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A Double Blind, Placebo Controlled, Randomized Phase II Study Evaluating Gemcitabine With or Without Ramucirumab , for II Line Treatment MPM

Brief Summary

Study RAMES is a multicentre, double-blind, randomized Phase II study exploring the efficacy and evaluating the safety of the addition of ramucirumab to gemcitabine as the second-line treatment of patients with diffuse pleural mesothelioma. Patients will be randomly assigned (1:1) to receive intravenous gemcitabine 1000 mg/m2 on days 1 and 8 every 21 days with placebo or combined with intravenous ramucirumab 10 mg/Kg (ramucirumab group) on day 1 of a 21 day cycle until PD. Randomisation will be done via a centralized system and will stratified by performance status (0-1 vs 2), age (≤70 vs >70), histology (epithelioid vs others), time to progression (TTP) after a previous treatment (first line therapy, adjuvant or neoadjuvant therapy) (< 6 months vs ≥6 months).

Tracking Information
First Received DateMay 18, 2018
Last Changed DateAugust 29, 2018
Start DateDecember 22, 2016
Anticipated Primary Completion DateDecember 22, 2018
Primary Outcome Measures

OS [Time Frame: 36 months]

Secondary Outcome Measures

PFS [Time Frame: 36 months]

Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]). [Time Frame: 36 months]

ORR [Time Frame: 36 months]

DCR [Time Frame: 36 months]

Predictive molecular markers [Time Frame: 36 months]

Quality life [Time Frame: 36 months]

Predictive molecular markers [Time Frame: 36 months]

Predictive molecular markers [Time Frame: 36 months]

Descriptive Information
PhasePhase 2
Study TypeInterventional
Condition
  • Mesothelioma
Intervention
  • Drug: Gemcitabine
  • Drug: Ramucirumab
Study Arms / Comparison Groups2 / 0
Recruitment Information
Recruitment StatusActive, not recruiting
Actual Enrollment164
GenderAll
Ages18 Years - N/A
Accepts Healthy VolunteersNo
Eligibility Criteria

Inclusion Criteria:

1. The patient has a histopathologically or cytologically confirmed diagnosis of malignant pleural mesothelioma.

2. The patient has documented disease progression after the last dose of first-line chemotherapy for metastatic disease,

a. Patients who are intolerant to first-line chemotherapy regimens are eligible. Disease progression must be assessed after the last dose of first-line therapy.

3. The patient received combination chemotherapy prior to disease progression.

1. Prior chemotherapy regimens must include a platinum or pemetrexed component. Exposure to antineoplastic therapy, in addition to platinum and/or pemetrexed, is acceptable if the agents were used in the first-line metastatic or neoadjuvant/adjuvant setting.

2. Patients who have had one or more components of first-line chemotherapy discontinued because of toxicity, but continued to receive the other component(s), are eligible following disease progression.

4. The patient has metastatic disease or locally advanced disease that is measurable, or nonmeasurable but evaluable, by radiological imaging per Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1) (Eisenhauer et al. 2009 Baseline tumor assessment should be performed using a high resolution computed tomography (CT) scan using intravenous and oral contrast unless clinically contraindicated. Magnetic resonance imaging (MRI) is acceptable if a CT cannot be performed.

5. The patient has an ECOG performance status of 0-2

6. The patient has adequate organ function.

7. The patient is at least 18 years old or of an acceptable age according to local regulations, whichever is older.

8. The patient has provided written informed consent prior to any study-specific procedures and is amenable to compliance with protocol schedules and testing.

9. The patient has an estimated life expectancy of 12 weeks in the judgment of the investigator.

10. The patient has resolution to Grade 1 by Common Terminology Criteria for Adverse Events CTCAE Version 4 NCI 2009, of all clinically significant toxic effects of previous anticancer therapy.

11. The patient, if male, is sterile (including vasectomy confirmed by post-vasectomy semen analysis) or agrees to use a reliable method of birth control and to not donate sperm during the study and for at least 12 weeks following the last dose of study treatment.

12. The patient, if female, is surgically sterile, is postmenopausal, or agrees to use a highly effective method of birth control during the study and for 12 weeks following the last dose of study treatment. A highly effective method of birth control is defined as one that results in a low failure rate when used consistently and correctly.

13. The patient, if female and of child-bearing potential, must have a negative serum or urine pregnancy test within 7 days prior to randomization.

