A Study of HDC/IL-2 Treatment in Chronic Myelomonocytic Leukemia (CMML)

Phase 1

• Conditions: Leukemia, Myelomonocytic, Chronic
• Interventions: Drug: Cohort 1, Ceplene® and Proleukin®; Drug: Cohort 2, Ceplene® and Proleukin®; Drug: Cohort 3, Ceplene® and Proleukin®

• Registration Number: NCT03040401
• Lead Sponsor: Vastra Gotaland Region

Brief Summary

Enrolled subjects will receive histamine dihydrochloride (HDC; Ceplene®) and/or IL-2 (Proleukin®) subcutaneously (s.c.) twice daily (BID) in 3-week periods followed by 3- or 6 week rest periods.

All subjects will be assigned to one of three consecutive cohorts, each comprising five patients.

Cohort 1 will receive HDC without IL-2 for the first treatment cycle, to enable the assessment of short-term impact of HDC alone on clonal and immunological markers. For all remaining cycles the combination of HDC and IL-2 will be given.

Cohort 2 will receive the combination of Ceplene and Proleukin in all cycles. After all patients in cohorts 1 and 2 have completed 4 treatment cycles, immunological and clinical response and toxicity will be evaluated. On the basis of the results for the first 4 cycles of cohorts 1 and 2, a third cohort of 5 patients will be enrolled receiving either the combination of HDC/IL-2 or HDC alone.

In case of a beneficial response\* after 4 cycles, treatment may be continued to a total of 10 cycles. Treatment cycles 5-10 will comprise 3 weeks of treatment and 6-week rest periods.

IL-2 will be administered s.c., 1 µg/kg (=16400 IU/kg) body weight twice daily (BID) during treatment periods. Ceplene® will be administered s.c. 0.5 mg BID after IL-2. The patient or a family member/significant other will be instructed to administer injections of both study drugs to allow safe treatment at home.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-01-24
• Study First Submitted QC: 2017-01-31
• Study First Posted: 2017-02-02
• Study Start: 2017-02-15
• Status Verified: 2017-12
• Last Update Submitted: 2017-12-18
• Last Update Posted: 2017-12-19
• Primary Completion: 2018-12-15
• Study Completion: 2019-12-15

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

• ≥18 years of age at the time of signing the informed consent form.

• CMML-1 with indication for treatment according to NMDSG guidelines*.

• Life expectancy of more than three months and ability to undergo routine outpatient evaluations for efficacy, safety, and compliance.

• The patient must be informed of the investigational nature of the study and written informed consent obtained and signed.

  • including, but not limited to increasing WBC, transfusion dependence, B-symptoms, splenomegaly.

Exclusion Criteria

• Acute myeloid leukemia.

• CMML-2 according to WHO criteria.

• Systemic mastocytosis.

• Previous or intended allogeneic stem cell transplantation.

• Concomitant or intended cytostatic or cytoreductive therapy other than hydroxyurea (HU) *.

• ECOG performance status ≥3.

• Platelet count (TPK) <30x109/L

• NYHA class III or IV cardiac disease, hypotension or severe hypertension, vasomotor instability, serious or uncontrolled cardiac dysrhythmias (including ventricular arrhythmias) at any time, acute myocardial infarction within the past 12 months, angina pectoris or symptomatic arteriosclerotic blood vessel disease.

• Other active malignancies except in situ carcinoma of the cervix, localized squamous or basal cell carcinoma of the skin.

• Serious concurrent or recent non-malignant medical conditions which, in the opinion of the Investigator, makes the patient unsuitable for participation in this study.

• History of seizures, central nervous system disorders, stroke within the last 12 months, or psychiatric disability thought to be clinically significant in the opinion of the Investigator and adversely affecting compliance to protocol.

• Serum creatinine > 1.5 times the upper normal limit.

• Serum aminotransferase (AST), alanine transaminase (ALT) and bilirubin >2.0 times the upper normal limit

• Active autoimmune disease (including but not limited to systemic lupus, inflammatory bowel disease, and psoriasis).

• Patients with active peptic or esophageal ulcer disease or with past peptic ulcer or esophageal disease with a history or bleeding.

• Patients requiring active treatment for hypotension.

• Patients continuing systemic treatment with clonidine, steroids, and/or H2 receptor blocking agents.

• Patients with a history of histamine hypersensitivity, severe allergies to food or contrast media requiring treatment within the last five years.

