using interferon-alpha (Roferon) and Isotretinoin (Accutane).

Condition or Disease	Intervention/Treatment	Phase
Lymphoma, T-Cell Mycosis Fungoides Hematologic Neoplasms	Drug: Isotretinoin (Accutane) Drug: Interferon Alpha	Phase 2

Detailed Description

Retinoids have shown activity in T-cell malignancies in past studies (both isotretinoin and etretinate) with an overall response rate of about 60%. One third of those responses were complete responses. Interferon-alpha has proven efficacy in wide ranges of human malignancies including T-cell lymphomas as a single agent. A clinical trial was needed to evaluate the response rate of these two agents combined.

Interferon is a normal body protein, which is made by cells after exposure to viruses. It acts as a messenger to warn surrounding cells of invasions by viruses and, possibly, by cancer cells. Isotretinoin is a synthetic form of Vitamin A which effects the growth of normal cells and cancer cells.

Participants participating in this study will receive a combination of alpha-interferon and isotretinoin. Alpha-interferon will be given once a day for an initial period of 12 weeks. Participants will take the drug home, where a nurse or family member of the participant (who can be trained at UTMDACC) will inject it just under the skin (SQ). Isotretinoin will be given by mouth twice a day.

If a participant's disease does not show a response, the alpha-interferon and the isotretinoin will be increased. If side effects occur, the dose of alpha-interferon and/or isotretinoin will be decreased by 50%. If the side effects are severe, therapy will be discontinued. If the participant's disease is unresponsive or worsens, the participant will be taken off study and other treatments will be recommended.

Responding participants will be placed on a maintenance schedule for as long as they respond. Up to 60 participants will be studied at UT M.D. Anderson Cancer Center to test the effectiveness of this drug combination.

This is an investigational study. Alpha-interferon and isotretinoin are FDA approved and commercially available.

Study Design

Study Type:

Interventional

Actual Enrollment :

56 participants

Allocation:

Non-Randomized

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Phase II Study of Interferon Alpha and Isotretinoin in Patients With T-Cell Malignancies

Actual Study Start Date :

May 8, 1990

Actual Primary Completion Date :

Jun 30, 2005

Actual Study Completion Date :

Jun 30, 2005

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 1 Alpha-interferon + Isotretinoin	Drug: Isotretinoin (Accutane) 0.5 mg/k (1.0 mg/k total) by mouth twice a day Other Names: 13-cis-Retinoic Acid Drug: Interferon Alpha Starting dose of 3 MU injected under skin once a day for 12 weeks. Other Names: Intron A Interferon alfa-2b

Arm

Intervention/Treatment

Experimental: 1

Alpha-interferon + Isotretinoin

Drug: Isotretinoin (Accutane)

0.5 mg/k (1.0 mg/k total) by mouth twice a day

Other Names:

13-cis-Retinoic Acid

Drug: Interferon Alpha

Starting dose of 3 MU injected under skin once a day for 12 weeks.

Other Names:

Intron A

Interferon alfa-2b

Outcome Measures

Primary Outcome Measures

To determine if the drug combination of alpha-interferon and isotretinoin is effective in controlling T-cell malignancies. [15 Years]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Patients with histologic proof of incurable T-cell malignancy or Hodgkin's disease, and not eligible for existing/higher priority protocols. Patients with Hodgkin's disease will be eligible only if they have failed at least a MOPP-like and ABVD-like regimen.
Patients should not have received chemotherapy, immunotherapy, hormonal therapy, or radiation therapy within three weeks of entry into the study and must have recovered from acute toxic effects of prior therapy.
Patients must have a life expectancy of at least 12 weeks and a performance status of less than or equal to 2 (Zubrod scale: Appendix A).
Patients must sign an informed consent indicating that they are aware of the investigational nature of this study, in keeping with policies of the hospital. The only approved consent form is appended to this protocol.
Patients must have measurable or evaluable disease.
Patients must be greater than or equal to 18 years old.
Patients may receive no other concurrent chemotherapy, immunotherapy, or radiotherapy.
Patients should have adequate hepatic function with bilirubin of less than or equal to 2.0 mg%, and SGPT of less than or equal to 4 times the upper limits of normal.
Patients should have adequate renal function (defined as serum creatinine of less than or equal to 2.0 mg%).
Patients should have serum triglyceride level less than or equal to 2.5 times the upper limits of normal.
Patients may not have serious intercurrent medical illness.
Patients of child bearing potential must be practicing adequate contraception.
Patients will be eligible regardless of the extent of prior chemotherapy.