UARK 2010-35, A Study of Expanded Natural Killer Cell Therapy for Multiple Myeloma

Inclusion Criteria

• Patient (Recipient of NK Cells) Inclusion Criteria
• Relapsed patients must have high risk disease as defined by GEP risk score of ≥ 0.66 or metaphase cytogenetic abnormalities or LDH ≥ 360 U/L (Rule out hemolysis, infection and contact PI for clarification if any doubt) Patients must have had at least 1 line of prior chemotherapy and/or have relapsed after auto- PBSCT.
• For subjects who have had a prior transplant, ≥2 months must have relapsed after the last transplant prior to enrollment.
• Zubrod ≤ 2, unless solely due to symptoms of MM-related (bone) disease.
• Patients must have a platelet count of ≥ 50,000/µL within 35 days of registration, unless lower levels are explained by extensive bone marrow plasmacytosis or extensive prior therapy.
• Patients must be at least 18 years of age and not older than 75 years of age at the time of registration.
• Participants must have preserved renal function as defined by a serum creatinine level of ≤ 3 mg/dL within 35 days of registration.
• Participants must have an ejection fraction by ECHO or MUGA scan ≥ 40% within 90 days prior to registration.
• Patients must have adequate pulmonary function studies > 50% of predicted on mechanical aspects (FEV1, FVC, etc) and diffusion capacity (DLCO) > 50% of predicted within 90 days prior to registration. If the patient is unable to complete pulmonary function tests due to MM related pain or condition, exception may be granted if the principal investigator documents that the patient is a candidate for high dose therapy.
• Patients must have signed an IRB-approved informed consent and HIPAA authorization form.
• Either a haploidentical family donor fit to undergo leukapheresis is available or the recipient is fit to undergo leukapheresis for exp-NK cell generation (see donor selection).
• Patient (Recipient of NK Cells) Exclusion criteria
• History of poorly controlled hypertension, diabetes mellitus, or any other serious medical illness or psychiatric illness that could potentially interfere with the completion of treatment according to this protocol or could be considered to be an exclusion criterion deemed by the PI.
• Patients must not have prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer for which the patient has not received treatment for one year prior to enrollment. Other cancers will only be acceptable if the patient's life expectancy exceeds three years as determined by the PI.
• Pregnant or nursing women may not participate. Women of childbearing potential must have a negative pregnancy documented within one week of registration. Women/men of reproductive potential may not participate unless they have agreed to use an effective contraceptive method.
• Donor Inclusion Criteria
• The source of the NK cells will be either A) a family member who is HLA haploidentical to the recipient, or B) if a suitable haploidentical donor is not available, the recipient may be the source of the NK cells.
• HLA typing will be performed by the Arkansas Children's Hospital clinical laboratory.
• If the recipient expresses HLA-C group I, HLA-C group II, and Bw4 KIR ligands, then a KIR-ligand mismatched haploidentical donor cannot be found, and the recipient will be the source of the NK cells.
• If the recipient fails to express one or more of the primary KIR ligands (HLA-C group I, HLA-C group II, and Bw4) then family member donors will be HLA typed in an effort to find a haploidentical donor. If multiple haploidentical donors are available, KIR phenotyping will be performed in Dr. van Rhee's research laboratory to select a KIR mismatched donor whenever possible.
• Donor selection will be performed by the PI or one of the MD co-investigators if Dr. van Rhee is not available.
• Signed IRB approved consent and HIPAA authorization form.
• Donor is not HIV I/II (+).
• Donor is not HTLV-I/II (+).
• Donor is not Hepatitis B or C (+) unless positive due to p