Intensity-modulated Radiotherapy for Locally Advanced Cervical Cancer (DEPICT)

This study is currently recruiting participants. (see Contacts and Locations)
Verified February 2013 by Queen Mary University of London
Sponsor:
Collaborators:
Barts & The London NHS Trust
Barts Cancer Institute
Information provided by (Responsible Party):
Centre of Experimental Medicine, Queen Mary University of London
ClinicalTrials.gov Identifier:
NCT01793701
First received: February 14, 2013
Last updated: NA
Last verified: February 2013
History: No changes posted
  Purpose

This will be the first study to assess the clinical feasibility of dose escalation with simultaneous integrated boost intensity-modulated radiotherapy for patients with locally advanced cervical cancer. Following screening to confirm eligibility patients will commence a six week treatment period. After this, patients will be followed up by visits to clinic every 3 months for a period of 24 months (2 years). End of study is defined as 24 months after treatment. Patients will be followed up for a minimum of 5 years (as per local policy) after treatment.


Condition Intervention Phase
Locally Advanced Cervical Cancer
Radiation: intensity modulated radiotherapy
Procedure: Intracavitary brachytherapy
Drug: Cisplatin
Phase 1
Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Phase I/II, Multi-centre Dose Escalation Study of Simultaneous Boost Intensity-modulated Radiotherapy for Locally Advanced Cervical Cancer

Resource links provided by NLM:


Further study details as provided by Queen Mary University of London:

Primary Outcome Measures:
  • severe gastrointestinal toxicity assessed according to Common Terminology for Adverse Event Criteria (CTCAE) v 3.0. [ Time Frame: six months of completing radiotherapy ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Objective tumour response rate [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • 2 year local control rate [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 44
Study Start Date: July 2010
Estimated Primary Completion Date: July 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Dose escalation study
This is a dose escalation study of IMRT for women with locally advanced cervical cancer. Three dose levels will be investigated, (although, the first dose level is considered to be the equivalent to a standard pelvic dose with parametrial boost). Before moving to the next dose level it must be confirmed by the Chief Investigator that the Maximum Administrable Dose (MAD) has not been met in the previous dose level (see section 6.3). If MAD is reached before dose level 3 the study will stop. All patients enrolled on the study will undergo the same procedures at the same time points, regardless of the dose level they are being given (see section 5).
Radiation: intensity modulated radiotherapy

Patients in this trial will receive radiotherapy to the pelvic area with additional chemotherapy (chemoradiotherapy).

This is the standard treatment for cervix cancer and will be almost identical to patients not taking part in this study. As patients in the study will be treated with IMRT, the total radiation dose will be slightly higher but without increasing the dose to normal tissue in the pelvis. This will mean the number of radiotherapy treatments that each patient receives in the study is between 27 and 30 compared with the usual 28. Each patient will undergo 6 weeks of radiotherapy treatment and must attend the radiotherapy department hospital once daily (Monday to Friday) over 6 weeks. Each treatment lasts for approximately 10 15 minutes. This is exactly the same as standard practice if patients were not participating in the trial.

Other Name: IMRT
Procedure: Intracavitary brachytherapy
Intracavitary brachytherapy will be given towards the end of external beam radiotherapy usually weeks five and six. This is routine treatment and will be given according to local practice As is the convention patients will be reviewed weekly (more frequently if necessary) by their study doctor and will have weekly blood tests to measure full blood count and urea and electrolytes
Drug: Cisplatin
Each patient will also receive chemotherapy with a drug called cisplatin, which is given intravenously through a drip in the arm once a week during their 6 week radiotherapy treatment. Again this is standard treatment for any patient with cervix cancer.

Detailed Description:
  1. Primary objective

    - To determine the feasibility of dose escalation with simultaneous boost intensity-modulated radiotherapy (IMRT) in locally advanced cervical cancer

  2. Secondary Objectives

    • To assess objective response rates
    • To assess local control
    • To correlate toxicity with dose-volume histogram data
  3. Primary endpoint

    - Grade 3 gastrointestinal toxicity at 6 months as defined by CTCAE v3.0 (Common Terminology for Adverse Events)

  4. Secondary endpoints

    • Response rate assessed radiologically at 3 months and 12 months
    • Local control at 2 years
    • Late toxicity at 2 years as defined by CTCAE v3.0
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Histologically confirmed squamous cell carcinoma, adenocarcinoma or poorly differentiated carcinoma of the cervix
  2. FIGO stage IIB-IVA (any pelvic nodal status) and FIGO stage 1B2 and IIA with pelvic nodal involvement
  3. Measurable disease on MRI
  4. Age > 18 years (no upper limit)
  5. WHO performance status 0,1
  6. Adequate renal function with EDTA clearance> 55ml/min
  7. Adequate liver function, as defined by ALT or AST less than 2.5 x ULN, and bilirubin less than 1.25 x ULN
  8. Adequate bone marrow function, defined by WCC >3.0 x 109/litre, neutrophils > 1.5 x 109/litre and platelets > 100 x 109 /litre
  9. Able to understand and give written informed consent

Exclusion Criteria:

  1. Evidence of common iliac or para-aortic nodal involvement, or distant metastases
  2. Previous history of cancer except skin tumour
  3. Previous pelvic radiotherapy or surgery other than toparoscopic node disection
  4. Previous history of pelvic adhesions, inflammatory bowel disease, pelvic inflammatory disease or diabetes mellitus
  5. Females of childbearing potential must have a negative pregnancy test within 7 days prior to being registered for protocol therapy if required. Acceptable contraception should be used such as barrier or hormonal methods.
  6. Females must not be pregnant or breastfeeding

Other protocol-defined inclusion/exclusion criteria may apply

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01793701

Contacts
Contact: Sofia Fernandes 0044(0)2078828487 depict@qmcr.qmul.ac.uk

Locations
United Kingdom
Barts Health NHS Trust Recruiting
London, United Kingdom
Contact: Sofia Fernandes, MSc    0044(0)2078828487    depict@qmcr.qmul.ac.uk   
Principal Investigator: Dr Melanie Powell         
Royal Marsden Recruiting
London, United Kingdom
Principal Investigator: Dr Susan Lalondrelle         
Hammersmith Hospital Recruiting
London, United Kingdom
Principal Investigator: Dr Steven Mangar         
Sponsors and Collaborators
Queen Mary University of London
Barts & The London NHS Trust
Barts Cancer Institute
Investigators
Principal Investigator: Dr Melanie Powell Barts & The London NHS Trust
  More Information

Additional Information:
No publications provided

Responsible Party: Centre of Experimental Medicine, Dr Melanie Powell, Queen Mary University of London
ClinicalTrials.gov Identifier: NCT01793701     History of Changes
Other Study ID Numbers: 6883, 28435, 09/H0706/90
Study First Received: February 14, 2013
Last Updated: February 14, 2013
Health Authority: United Kingdom: Research Ethics Committee

Keywords provided by Queen Mary University of London:
Cervical Cancer, Intensity-modulated radiotherapy

Additional relevant MeSH terms:
Uterine Cervical Diseases
Uterine Cervical Neoplasms
Uterine Neoplasms
Genital Neoplasms, Female
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Uterine Diseases
Genital Diseases, Female
Cisplatin
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions
Radiation-Sensitizing Agents

ClinicalTrials.gov processed this record on August 20, 2014