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Metronomic Cyclophosphamide in Combination With Standard Chemotherapy for Squamous Cell Lung Carcinoma

Primary Purpose

Lung Cancer, Squamous Cell Carcinoma of the Lung, Locally Advanced and Metastatic Squamous Cell Carcinoma of the Lung

Status
Unknown status
Phase
Phase 3
Locations
India
Study Type
Interventional
Intervention
Intravenous Cisplatin & etoposide
Intravenous Cisplatin & etoposide along with oral cyclophosphamide
Sponsored by
Swami Rama Cancer Hospital and Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Cancer focused on measuring NSCLC, Metronomic chemotherapy, Metronomic cyclophosphamide

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histopathologically proven squamous cell carcinoma of the lung
  • Surgically unresectable or metastatic disease

Exclusion Criteria:

  • Severe life limiting diabetes, hypertension or cardiac co-morbidities
  • Co-existing tuberculosis
  • Brain metastases at presentation
  • Non-consenting patients
  • Previously treated with any regimen of chemotherapy for existing or previous malignancy

Sites / Locations

  • Swami Rama Cancer Hospital & Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard intravenous chemotherapy

Intravenous with metronomic chemotherapy

Arm Description

Patients will receive standard intravenous chemotherapy based on cisplatin and etoposide.

Patients will receive both intravenous (cisplatin and etoposide based) and metronomic chemotherapy (with oral cyclophosphamide).

Outcomes

Primary Outcome Measures

Progression free survival

Secondary Outcome Measures

Response rate

Full Information

First Posted
September 10, 2013
Last Updated
September 17, 2013
Sponsor
Swami Rama Cancer Hospital and Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01947062
Brief Title
Metronomic Cyclophosphamide in Combination With Standard Chemotherapy for Squamous Cell Lung Carcinoma
Official Title
Evaluation of the Benefits of Oral Metronomic Cyclophosphamide in Combination With Standard Cisplatin-etoposide Based Chemotherapy for Squamous Cell Lung Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Unknown status
Study Start Date
October 2013 (undefined)
Primary Completion Date
June 2014 (Anticipated)
Study Completion Date
October 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Swami Rama Cancer Hospital and Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Treatment of locally advanced and metastatic squamous cell carcinoma of the lung involves the use of chemotherapy as the therapeutic mainstay. Platinum-etoposide regimens (such as cisplatin-etoposide) are the most commonly used chemotherapeutic regimen, which is delivered intravenously in the standard three-weekly intervals. Recent interest in oral metronomic chemotherapy has arisen, especially due to its beneficial effects in delaying disease progression among heavily pre-treated patients with various malignancies. This study attempts to combine the use of metronomic chemotherapy concurrently during standard intravenous chemotherapy.
Detailed Description
Adenocarinoma and squamous cell carinoma are the two major types of non-small cell lung carcinoma. While patients with adenocarcinoma of the lung have the feasibility of treatment with tyrosine kinase inhibitors, the patients with squamous cell carcinoma can only be treated with standard chemotherapy due to the ineffectiveness of tyrosine kinase inhibitors. Thus, the current standard is to treat patients of squamous cell lung cancers with standard intravenous chemotherapy, which is mostly delivered once in three weeks. Metronomic chemotherapy, meaning the delivery of low doses of chemotherapy, often by an oral approach, on a daily basis so as to maintain a low but definite level of the chemotherapy has received great interest in recent times due to its beneficial effects in terms of extending progression free survival among patients of various malignancies, even after failure with previous conventional therapies. Metronomic chemotherapy is proposed to be active by alternate mechanisms, such as the predominant anti-angiogenic effect, in contrast to the cytotoxic and genotoxic effects of standard chemotherapy. Metronomic chemotherapy with oral cyclophosphamide has been shown to extend progression free survival when used as a single agent in various malignancies. Given the fact that progression after varying time spans is a rule (rather than the exception) among patients of squamous cell lung cancer being treated with conventional chemotherapy, we have intended to combine the use of oral metronomic chemotherapy given concurrently with standard intravenous cisplatin-etoposide based chemotherapy. We intend to observe a prolongation of progression free survival.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Squamous Cell Carcinoma of the Lung, Locally Advanced and Metastatic Squamous Cell Carcinoma of the Lung
Keywords
NSCLC, Metronomic chemotherapy, Metronomic cyclophosphamide

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard intravenous chemotherapy
Arm Type
Active Comparator
Arm Description
Patients will receive standard intravenous chemotherapy based on cisplatin and etoposide.
Arm Title
Intravenous with metronomic chemotherapy
Arm Type
Experimental
Arm Description
Patients will receive both intravenous (cisplatin and etoposide based) and metronomic chemotherapy (with oral cyclophosphamide).
Intervention Type
Drug
Intervention Name(s)
Intravenous Cisplatin & etoposide
Other Intervention Name(s)
Control arm, Standard intravenous chemotherapy
Intervention Description
Patients will receive standard intravenous cisplatin and etoposide based chemotherapy, for a total of six cycles, delivered at three-weekly intervals. In each cycle, the dose of cisplatin will be at 50mg/m2 on days 1 & 2. The dose of etoposide will be 100mg/m2 on days 1, 2 & 3.
Intervention Type
Drug
Intervention Name(s)
Intravenous Cisplatin & etoposide along with oral cyclophosphamide
Other Intervention Name(s)
Experimental arm, Intravenous with metronomic chemotherapy
Intervention Description
Patients will be treated with oral cyclophosphamide at a daily dose of 50mg. Patients will also receive standard intravenous cisplatin and etoposide based chemotherapy, for a total of six cycles, delivered at three-weekly intervals. In each cycle, the dose of cisplatin will be at 50mg/m2 on days 1 & 2. The dose of etoposide will be 100mg/m2 on days 1, 2 & 3.
Primary Outcome Measure Information:
Title
Progression free survival
Time Frame
12 months on average
Secondary Outcome Measure Information:
Title
Response rate
Time Frame
12 months on average

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histopathologically proven squamous cell carcinoma of the lung Surgically unresectable or metastatic disease Exclusion Criteria: Severe life limiting diabetes, hypertension or cardiac co-morbidities Co-existing tuberculosis Brain metastases at presentation Non-consenting patients Previously treated with any regimen of chemotherapy for existing or previous malignancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Swaroop Revannasiddaiah, MD
Phone
+91
Ext
8971862565
Email
swarooptheone@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Kailash C Pandey, MD
Phone
+91
Ext
9634652758
Email
drkcp89@gmail.com
Facility Information:
Facility Name
Swami Rama Cancer Hospital & Research Institute
City
Haldwani, Nainital
State/Province
Uttarakhand
ZIP/Postal Code
263139
Country
India
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Swaroop Revannasiddaiah, MD
Phone
91
Ext
8971862565
Email
swarooptheone@gmail.com
First Name & Middle Initial & Last Name & Degree
Swaroop Revannasiddaiah, MD
First Name & Middle Initial & Last Name & Degree
Kailash C Pandey, MD
First Name & Middle Initial & Last Name & Degree
Sridhar P Susheela, MD

12. IPD Sharing Statement

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Metronomic Cyclophosphamide in Combination With Standard Chemotherapy for Squamous Cell Lung Carcinoma

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