Combination of MK3475 and Metronomic Cyclophosphamide in Patients With Advanced Sarcomas : Multicentre Phase II Trial

Sarcoma Clinical Trial

— PEMBROSARC  

Official title:

Combination of MK3475 and Metronomic Cyclophosphamide in Patients With Advanced Sarcomas : Multicentre Phase II Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02406781
• Other study ID #: IB 2014-04
• Secondary ID: 2014-004568-39
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: June 2015
• Est. completion date: August 2021

Study information

• Verified date: May 2021
• Source: Institut Bergonié
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multicenter study assessing the efficacy of different therapeutic strategy in patients with advanced sarcomas.

Description:

This is a phase 2 trial with 7 strata :

• Leiomyosarcoma (strata 1) : 33 patients

• Undifferentiated sarcoma (strata 2): 33 patients

• Sarcomas others (strata 3) : 33 patients

• Osteosarcoma (strata 4) : 33 patients

• GIST (strata 5): 31 patients

• Advanced soft-tissue sarcoma with immune signature (strata 6): 32 patients

• Metastatic soft-tissue sarcoma (strata 7): 32 patients

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 227
• Est. completion date: August 2021
• Est. primary completion date: November 24, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Histology : Leiomyosarcoma, or UPS, or other sarcoma, or GIST or osteosarcoma, or soft-tissue sarcoma with presence of tertiary lymphoid structures (stratum 6) histologically confirmed by central review.

2. Advanced non resectable / metastatic disease for strata 1 to 6. For stratum 7: locally advanced or metastatic disease with at least one injectable lesion.

3. Documented progression according to RECIST criteria. Progression on the last line of treatment should be confirmed by central review with two radiological assessments identical obtained at less than 6 months interval within the 12 months before inclusion.

4. For stratum 5, documented disease progression according to RECIST criteria after the first line imatinib and second line sunitinib.

5. Have provided tissue of a tumor lesion from an archival tissue sample obtained on metastasis or on locally advanced disease, or newly obtained core or excisional biopsy. For strata 6 and 7, tissue < 3 months old and with no subsequent treatment since or from a newly obtained biopsy.

6. For strata 1, 2, 3 and 6: no more of four previous lines of systemic therapy for metastatic disease and no more than 2 previous line for stratum 7.

7. Age = 18 years.

8. ECOG performance status = 1.

9. Measurable disease according to RECIST v1.1 outside any previously irradiated field. At least one site of disease must be uni-dimensionally = 10 mm.

10. Life expectancy > 3 months (except for stratum 7 > 6 months).

11. = 1 previous line (s) of chemotherapy in the palliative setting for strata 1 to 5. For other strata, participant must have advanced disease and must not be a candidate for other approved therapeutic regimen known to provide significant clinical benefit based on investigator judgement.

12. No symptomatic central nervous system disease.

13. No chronic use of glucocorticoids.

14. Adequate hematological, renal, metabolic and hepatic function:

1. Hemoglobin = 9 g/dl (patients may have received prior red blood cell transfusion); ANC = 1.5 x 109/l and platelet count = 100 x 109/l. For stratum 7: lymphocyte count = 0.5.109 /l

2. ALT and AST = 2.5 x upper limit of normality (ULN) (= 5 in case of liver metastasis)

3. Total bilirubin = 1.5 x ULN OR Direct bilirubin = ULN for subjects with total bilirubin levels = 1.5 x ULN

4. Albumin = 25g/l

5. Serum creatinine = 1.5 x ULN OR CrCl = 60 ml/min for subject with creatinine levels = 1.5 x ULN,

6. Creatine phosphokinase = 2.5 x ULN

7. INR = 1.5 x ULN unless subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants

8. aPTT = 1.5 X ULN unless subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants

15. No prior or concurrent malignant disease diagnosed or treated in the last 2 years except for adequately treated in situ carcinoma of the cervix, basal or squamous skin cell carcinoma, or in situ transitional bladder cell carcinoma.

16. At least three weeks since last chemotherapy, immunotherapy or any other pharmacological treatment and/or radiotherapy.

17. Recovery to grade = 1 from any adverse event from previous treatment (excluding alopecia of any grade and non-painful peripheral neuropathy grade = 2 (NCI-CTCAE, v 4.0).

18. Women of childbearing potential must have a negative serum pregnancy test within 72 hours prior to receiving the first dose of study medication. Both women and men must agree to use a medically acceptable method of contraception throughout the treatment period and for four months after discontinuation of treatment. Acceptable methods for contraception include intrauterine device, oral contraceptive, subdermal implant and double barrier. Subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for = 1 year.

19. Voluntary signed and dated written informed consents prior to any specific study procedure.

20. Patients with a French social security in compliance with the Law relating to biomedical research (Article 1121-11 of French Public Health Code).

Exclusion Criteria:

1. Previous treatment with MK3475 or CP or G100.

2. Has received prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-CTLA-4 antibody (including ipilimumab or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways).

3. Evidence of progressive or symptomatic central nervous system (CNS) or leptomeningeal metastases.

4. Men or women of childbearing potential who are not using an effective method of contraception as previously described; women who are pregnant or breast feeding.

5. Participation to a study involving a medical or therapeutic intervention in the last 30 days.

6. Previous enrolment in the present study.

7. Patient unable to follow and comply with the study procedures because of any geographical, familial, social or psychological reasons.

8. Known hypersensitivity to any involved study drug or of its formulation components.

9. Has an active autoimmune disease requiring systemic treatment within the past 3 months or a documented history of clinically severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents. Subjects with vitiligo or resolved childhood asthma/atopy would be an exception to this rule. Subjects that require intermittent use of bronchodilators or local steroid injections would not be excluded from the study. Subjects with hypothyroidism stable on hormone replacement or Sjorgen's syndrome will not be excluded from the study.

10. Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment.

11. History of idiopathic pulmonary fibrosis (including pneumonitis), drug-induced pneumonitis, organizing pneumonia, or evidence of active pneumonitis on screening chest CT scan. History of radiation pneumonitis in the radiation field (fibrosis) is permitted.

12. Has known active hepatitis B or hepatitis C.

13. Has a known history of HIV (HIV1/2 antibodies).

14. Has received a live vaccine within 30 days prior to the first dose of trial treatment.

15. For strata 6 to 7:

• patients with oral anticoagulation therapy

• known urinary tract obstruction

• previous allogenic bone marrow transplant

• has an active infection requiring systemic treatment within 14 days prior to study

Related Conditions & MeSH terms

• Sarcoma

Intervention

Drug:
• Combination of MK3475 with Metronomic CP
Combination of MK3475 with Metronomic CP. Metronomic CP (cyclophosphamide) will be administered per os bi-daily (50 mg x 2), and given on a week on/ week off schedule. MK3475 will be administered intraveinously, and given every 3 weeks on day 8. A treatment cycle consists of 3 weeks. Treatment may continue until disease progression or study discontinuation.
• Combination of MK3475 with Metronomic CP and G100
Combination of MK3475 with Metronomic CP and G100. Metronomic CP (cyclophosphamide) will be administered per os bi-daily (50 mg x 2), and given on a week on/ week off schedule. MK3475 will be administered intravenously (200 mg), and given every 3 weeks on day 8. G100 will be administered by intra-tumoral injection (20µg), one weekly injection for at least 6 weeks and for a maximum of 12 weeks. G100 will start one week before CP administration (impregnation phase). A treatment cycle consists of 3 weeks. Treatment may continue until disease progression or study discontinuation.

Locations

Country	Name	City	State
France	Institut Bergonié	Bordeaux
France	Centre Oscar Lambret	Lille
France	Centre Léon Bérard	Lyon
France	Institut Paoli Calmettes	Marseille
France	Institut Curie	Paris
France	Institut de Cancérologie de l'Ouest	Saint-Herblain
France	Institut Claudius Regaud	Toulouse
France	Institut Gustave Roussy	Villejuif

Sponsors (4)

Lead Sponsor	Collaborator
Institut Bergonié	Immune Design, Merck Sharp & Dohme Corp., Ministry of Health, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of the efficacy of MK3475 associated with Metronomic Cyclophosphamide per RECIST v1.1 criteria	This primary objective of this study is to assess the efficacy of MK3475 and Metronomic Cyclophosphamide (CP) independently for 6 strata as per RECIST v1.1 criteria : In terms of 6-month objective response and 6-months non progression for: Advanced leiomyosarcoma; Advanced undifferentiated sarcoma; Advanced other sarcoma; Advanced osteosarcoma; In terms of·6-month non progression for: Advanced GIST; Advanced soft-tissue sarcoma with immune signature	6 months
Primary	Assessment of the efficacy of MK3475 associated with Metronomic Cyclophosphamide and G100 per RECIST v1.1 criteria	This primary objective of this study is to assess the efficacy of MK3475 and Metronomic Cyclophosphamide (CP) and G100 as per RECIST v1.1 criteria, in terms of 6-months non progression for metastatic soft-tissue sarcoma.	6 months
Secondary	Efficacy of the treatment strategy in terms of Best overall response	Assessment of the efficacy of the treatment strategy in terms of best overall response (as per RECIST v1.1 criteria)	participants will be followed for the duration of treatment, an expected average of 6-months
Secondary	Efficacy of the treatment strategy in terms of Progression-free Survival	Assessment of the efficacy of the treatment strategy in terms of 1-year progression-free survival (as per RECIST v1.1 criteria)	Progression-free survival assessed at 12 months
Secondary	Efficacy of the treatment strategy in terms of Immune_related Response	Assessment of the efficacy of the treatment strategy in terms of 6-months immune-related response (as per Wolchok 2009)	Immune-related response assessed at 6 months
Secondary	Efficacy of the treatment strategy in terms of Overall Survival.	Assessment of the efficacy of the treatment strategy in terms of 1-year overall survival	Overall survival assessed at 12 months
Secondary	Safety profile of the treatment strategy.Toxicity graded using the Common Terminology Criteria for Adverse Events version 4	Toxicity graded using the Common Terminology Criteria for Adverse Events version 4	Throughout the treatment period, an average of 6 months
Secondary	Exploration of blood cytokines levels (TNF?, TNFa, TGFß, IL2, 4, 6, 10) (ELISA)		Blood samples collected at different time points : Baseline, Day 8 cycle 1, Day 8 cycle 2, Day 8 cycle 3, Day 8 cycle 4, Day 8 Cycle 6 and at progression
Secondary	Exploration of blood VEGF, Svegfr2 and TPS-1 levels (ELISA)		Blood samples collected at different time points : Baseline, Day 8 cycle 1, Day 8 cycle 2, Day 8 cycle 3, Day 8 cycle 4, Day 8 Cycle 6 and at progression
Secondary	Exploration of lymphocytes subpopulations monitoring, CD8+/Treg ratio (flow cytometry)		Blood samples collected at different time points : Baseline, Day 8 cycle 1, Day 8 cycle 2, Day 8 cycle 3, Day 8 cycle 4, Day 8 Cycle 6 and at progression
Secondary	Exploration of Plasma levels of Kynurenine and Kynurenine to Tryptophan ratio (ELISA and LC/MS)		Blood samples collected at different time points : Baseline, Day 8 cycle 1, Day 8 cycle 2, Day 8 cycle 3, Day 8 cycle 4, Day 8 Cycle 6 and at progression