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CompletedNCT00759824Updated Feb 12, 2015

A Phase II Study of Doxorubicin, Cyclophosphamide and Vindesine With Valproic Acid in Patients With Refractory or Relapsing Small Cell Lung Cancer After Platinum Derivatives and Etoposide

A Phase 2 interventional study of Adriamycin, cyclophosphamide, vindesine, valproic acid in Small Cell Lung Carcinoma, sponsored by European Lung Cancer Working Party. Completed at 5 sites in Belgium. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-02-12.

Sponsored by European Lung Cancer Working Party · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
64
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
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Study summary

The primary aim of this study is to determine if the addition of valproic acid to a combination of adriamycin, cyclophosphamide and vindesine could increase progression-free survival in patients relapsing after first-line chemotherapy including platinum derivatives, cisplatin or carboplatin, and etoposide.

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Conditions studied

  • Small Cell Lung Carcinoma

Keywords

  • Small cell lung carcinoma
  • Valproic acid
  • Adriamycin
  • Cyclophosphamide
  • Vindesine
  • Second-line chemotherapy
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In context

Small Cell Lung Carcinoma

1,203 studies on the registry are indexed under Small Cell Lung Carcinoma; 342 are open to participants now.

This study's enrollment of 64 is above the median of 56 across 1,031 interventional studies indexed under Small Cell Lung Carcinoma.

Browse Small Cell Lung Carcinoma studies →

Lead sponsor

European Lung Cancer Working Party is the lead sponsor of 12 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Histological or cytological diagnosis of small-cell lung cancer (SCLC)
  • SCLC refractory to prior chemotherapy regimen including platinum derivatives (cisplatin or carboplatin) and etoposide, either primary refractory (immediate progression or recurrence less than 3 months after the end of previous chemotherapy) or secondary refractory (sensitive patients to platinum plus etoposide in first-line, progressing or recurring less than 3 months after reintroduction of the same chemotherapy).
  • At least one evaluable or measurable lesion
  • Availability for participating in the detailed follow-up of the protocol
  • Signed informed consent.

Exclusion criteria

Exclusion Criteria:

  • Patient who were previously treated with anthracyclin or vinca-alcaloid derivatives or cyclophosphamide
  • Performance status \< 60 on the Karnofsky scale
  • A history of prior malignant tumour, except non-melanoma skin cancer or in situ carcinoma of the cervix or of the bladder or cured malignant tumour (more than 5-year disease free interval)
  • A history of prior HIV infection
  • Polynuclear cells \< 2,000/mm³
  • Platelet cells \< 100,000/mm³
  • Abnormal coagulation tests (aPTT, PTT, prothrombin time) and/or decreased fibrinogen
  • Serum bilirubin >1.5 mg/100 ml
  • Transaminases more than twice the normal range
  • Serum creatinine > 1.5 mg/100 ml
  • Recent myocardial infarction (less than 3 months prior to date of diagnosis)
  • Congestive cardiac failure (ejection fraction of the left ventricle \< 50%) or uncontrolled cardiac arrhythmia
  • Uncontrolled infectious disease
  • Active epilepsy needing a specific treatment
  • Concomitant treatment with IMAO, carbamazepine, mefloquine, phenobarbital, primidone, phenytoïn, lamotrigine, zidovudine
  • Pregnancy or refusal to use active contraception
  • A known allergy to valproic acid and/or doxorubicin, cyclophosphamide, vindesine
  • Serious medical or psychological factors which may prevent adherence to the treatment schedule.
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Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
64 participants (actual)

Study arms

  • Experimental
    1

    Chemotherapy regimen (adriamycin, cyclophosphamide, vindesine) plus valproic acid

    Drug: Adriamycin, cyclophosphamide, vindesine, valproic acid

Interventions

  • DrugAdriamycin, cyclophosphamide, vindesine, valproic acid

    Adriamycin 45 mg/m² day 1 IV Cyclophosphamide 1 g/m² day 1 IV Vindesine 3 mg/m² day 1 IV Valproic acid 20-30 mg/kg/day from day -7 until the end of treatment, orally

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What researchers measure

Primary outcomes

  1. Six-months progression-free survival

    Time frame: The period between the day of registration and the date of first progression

Secondary outcomes

  1. Survival

    Time frame: Survival will be dated from the date of registration

  2. Response rate

    Time frame: Every three cycles of chemotherapy

  3. Toxicity

    Time frame: After each course of chemotherapy and at the end of treatment

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Study locations

5 sites
  • Department of Intensive Care Unit and Thoracic Oncology Institut Jules Bordet
    Brussels, 1000, Belgium
  • Department of Pneumology CHU Charleroi
    Charleroi, 6000, Belgium
  • Department of Pneumology Hôpital Saint-Joseph
    Gilly, 6060, Belgium
  • Hôpital Ambroise Paré
    Mons, 7000, Belgium
  • Department of Pneumology Centre Hospitalier de Mouscron
    Mouscron, 7700, Belgium
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 12, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00759824
Lead sponsor
European Lung Cancer Working Party
Responsible party
Sponsor
First posted
Sep 25, 2008
Start date
Sep 2008
Primary completion
Dec 2013
Completion
Jun 2014
Last update
Feb 12, 2015

Study contacts

Thierry Berghmans, MD
study chair · European Lung Cancer Working Party

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2015. You cannot join it, but the record below documents what was studied.

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