Oligometastases of the LIVer Treated With Chemotherapy With ou Without Extracranial Stereotactic Body Radiation Therapy in Patients With Colorectal Cancer

NCT ID: NCT03532204

Last Updated: 2019-05-22

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-04-15
• Study Completion Date: 2023-08-15

Brief Summary

The role of radiotherapy in metastatic cancer has historically been limited to palliation while metastasectomy or radiofrequency has emerged as playing a major role in disease control. Although resection is the standard of care for liver metastasis, 80-90% of patients are not resectable at diagnosis in particular because of the presence of oligometastases. Factors that favour a truly oligometastatic state include a long latent interval between the treatment of the primary tumor and the appearance of metastases.

Oligometastatic cancer is a very heterogeneous disease with respect to several factors including the location of the primary tumor. With the advent of extracranial stereotactic body radiation therapy (SBRT), higher biological equivalent doses can be safely delivered in 3 to 5 fractions, thus potentially ablating all the tissue in the treated area while protecting more efficiently the hosting organ and healthy tissues surrounding the tumors.

In patients with liver oligometastases, in-field local control rates at 2 years range from 70% to 90% with less than 5% severe grade 3 or higher toxicity rates. Retrospective studies indicate that roughly 20% of the patients remain disease-free 2 to 4 years after SBRT.

For patients treated with SBRT some authors found that half of the patients had either no metastatic progression or very little progression in terms of number and site of metastases. The patterns of failure after SBRT for oligometastases in one organ showed that 73% of patients eventually developed new metastases with higher than 80% occurring as new metastases in the same index organ. These findings support the idea of an oligometastatic state in which aggressive local therapy could improve progression-free survival (PFS).

With this phase III study, we sought to evaluate the impact of SBRT on PFS at 2 years in patients with synchronous or metachronous liver-only oligometastases from colorectal cancers patients after a first line chemotherapy for metastatic disease but not having progressed during first line chemotherapy and up to 1 year

Conditions

Liver Metastases; Colorectal Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Chemotherapy + SBRT

Patients will received 2 courses of chemotherapy before SBRT if no hepatic or extra-hepatic progression identified.

All liver metastases will be irradiated. 4 doses prescription are allowed (according to the center, and the technique uded and the dosimetric constraints): 3x15 Gy, 4 x 15 Gy, 5 x10 Gy or 5 x 8 Gy.

The remaining courses of chemotherapy 2 to 3 weeks after completion of SBRT will be administered

Group Type: EXPERIMENTAL

SBRT

Intervention Type: RADIATION

Patients will received 2 courses of chemotherapy before SBRT if no hepatic or extra-hepatic progression identified.

All liver metastases will be irradiated. 4 doses prescription are allowed (according to the center, and the technique uded and the dosimetric constraints): 3x15 Gy, 4 x 15 Gy, 5 x10 Gy or 5 x 8 Gy.

The remaining courses of chemotherapy 2 to 3 weeks after completion of SBRT will be administered

Chemotherapy

Intervention Type: DRUG

At investigator's discretion

Chemotherapy

Patients will receive chemotherapy as initially scheduled

Group Type: ACTIVE_COMPARATOR

Chemotherapy

Intervention Type: DRUG

At investigator's discretion

Interventions

SBRT

Patients will received 2 courses of chemotherapy before SBRT if no hepatic or extra-hepatic progression identified.

All liver metastases will be irradiated. 4 doses prescription are allowed (according to the center, and the technique uded and the dosimetric constraints): 3x15 Gy, 4 x 15 Gy, 5 x10 Gy or 5 x 8 Gy.

The remaining courses of chemotherapy 2 to 3 weeks after completion of SBRT will be administered

Intervention Type: RADIATION

Chemotherapy

At investigator's discretion

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male or female with age ≥18 years and <85 years;

2. Patient with histologically proven colorectal cancer;

3. Patient with a curative surgical treatment (R0) of the primary tumor performed;

4. Oligometastatic disease defined as 1 to 3 liver-only metastases (measurable lesion as per RECIST 1.1);

5. Patient unfit for surgery or with unresectable metastases;

6. Maximal diameter of largest metastasis: 30 mm;

7. Patient naïve of chemotherapy in the metastatic setting or after a first-line of chemotherapy for metastatic disease but not having progressed up to 1 year (i.e. slowly progressing disease);

8. WHO status 0-1;

9. Adequate liver function: bilirubin <3 mg/dL, albumin >2.5 g/dL;

10. Adequate hematological function: absolute neutrophil count (ANC) >1.5 x 10⁹/L; platelets >100 x 10⁹/L, hemoglobin (Hb) >9 g/dL;

11. Normal PT (>70%) and PTT except if the patient uses anticoagulants;

12. Liver enzymes <3 times upper limit of normal;

13. Renal function must be adequate for infusion of iv. contrast agent for CT-scan according to the local policy;

14. Woman of childbearing potential and male patients must agree to use adequate contraception for the duration of study and up to 3 months following completion of therapy;

15. Patient who have received the information sheet, dated and signed the informed consent form;

16. Affiliated to the social security system.

Exclusion Criteria

1. Healthy liver volume<700 mL

2. Life expectancy <3 months;

3. Patient fit for metastasectomy or hepatectomy;

4. Extrahepatic metastases;

5. Cirrhosis with Child Pugh score B or C;

6. More than one line of chemotherapy in the metastatic setting or rapidly progressing disease;

7. Previous local treatment of liver metastases;

8. Treatment with any other investigational agent against cancer;

9. Malignancies other than mCRC within 5 years prior to randomization, except for adequately treated carcinoma in situ of the cervix, basal or squamous cell skin cancer, localized prostate cancer treated surgically with curative intent, and ductal carcinoma in situ treated surgically with curative intent;

10. Pregnant woman or breast feeding mother;

11. Patient deprived of liberty or placed under the authority of a tutor. Patient with any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial. Patient unable to understand the purpose of the study (language, etc.).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

UNICANCER

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stéphanie SERVAGI, MD

Role: PRINCIPAL_INVESTIGATOR

INSTITUT JEAN GODINOT, REIMS

Gilles CREHANGE, MD

Role: PRINCIPAL_INVESTIGATOR

CENTRE GEORGES FRANCOIS LECLERC, DIJON

Other Identifiers

UC-0107/1602

Identifier Type: -

Identifier Source: org_study_id

NCT03296839

Identifier Type: -

Identifier Source: nct_alias