Carfilzomib, Pegylated Liposomal Doxorubicin Hydrochloride, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma

Multiple Myeloma Clinical Trial

Official title:

A Phase I/II Trial of Carfilzomib, Pegylated Liposomal Doxorubicin, and Dexamethasone for the Treatment of Relapsed/Refractory Multiple Myeloma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01246063
• Other study ID #: 201102043
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: May 14, 2012
• Est. completion date: March 23, 2018

Study information

• Verified date: April 2019
• Source: Washington University School of Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this phase I/II trial is to determine the maximal tolerated dose (MTD) of carfilzomib together with pegylated liposomal doxorubicin hydrochloride (PLD) with or without dexamethasone, and then to establish the efficacy and safety of this novel combination in patients with relapsed or refractory multiple myeloma

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: March 23, 2018
• Est. primary completion date: December 28, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed diagnosis of multiple myeloma with a measurable disease parameter at time of screening; a measurable disease parameter is defined as one or more of the following:

• Serum monoclonal protein >= 0.5 g/dl

• 24 hour urine monoclonal protein >= 0.2 g/24 hour

• Serum free light chain ratio > 5 x normal ratio with an absolute difference of 10mg/dl between the involved and uninvolved free light chain

• Soft tissue plasmacytoma >= 2 cm measurable by either physical examination and/or applicable radiographs (e.g. magnetic resonance imaging [MRI], computed tomography [CT], etc)

• Bone Marrow Plasma Cells >= 30%

• Documentation of at least one line of prior myeloma therapy now with relapsed or refractory disease requiring re-treatment

• At least 18 years of age at the time of signing the informed consent.

• Performance status of Eastern Cooperative Oncology Group (ECOG) =< 2 or Karnofsky >= 60%; participants with lower performance status based solely on bone pain secondary to multiple myeloma will be eligible

• Required laboratory values

• Alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) and aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) < 2.5 x the upper limit of the institutional normal value (ULN)

• Total bilirubin =< 1.5 x upper limit of normal (ULN)

• Absolute neutrophil count (ANC) >= 1,000

• Hemoglobin >= 8 g/dl

• Platelets >= 50,000

• Creatinine clearance > 15 ml/minute using Cockcroft-Gault formula

• For those participants receiving warfarin (Coumadin), unfractionated heparin, or low-molecular weight heparin therapy, the applicable coagulation parameter that is being monitored must be within the accepted therapeutic ranges for those indications

• Transfusions and/or growth factor dependent participants are not excluded if the above parameters can be achieved with such support

• Females of childbearing potential (FCBP) must agree to refrain from becoming pregnant while on study drug and for 3 months after discontinuation from study drug, and must agree to use adequate contraception including hormonal contraception, (i.e. birth control pills, etc), barrier method contraception (i.e. condoms), or abstinence during that time frame; FCBP must agree to regular pregnancy testing during this timeframe; inclusion of FCBP requires two negative pregnancy tests prior to enrollment. All women, regardless of age, should be considered FCBP unless they are surgically sterile (post hysterectomy, post bilateral oophorectomy, etc) or have been naturally post menopausal for >= 24 consecutive months

• Men engaging in sexual intercourse with a FCBP must agree to use adequate contraception including hormonal contraception, (i.e. birth control pills, etc), barrier method contraception (i.e. condoms), or abstinence while on study drug and for 3 months after discontinuation from study drug

• Ability to understand and willing to sign a written informed consent document

Exclusion Criteria:

• POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes)

• Plasma Cell Leukemia

• Waldenstrom's macroglobulinemia

• Pregnant or lactating females

• Use of any anti-myeloma drug therapy within 14 days of initiation of study drug treatment excluding corticosteroids if given for an indication other than myeloma; bisphosphonates are not considered anti-myeloma drugs

• Participation in an investigational therapeutic study within 14 days of initiation of study drug treatment

• Radiotherapy to multiple sites or immunotherapy within 14 days of initiation of study drug treatment (localized radiotherapy to a single site at least 7 days before start is permissible)

• Major surgery within 14 days of initiation of study drug treatment

• Participants in whom the required program of oral (PO) and IV fluid hydration is contraindicated

