Inclusion Criteria:
1. Transplant eligible patients with newly diagnosed multiple myeloma (NDMM).
2. High-risk multiple myeloma*
3. Participants with disease response ≥ PR to induction therapy. 4. Age ≥ 18 and ≤ 75. Non-English-speaking participants are eligible.
5. Karnofsky performance status ≥70 (Appendix A).
6. Adequate liver function (total bilirubin ≤1.5X ULN; ALT ≤2.5 X ULN)
7. Estimated creatinine clearance ≥40 mL/min. Creatinine clearance may be calculated
using Cockcroft-Gault, estimated glomerular filtration rate (Modification of Diet in
Renal Disease [MDRD]), or Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI)
formula). *
8. Participant agrees to not donate blood while taking lenalidomide and for 28 days after
stopping lenalidomide.
9. Participant agrees to enroll in the lenalidomide REMS program.
10. Women of child-bearing potential (WOCPB) must abstain from heterosexual intercourse or
agree to use a contraceptive method that is highly effective (with a failure rate of
<1% per year), preferably with low user dependency (as described in Appendix B), plus
one additional effective method at least 28 days before starting therapy, during the
intervention period, at least 28 days after the last dose of lenalidomide and at least
4 months after the last dose of elranatamab, 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.
Non Nonchildbearing potential is defined as follows (by other than medical reasons):
- - ≥ 45 years of age and has not had menses for >1 year.
- - Participants 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.
11. 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 1 (for lenalidomide) to 4 (for
elranatamab) 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 and 4
months after the last dose of elranatamab.
PLUS, either:
- - 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 as detailed in Appendix B.
*Definition of
high-risk and ultra-high-risk MM15:
- - High-risk MM:
o Presence of a high-risk chromosomal abnormality (HRCA) including: 17p13
deletion; t(4;14); t(14;16); t(14;20); Gain or amplification 1q by FISH.
Exclusion Criteria:
• History of allergic reactions attributed to compounds of similar chemical or
biologic composition to elranatamab or other agents used in study.
• Drug interactions (Prohibited unless considered medically necessary):
a. At projected clinical doses, TMDD (target mediated drug disposition) of elranatamab
is expected. If concomitant medication alters target expression, it can potentially
impact the PK of elranatamab. Drugs like anti-thymocyte globulin (ATG) can deplete
T-cells and can potentially impact the PK of drugs targeting CD3. b. Elranatamab has
been shown to increase T-cell activation and induce cytokine production (including
IL-2, IL-6, IL-10, TNF-alpha and IFN-gamma). Cytokines have been shown to modulate
expression of CYP enzymes and transporters, therefore, elranatamab can potentially
affect CYP enzyme and transporter expression levels, and consequently modulate the
clearance of concomitant medications that are substrates for these enzymes or
transporters. When administering elranatamab, it is important to exercise caution with
concomitant medications, especially those that are sensitive substrates of the
cytochrome P450 (CYP) enzyme system and have a narrow therapeutic index. Increased
exposure of CYP substrates is more likely to occur after the first dose of elranatamab
on Day 1 and up to 14 days after the 32 mg dose on Day 4 and during and after CRS.
Examples of such medications include cyclosporine. During this critical window, it's
imperative to closely monitor the toxicity or concentrations of these concomitant
drugs. If necessary, dose adjustments for these co-administered drugs should be
considered to ensure patient safety. c. Cytochrome P450 (CYP) enzyme system is
responsible for the metabolism of a vast number of drugs. Below are examples of drugs
metabolized by specific CYP enzymes that could be impacted if elranatamab alters the
activity or expression of these enzymes. Exercise caution when using these drugs: i.
CYP2C9 substrates:
1.
2.
3.
4.
CYP3A4 substrates:
1.
- - Statins: simvastatin, atorvastatin, lovastatin.
2.
- - Calcineurin inhibitors: cyclosporine, tacrolimus.
3.
- - Antiretroviral drugs: ritonavir, saquinavir, nelfinavir.
4.
- - Benzodiazepines: diazepam, alprazolam.
5.
- - Calcium channel blockers: nifedipine, verapamil, diltiazem.
6.
- - Macrolide antibiotics: erythromycin, clarithromycin iii.
CYP2D6 substrates:
1.
- - Antipsychotics: aripiprazole, risperidone, haloperidol.
2.
- - Tricyclic antidepressants: amitriptyline, nortriptyline, imipramine.
3.
- - Beta-blockers: metoprolol, propranolol, carvedilol.
4.
5.
CYP1A2 substrates:
1.
CYP2C19 substrates:
1.
2.
3.
For participants on digoxin, monitor digoxin plasma levels periodically
with the concomitant use of lenalidomide. Refer to lenalidomide USPI for additional
information.
• History of progressive disease at any time before starting maintenance.
• Participants with non-secretory MM (no measurable disease on electrophoresis and
immunofixation). Participants with a measurable disease on PET scan or bone marrow
will be eligible.
• Participants with Waldenströms macroglobulinemia.
• Participants with POEMS syndrome.
• Participants with smoldering MM (IMWG criteria)
• Participants with plasma cell leukemia.
• Participants with standard-risk MM.
• Participants with relapsed and/or refractory MM.
• 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
fulfil inclusion criteria.
• Participant must not have current unstable liver or biliary disease defined by the
presence of ascites, encephalopathy, coagulopathy, 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.
• Uncontrolled and active pulmonary disease.
• 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 any evidence of active mucosal or internal bleeding.
• Participant must not have an uncontrolled infection.
• Participant must not have evidence of cardiovascular risk, including any of the
following:
- - Evidence of current clinically significant uncontrolled arrhythmias, including
clinically significant 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.
16.
- - Uncontrolled hypertension (blood pressure that remains above goal despite the
concurrent use of three antihypertensive drug classes).
• Participant must not
have known HIV infection. • Participant must not have active Hepatitis B and/or C
infection. • 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. • Patients with cognitive impairments and/or 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.
