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Oxaliplatin and 5-Fluorouracil With or Without Docetaxel in Elderly Patients (>65 y) With Stomach and Esophagus Cancer

Primary Purpose

Gastric Cancer, Adenocarcinoma of the Esophagogastric Junction

Status
Completed
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
Docetaxel
5-Fluorouracil
Oxaliplatin
folinic acid
Sponsored by
Krankenhaus Nordwest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • metastatic or locally advanced gastric cancer or adenocarcinoma of the esophagogastric junction
  • no prior chemotherapy in metastatic state
  • adequate blood and biochemistry parameters

Exclusion Criteria:

  • hypersensitivity for 5-FU, Leucovorin, Oxaliplatin or Docetaxel
  • KHK, cardiomyopathy or cardiac insufficiency
  • malignancy <5 years ago
  • brain metastases
  • severe internal disease or inadequate blood and biochemistry parameters

Sites / Locations

  • Krankenhaus Nordwest

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

FLOT

FLO

Outcomes

Primary Outcome Measures

response (WHO criteria)

Secondary Outcome Measures

Full Information

First Posted
August 18, 2008
Last Updated
September 18, 2012
Sponsor
Krankenhaus Nordwest
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1. Study Identification

Unique Protocol Identification Number
NCT00737373
Brief Title
Oxaliplatin and 5-Fluorouracil With or Without Docetaxel in Elderly Patients (>65 y) With Stomach and Esophagus Cancer
Official Title
A Multicenter, Randomised Phase II Trial on the Therapy of Advanced Gastric Cancer or Adenocarcinoma of the Esophagogastric Junction in Patients Older Than 65 Years With Specific Regard of Quality of Life and Pharmacogenetic Risk Profile
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
March 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Krankenhaus Nordwest

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In this trial, FLOT will be evaluated as therapy option for elderly patients (>65 years) with advanced gastric cancer in comparison to the well established FLO scheme. The hypothesis is that FLOT is more effective than FLO in elderly patients with acceptable side effects.
Detailed Description
Patients with locally advanced, potentially operable or metastatic gastric cancer or adenocarcinoma of the esophagogastric junction without prior therapy in the palliative setting are treated with: Arm A: FLO Arm B: FLOT max. 12 cycles Evaluation of quality of life by standard forms at baseline and then every 2 months until progress of disease. Pharmacogenetic analyses will be done to evaluate a risk profile for platin-based therapies. 140 patients will be treated (70 per arm) primary endpoint: Response Rate secondary endpoints: Prospective Validation of a pharmacogenetic risk profile for patients with advanced GC under first-line therapy with platin/docetaxel Evaluation of quality of life safety and tolerability progression free survival (PFS), time to treatment failure (TTF), overall survival (OS)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer, Adenocarcinoma of the Esophagogastric Junction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
143 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
FLOT
Arm Title
2
Arm Type
Active Comparator
Arm Description
FLO
Intervention Type
Drug
Intervention Name(s)
Docetaxel
Intervention Description
50mg/m2 qd15
Intervention Type
Drug
Intervention Name(s)
5-Fluorouracil
Intervention Description
2600mg/m2 qd15
Intervention Type
Drug
Intervention Name(s)
Oxaliplatin
Intervention Description
85mg/m2 qd15
Intervention Type
Drug
Intervention Name(s)
folinic acid
Intervention Description
200mg/m2 qd15
Primary Outcome Measure Information:
Title
response (WHO criteria)
Time Frame
staging every 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: metastatic or locally advanced gastric cancer or adenocarcinoma of the esophagogastric junction no prior chemotherapy in metastatic state adequate blood and biochemistry parameters Exclusion Criteria: hypersensitivity for 5-FU, Leucovorin, Oxaliplatin or Docetaxel KHK, cardiomyopathy or cardiac insufficiency malignancy <5 years ago brain metastases severe internal disease or inadequate blood and biochemistry parameters
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Salah Al-Batran, MD
Organizational Affiliation
Krankenhaus Nordwest
Official's Role
Study Chair
Facility Information:
Facility Name
Krankenhaus Nordwest
City
Frankfurt
ZIP/Postal Code
60488
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
18349393
Citation
Al-Batran SE, Hartmann JT, Probst S, Schmalenberg H, Hollerbach S, Hofheinz R, Rethwisch V, Seipelt G, Homann N, Wilhelm G, Schuch G, Stoehlmacher J, Derigs HG, Hegewisch-Becker S, Grossmann J, Pauligk C, Atmaca A, Bokemeyer C, Knuth A, Jager E; Arbeitsgemeinschaft Internistische Onkologie. Phase III trial in metastatic gastroesophageal adenocarcinoma with fluorouracil, leucovorin plus either oxaliplatin or cisplatin: a study of the Arbeitsgemeinschaft Internistische Onkologie. J Clin Oncol. 2008 Mar 20;26(9):1435-42. doi: 10.1200/JCO.2007.13.9378.
Results Reference
background
PubMed Identifier
18669868
Citation
Al-Batran SE, Hartmann JT, Hofheinz R, Homann N, Rethwisch V, Probst S, Stoehlmacher J, Clemens MR, Mahlberg R, Fritz M, Seipelt G, Sievert M, Pauligk C, Atmaca A, Jager E. Biweekly fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT) for patients with metastatic adenocarcinoma of the stomach or esophagogastric junction: a phase II trial of the Arbeitsgemeinschaft Internistische Onkologie. Ann Oncol. 2008 Nov;19(11):1882-7. doi: 10.1093/annonc/mdn403. Epub 2008 Jul 31.
Results Reference
background
PubMed Identifier
14966088
Citation
Al-Batran SE, Atmaca A, Hegewisch-Becker S, Jaeger D, Hahnfeld S, Rummel MJ, Seipelt G, Rost A, Orth J, Knuth A, Jaeger E. Phase II trial of biweekly infusional fluorouracil, folinic acid, and oxaliplatin in patients with advanced gastric cancer. J Clin Oncol. 2004 Feb 15;22(4):658-63. doi: 10.1200/JCO.2004.07.042.
Results Reference
background
PubMed Identifier
23063354
Citation
Al-Batran SE, Pauligk C, Homann N, Hartmann JT, Moehler M, Probst S, Rethwisch V, Stoehlmacher-Williams J, Prasnikar N, Hollerbach S, Bokemeyer C, Mahlberg R, Hofheinz RD, Luley K, Kullmann F, Jager E. The feasibility of triple-drug chemotherapy combination in older adult patients with oesophagogastric cancer: a randomised trial of the Arbeitsgemeinschaft Internistische Onkologie (FLOT65+). Eur J Cancer. 2013 Mar;49(4):835-42. doi: 10.1016/j.ejca.2012.09.025. Epub 2012 Oct 11.
Results Reference
derived

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Oxaliplatin and 5-Fluorouracil With or Without Docetaxel in Elderly Patients (>65 y) With Stomach and Esophagus Cancer

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