Chloroquine as an Anti-Autophagy Drug in Stage IV Small Cell Lung Cancer (SCLC) Patients

Small Cell Lung Cancer Clinical Trial

— Chloroquine IV  

Official title:

Chloroquine as an Anti-autophagy Drug in Stage IV Small Cell Lung Cancer (SCLC) Patients: A Phase 1 Trial

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00969306
• Other study ID #: Chloroquine IV
• Status: Terminated
• Phase: Phase 1
• Start date: September 2013
• Est. completion date: June 2016

Study information

• Verified date: February 2019
• Source: Maastricht Radiation Oncology
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chloroquine might very well be able to increase overall survival in small cell lung cancer by sensitizing cells resistant to chemotherapy and radiotherapy.

Description:

Tumor hypoxia is a well-known factor negatively influencing outcome in many solid tumors, including small cell lung cancer. Hypoxic cells are more radio-resistant, more chemo-resistant and more prone to develop distant metastases than normoxic cells.

One of the mechanisms responsible for survival of these therapy-resistant hypoxic cells is (macro-)autophagy: a phenomenon in which cells provide themselves with energy (ATP) by digesting their own cell-organelles. Chloroquine is a potent blocker of autophagy and has been demonstrated in a lab setting to dramatically enhance tumor response to radiotherapy, chemotherapy and even anti-hormonal therapy.

Thus, chloroquine might very well be able to increase overall survival in small cell lung cancer by sensitizing cells resistant to chemotherapy and radiotherapy.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 5
• Est. completion date: June 2016
• Est. primary completion date: June 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

• Histologically or cytologically confirmed ``extensive disease`` (Stage T0-4 N0-3 M1) small cell lung cancer

• At least one measurable disease site, defined as lesion of = 1 cm unidimensionally on CT-scan.

• WHO performance status 0-2

• Absolute neutrophil count at least 1800/µl and platelets at least 100000/µl and hemoglobin at least 6.2 mmol/l.

• Calculated creatinine clearance at least 60 ml/min

• Adequate hepatic function: Total bilirubin = 1.5 x upper limit of normal (ULN) for the institution; ALT, AST, and alkaline phosphatase = 2.5 x ULN for the institution (in case of liver metastases = 5 x ULN for the institution)

• No previous platinum chemotherapy or topo-isomerase-inhibitors for SCLC.

• Life expectancy more than 6 months

• Willing and able to comply with the study prescriptions

• 18 years or older

• Not pregnant or breast feeding and willing to take adequate contraceptive measures during the study

• Ability to give and having given written informed consent before patient registration

• No mixed pathology, e.g. non-small cell plus small cell cancer

• No recent (< 3 months) severe cardiac disease (NYHA class >1) (congestive heart failure, infarction)

• No history of cardiac arrythmia (multifocal premature ventricular contractions, uncontrolled atrial fibrillation, bigeminy, trigeminy, ventricular tachycardia) which is symptomatic and requiring treatment (CTC AE 4.0), or asymptomatic sustained ventricular tachycardia. Asymptomatic atrial fibrillation controlled on medication is allowed.

• No cardiac conduction disturbances or medication potentially causing them:

• QTc interval prolongation with other medications that required discontinuation of the treatment

• Congenital long QT-syndrome or unexplained sudden death of first degree relative under 40 years of age

• QTc interval > 480 msec (note: when this is the case on screening ECG, the ECG may be repeated twice. If the average QT-interval of these 3 measurements remains below 480 msec, patient is eligible)

• Patients on medication potentially prolongating the QT-interval are excluded if the QT-interval is > 460 msec (Appendix, table 2).

• Medication that might cause QT-prolongation or Torsades de pointes tachycardia is not allowed (Appendix, Table 1). Drugs with a risk of prolongating the QT-interval that cannot be discontinued are allowed, however, under close monitoring by the treating physician (Appendix, table 2).

• No uncontrolled infectious disease

• No other active malignancy

• No major surgery (excluding diagnostic procedures like e.g., mediastinoscopy) in previous 4 weeks

• No treatment with investigational drugs in 4 weeks prior to or during this study

• No chronic systemic immune therapy

• No known G6PD deficiency

Exclusion Criteria:

• The opposite of the above

Related Conditions & MeSH terms

• Lung Neoplasms
• Small Cell Lung Cancer
• Small Cell Lung Carcinoma

Intervention

Drug:
• Chloroquine, A-CQ 100
Administration: Orally Timing: Once daily Tablets of 100 mg During or after meals In case of missed dose: intake of the missed dose is still possible up until 12 hours before the next dose. Patients should always note date and time of intake on the chloroquine monitoring form.

Locations

Country	Name	City	State
Netherlands	NKI/AvL	Amsterdam
Netherlands	VU Medical Center	Amsterdam
Netherlands	Maastricht Radiation Oncology	Maastricht
Netherlands	Maastricht University Medical Center	Maastricht

Sponsors (3)

Lead Sponsor	Collaborator
Maastricht Radiation Oncology	Maastricht University Medical Center, National Cancer Institute (NCI)

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To determine the toxicity of adding chloroquine in escalating doses in SCLC patients: to standard dose cisplatin-etoposide in extensive disease SCLC; to standard dose concurrent radiotherapy and cisplatin-etoposide in limited disease SCLC		6 years
Secondary	Tumor response (according to RECIST)		6 years
Secondary	Overall survival		6 years