Continued, Long-Term Follow-Up and Lenalidomide Maintenance Therapy for Patients on BMT CTN 0702 Protocol (BMT CTN 07LT)

This study is designed to compare long-term outcomes among patients randomized on the BMT CTN 0702 protocol (NCT01109004). All patients who consent will be followed for death, progression, Second Primary Malignancies (SPMs), and Quality of Life (QOL). Patients who do not consent to the long-term follow-up mechanism or who have experienced progression on the BMT CTN 0702 study will be followed through the standard Center for International Blood and Marrow Transplant Research (CIBMTR) long-term follow-up mechanism. Additionally, patients who are eligible and are willing to continue with lenalidomide as maintenance therapy will be provided lenalidomide free of charge. These patients will continue to receive lenalidomide as maintenance therapy until disease progression or discontinuation due to toxicity, death, or withdrawal from the study. The endpoints assessed will include progression-free survival (PFS), overall survival (OS), event-free survival (EFS), incidence of second primary malignancies (SPM) and health quality of life (QOL).

Inclusion criteria

Patients fulfilling the following criteria will be eligible to provide continued long-term follow-up data as part of this study:

• Enrolled and randomized on the BMT CTN 0702 protocol.
• Alive at the completion of BMT CTN 0702 protocol specified follow-up defined as 4 years post-randomization.
• Patients without evidence of disease progression at the completion of BMT CTN 0702 protocol specified follow up.
• Signed Informed Consent Form.
• Patients with the ability to speak English or Spanish are eligible to participate in the HQL component of this trial.

Inclusion criteria

for Optional Long-term Lenalidomide Maintenance Therapy:

Patients fulfilling the following criteria will be eligible to provide continued long-term follow-up data AND receive long-term lenalidomide maintenance therapy as part of this study:

• Enrolled and randomized to BMT CTN 0702.
• Completion of 3 years of maintenance therapy on BMT CTN 0702.
• Registered in the mandatory Revlimid REMS® program (formerly the RevAssist® for Study Participants (RASP) program), and be willing and able to comply with the requirements of the Revlimid REMS® program, including counseling, pregnancy testing, and phone surveys.
• Signed informed consent form.
• Patients with the ability to speak English or Spanish are eligible to participate in the HQL component of this trial.

Exclusion criteria

Patients who meet any of the following criteria will be ineligible to receive long-term lenalidomide maintenance therapy as part of this study:

• Patients who have evidence of disease progression prior to enrollment.
• Patients who were discontinued from BMT CTN 0702 lenalidomide maintenance therapy, for any reason, prior to the completion of the 3 years of 0702 maintenance.
• Female patients who are pregnant (positive - Beta Human Chorionic Gonadotropin) or breastfeeding.
• Females of childbearing potential (FCBP) or men who have sexual contact with FCBP unwilling to use contraceptive techniques during the length of lenalidomide maintenance therapy.
• Patients who experienced thromboembolic events while on full anticoagulation during prior therapy with lenalidomide.
• Patients unwilling to take Deep Vein Thrombosis (DVT) prophylaxis.
• Patients who developed a second primary malignancy, excluding non-melanoma skin cancers after initiation of lenalidomide maintenance therapy on BMT CTN 0702.