Dose Escalation of Cisplatin Hyperthermic Intraperitoneal Chemotherapy After Surgery in Patients With Unresectable Stage IIIC Ovarian, Tube or Peritoneal Primary Adenocarcinoma

Primary Peritoneal Carcinoma Clinical Trial

— CHIPASTIN  

Official title:

Phase I Study of Cisplatin Hyperthermic Intraperitoneal Chemotherapy Dose Escalation After Surgery in Patients With Unresectable Stage IIIC Ovarian, Tube or Peritoneal Primary Adenocarcinoma Previously Treated by Chemotherapy and Completed by Bevacizumab for 15 Months

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02217956
• Other study ID #: 2010-024361-51
• Secondary ID: 2010/1699
• Status: Completed
• Phase: Phase 1
• First received: August 14, 2014
• Last updated: January 25, 2016
• Start date: June 2011
• Est. completion date: June 2015

Study information

• Verified date: January 2016
• Source: Gustave Roussy, Cancer Campus, Grand Paris
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Agence Nationale de Sécurité du Médicament et des produits de santé
• Study type: Interventional

Clinical Trial Summary

HCIP has shown efficacy in treatment of peritoneal carcinosis from colorectal background. Few studies have been published on the use of HCIP in peritoneal carcinosis from ovarian background but most of them were non-randomized phase II studies on a small population using different type of drugs and dosage. before this heterogeneity it seems necessary to standardize the utilization modalities of HCIP in peritoneal carcinosis from ovarian background

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: June 2015
• Est. primary completion date: June 2015
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Stage IIIC unresectable ovarian, tubes or peritoneal primitive adenocarcinoma according to FIGO classification previously treated with 6 cycles of carboplatin-cisplatin neoadjuvant chemotherapy with a response allowing complete surgery after the 6 cycles

2. Time frame between the sixth platin injection and the CRS + HCIP < 10 weeks

3. No disease progression during the neoadjuvant chemotherapy

4. 18 </= âge </= 65 ans

5. Performance Status OMS < 2

6. Hematological function : PNN >/= 1.5x10^9/L, platelets >/= 150x10^9/L, hemoglobin > 9 g /dl (transfusion allowed)

7. Hepatic function : Bilirubin </= 1,5 x LSN, ASAT (SGOT) and ALAT (SGPT) </= 3 x LSN, Phosphatases alkaline </= 3 x LSN

8. No kidney related pathology, plasmatic creatinine < 140 µmol/l, creatinine clearance > 60 ml/min (Cockcroft formula) and urinary strip <2 (If urinary strip >/= 2, proteinuria < 1g/24h)

9. Plasmatic albumine > 25 g/l

10. HIV negative status

11. Affiliation to social security

12. Signed informed consent

Exclusion Criteria:

1. Incomplete cell kill surgery

2. Non-epithelial ovarian cancer

3. Borderline tumors

4. Non in complete remission previous cancer for more than 5 five years before inclusion

5. Uncontrolled high blood pressure (blood pressure > 150/100 mm Hg despite antihypertensive treatment)

6. Previous abdominal or pelvic radiotherapy

7. Previous pathology of the central nervous system, except for well controlled pathology like epilepsy

8. Previous stroke, transient ischemic attacks or subarachnoid hemorrhage

9. Previous pulmonary embolism

10. Pregnant or breastfeeding women (Women in age must have a blood negative pregnancy test at least 15 days before going under surgery)

11. Participation to an other clinical trial within 30 days before inclusion in the study

12. Known hypersensitivity to platin or bevacizumab

13. Not healed wound, ulcer or bone fracture

14. Previous haemorrhagic or thrombotic malfunction < 6 months

15. Significant CArdiovascular disorder including:

• Heart attack or unstable angina within the 6 months before inclusion

• Grade > 1 congestive heart failure according to the NYHA classification

• Uncontrolled cardiac arrhythmia despite of treatment (patients with atrial fibrillation for which the pace is under control can be include)

16. Long term or recent (within 10 days before inclusion) medication using Aspirin at dosage > 325 mg/day

17. Long term or recent (within 10 days before inclusion) medication using anticoagulant per os or parenteral or thrombolytic given at full dosage for therapeutic purpose.

18. Grade > 1 previous sensory and motor neuropathies according to CTC AE V4.0

19. Previous abdominal fistula, GI perforation or intra-abdominal abscess within 6 months before first administration of bevacizumab

20. Proof of any other disease, metabolic malfunction, physical or laboratory exam showing any possibility of disease or condition contraindicating administration of the drug under trial or exsposing the patient to several complications related to the treatment.

21. Persons deprived of liberty

22. Impossibility to comply with the medical following of the treatment for geographical, social or mental reason

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Adenocarcinoma
• Fallopian Tube Adenocarcinoma
• Neoplasms, Glandular and Epithelial
• Ovarian Adenocarcinoma
• Ovarian Neoplasms
• Primary Peritoneal Carcinoma

Intervention

Drug:
• Cisplatin

• Bevacizumab

Locations

Country	Name	City	State
France	Gustave Roussy	Villejuif	Val de Marne

Sponsors (1)

Lead Sponsor	Collaborator
Gustave Roussy, Cancer Campus, Grand Paris

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Toxicity	Using NCI CTCV4	Assessed at week 4 and 8 after HCIP then every 3 weeks up to 15 months	Yes
Secondary	Progression Free Survival		Assessed every 3 weeks from HCIP until progression up to 30 months	No