Exclusion Criteria:

14. The patient has cancer with histology other than mesothelioma.

15. The patient is receiving chronic therapy with any of the following within 7 days prior to randomization:

1. nonsteroidal anti-inflammatory agents (NSAIDs; such as indomethacin, ibuprofen, naproxen, or similar agents)

2. other anti-platelet agents (such as clopidogrel, ticlopidine, dipyridamole, or anagrelide) Aspirin use at doses up to 325 mg/day is permitted.

16. The patient received radiotherapy within 14 days prior to randomization. Any lesion requiring palliative radiotherapy or which has been previously irradiated cannot be considered for response assessment.

17. The patient received >1 line of prior therapy for the treatment MPM.

18. The patient received previous treatment with agents targeting the VEGF/VEGF Receptor 2 signaling pathway, including previous exposure to ramucirumab.

19. The patient has documented brain metastases, leptomeningeal disease, or uncontrolled spinal cord compression. Screening of asymptomatic patients is not required.

20. The patient has a significant bleeding disorder or vasculitis or had a Grade 3 bleeding episode within 12 weeks prior to randomization.

21. The patient experienced any arterial thromboembolic event (ATE), including myocardial infarction, unstable angina, cerebrovascular accident, or transient ischemic attack, within 6 months prior to randomization.

22. The patient has symptomatic congestive heart failure (CHF; New York Heart Association II-IV) or symptomatic or poorly controlled cardiac arrhythmia.

23. The patient has uncontrolled hypertension, as defined in CTCAE Version 4.0, prior to initiating study treatment, despite antihypertensive intervention. CTCAE Version 4.0 defines uncontrolled hypertension as Grade >2 hypertension; clinically, the patient continues to experience elevated blood pressure (systolic >160 mmHg and/or diastolic >100 mmHg) despite medications).

24. The patient underwent major surgery within 28 days prior to randomization or central venous access device placement within 7 days prior to randomization. The patient has a serious or nonhealing wound, ulcer or bone fracture within 28 days prior to enrollment.

25. The patient has selective or planned major surgery to be performed during the course of clinical trial.

26. The patient has a history of gastrointestinal (GI) perforation or fistula within 6 months prior to randomization.

27. The patient has a history of inflammatory bowel disease or Crohn's disease requiring medical intervention (immunomodulatory or immunosuppressive medications or surgery) 12 months prior to randomization.

28. The patient has an acute or subacute bowel obstruction or history of chronic diarrhoea that is considered clinically significant in the opinion of the investigator.

29. The patient has either of the following:

1. cirrhosis at a level of Child-Pugh B (or worse)

2. cirrhosis (any degree) and a history of hepatic encephalopathy or clinically meaningful ascites resulting from cirrhosis. Clinically meaningful ascites is defined as ascites resulting from cirrhosis and requiring ongoing treatment with diuretics and/or paracentesis.

30. The patient has known allergy or hypersensitivity to any components of study treatment.

31. The patient received any previous investigational therapy within 4 half -lives of the investigational agent prior to randomization.

32. The patient has a serious illness or medical condition including, but not limited to, the following:

1. known human immunodeficiency virus infection or acquired immunodeficiency syndrome-related illness

2. active or uncontrolled clinically serious infection

33. The patient is pregnant or breast-feeding.

34. The patient has a concurrent active malignancy other than the following:

1. adequately treated not melanomatous skin cancer

2. curatively treated in situ carcinoma of the cervix or other not invasive carcinoma or in situ neoplasm A patient with a history of prior malignancy is eligible if he or she has been disease free for 3 years prior to randomization.

35. The patient has a serious nonhealing: (a) wound, (b) peptic ulcer, or (c) bone fracture, within 28 days prior to randomization.

36. The patient experienced any Grade 3 or 4 venous thromboembolic event (VTE) that is considered by the investigator to be life-threatening or that is symptomatic and not adequately treated by anticoagulation therapy, within 6 months prior to randomization (venous port or catheter thrombosis or superficial venous thrombosis are not considered "significant")

37. The patient has any condition (for example, psychological, geographical, or medical) that does not permit compliance with the study and follow-up procedures or suggests that the patient is, in the investigator's opinion, not an appropriate candidate for the study.

Administrative Information
NCTIDNCT03560973
Responsible PartySponsor
SponsorGruppo Oncologico Italiano di Ricerca Clinica
Verification DateJune 2018
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