Belantamab Mafodotin and Lenalidomide After Stem Cell Transplant in Patients With Newly Diagnosed Multiple Myeloma.

Inclusion Criteria

• Patients with newly diagnosed multiple myeloma status post 1st auto-HCT (day 60 – 180 post-transplant)
• Disease status (MRD positive or negative), partial response, or better
• Age > 18-year and =< 75-year. Non-English speaking patients are eligible.
• Karnofsky performance status >= 70
• Absolute neutrophil count (ANC) >= 1.5 X 10^9/L
• Hemoglobin >= 8.0 g/dL
• Platelets >= 75 X 10^9/L
• Total bilirubin =< 1.5 X upper limit of normal (ULN) (Isolated bilirubin >= 1.5 x ULN is acceptable if bilirubin is fractionated and direct bilirubin < 35%)
• Alanine aminotransferase (ALT) =< 2.5 X ULN
• Estimated glomerular filtration rate (eGFR) >= 40 mL/min/1.73 m^2, as calculated by the Modified Diet in Renal Disease (MDRD) formula
• Spot urine (albumin/creatinine) ratios (spot urine) < 500 mg/g (56 mg/mmol) OR Urine dipstick Negative/trace (if >= 1+ only eligible if confirmed < 500 mg/g (56 mg/mmol) by albumin/creatinine ratio (spot urine from first void)
• Participant agrees to not donate blood while taking lenalidomide and for 28 days after stopping lenalidomide
• Patient agrees to enroll in the lenalidomide risk evaluation and mitigation strategy (REMS) program
• Woman of child-bearing potential (WOCBP) must abstain from heterosexual sexual contact or agrees to use a contraceptive method that is highly effective (with a failure rate of < 1% per year), preferably with low user dependency, plus one additional effective method at least 28 days before starting therapy (for lenalidomide), during the intervention period, at least 28 days after the last dose of lenalidomide and at least 4 months after the last dose of belantamab mafodotin, and agrees not to donate eggs (ova, oocytes) for reproduction during this period. The investigator should evaluate the effectiveness of the contraceptive method in relation to the first dose of the study intervention. A WOCBP must have a negative highly sensitive serum pregnancy test (as required by local regulations) within 10-14 days and also within 24 hours before the first dose of the study intervention Nonchildbearing potential is defined as follows (by other than medical reasons): * >= 45 years of age and has not had menses for > 1 year * Patients who have been amenorrhoeic for < 2 years without a history of a hysterectomy and oophorectomy must have a follicle-stimulating hormone value in the postmenopausal range upon screening evaluation * Post-hysterectomy, post-bilateral oophorectomy, or post-tubal ligation
• Male participant agrees to contraceptive use that should be consistent with institutional guidelines regarding the methods of contraception for those participating in clinical studies. Male participants are eligible to participate if they agree to the following during the intervention period and for 6 months after the last dose of study treatment to allow for clearance of any altered sperm: * Refrain from donating sperm during treatment (including dose interruptions) and for 4 weeks after their last dose of lenalidomide * Be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long term and persistent basis) and agree to remain abstinent * Or must agree to use contraception/barrier
• All prior auto-HCT-related toxicities (defined by National Cancer Institute – Common Toxicity Criteria for Adverse Events (NCI-CTCAE), version 5 must be =< Grade 1 at the time of enrollment except for alopecia, fatigue, and amenorrhea

Exclusion Criteria

• History of progressive disease at any time before starting maintenance
• Patients with smoldering multiple myeloma (MM)
• Patients with plasma cell leukemia
• Patients with non-secretory MM (no measurable disease on electrophoresis and immunofixation). Patients with a measurable disease on positron emission tomography (PET) scan or bone marrow will be eligible
• Participant must not have current unstable liver or biliary disease defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia due to underlying liver disease (serum albumin < 3 gm/dL), esophageal or gastric varices, persistent jaundice, or cirrhosis. Note: Stable non-cirrhotic chronic liver disease (including Gilbert’s syndrome or asymptomatic gallstones) or hepatobiliary involvement of malignancy is acceptable if otherwise meets entry criteria
• Participant must not have presence of active renal condition (infection, requirement for dialysis or any other condition that could affect participant’s safety). Participants with isolated proteinuria resulting from MM are eligible, provided they fulfill inclusion criteria
• Current corneal or epithelial disease (except mild punctate keratopathy)
• Participant must not use contact lenses while participating in this study
• Participant must not have used an investigational drug or approved systemic anti-myeloma therapy (including systemic steroids) within 14 days or five half-lives, whichever is shorter, preceding the first dose of study drug
• Participant must not have received prior treatment with a monoclonal antibody within 30 days of receiving the first dose of study drugs
• Participant must not have had major surgery =< 4 weeks before initiating study treatment
• The participant must not have any evidence of active mucosal or internal bleeding
• Participant must not have known immediate or delayed hypersensitivity reaction or idiosyncratic reactions to belantamab mafodotin or drugs chemically related to belantamab mafodotin, or any of the components of the study treatment
• Participant must not have an active infection requiring treatment
• Participant must not have evidence of cardiovascular risk, including any of the following: * Evidence of current clinically significant uncontrolled arrhythmias, including clinically significant electrocardiogram (ECG) abnormalities such as 2nd degree (Mobitz Type II) or 3rd degree atrioventricular (AV) block * History of myocardial infarction, acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting or bypass grafting within three (3) months of screening * Class III or IV heart failure as defined by the New York Heart Association functional classification system. * Uncontrolled hypertension (blood pressure that remains above goal despite the concurrent use of three antihypertensive drug classes)
• Participant must not have known human immunodeficiency virus (HIV) infection
• Patients will hepatitis B will be excluded unless certain criteria can be met
• Positive hepatitis C antibody test result or positive hepatitis C ribonucleic acid (RNA) test result at screening or within 3 months prior to first dose of study treatment unless the participant can meet the following criteria: * RNA test negative * Successful anti-viral treatment (usually 8 weeks duration) is required, followed by a negative hepatitis C virus (HCV) RNA test after a washout period of at least 4 weeks.
• Participant must not have invasive malignancies other than disease under study, unless the second malignancy has been medically stable for at least 2 years and, in the opinion of the principal investigators, will not affect the evaluation of the effects of clinical trial treatments on the currently targeted malignancy. Participants with curatively treated non-melanoma skin cancer may be enrolled without a 2-year restriction
• Participants must not be pregnant or lactating
• Any serious unstable pre-existing medical condition or psychiatric disorder that can interfere with safety or with obtaining informed consent or compliance with study procedures
• All prior treatment-related toxicities (defined by National Cancer Institute-Common Toxicity Criteria for Adverse Events (NCI-CTCAE), version 5 must be =< grade 1 at the time of enrollment except for alopecia