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LEE011 in Neuroendocrine Tumors of Foregut Origin

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT02420691
Recruitment Status : Active, not recruiting
First Posted : April 20, 2015
Last Update Posted : January 30, 2019
Information provided by (Responsible Party):
M.D. Anderson Cancer Center

Brief Summary:
The goal of this clinical research study is to learn if LEE011 can help to control advanced neuroendocrine tumors of the foregut. The safety of this drug will also be studied.

Condition or disease Intervention/treatment Phase
Gastrointestinal Cancer Drug: LEE011 Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 21 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase II Study of LEE011 (Ribociclib) in Patients With Advanced Neuroendocrine Tumors of Foregut Origin (CLEE011 XUS02T)
Actual Study Start Date : August 2015
Estimated Primary Completion Date : August 2019
Estimated Study Completion Date : August 2019

Resource links provided by the National Library of Medicine

Drug Information available for: Ribociclib

Arm Intervention/treatment
Experimental: LEE011
Patients treated with LEE011 600 mg by mouth daily 3 weeks on/1 week off in 28 day cycles. Participants allowed to remain on study until disease progression or unacceptable toxicities
Drug: LEE011
600 mg by mouth daily on Days 1 - 21 of a 28 day cycle.

Primary Outcome Measures :
  1. Overall Response of LEE011 in Participants With Foregut Neuroendocrine Tumors (NETs) [ Time Frame: After 3, 21 day cycles ]
    Overall response is best response recorded from the start of treatment until disease progression/recurrence (taking as reference for progressive disease the smallest measurements recorded since the treatment started). Participant's response assignment depends on achievement of both measurement and confirmation criteria. Progressive disease (PD) defined as appearance of one or more new lesions and/or unequivocal progression of existing non-target lesions. Response and progression evaluated using Response Evaluation Criteria in Solid Tumors (RECIST) (per version 1.1).

Secondary Outcome Measures :
  1. Clinic Benefit Rate of LEE011 in Participants With Foregut Neuroendocrine Tumors (NETs) [ Time Frame: 6 months ]
    Clinic benefit rate defined as complete response plus partial response plus stable disease with LEE011 among patients with advanced foregut NETs. Complete Response (CR): Disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. Stable Disease (SD): Neither sufficient shrinkage to qualify for partial response (PR) nor sufficient increase to qualify for progressive disease (PD), taking as reference the smallest sum diameters while on study. Partial Response (PR): At least a 30% decrease in the sum of the diameters of target lesions, taking as reference the baseline sum diameters.

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Histologically or cytologically confirmed low or intermediate grade, unresectable well differentiated foregut neuroendocrine tumors (thymic, bronchopulmonary, gastric, duodenal and pancreatic). Patients with multiple neuroendocrine tumors associated with MEN1 syndrome will be eligible.
  2. Patients must have radiographically measurable disease.
  3. Pancreatic neuroendocrine patients must have had progression after prior therapy. Patients with other foregut neuroendocrine tumors must have had progressive disease over the last 12 months, irrespective of prior therapy. Patients with both functional (who may continue somatostatin analogues as required for control of related symptoms) and non-functional tumors are eligible. In patients who have previously received therapy, the number of prior lines of therapy should not be more than 2 lines of systemic therapy not including somatostatin analogues.
  4. Written informed consent must be obtained prior to any screening procedures.
  5. Age greater than or equal to 18 years.
  6. Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 1.
  7. A sufficient interval must have elapsed between the last dose of prior anti-cancer therapy (including cytotoxic and biological therapies and major surgery) and enrollment, to allow the effects of prior therapy to have abated: a) Cytotoxic or targeted chemotherapy: greater than or equal to the duration of the cycle of the most recent treatment regimen (a minimum of 3 weeks for all regimens, except 6 weeks for nitrosoureas and mitomycin-C). b) Biologic therapy (e.g., antibodies): greater than or equal to 4 weeks.
  8. Patients must have adequate organ function, as defined by the following parameters: a. Bone marrow: Absolute Neutrophil Count (ANC) greater than or equal to 1.5 x 10^9/L; Hemoglobin (Hgb) greater than or equal to 9 g/dL; Platelets greater than or equal to 100 x 10^9/L. b. Hepatic function: Serum total bilirubin less than or equal to 1.5 x upper limit of normal (ULN); Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) and ALT (SGPT) less than or equal to 2.5 x ULN, except in patients with tumor involvement of the liver who must have AST and ALT less than or equal to 5 x ULN.
  9. (continued from above) c. Renal function: Serum creatinine less than or equal to 1.5 x ULN or 24-hour clearance greater than or equal to 50 mL/min; Serum potassium, sodium, magnesium, phosphorus, and total calcium (corrected for serum albumin) must be within clinically relevant limits (e.g., a patient can be enrolled if a lab value may be outside the normal laboratory range but the abnormality is not clinically relevant or can be repleted.)
  10. Negative pregnancy test (serum B-HCG) within 7 days of starting study treatment is required in women of childbearing potential. B-HCG may be secreted by a small percentage of NETs and be a tumor marker. Thus, NET patients with positive B-HCG are eligible if pregnancy can be excluded by vaginal ultrasound or lack of expected doubling of B-HCG.

