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JOURNAL ONKOLOGIE – STUDIE

A Trial of Doxycycline vs. Standard Supportive Therapy in Newly-diagnosed Cardiac AL Amyloidosis Patients Undergoing Bortezomib-based Therapy

Rekrutierend

NCT-Nummer:
NCT03474458

Studienbeginn:
Februar 2019

Letztes Update:
26.01.2021

Wirkstoff:
Doxycycline, Standard of care therapy

Indikation (Clinical Trials):
Amyloidosis, Immunoglobulin Light-chain Amyloidosis

Geschlecht:
Alle

Altersgruppe:
Erwachsene (18+)

Phase:
-

Sponsor:
IRCCS Policlinico S. Matteo

Collaborator:
-

Kontakt

Studienlocations
(3 von 8)

Alle anzeigen

Studien-Informationen

Brief Summary:

Systemic amyloidoses are rare diseases affecting approximately 1 in 100,000 persons each

year.

In systemic amyloidoses abnormal proteins deposit in bodily organs and severely impair their

function, causing death if not treated effectively. Light chain (AL) amyloidosis is caused by

a usually small population of plasma cells (the cells that produce antibodies). These cells

produce part of antibodies, the light chains (LC) that form amyloid deposits. Almost every

organ, with the exception of the brain, can be affected by AL amyloidosis. The heart is

involved in three fourths of patients and is responsible for almost all the deaths occurring

in the first 6 months after diagnosis. Current therapy of AL amyloidosis is based on drugs

targeting the plasma cells producing the amyloid-forming LC. At present, most patients

receive a powerful anti-plasma cell drug, bortezomib, as part of their initial treatment.

However, bortezomib-based therapy, can improve heart involvement only in less than one third

of patients with AL amyloidosis, and many patients (approximately one third) still die within

12 months from diagnosis. Early cardiac deaths remain an acute unmet need and the major

determinant of overall outcome in this disease. Thus, there is the need of alternative means

to treat heart involvement in AL amyloidosis. Doxycycline is a widely used, well tolerated,

antibiotic that has been marketed for decades and used to treat a number of different

infectious diseases caused by bacteria. This molecule has been extensively studied in the

laboratory, in animal models and, more recently, in small studies involving patients, for its

potential of improving cardiac damage in amyloidosis. These studies showed that doxycycline

disrupts amyloid deposits, reduces the amyloid load in a mouse model, and counteracts the

toxicity exerted by amyloid-forming LCs on C. elegans, a worm whose pharynx is used as a

model resembling human heart. In a small clinical study, doxycycline was given to patients

with cardiac AL amyloidosis during treatment for their underlying plasma cell disease. This

resulted in a remarkable improvement of survival compared to "matched historical controls"

(i.e. similar patients who had received only anti-plasma cell therapy without doxycycline in

the past). Based on these promising preliminary results, we designed the present clinical

trial to assess whether the addition of doxycycline to anti-plasma cell therapy can improve

survival in patients with cardiac AL amyloidosis who were not previously treated. The rate of

survival at 12 months will be compared in patients receiving doxycycline and in controls

receiving standard antibiotic therapy, together with anti-plasma cell therapy. Patients will

be assessed for parameters of plasma cell disease, heart involvement and possible involvement

of other organs, as well as for quality of life. To make sure that patients who will receive

doxycycline and those who will not have comparable severity of cardiac disease, patients will

be stratified according to the stage of cardiac involvement. Patients with very advanced

heart dysfunction will not be enrolled in the trial, because preliminary data indicate that

doxycycline is of little or no benefit in these subjects. Patients will be randomized to

receive doxycycline or standard antibiotics in combination with anti-plasma cell therapy.

Bortezomib-based treatment directed against plasma cells will be delivered according to each

participating institutions' guidelines. Doxycycline will be administered at a dosage of 100

mg two times a day, which is usual in the treatment of bacterial diseases. Standard

antibiotics will be delivered according to each participating institutions' guidelines

(provided that drugs of the same class as doxycycline are not administered) in the control

arm. Patients will be provided a diary to record possible adverse events and will be

instructed accordingly. Patients will be evaluated at trial centers every 2 months for

treatment efficacy and toxicity. In case of unsatisfactory response second-line therapy will

be initiated. In the absence of unacceptable toxicity, doxycycline administration will be

continued for the entire duration of follow-up (12 months).

Ein-/Ausschlusskriterien

INCLUSION CRITERIA

1. Age ≥ 18.

2. Newly-diagnosed AL amyloidosis.

3. Confirmed diagnoses of AL amyloidosis by the following:

1. histochemical diagnoses of AL amyloidosis determined by polarizing light

microscopy of green birefringent material in Congo red stained issue specimens OR

characteristic electron microscopy appearance AND

2. confirmatory electron microscopy immunohistochemistry OR mass spectroscopy of AL

amyloidosis. Confirmation of amyloid type can be omitted in patients with a

clear-cut clinical evidence of AL amyloidosis (e.g. cardiac and renal

involvement, soft tissue involvement) in the presence of a monoclonal component.

4. Cardiac involvement as defined by ALL of the following:

1. Either an endomyocardial biopsy consistent with AL amyloidosis OR an

echocardiogram demonstrating a mean left ventricular wall thickness in diastole

>12 mm in the absence of other causes (e.g., severe hypertension, aortic

stenosis) which would adequately explain the degree of wall thickening .

2. Cardiac stage II disease: either cTnT > 0.035 ng/mL (or in place of cTnT the cTnI

> 0.10 ng/mL or hs-cTnT >77 ng/L) or simultaneous NT-proBNP >332 ng/L OR patients

with cardiac stage IIIa: both cTnT > 0.035 ng/mL (or in place of cTnT the cTnI >

0.10 ng/mL or hs-cTnT >77 ng/L) and simultaneous NT-proBNP >332 ng/L and

NT-proBNP ≤8500 ng/L.

5. Planned bortezomib-based therapy.

6. Total bilirubin <1.5 × upper reference limit (url), patients with Gilbert disease who

have a total bilirubin, predominantly unconjugated >1.5 × url without any other liver

function test abnormalities are still eligible.

7. Alkaline phosphatase <5 × url.

8. Alanine aminotransferase <3 × url.

9. Systolic blood pressure 90-180 mmHg.

10. Women of childbearing potential (WOCBP) must have a negative serum pregnancy test

within 14 days prior to the first administration of study drug and perform a pregnancy

test every 4 weeks to rule out pregnancy, they must agree to use highly effective

physician-approved contraception 30 days prior to the first study drug administration.

Highly-effective contraceptive methods with a Pearl Index lower than 1 are: Oral

hormonal contraception ('pill') (as far as its efficacy is not expected to be impaired

during the trial, e.g. with IMPs that cause vomiting and diarrhoea or interfere with

hormone metabolism, adequate safety cannot be assumed), Dermal hormonal contraception

(e.g. contraceptive patch), Vaginal hormonal contraception (NuvaRing®), Long-acting

injectable contraceptives, Tubal ligation (female sterilisation), Double barrier

methods. This means that the following are not regarded as safe: condom plus

spermicide, simple barrier methods (vaginal pessaries, condom, female condoms), copper

spirals, the rhythm method, basal temperature method, and the withdrawal method

(coitus interruptus).

The following duration of highly effective contraception is necessary: Bortezomib:

during and until 3 months after the end of therapy, Melphalan: during and 6 months

after the end of therapy, Cyclophosphamide: during and 12 months after the end of

therapy

11. Males must be surgically sterile or must agree to use highly effective physician

approved contraception from 30 days prior to the first study drug administration to 90

days following the last study drug administration.

12. Ability to understand and willingness to sign an informed consent form prior to

initiation of any study procedures.

13. Patient was assessed to determine ineligibility for ASCT. Patients who are eligible

for high-dose chemotherapy and ASCT but decline the procedure, can be enrolled in the

study.

EXCLUSION CRITERIA

1. Non-AL amyloidosis.

2. Stage IIIb (NT-proBNP >8500 ng/L and cTnI >0.1 ng/mL, or cTnT >0.035 ng/mL, or hs-cTnT

>77 ng/L.

3. Previous treatment for AL amyloidosis.

4. Clinically overt multiple myeloma with lytic bone lesions.

5. Symptomatic orthostatic hypotension that in the medical judgment of the Investigator

would interfere with subject's ability to safely receive treatment or complete study

assessments.

6. Patients with uncontrolled infection or active malignancy with the exception of

adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer,

adequately treated Stage I cancer from which the patient is currently in complete

remission, or any other cancer from which the patient has been disease-free for 5

years.

7. Known HIV positive.

8. Pregnant or nursing women.

9. Known hypersensitivity to doxycycline, bortezomib, boron, or mannitol.

10. Treatment with drugs potentially affecting doxycycline absorption.

11. Significant acute gastrointestinal symptoms.

12. Active peptic ulceration and/or esophageal reflux disease.

13. Patients with serious medical or psychiatric illness likely to interfere with

participation in this clinical study.

14. Contraindication to bortezomib based therapy

Studien-Rationale

Primary outcome:

1. proportion surviving (Time Frame - 12 months):
proportion surviving

Studien-Arme

  • Experimental: Experimental intervention
    doxycycline (100 mg bid)
  • Active Comparator: Control intervention
    Standard of care therapy

Geprüfte Regime

  • Doxycycline:
    Doxycycline
  • Standard of care therapy:
    Standard of care therapy

Quelle: ClinicalTrials.gov


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