NCT03117361 · REGISTRY CONDITION SEARCH

Trial of Plitidepsin (Aplidin®) in Combination With Bortezomib and Dexamethasone in Multiple Myeloma Patients Double Refractory to Bortezomib and Lenalidomide

Found through the registry condition index, not selected as a treatment recommendation. This discovery collection was restricted to studies with posted results.

Phase: PHASE2
Status at capture: TERMINATED
Registry last update: 2020-12-02

This is a multi-center, open-label, single arm, non-comparative phase II trial, designed to evaluate the efficacy of plitidepsin in combination with bortezomib and dexamethasone in patients with Multiple Myeloma (MM) double refractory to bortezomib and lenalidomide.

Open the original ClinicalTrials.gov record → · Download preserved record

What did the study report?

Outcomes, safety and baseline populations are separate source sections. Quality-of-life measures appear under their original outcome titles.

flow

Participant flow

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baseline

Baseline characteristics

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outcome · POSTED

Overall Response

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outcome · POSTED

Overall Response Rate

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outcome · POSTED

Clinical Benefit Rate

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outcome · POSTED

Disease Control Rate

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outcome · POSTED

Duration of Response

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outcome · POSTED

Time to Progression

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outcome · POSTED

Percentage of Participants With Progression Disease at 3 Months

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outcome · POSTED

Percentage of Participants With Progression Disease at 6 Months

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outcome · POSTED

Percentage of Participants With Progression Disease at 12 Months

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outcome · POSTED

Progression-free Survival

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outcome · POSTED

Percentage of Participants With Progression-free Survival at 3 Months

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outcome · POSTED

Percentage of Participants With Progression-free Survival at 6 Months

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outcome · POSTED

Percentage of Participants With Progression-free Survival at 12 Months

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outcome · POSTED

Event-free Survival

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outcome · POSTED

Percentage of Participants With Event-free Survival at 3 Months

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outcome · POSTED

Percentage of Participants With Event-free Survival at 6 Months

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outcome · POSTED

Percentage of Participants With Event-free Survival at 12 Months

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outcome · POSTED

Overall Survival

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outcome · POSTED

Percentage of Participants With Overall Survival at 6 Months

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outcome · POSTED

Percentage of Participants With Overall Survival at 12 Months

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adverse events

Adverse events

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more info

Limitations, agreements, and source contact

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Who could take part

eligibility Criteria: Inclusion Criteria: 1. Patients must give written informed consent (IC) in accordance with institutional and local guidelines. 2. Age ≥ 18 years. 3. Patients must have a confirmed diagnosis of MM according to the Durie and Salmon criteria. 4. Patients must have measurable disease defined as any of the following: 1. Serum M-protein ≥ 0.5 g/dL or ≥ 0.2 g/24-h urine light chain (UFLC) excretion. 2. In patients who lack measureable M-protein in serum or urine, i.e., serum M-protein \< 0.5 g/dL and urine M-protein \< 0.2 g/24 h, serum free light chain (SFLC) levels are most informative. SFLC levels can be used only if the baseline SFLC ratio is abnormal (\<0.26 or \>1.65), indicating clonality. In addition, the baseline SFLC level must be ≥10 mg/dl of the appropriate involved light chain isotype. 3. When applicable, measurable soft tissue plasmacytoma ≥ 2 cm, by either physical examination and/or applicable radiological evaluation (i.e., magnetic resonance imaging \[MRI\], computed tomography \[CT\]-scan). 5. Prior autologous and/or allogeneic hematopoietic stem cell transplantation (HSCT) patients are allowed. Patients must not have acute/chronic graft-versus-host disease (GVHD) or be receiving immunosuppressive therapy at least 90 days before the onset of treatment with the trial drug(s). 6. Patients must have received previous treatment with bortezomib and lenalidomide and be refractory to both. 7. Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 2. 8. Recovery to grade ≤ 1 from any non-hematological adverse event (AE) derived from previous treatment (if present, alopecia and peripheral neuropathy must be grade \<1). 