• Pregnancy. Women of childbearing potential (WCBP) and males having intercourse with WCBP must agree to comply with using an effective contraceptive method for the duration of the treatment (WCBP is a sexually mature woman who is not surgically sterile or has not been naturally postmenopausal for at least 12 consecutive months).

• Nursing

  • Note that treatment with HU is allowed if treatment has been ongoing for at least 3 months prior to enrollment. The use of HU is also allowed to control myeloproliferation after starting study treatment, preferably during resting periods.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Cohort 1: Ceplene® and Proleukin®	Cohort 1, Ceplene® and Proleukin®	Enrolled subjects will receive histamine dihydrochloride (HDC; Ceplene®) and IL-2 (Proleukin®) subcutaneously (s.c.) twice daily (BID) in 3-week periods followed by 3 week rest periods for a total of 4 treatment cycles. IL-2 will be administered s.c., 1 µg/kg (=16400 IU/kg) body weight twice daily (BID) during treatment periods. Ceplene® will be administered s.c. 0.5 mg BID after IL-2 injections. Cohort 1 will receive only Ceplene® during the first treatment cycles and Ceplene® in combination with Proleukin® during treatment cycles 2-4.
Cohort 2: Ceplene® and Proleukin®	Cohort 2, Ceplene® and Proleukin®	Enrolled subjects will receive histamine dihydrochloride (HDC; Ceplene®) and IL-2 (Proleukin®) subcutaneously (s.c.) twice daily (BID) in 3-week periods followed by 3 week rest periods for a total of 4 treatment cycles. IL-2 will be administered s.c., 1 µg/kg (=16400 IU/kg) body weight twice daily (BID) during treatment periods. Ceplene® will be administered s.c. 0.5 mg BID after IL-2 injections. Cohort 2 will receive Ceplene® in combination with Proleukin® during all treatment cycles (1-4).
Cohort 3: Ceplene® and Proleukin®	Cohort 3, Ceplene® and Proleukin®	Enrolled subjects will receive histamine dihydrochloride (HDC; Ceplene®) and IL-2 (Proleukin®) subcutaneously (s.c.) twice daily (BID) in 3-week periods followed by 3 week rest periods for a total of 4 treatment cycles. IL-2 will be administered s.c., 1 µg/kg (=16400 IU/kg) body weight twice daily (BID) during treatment periods. Ceplene® will be administered s.c. 0.5 mg BID after IL-2 injections. Cohort 3 will receive either only Ceplene® during treatment cycles 1-4 or Ceplene® in combination with Proleukin® during treatment cycles 1-4. Treatment will be decided by the study committee based on the safety profile of treatment administered to cohort 1 and 2.

Primary Outcome Measures

Name	Time	Method
Adverse events as defined by CTCAE v4.03.	3 weeks after last treatment cycle

Secondary Outcome Measures

Name	Time	Method
Percentage of circulating CD8+ T cells i peripheral blood	3 weeks after last treatment cycle	Percentage of CD8+ T cells in peripheral blood will be assessed by flow cytometry. End-of-treatment percentage will be compared to values pre-study.
Proportion of participants with overall survival at 2 years.	2 years after last treatment cycle
Disease progression according to IWG criteria for MDS/MPN	3 weeks after last treatment cycle
Percentage of blasts in peripheral blood	3 weeks after last treatment cycle	Percentage of blasts (CD34+ cells and promonocytes) will be assessed by flow cytometry. End-of-treatment percentage will be compared to values pre-study.
Percentage of monocytes in peripheral blood	3 weeks after last treatment cycle	Percentage of CD14+ monocytes will be assessed by flow cytometry. End-of-treatment percentage will be compared to values pre-study.
Number of treated patients that transform to AML	2 years after last treatment cycle
Percentage of circulating NK cells i peripheral blood	3 weeks after last treatment cycle	Percentage of NK cells in peripheral blood will be assessed by flow cytometry. End-of-treatment percentage will be compared to values pre-study.
Percentage of circulating CD4+ T cells i peripheral blood	3 weeks after last treatment cycle	Percentage of CD4+ T cells in peripheral blood will be assessed by flow cytometry. End-of-treatment percentage will be compared to values pre-study.

Trial Locations

Locations (2)

Sahlgrenska University Hospital; 🇸🇪 Gothenburg, Sweden

Karolinska University Hospital, Huddinge; 🇸🇪 Stockholm, Sweden