• Prior history of a hypersensitivity reaction to PLD, doxorubicin, bortezomib, carfilzomib, or liposomal drug formulations other than PLD; history of reactions to liposomal drug formulations other than PLD should be evaluated individually and if their reactions were felt to have been due to the encapsulated agent, rather than the liposomal component itself they should be excluded at the discretion of the investigators

• Participants who are known to have active hepatitis A, B, or C viral infection may not participate in this study; active disease is defined as participants with a known viral hepatitis whose liver function tests are elevated

• Known human immunodeficiency virus (HIV)-seropositive and are taking anti-retrovirals may not participate in this study; participants who are HIV-seropositive and not on anti-retroviral therapy and who otherwise meet the inclusion/exclusion criteria will be eligible for the study

• Compromised cardiovascular function defined as any of the following:

• Electrocardiogram (EKG) evidence of acute ischemia

• EKG evidence of medically significant conduction system abnormalities

• History of myocardial infarction within the last 6 months

• Unstable angina pectoris or cardiac arrhythmia

• History of Class 3 or Class 4 New York Heart Association Congestive Heart Failure within 6 months of enrollment on study

• Left ventricular ejection fraction (LVEF) < 45% by either echocardiography or radionuclide-based multiple gated acquisition (Echo or MUGA)

• Uncontrolled concurrent illness including: other hematologic or non-hematologic malignancy, active infection, or uncontrolled diabetes

• Any significant psychological, medical, or surgical condition thought to compromise the participant, the study, or prevent informed consent

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell

Intervention

Drug:
• carfilzomib

• pegylated liposomal doxorubicin (PLD)

• Dexamethasone

Locations

Country	Name	City	State
United States	Washington University School of Medicine	Saint Louis	Missouri

Sponsors (1)

Lead Sponsor	Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Tolerated Dose (MTD) of Carfilzomib and Pegylated Liposomal Doxorubicin (Phase I - Part 1).	MTD is the maximum tolerated dose level tested unless dose limiting toxicity (DLT) are observed during Cycle 1. If DLT is observed, MTD will be the next lower dose level.; Please note that the maximum tolerated dose of carfilzomib and pegylated liposomal doxorubicin was not reached. The data below is the recommended dosage for further studies.	28 days (completion of first cycle of all Phase I - Part 1 patients)
Primary	Maximum Tolerated Dose (MTD) of Carfilzomib and PLD (Phase I - Part 2).	-MTD is the maximum tolerated dose level tested unless dose limiting toxicity (DLT) are observed during Cycle 1. If DLT is observed, MTD will be the next lower dose level.	28 days (completion of first cycle of all Phase I - Part 2 patients)
Primary	Maximum Tolerated Dose (MTD) of Dexamethasone (Phase I - Part 2).	-MTD is the maximum tolerated dose level tested unless dose limiting toxicity (DLT) are observed during Cycle 1. If DLT is observed, MTD will be the next lower dose level.	28 days (completion of first cycle of all Phase I - Part 2 patients)
Primary	Phase 2 - Efficacy of Carfilzomib in Combination With PLD and Dexamethasone as Measured by the Percentage of Participants With Confirmed Tumor Responses	-A confirmed response is defined to be a complete response (CR), very good partial response (VGPR), or partial response (PR) per IMWG Criteria.	Completion of treatment (median number of cycles was 9.5 (range 1-34))
Primary	Phase 2 - Toxicity of Carfilzomib in Combination With PLD and Dexamethasone as Measured by Number of Participants Who Experience Grade 3/4 Toxicity		Through 30 days after completion of treatment (median number of cycles was 9.5 (range 1-34))
Secondary	Median Overall Survival		Completion of follow-up (median of 23.3 months)
Secondary	Progression-free Survival Time (Phase 2 Only)	-Progression per IMWG Criteria	Through completion of follow-up (median follow-up was 23.3 months)
Secondary	Median Duration of Overall Response	For participants with confirmed tumor responses; A confirmed response is defined to be a complete response (CR), very good partial response (VGPR), or partial response (PR) per IMWG Criteria	Through completion of follow-up (median follow-up was 23.3 months)

External Links

•   Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine