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NCT02728102 · OUTCOME

Number of Grade ≥ 3 Toxicities

Dendritic Cell/Myeloma Fusion Vaccine for Multiple Myeloma (BMT CTN 1401) · Source last updated 2024-05-07

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
NUMBER
Unit
Toxicities
Interval / dispersion
Not reported
Time frame
2 years

What was measured

Toxicities are evaluated using NCI CTCAE version 4.0 at pre-maintenance initiation and during maintenance therapy monthly for the first 4 cycles and then at cycles 6, 9, 15, 21, 24, which correspond to Day 1, 29, 57, 85, 141, 225, 393, 561, and 645 post maintenance initiation. All Grade ≥ 3 toxicities will be tabulated for treatment arms. Toxicities are categorized by organ system according to the CTCAE. Toxicities that involve multiple questions per organ system are combined in one category.

Analysis population: The randomized participants are included in the analysis

Groups in this outcome

Lenalidomide, Vaccine, and GM-CSF

Patients will undergo tumor cell collection and autologous stem cell transplant with melphalan. Patients will undergo leukapheresis and then will receive maintenance lenalidomide with myeloma vaccine and GM-CSF. Tumor Cell Collection: Patients will undergo aspiration of 30 mL of bone marrow from which myeloma cell will be isolated and frozen for subsequent vaccine generation. Autologous Stem Cell Transplant: Patients will receive an autologous graft of a minimum cell dose of 2.0 x 10\^6 CD34+ cells/kg patient actual body weight per transplantation with high-dose melphalan of 200mg/m\^2 at the schedule and timing according to institutional practices. Leukapheresis: Blood samples will be collected through a catheter in the neck or chest and leukapheresis will be performed using standard clinical procedures. Lenalidomide: Maintenance therapy with lenalidomide will begin between 90 and 100 days after stem cell infusion. Lenalidomide will be administered initially at a dose of 10 mg per day continuously. Cycle duration during maintenance therapy is 28 days. Patients will continue lenalidomide for two years from initiation of therapy. Myeloma vaccine: The target dose is 3 x 10\^6 fusion cells per vaccine. A minimum of 3 x 10\^6 total fusion cells will be required to proceed with vaccine administration. Patients will receive the DC/MM fusion vaccine on day 1 of cycles 2, 3, and 4 of lenalidomide maintenance. GM-CSF: 100 ug GM-CSF will be given for a total of 4 days of each cycle.

Lenalidomide and GM-CSF

Patients will undergo tumor cell collection and autologous stem cell transplant with melphalan. Patients will receive maintenance lenalidomide with GM-CSF. Tumor Cell Collection: Patients will undergo aspiration of 30 mL of bone marrow from which myeloma cell preparations will be generated. Myeloma cells will be isolated and frozen for subsequent vaccine generation for patients randomized to the vaccine arm (randomization occurs after transplant and recovery). Autologous Stem Cell Transplant: Patients will receive an autologous graft with a minimum cell dose of 2.0 x 10\^6 CD34+ cells/kg patient actual body weight per autologous transplantation. Melphalan: Autologous hematopoietic cell transplant will be done with high-dose melphalan of 200mg/m\^2 at the schedule and timing according to institutional practices. Lenalidomide: Maintenance therapy with lenalidomide will begin between 90 and 100 days after stem cell infusion. Lenalidomide will be administered initially at a dose of 10 mg per day continuously. Cycle duration during maintenance therapy is 28 days. Patients will continue lenalidomide for two years from initiation of therapy. GM-CSF: 100 ug GM-CSF will be given subcutaneously in the upper thigh and daily for a total of 4 days of each cycle.

Maintenance Lenalidomide

Patients will undergo tumor cell collection and autologous stem cell transplant with melphalan. Patients will receive maintenance lenalidomide. Tumor Cell Collection: Patients will undergo aspiration of 30 mL of bone marrow from which myeloma cell preparations will be generated. Myeloma cells will be isolated and frozen for subsequent vaccine generation for patients randomized to the vaccine arm (randomization occurs after transplant and recovery). Autologous Stem Cell Transplant: Patients will receive an autologous graft with a minimum cell dose of 2.0 x 10\^6 CD34+ cells/kg patient actual body weight per autologous transplantation. Melphalan: Autologous hematopoietic cell transplant will be done with high-dose melphalan of 200mg/m\^2 at the schedule and timing according to institutional practices. Lenalidomide: Maintenance therapy with lenalidomide will begin between 90 and 100 days after stem cell infusion. Lenalidomide will be administered initially at a dose of 10 mg per day continuously. Cycle duration during maintenance therapy is 28 days. Patients will continue lenalidomide for two years from initiation of therapy.

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Lenalidomide, Vaccine, and GM-CSF68
Lenalidomide and GM-CSF37
Maintenance Lenalidomide35

Reported measurements

Auditory Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF1Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF0Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide0Not reportedNot reportedNot reportedNot reported
Blood and Lymphatic Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF81Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF40Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide38Not reportedNot reportedNot reportedNot reported
Cardiovascular Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF4Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF3Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide2Not reportedNot reportedNot reportedNot reported
GI Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF15Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF4Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide2Not reportedNot reportedNot reportedNot reported
General Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF5Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF2Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide2Not reportedNot reportedNot reportedNot reported
Hepatobiliary/Pancreas Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF4Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF1Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide1Not reportedNot reportedNot reportedNot reported
Immune System Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF2Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF0Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide0Not reportedNot reportedNot reportedNot reported
Investigations
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF2Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF0Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide1Not reportedNot reportedNot reportedNot reported
Metabolism and Nutrition Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF7Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF1Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide3Not reportedNot reportedNot reportedNot reported
Musculoskeletal and Connective Tissue Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF1Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF1Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide2Not reportedNot reportedNot reportedNot reported
Nervous System Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF14Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF5Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide1Not reportedNot reportedNot reportedNot reported
Renal Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF1Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF0Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide2Not reportedNot reportedNot reportedNot reported
Respiratory, Thoracic and Mediastinal Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF5Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF1Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide2Not reportedNot reportedNot reportedNot reported
Skin and Subcutaneous Tissue Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF4Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF5Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide7Not reportedNot reportedNot reportedNot reported
Vascular Disorders
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF6Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF11Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide3Not reportedNot reportedNot reportedNot reported
Abnormal Liver Symptoms
Values in Toxicities · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Lenalidomide, Vaccine, and GM-CSF0Not reportedNot reportedNot reportedNot reported
Lenalidomide and GM-CSF1Not reportedNot reportedNot reportedNot reported
Maintenance Lenalidomide0Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        1
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
    title
    Auditory Disorders
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        81
      2. group Id
        OG001
        value
        40
      3. group Id
        OG002
        value
        38
    title
    Blood and Lymphatic Disorders
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        4
      2. group Id
        OG001
        value
        3
      3. group Id
        OG002
        value
        2
    title
    Cardiovascular Disorders
  4. categories
    1. measurements
      1. group Id
        OG000
        value
        15
      2. group Id
        OG001
        value
        4
      3. group Id
        OG002
        value
        2
    title
    GI Disorders
  5. categories
    1. measurements
      1. group Id
        OG000
        value
        5
      2. group Id
        OG001
        value
        2
      3. group Id
        OG002
        value
        2
    title
    General Disorders
  6. categories
    1. measurements
      1. group Id
        OG000
        value
        4
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        1
    title
    Hepatobiliary/Pancreas Disorders
  7. categories
    1. measurements
      1. group Id
        OG000
        value
        2
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
    title
    Immune System Disorders
  8. categories
    1. measurements
      1. group Id
        OG000
        value
        2
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        1
    title
    Investigations
  9. categories
    1. measurements
      1. group Id
        OG000
        value
        7
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        3
    title
    Metabolism and Nutrition Disorders
  10. categories
    1. measurements
      1. group Id
        OG000
        value
        1
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        2
    title
    Musculoskeletal and Connective Tissue Disorders
  11. categories
    1. measurements
      1. group Id
        OG000
        value
        14
      2. group Id
        OG001
        value
        5
      3. group Id
        OG002
        value
        1
    title
    Nervous System Disorders
  12. categories
    1. measurements
      1. group Id
        OG000
        value
        1
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        2
    title
    Renal Disorders
denoms
  1. counts
    1. group Id
      OG000
      value
      68
    2. group Id
      OG001
      value
      37
    3. group Id
      OG002
      value
      35
    units
    Participants
description
Toxicities are evaluated using NCI CTCAE version 4.0 at pre-maintenance initiation and during maintenance therapy monthly for the first 4 cycles and then at cycles 6, 9, 15, 21, 24, which correspond to Day 1, 29, 57, 85, 141, 225, 393, 561, and 645 post maintenance initiation. All Grade ≥ 3 toxicities will be tabulated for treatment arms. Toxicities are categorized by organ system according to the CTCAE. Toxicities that involve multiple questions per organ system are combined in one category.
groups
  1. description
    Patients will undergo tumor cell collection and autologous stem cell transplant with melphalan. Patients will undergo leukapheresis and then will receive maintenance lenalidomide with myeloma vaccine and GM-CSF. Tumor Cell Collection: Patients will undergo aspiration of 30 mL of bone marrow from which myeloma cell will be isolated and frozen for subsequent vaccine generation. Autologous Stem Cell Transplant: Patients will receive an autologous graft of a minimum cell dose of 2.0 x 10\^6 CD34+ cells/kg patient actual body weight per transplantation with high-dose melphalan of 200mg/m\^2 at the schedule and timing according to institutional practices. Leukapheresis: Blood samples will be collected through a catheter in the neck or chest and leukapheresis will be performed using standard clinical procedures. Lenalidomide: Maintenance therapy with lenalidomide will begin between 90 and 100 days after stem cell infusion. Lenalidomide will be administered initially at a dose of 10 mg per day continuously. Cycle duration during maintenance therapy is 28 days. Patients will continue lenalidomide for two years from initiation of therapy. Myeloma vaccine: The target dose is 3 x 10\^6 fusion cells per vaccine. A minimum of 3 x 10\^6 total fusion cells will be required to proceed with vaccine administration. Patients will receive the DC/MM fusion vaccine on day 1 of cycles 2, 3, and 4 of lenalidomide maintenance. GM-CSF: 100 ug GM-CSF will be given for a total of 4 days of each cycle.
    id
    OG000
    title
    Lenalidomide, Vaccine, and GM-CSF
  2. description
    Patients will undergo tumor cell collection and autologous stem cell transplant with melphalan. Patients will receive maintenance lenalidomide with GM-CSF. Tumor Cell Collection: Patients will undergo aspiration of 30 mL of bone marrow from which myeloma cell preparations will be generated. Myeloma cells will be isolated and frozen for subsequent vaccine generation for patients randomized to the vaccine arm (randomization occurs after transplant and recovery). Autologous Stem Cell Transplant: Patients will receive an autologous graft with a minimum cell dose of 2.0 x 10\^6 CD34+ cells/kg patient actual body weight per autologous transplantation. Melphalan: Autologous hematopoietic cell transplant will be done with high-dose melphalan of 200mg/m\^2 at the schedule and timing according to institutional practices. Lenalidomide: Maintenance therapy with lenalidomide will begin between 90 and 100 days after stem cell infusion. Lenalidomide will be administered initially at a dose of 10 mg per day continuously. Cycle duration during maintenance therapy is 28 days. Patients will continue lenalidomide for two years from initiation of therapy. GM-CSF: 100 ug GM-CSF will be given subcutaneously in the upper thigh and daily for a total of 4 days of each cycle.
    id
    OG001
    title
    Lenalidomide and GM-CSF
  3. description
    Patients will undergo tumor cell collection and autologous stem cell transplant with melphalan. Patients will receive maintenance lenalidomide. Tumor Cell Collection: Patients will undergo aspiration of 30 mL of bone marrow from which myeloma cell preparations will be generated. Myeloma cells will be isolated and frozen for subsequent vaccine generation for patients randomized to the vaccine arm (randomization occurs after transplant and recovery). Autologous Stem Cell Transplant: Patients will receive an autologous graft with a minimum cell dose of 2.0 x 10\^6 CD34+ cells/kg patient actual body weight per autologous transplantation. Melphalan: Autologous hematopoietic cell transplant will be done with high-dose melphalan of 200mg/m\^2 at the schedule and timing according to institutional practices. Lenalidomide: Maintenance therapy with lenalidomide will begin between 90 and 100 days after stem cell infusion. Lenalidomide will be administered initially at a dose of 10 mg per day continuously. Cycle duration during maintenance therapy is 28 days. Patients will continue lenalidomide for two years from initiation of therapy.
    id
    OG002
    title
    Maintenance Lenalidomide
param Type
NUMBER
population Description
The randomized participants are included in the analysis
reporting Status
POSTED
time Frame
2 years
title
Number of Grade ≥ 3 Toxicities
type
SECONDARY
unit Of Measure
Toxicities

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Preserved source evidence · Not medical advice