Venetoclax, Daratumumab, and Dexamethasone for Systemic Light-Chain Amyloidosis With Translocation (11;14) (ALTITUDE)

Exclusion Criteria

• •6. Measurable disease of light chain amyloidosis as defined by at least ONE of the following:
• •1. Serum M-protein \>= 0.5 g/dL by protein electrophoresis (routine serum protein electrophoresis and immunofixation (IFE) performed at a local laboratory),
• •2. Serum free light chain \>= 40mg/L with an abnormal kappa:lambda ratio or
• •3. The difference between involved and uninvolved free light chains (dFLC) \>= 20 mg/L.
• •7. One or more organs impacted by AL amyloidosis according to consensus guidelines.
• •8. Eastern Cooperative Oncology Group (ECOG) performance status =\< 2.
• •9. Pretreatment clinical laboratory values meeting the following criteria during the Screening Phase (within 1 day of C1D1):
• •1. Absolute neutrophil count \>= 1.0 × 10\^9/L without growth factor support for 7 days (14 days if pegfilgrastim).
• •2. Hemoglobin level \>= 8.0 g/dL (\>= 5 mmol/L).
• •3. Platelet count \>= 100 × 10\^9/L without transfusion for 14 days.
• •4. Alanine aminotransferase level (ALT) =\< 2.5 times the upper limit of normal (ULN).
• •5. Aspartate aminotransferase (AST) =\< 2.5 times the ULN.
• •6. Total bilirubin level =\< 3 × ULN except for subjects with Gilbert syndrome, in which case direct bilirubin =\< 2 × ULN.
• •7. Creatinine clearance of ≥ 30 mL/min based upon Cockcroft-Gault formula calculation or a 24-hour urine collection.
• •10. Patients must have completed other systemic therapy \>= 14 days or investigational drug/vaccine \>= 28 days prior to treatment, focal radiation therapy \>= 14 days, surgery (other than biopsies) \>= 21 days prior to treatment, and any autologous stem cell transplant (ASCT) \>= 100 days prior to start of treatment.
• •11. Patients must not have received any medications or supplements which have been known to have some anti-amyloidogenic effect (such as: doxycycline; curcumin; prednisone; dexamethasone; epigallocatechin gallate) within 14 days prior to start of treatment.
• •12. Women of childbearing potential must commit to either abstain continuously from heterosexual sexual intercourse (if this is the preferred and usual lifestyle of the subject) or to use 2 methods of reliable birth control simultaneously. This includes one highly effective form of contraception (tubal ligation, intrauterine device, hormonal \[birth control pills, injections, hormonal patches, vaginal rings or implants\] or partner's vasectomy) and one additional effective contraceptive method (male latex or synthetic condom, diaphragm, or cervical cap). Contraception must begin 4 weeks prior to treatment and continue for 30 days after discontinuation of venetoclax or 3 months after discontinuation of DARA SC, whichever is longer. Reliable contraception is indicated even where there has been a history of infertility, unless due to hysterectomy or bilateral oophorectomy.
• •13. During the study and for 30 days after stopping VEN or 3 months after receiving the last dose of DARA SC, whichever is longer, a woman must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction.
• •14. A man who is sexually active with a woman of childbearing potential and has not had a vasectomy must agree to use a barrier method of birth control; e.g., either condom with spermicidal foam/gel/film/cream/suppository or partner with occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository during and up to 30 days after discontinuation of VEN or 3 months after discontinuation DARA SC, whichever is longer. All men must also not donate sperm during the study and for 30 days after discontinuation of VEN or 3 months after discontinuation of DARA SC, whichever is longer.
• •15. Patients must have documentation of yearly flu vaccination and a pneumococcus vaccination. Note: If the patient is due for 2 doses of pneumococcus vaccination, patients must have documentation of having received one dose of vaccine. Live attenuated vaccines are not allowed
• •16. Ability to understand a written informed consent document, and the willingness to sign it.
• •1. Any prior hematologic progression to CD38 antibody therapy (regardless of presence of a response) while on treatment or within 90 days of the last dose. Hematologic progression is defined as any ONE of the following:
• •1. From CR, any detectable monoclonal protein or abnormal free light chain ratio (the absolute concentration of the light chains must double)
• •2. From PR, 50% increase in serum M protein to \>0.5 g/dl or 50% increase in urine M protein to 4200 mg/day (a visible peak must be present)
• •3. Free light chain increase of 50% to \>100 mg/l
• •2. Prior exposure to BCL-2 inhibitors.
• •3. Intolerance to anti-CD38 antibody therapy, monoclonal antibodies, or hyaluronidase
• •4. Previous or current diagnosis of multiple myeloma by International Myeloma Working Group (IMWG) criteria, including the presence of lytic bone disease, plasmacytomas, \>= 60% plasma cells in the bone marrow, or hypercalcemia.
• •5. Systemic AL amyloidosis from a lymphoma.
• •6. Any form of non-AL amyloidosis, including wild type or mutated (ATTR) amyloidosis.
