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Carcinoma, Non-Small-Cell LungPhase 2SELECT-ANCT01674738

TS Stratified Chemotherapy and VEGF Inhibition in Non-Squamous Non-Small Cell Lung Cancer - Stage IV

A Phase 2 study testing Pemetrexed, Cisplatin and Bevacizumab in people with Carcinoma, Non-Small-Cell Lung, run by Aktion Bronchialkarzinom e.V..

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This study wants to determine the activity of a first-line treatment related to Thymidylate Synthetase (TS) Expression. Patients with the diagnosis of non-squamous advanced Non-Small-Cell Lung-Cancer (Stage IV) and without evidence of EGFR mutation may be enclosed in this clinical trial. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Carcinoma, Non-Small-Cell Lung
What is being tested?
Pemetrexed, Cisplatin and Bevacizumab
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
No sites listed yet
Study dates
Start not givento not given
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Histological confirmed Non-Small-Cell lung cancer
  • Tumor stage IV (UICC 7th Version)
  • The following histological tumor types are eligible:
  • Adenocarcinoma (including adenocarcinomas with bronchioloalveolar differentiation)
  • Large Cell carcinoma without neuroendocrine differentiation
  • Mixed Cell Carcinoma without small cell fraction and without predominant squamous cell fraction
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  • undifferentiated non-small-cell-carcinoma
  • No previous chemotherapy for stage IV NSCLC
  • Adjuvant or neoadjuvant chemotherapy for NSCLC must be completed at least one year prior to study enrolment (from end of chemotherapy)
  • No previous treatment with Pemetrexed or Bevacizumab
  • Patients with prior radiation therapy may be eligible for this study if they meet the following guidelines:
  • Previous radiation therapy is allowed to <25% of the bone marrow (Cristy and Eckerman 1987), but should have been limited and must not have included whole pelvis radiation.
  • Patients must have recovered from the toxic effects of the treatment prior to study enrollment (except for alopecia).
  • Prior thoracic radiotherapy must be completed 30 days before study enrollment.
  • Lesions that have been radiated cannot be included as sites of measurable disease unless clear tumor progression has been documented in these lesions since the end of radiation therapy.
  • Palliative extrathoracic radiotherapy to preexisting lesions may continue on study; however, these lesions may not be included as sites of measurable disease.
  • At least 4 weeks since last major surgery
  • Age ≥ 18 and ≤ 70 years
  • ECOG ≤ 1
  • Adequate hematological laboratory parameters:
  • Hemoglobin ≥9 g/dl
  • Neutrophils ≥ 1.500 µl
  • WBC ≥3.000 µl
  • Platelets ≥100.000 µl
  • Adequate hepatic laboratory parameters:
  • Total Bilirubin ≤ 1,5 x ULN
  • Alkaline phosphatase ≤ 3 x ULN
  • AST(GOT) < 2,5 ULN in patients without liver metastasis < 5 x ULN in patients with liver metastasis ULN = (upper limit of normal)
  • ALT(GPT) < 2,5 ULN in patients without liver metastasis < 5 x ULN in patients with liver metastasis ULN = (upper limit of normal)
  • Adequate renal laboratory parameters:
  • Creatinine Clearance > 50 ml/min
  • Urine dipstick for proteinuria < 2+ Patients discovered to have ≥ 2+ proteinuria on dipstick urinalysis at baseline should undergo a 24-hour urine collection and must demonstrate <1 g of protein in 24 hours
  • Normal cardiac function defined by New York Heart Association - NYHA Class I and Class II
  • Electrocardiogram without significant signs of cardiac arrhythmias
  • Provision of informed consent according to local regulatory requirements prior to any protocol specific treatment.
  • Measurable lesion according to RECIST 1.1
  • Negative pregnancy test for women of childbearing potential unless they are postmenopausal at baseline. (Postmenopausal women must have been amenorrheic at least for 12 months to be considered of non childbearing potential)
  • Women of child bearing potential to be willing to use an acceptable method to avoid pregnancy at least one month before study start. Examples: oral contraceptives (sole application of oral contraceptives is not sufficient), diaphragm pessary, intrauterine device (spiral), condom plus diaphragm pessary plus spermicide.