9. Laboratory data: 1. Hemoglobin ≥ 8 g/dL. 2. Absolute neutrophil count (ANC) ≥ 1,000 cells/mm3 (1.0 x 109/L) (≥ 0.5 x 109/L if due to extensive bone marrow \[BM\] involvement by ≥ 50% of plasma cells in BM biopsy). Screening of ANC should be independent of granulocyte- and granulocyte/macrophage-colony stimulating factor (G-CSF and GM-CSF) support for at least one week and of pegylated G-CSF for at least two weeks. 3. Platelet count ≥ 50,000/mm3 (50.0 x 109/L) for patients in whom \< 50% of the BM nucleated cells are plasma cells. 4. Platelet count ≥ 25,000/mm3 (25.0 x 109/L) for patients in whom ≥ 50% of BM nucleated cells are plasma cells. 5. Serum total bilirubin \< 1.5 x institutional upper limit of normal (ULN) (except when Gilbert syndrome is clearly documented and other liver function tests are within normal levels). 6. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3.0 x institutional ULN and alkaline phosphatase (AP) ≤ 2.5 x institutional ULN. 7. Creatinine clearance (CrCl) \> 30 mL/min, measured or calculated according to Cockcroft and Gault's formula. 8. Albumin ≥ 2.5 g/dl. 10. Evidence of non-childbearing status for women of childbearing potential (WOCBP): WOCBP must have a negative serum or urine pregnancy test within seven days prior to enrolment and must agree to use a highly effective contraceptive measure throughout the trial and during six months after treatment discontinuation. Male patients enrolled in the study should also use contraceptive methods during and after treatment discontinuation. 11. Left ventricular ejection fraction (LVEF) ≥ 45%. 12. Patients must have a BM assessment within three weeks prior to enrolment. Exclusion Criteria: 1. Previous treatment with plitidepsin. 2. Active or metastatic primary malignancy other than MM. 3. Serious concomitant systemic disorders that would compromise the safety of the patient or the patient's ability to complete the trial, including the following specific conditions: 1. Uncontrolled psychiatric illness or medical illness that the Investigator feels will compromise the patient's tolerance of the trial medication. 2. Significant non-neoplastic liver disease. 3. Uncontrolled endocrine diseases (i.e., requiring relevant changes in medication within the last month, or hospital admission within the last three months). 4. Uncontrolled systemic infection. 5. Acute infiltrative pulmonary and pericardial disease. 4. Other relevant cardiac conditions: 1. Symptomatic arrhythmia (excluding anemia-related grade ≤ 2 sinusal tachycardia) or any arrhythmia requiring ongoing treatment, and/or prolonged grade ≥ 2 QT-QTc; or presence of unstable atrial fibrillation (according to the National Cancer Institute Common Terminology Criteria for the Classification of Adverse Events \[NCI-CTCAE\] v4.0). Patients on treatment for stable atrial fibrillation are allowed, provided they do not meet any other cardiac or prohibited drug exclusion criterion. 2. History or presence of unstable angina, myocardial infarction, valvular heart disease, cardiac amyloidosis or congestive heart failure within the last 12 months. 3. Uncontrolled arterial hypertension (≥ 150/100 mmHg) despite optimal medical therapy. 4. Previous treatment with doxorubicin at cumulative doses of \> 400 mg/m², or equivalent. 5. History of hypersensitivity reactions and/or intolerance to bortezomib, polyoxyl 35 castor oil, mannitol, boron or dexamethasone. 6. Myopathy or any clinical situation that causes significant and persistent elevation of creatine phosphokinase (CPK) (\> 2.5 ULN) in two different determinations performed within one week of each other. 7. Grade ≥ 1 neuropathy (either bortezomib-related or not) according to NCI-CTCAE v4.0. 8. Any other major illness that, in the Investigator's judgment, will substantially increase the risk associated with the patients' participation in this trial. 9. Pregnant and/or lactating women. 10. Known active human immunodeficiency virus (HIV) infection (HIV testing is not required unless infection is clinically suspected). 11. Active hepatitis B or C virus (HBV or HCV) infection. 12. Treatment with any Investigational Medicinal Product (IMP) in the 30 days before inclusion in the trial. 13. Concomitant medications that include corticosteroids, chemotherapy (CT), or other therapy that is or may be active against myeloma. Concurrent corticosteroids are allowed as an equivalent to a prednisone dose of ≤ 10 mg daily, administered as an antiemetic or as premedication for blood products. 14. Wash-out periods after the end of the previous therapy: 1. Nitrosoureas must be discontinued six weeks prior to Cycle (C) 1, D1. 2. Thirty days for other CTs and 15 days for other biological agents prior to C1 D1. 3. Thirty days after the end of any prior radiation or radionuclide therapy (six weeks in the case of prior extensive external beam radiation, with more than 25% of BM distribution). 15. Plasma cell leukemia at the time of trial entry. 16. Disease-related symptomatic hypercalcemia despite optimal medical therapy. 17. Limitation of the patient's ability to comply with the treatment or follow-up protocol. 18. Contraindication to use steroids.
healthy Volunteers: false
minimum Age: 18 Years
sex: ALL
std Ages: ADULT
OLDER_ADULT