• •7. Evidence of significant cardiovascular conditions as specified below:
• •1. Troponin I \>0.1 ng/ml and B-type natriuretic peptide (BNP) \>700 pg/ml (cardiac stage 3B)
• •2. Left ventricular ejection fraction (LVEF) \<40%
• •3. New York Heart Association (NYHA) classification IIIB or IV heart failure
• •4. Heart failure that in the opinion of the investigator is on the basis of ischemic heart disease (e.g. prior myocardial infarction with documented history of cardiac enzyme elevation and electrocardiogram \[ECG\] changes) or uncorrected valvular disease and not primarily due to AL amyloid cardiomyopathy
• •5. Inpatient admission to a hospital for unstable angina or myocardial infarction within the last 6 months prior to first dose or percutaneous cardiac intervention with recent stent within 6 months or coronary artery bypass grafting within 6 months
• •6. For patients with congestive heart failure, cardiovascular-related hospitalizations within 4 weeks prior to Cycle 1 Day 1.
• •7. Patients with a history of sustained ventricular tachycardia or aborted ventricular fibrillation or with a history of atrioventricular nodal or sinoatrial (SA) nodal dysfunction for which a pacemaker/implantable cardioverter-defibrillator (ICD) is indicated but not placed. Note: Patients who do have a pacemaker/ICD are allowed on study.
• •8. Screening 12-lead ECG showing a baseline QT interval as corrected by Fridericia's formula (QTcF) \>500 msec. Note: Patients who have a pacemaker may be included regardless of calculated QTc interval.
• •9. Supine systolic blood pressure \<90 mm Hg, or symptomatic orthostatic hypotension, defined as a decrease in systolic blood pressure upon standing of \>20 mmHg despite medical management (e.g., midodrine, fludrocortisones) in the absence of volume depletion.
• •8. Planned stem cell transplant. Note: Stem cell collection is permitted. Timing should be discussed with sponsor-investigator.
• •9. History of malignancy (other than AL amyloidosis) within 3 years before the date of study enrollment. Note: Exceptions are squamous and basal cell carcinomas of the skin, carcinoma in situ of the cervix or breast, or other non-invasive lesion that in the opinion of the investigator, with concurrence with the sponsor's medical monitor, is considered cured with minimal risk of recurrence within 3 years).
• •10. For patients with known or suspected COPD, chronic obstructive pulmonary disease (COPD) with a forced expiratory volume in 1 second (FEV1) \< 50% of predicted normal are excluded. Note: FEV1 testing is required only for patients known or suspected of having COPD and patients must be excluded if FEV1 is \< 50% of predicted normal.
• •11. Moderate or severe persistent asthma within the past 2 years, or currently has uncontrolled asthma of any classification. Note: Patients who currently have controlled intermittent asthma or controlled mild persistent asthma are allowed to participate.
• •12. Participant meets one of the following criteria:
• •1. Known history of human immunodeficiency virus (HIV).
• •2. Seropositive for hepatitis B (defined by a positive test for hepatitis B surface antigen (HBsAg)). Note: Patients with resolved infection (i.e., patients who are HBsAg negative with antibodies to total hepatitis B core antigen (anti-HBc) with or without the presence of hepatitis B surface antibody (anti-HBs)) must be screened using real-time polymerase chain reaction (PCR) measurement of hepatitis B virus (HBV) DNA levels. Those who are PCR positive will be excluded. However, patients with serologic findings suggestive of HBV vaccination (anti-HBs positivity as the only serologic marker) AND a known history of HBV vaccination, do not need to be testing for HBV DNA by PCR, and will not be excluded.
• •3. Seropositive for hepatitis C (except in the setting of a sustained virologic response (SVR), defined as aviremia at least 12 weeks after completion of antiviral therapy).
• •13. Concurrent medical condition or disease (e.g., active systemic infection) that is likely to interfere with study procedures or results, or that in the opinion of the investigator would constitute a hazard for participating in this study.
• •14. Has not recovered from adverse events due to prior anti-cancer therapy to \<= grade 1 or baseline (other than alopecia).
• •15. Systemic treatment with any of the following within 7 days prior to the first dose of study drug:
• •* Steroid therapy for anti-neoplastic intent
• •* Known moderate or strong cytochrome P450 3A (CYP3A) inhibitors
• •* Known moderate or strong CYP3A inducers \*\* Note: Patients who are taking strong CYP3A4 inducers must discontinue their use at least 5 half-lives prior to the first dose of study treatment
• •16. Administration or consumption of any of the following within 3 days prior to the first dose of study drug:
• •* Grapefruit or grapefruit products
• •* Seville oranges (including marmalade containing Seville oranges)
• •* Starfruit
• •17. Patient anticipates use of prohibited medications or foods during study participation.
• •18. Major surgery within 2 weeks before Cycle 1 Day 1, or will not have fully recovered from surgery, or has surgery planned during the time the subject is expected to participate in the study or within 2 weeks after the last dose of study treatment administration.
• •\* Note: Patients with planned surgical procedures to be conducted under local anesthesia may participate.
• •19. Known or suspected of not being able to comply with the study protocol or the patient has any condition for which, in the opinion of the investigator, participation would not be in the best interest of the patient (e.g., compromise their well-being) or that could prevent, limit, or confound the protocol-specified assessments.
• •20. Woman who is pregnant or breastfeeding or planning to become pregnant while enrolled in this study or within 3 months following discontinuation of daratumumab or venetoclax.
• •21. Have received vaccination with live attenuated vaccines within 4 weeks of first study agent administration.