Who cannot join

  • Histological confirmed predominant squamous cell carcinoma
  • Presence of activating EGFR mutations in exons 18-21
  • Pregnancy or lactation period
  • Have known central nervous system (CNS) disease, other than stable, treated brain metastasis. Stable, treated brain metastasis is defined as metastasis having no evidence of progression or hemorrhage after treatment and no ongoing requirement for dexamethasone, as ascertained by clinical examination and post-treatment brain imaging (CT scan or magnetic resonance imaging [MRI]). Patients should be off corticosteroids for 1 week (7 days) at the time of the post-treatment brain CT/MRI. Anticonvulsants (stable dose) are allowed. Treatment for brain metastases may include whole brain radiotherapy, (stereotactic) radiosurgery (Gamma Knife, linear particle accelerator, or equivalent), or a combination as deemed appropriate by the treating physician, and must have been completed > 8 days prior to Day 1 of Cycle 1. Patients with signs of a fresh bleeding into one or more cerebral metastases or with CNS metastases treated by neurosurgical resection or brain biopsy performed within 8 weeks prior to Day 1 of Cycle 1 will be excluded.
  • Evidence of tumor invading or abutting major blood vessels
  • Presence of a tracheobronchial fistula
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  • History of abdominal fistula or fistulisation of urogenital tract, gastrointestinal perforation or intra-abdominal abscess, inflammatory bowel disease, or diverticulitis within 6 months prior to study start
  • Other co-existing malignancies or malignancies diagnosed within the last 5 years with the exception of a CIS of the cervix, non-melanomatous skin cancer, stable chronic lymphatic leukaemia, non-muscle invasive bladder cancer or surgically treated or irradiated prostate cancer with no signs of recurrence for one year. Patients with other malignancies curatively treated and free of disease for at least 5 years will be discussed with the Principal Investigator (LKP) before inclusion.
  • Treatment with an investigational new drug, currently or within the last 28 days, and/or participation in another clinical trial, currently or during the last 12 weeks, and/or previous participation in this study.
  • History or presence of a mental disease or condition such as to interfere with the patient's ability to understand the requirements of the study and the intake of study medication according to study protocol.
  • Patients with any clinically significant disease that in the opinion of the investigator is likely to put the patient at risk or to interfere with the evaluation of the patient's safety and of the study outcome. This includes, but is not limited to:
  • Immediate need for therapeutic intervention (e.g.: upper inflow congestion or poststenotic pneumonia).
  • Clinically significant cardiac disease (e.g. right-sided heart failure, symptomatic coronary artery disease and cardiac arrhythmias not well controlled with medication) or myocardial infarction within the last 6 months.
  • Have a history of hypertension, unless hypertension is well controlled upon study entry (<150/90 mm Hg) and the patient is on a stable regimen of antihypertensive therapy. Patients should not have any prior history of hypertensive crisis or hypertensive encephalopathy.
  • Non healing wound, ulcer or bone fracture
  • Fresh thrombosis (within the last two weeks) under full dose therapy with anticoagulants.
  • History of thrombotic disorders within the last 6 months prior to entry.
  • Current or recent (within 10 days of first dose of study medication) full-dose oral or parenteral anticoagulants, or thrombolytic agents for therapeutic purposes.
  • Prophylactic use of anticoagulants is allowed; international normalized ratio (INR) should be <1.5 at study enrollment.
  • Current or recent (within 10 days of first dose of study medication) use of ASS - Dosage > 325 mg/day
  • Current or recent (within 10 days of first dose of study medication) use of Plavix/Clopidogrel, at doses >75 mg/d, dipyramidole, ticlopidine, cilostazol,
  • Hemorrhagic diathesis, Hemophilia A, Hemophilia B
  • Implantation of a central vein catheter (Implanted port catheter) within 24 h prior to application of study medication
  • Have a history of gross hemoptysis (bright red blood of ½ teaspoon per episode of coughing) <3 months prior to enrollment or history or evidence of inherited bleeding diathesis or coagulopathy with the risk of bleeding.
  • Peritoneal carcinomatosis.
  • Pleural effusion with the need of therapeutic pleurodesis
  • Ascites with the need of intervention
  • Any other uncontrolled infection
  • Organ allograft
  • Hardness of hearing that interferes with daily life
  • Sensory Neuropathy > grade I (CTCAE Version 4.0 )
  • Alcohol and drug abuse
  • Known hypersensitivity to any of the study drugs
  • Have a history of a serious reaction to a monoclonal antibody. Patients with known hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies are not eligible.
  • Have received a recent (within 30 days of enrollment) or are receiving concurrent yellow fever vaccination
  • Have had major surgery, open biopsy, or significant traumatic injury within 28 days prior to study enrollment, or anticipate the need for major surgical procedure during the course of the study.
  • Patients with creatinine clearance 45-79 ml/min must be able to interrupt NSAIDs 2 days before (5 days for long-acting NSAIDs ), the day of, and 2 days following administration of pemetrexed.
  • Are unable or unwilling to take folic acid, vitamin B12 supplementation, or corticosteroids.