Exclusion Criteria:

  1. Patient has a known hypersensitivity to LEE011 or any of its excipients.
  2. Patients with known or suspected brain metastases. However, if radiation therapy and/or surgery has been completed and serial evaluation by CT (with contrast enhancement) or MRI over a minimum of 3 months demonstrates the disease to be stable and if the patient remains asymptomatic, then the patient may be enrolled. Such patients must have no need for treatment with steroids or anti-epileptic medications.
  3. Patients with concurrent malignancies or malignancies within 3 years prior to starting study drug (with the exception of tumors common to a single genetic cancer syndrome, i.e. MEN1, MEN2, vHL, TSC etc., or adequately treated, basal cell skin cancer, squamous cell carcinoma, non-melanoma skin cancer or curatively resected cervical cancer).
  4. Patient is not able to swallow oral medication and/or has impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of the study drugs (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection).
  5. Known diagnosis of human immunodeficiency virus (HIV) or hepatitis C (testing is not mandatory).
  6. Patient has any other concurrent severe and/or uncontrolled medical condition that would, in the investigator's judgment, contraindicate patient participation in the clinical study (e.g. chronic pancreatitis, chronic active hepatitis, etc.).
  7. Patient who has received radiotherapy within less than or equal to 4 weeks or limited field radiation for palliation within less than or equal to 2 weeks prior to starting study drug, and who has not recovered to grade 1 or better from related side effects of such therapy (exceptions include alopecia) and/or in whom greater than or equal to 30% of the bone marrow was irradiated.
  8. Patient has had major surgery within 14 days prior to starting study drug or has not recovered from major side effects (tumor biopsy is not considered as major surgery).
  9. Impaired cardiac function or clinically significant cardiac diseases, including any of the following: a) History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty, or stenting) or symptomatic pericarditis less than 12 months prior to screening b) History of documented congestive heart failure (New York Heart Association functional classification III-IV) c) Documented cardiomyopathy d) Patient has a Left Ventricular Ejection Fraction (LVEF) less than 50% as determined by Multiple Gated acquisition (MUGA) scan or echocardiogram (ECHO) at screening e) History of ventricular, supraventricular, nodal arrhythmias, or any other cardiac arrhythmias, long QT Syndrome or conduction abnormality within 12 months prior to starting study drug
  10. (continued from above) f) Congenital long QT syndrome or a family history of QTc prolongation g) On screening, inability to determine the QTcF interval on the ECG (i.e.: unreadable or not interpretable) or QTcF >450 msec (using Fridericia's correction). All as determined by screening ECG (mean of triplicate ECGs)
  11. Systolic blood pressure greater than 160 mmHg or less than 90 mmHg at screening.
  12. Patients who are currently receiving treatment with agents that are known to cause QTc prolongation or inducing Torsades de Pointes in humans and are unable to discontinue or switch to an alternate medication.
  13. Patients who are currently receiving treatment (within 5 days prior to starting study drug) with agents that are known strong inducers or inhibitors of CYP3A4/5, or that have a narrow therapeutic window and are predominantly metabolized through CYP3A4/5.
  14. Patients with concurrent severe and/or uncontrolled concurrent medical conditions that could compromise participation in the study (e.g., uncontrolled diabetes mellitus defined by a glucose greater than 1.5 ULN in spite of adequate medical treatment, clinically significant pulmonary disease, clinically significant neurological disorder, active or uncontrolled infection)
  15. Patient has a history of non-compliance to medical regimen or inability to grant consent.
  16. Pregnant or lactating women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test (greater than 5 mIU/mL).
  17. Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using effective methods of contraception throughout the study and for 8 weeks after study drug discontinuation. Highly effective contraception methods include: Total abstinence when this is in line with the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception; Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment. In case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment.
  18. (continued from above) Male sterilization (at least 6 months prior to screening). For female patients on the study, the vasectomized male partner should be the sole partner for that patient; Combination of any of the two following (a+b or a+c or b+c) a. Use of oral, injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate <1%), for example hormone vaginal ring or transdermal hormone contraception b. Placement of an intrauterine device (IUD) or intrauterine system (IUS) c. Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/ vaginal suppository. In case of use of oral contraception, women should have been stable on the same pill before taking study treatment.Note: Oral contraceptives are allowed but should be used in conjunction with a barrier method of contraception due to unknown effect of drug-drug interaction.
  19. (continued from above) Women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks ago. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child bearing potential.
  20. Sexually active males unless they use a condom during intercourse while taking the drug and for 21 days after stopping treatment and should not father a child in this period. A condom is required to be used also by vasectomized men in order to prevent delivery of the drug via seminal fluid.
  21. Patients unwilling or unable to comply with the protocol.
  22. Patient is currently receiving warfarin or other coumarin-derived anticoagulant for treatment, prophylaxis or otherwise. Therapy with heparin, low molecular weight heparin (LMWH) or fondaparinux is allowed.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT02420691

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United States, Texas
University of Texas MD Anderson Cancer Center
Houston, Texas, United States, 77030
Sponsors and Collaborators
M.D. Anderson Cancer Center
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Principal Investigator: Nageshwara V. Dasari, MBBS M.D. Anderson Cancer Center

Additional Information:
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Responsible Party: M.D. Anderson Cancer Center Identifier: NCT02420691     History of Changes
Other Study ID Numbers: 2014-0371
NCI-2015-01017 ( Other Identifier: NCI CTRP )
First Posted: April 20, 2015    Key Record Dates
Last Update Posted: January 30, 2019
Last Verified: January 2019

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by M.D. Anderson Cancer Center:
Gastrointestinal cancer
Foregut neuroendocrine tumors
Additional relevant MeSH terms:
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Neuroendocrine Tumors
Gastrointestinal Neoplasms
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms, Nerve Tissue
Digestive System Neoplasms
Neoplasms by Site
Digestive System Diseases
Gastrointestinal Diseases