Treatment arms and interventions

arm Groups

description
Plitidepsin + bortezomib + dexamethasone Plitidepsin will be administered as a 3-hour intravenous (i.v.) infusion on Day(D) 1 and 15 , every four weeks (q4wk) Bortezomib will be administered as a bolus subcutaneous (s.c.) injection on D 1, 4, 8 and 11,q4wk Dexamethasone will be taken orally on D1,8,15 and 22, q4wk
intervention Names
Drug: plitidepsin
Drug: Bortezomib
Drug: Dexamethasone
label
Experimental
type
EXPERIMENTAL

interventions

arm Group Labels
Experimental
description
Patients received plitidepsin as a 3-hour i.v. infusion at a dose of 5 mg/m2 on Days 1 and 15 every Four Weeks.
name
plitidepsin
type
DRUG
arm Group Labels
Experimental
description
BTZ as a 3-5 second bolus s.c. injection at a dose of 1.3 mg/m2 on Days 1, 4, 8 and 11 every four weeks
name
Bortezomib
type
DRUG
arm Group Labels
Experimental
description
DXM orally at a dose of 40 mg/day on Days 1, 8, 15 and 22 every four weeks
name
Dexamethasone
type
DRUG

Study design

allocation

intervention Model

SINGLE_GROUP

masking Info

masking: NONE

primary Purpose

TREATMENT

Enrollment

count: 10
type: ACTUAL

Registered outcome plans (not posted results)

primary Outcomes

description
Partial response (PR): ≥50% reduction in serum M-protein and reduction of 24-hour urine M-protein by 90% or to \<200 mg/24h Minimal response (MR): ≥25% but ≤49% reduction of serum M-protein and reduction of 24h urine M-protein 50-89%. Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions Stable disease (SD): not meet the criteria for PR, MR or PD Primary analysis should have been done once a total of 64 patients have received plitidepsin+BTZ+DXM with one futility analysis planned after the inclusion of 20 evaluable patients that had completed two full treatment cycles. Only 10 patients were treatedand 8 evaluable for the primary endpoint (ORR according to IMWG criteria). As a result of slow patient accrual, the study was closed before reaching the target enrollment
measure
Overall Response
time Frame
From the date of first drug administration to the date of at least one disease assessment, up to 100 weeks
description
The primary endpoint was overall response rate (ORR) (including stringent complete response \[sCR\], complete response \[CR\], very good partial response \[VGPR\] and partial response \[PR\]), according to the IMWG response criteria.
measure
Overall Response Rate
time Frame
From the date of first drug administration to the date of at least one disease assessment, up to 100 weeks

secondary Outcomes

description
Clinical benefit rate defined as minimal response or better
measure
Clinical Benefit Rate
time Frame
From the date of first drug administration to the date of at least one disease assessment, up to 100 weeks
description
Disease control rate defined as stable disease \[SD\] or better
measure
Disease Control Rate
time Frame
From the date of first drug administration to the date of at least one disease assessment, up to 100 weeks
description
Duration of Response defined as the time, in months, from the date of first documentation of response to the date of disease progression. Response was assessed according to the IMWG classification response criteria.
measure
Duration of Response
time Frame
From the date of first documentation of response to the date of disease progression, up to 100 weeks
description
Time to progression (TTP) was defined as the time, in months, from the date of the first infusion to the date of documented PD or death due to PD. TTP was to be censored on the date of the last tumor assessment or on the date of the first drug administration if there were no tumor assessments. Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions.
measure
Time to Progression
time Frame
From the date of the first infusion to the date of documented PD or death due to PD, up to 100 weeks
description
Progression disease was defined as documented PD or death due to PD Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions.
measure
Percentage of Participants With Progression Disease at 3 Months
time Frame
From the date of the first infusion to the date of documented PD or death due to PD, up to 3 months
description
Progression disease was defined as documented PD or death due to PD. Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions
measure
Percentage of Participants With Progression Disease at 6 Months
time Frame
From the date of the first infusion to the date of documented PD or death due to PD, up to 6 months
description
Progression disease was defined as documented PD or death due to PD. Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions.
measure
Percentage of Participants With Progression Disease at 12 Months
time Frame
From the date of the first infusion to the date of documented PD or death due to PD, up to 12 months
description
Progression-free survival (PFS) was defined as the time, in months, from the date of first drug administration to the date of documented PD, or death (of any cause). If any patient was lost to follow-up before PD or received another antitumor therapy, PFS was to be censored on the date of the last tumor assessment. If there were no tumor assessments, these parameters were to be censored on the date of the first drug administration. Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions.
measure
Progression-free Survival
time Frame
From the date of first drug administration to the date of documented PD, or death (of any cause), up to 100 weeks
description
Progression-free Survival was defined as documented PD, or death of any cause. Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions.
measure
Percentage of Participants With Progression-free Survival at 3 Months
time Frame
From the date of first drug administration to the date of documented PD, or death (of any cause), up to 3 months
description
Progression-free Survival was defined as documented PD, or death of any cause. Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions.
measure
Percentage of Participants With Progression-free Survival at 6 Months
time Frame
From the date of first drug administration to the date of documented PD, or death (of any cause), up to 6 months
description
Progression-free survival (PFS) was defined as the time, in months, from the date of first drug administration to the date of documented PD, or death (of any cause). If any patient was lost to follow-up before PD or received another antitumor therapy, PFS was to be censored on the date of the last tumor assessment. If there were no tumor assessments, these parameters were to be censored on the date of the first drug administration Progressive disease (PD): 25% increase from the lowest response value in any of the following: serum M-protein, urine M-protein, BM plasma cell percentage, or difference in the kappa and lambda FLC. PD also diagnosed when an increase size or new bone lesions.
measure
Percentage of Participants With Progression-free Survival at 12 Months
time Frame
From the date of first drug administration to the date of documented PD, or death (of any cause), up to 12 months
description
Event-free survival (EFS) was defined as the time, in months, from the date of first drug administration to the date of onset of the first drug-related event leading to treatment discontinuation, documented PD or death. The censoring rules defined above for PFS were used for EFS
measure
Event-free Survival
time Frame
From the date of first drug administration to the date of onset of the first drug-related event leading to treatment discontinuation, documented PD or death, up to 100 weeks

Full study description

brief Summary: This is a multi-center, open-label, single arm, non-comparative phase II trial, designed to evaluate the efficacy of plitidepsin in combination with bortezomib and dexamethasone in patients with Multiple Myeloma (MM) double refractory to bortezomib and lenalidomide.
detailed Description: This is a multi-center, open-label, single arm, non-comparative phase II trial, designed to evaluate the efficacy of plitidepsin in combination with bortezomib and dexamethasone in patients with MM double refractory to bortezomib and lenalidomide.The primary endpoint will be overall response rate (ORR), including stringent complete response (sCR), complete response (CR), very good partial response (VGPR) and partial response (PR). Approximately 64 evaluable patients will be needed for the evaluation of the primary endpoint, ORR. An early futility analysis will be performed with the efficacy data collected from the first 20 evaluable patients. The futility analysis will commence once patient number 20 has completed two full treatment cycles. Patient recruitment will not be halted during the conduct of this futility analysis.

Source references

Source notices and limitations

Discovery and provenance

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Preserved source evidence · Not medical advice