About this study

This study wants to determine the activity of a first-line treatment related to Thymidylate Synthetase (TS) Expression. Patients with the diagnosis of non-squamous advanced Non-Small-Cell Lung-Cancer (Stage IV) and without evidence of EGFR mutation may be enclosed in this clinical trial.

Read the detailed description

During the screening procedure tumour specimens obtained by primary biopsy, will be analysed for EGFRmut and immunohistochemically for thymidylate synthetase (TS) expression. Employing the H-Score with a cut-off of 150, EGFR-wt patients will be stratified into a TS low (Stratum A) and TS high (Stratum B) group. This procedure is aiming to provide two equally sized strata.

After stratification according to the TS expression level patients will be treated with a combination of Pemetrexed, Cisplatin and Bevacizumab.

Pemetrexed/Cisplatin/Bevacizumab will be administered for a maximum of 4 cycles. Patients with a complete response (CR), partial response (PR) or stable disease (SD) will continue on maintenance therapy of Pemetrexed and Bevacizumab until disease progression or unacceptable toxicity.

  • Duration of treatment/patient: up to 1,5 years
  • Follow Up: at least 6 month
  • Planned number of patients: 146 treated patients
Keywords
Non Small Cell Lung Cancer, NSCLC Stage IV, Non-Squamous Advanced Non-Small-Cell Lung-Cancer (Stage IV)
Medical subject headings
Carcinoma, Non-Small-Cell Lung

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PemetrexedDrug

    500 mg/m2 i.v. on day 1 (three-week cycle)

  • CisplatinDrug

    75 mg/m2 i.v. on day 1 (three-week cycle)

  • BevacizumabDrug

    7,5 mg/kg i.v. on day 1 (three-week cycle)

Study groups in NCT01674738
Study groupRoleWhat they receive
Pemetrexed, Cisplatin, BevacizumabExperimentalStratum A
Receives: Drug: Pemetrexed; Drug: Cisplatin; Drug: Bevacizumab
Pemetrexed, Cisplatin, BevazizumabExperimentalStratum B:
Receives: Drug: Pemetrexed; Drug: Cisplatin; Drug: Bevacizumab

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Progression free survival

    Measured: Recruitment period 1,5 years, observation period 2 years

Secondary outcomes (4)

  1. Overall survival

    Measured: Recruitment period 1,5 years, observation period 2 years

  2. Quality of life

    Measured: Screening, day 1, end of cycle 1, end of treatment (for each patient)

  3. Response rate

    Measured: Screening, prior to cycle 3, end of cycle 4, evry 6 weeks after end of cycle 4, end of treatment (for each patient)

  4. Molecular investigations

    Measured: Day 1, prior to cycle 3, end of cycle 4, end of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Aug 2012 (estimated)

Why it stopped: Decision of the Sponsor, as the funding of the study was no longer guaranteed.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01674738
Sponsor's protocol ID
ABC-2011-NSCLC-03
Other IDs
2011-002145-35
Acronym
SELECT-A
Status last verified
Oct 2013
First submitted
23 Aug 2012
Last updated
11 Oct 2013
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Pemetrexed, Cisplatin and Bevacizumab in people with Carcinoma, Non-Small-Cell Lung, run by Aktion Bronchialkarzinom e.V..

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 38 inclusion and 38 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 11 Oct 2013. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Progression free survival (time frame: Recruitment period 1,5 years, observation period 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01674738.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Oct 2013.

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