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Multicenter prospective phase II study evaluating regorafenib in older patients with metastatic colorectal cancer
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Regorafenib 160 mg | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Regorafenib 160 mg | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Patients With a Tumoral Control Rate at 2 Months | Tumor control rate is defined as the percentage of patients with complete tumor response, partial tumor response, or tumor stability on regorafenib therapy at 2 months after initiation of therapy as determined by the investigator per Response Evaluation Criteria In Solid Tumors Criteria (RECIST V1.1 criteria) for target lesions and assessed by CT-Scan: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Stability : neither complete or partial response nor progression. | 2 months after the start of treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Overall Survival | Overall survival was defined as the time from the date of the patient's inclusion to the patient's death (all causes). For alive patients the date of the latest news wastaken into account. Overall survival was estimated also after the treatment stopped explaining the difference of time frame between this outcome and the adverse events outcome. | Up to approximatively 1 year after the end of the treatment |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Thomas APARICIO, Pr | Hôpital Avicenne BOBIGNY | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CH Victor Dupouy | Argenteuil | France | ||||
| Centre François Bacless |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32334940 | Result | Aparicio T, Darut-Jouve A, Khemissa Akouz F, Monterymard C, Artru P, Cany L, Romano O, Valenza B, Le Foll C, Delbaldo C, Falandry C, Norguet Monnereau E, Ben Abdelghani M, Smith D, Rinaldi Y, Pere Verge D, Baize N, Maillard E, Dohan A, Des Guetz G, Pamoukdjian F, Lepage C. Single-arm phase II trial to evaluate efficacy and tolerance of regorafenib monotherapy in patients over 70 with previously treated metastatic colorectal adenocarcinoma FFCD 1404 - REGOLD. J Geriatr Oncol. 2020 Nov;11(8):1255-1262. doi: 10.1016/j.jgo.2020.04.001. Epub 2020 Apr 22. |
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Before enrollement, standard examinations (biological, clinical, ECG) as well as geriatric questionnaires were done. In terms of imaging, abdominal and thoracic computed tomography scan or MRI were also done.
Between January 2016 to April 2017, 43 patients were enrolled in the trial by 25 centers in France.
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| ID | Title | Description |
|---|---|---|
| FG000 | Regorafenib 160 mg | Regorafenib monotherapy at an initial dose of 160 mg once daily orally (21 days on, 7 days off treatment) |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Aug 17, 2015 | Jun 24, 2022 |
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| Caen |
| France |
| Centre Oncologie et Radiothérapie | Dijon | France |
| Clinique du Cap d'Or | La Seyne-sur-Mer | France |
| Caluire et Cuire - Infirmerie Protestante de Lyon | Lyon | France |
| CH Lyon Sud (HCL) - Pierre Benite | Lyon | France |
| Hôpital privé Jean Mermoz | Lyon | France |
| Hôpital Européen | Marseille | France |
| CHRU - Hôpital Saint Eloi | Montpellier | France |
| CHR - Service HGE | Orléans | France |
| Saint Joseph | Paris | France |
| CH | Perpignan | France |
| Hôpital Haut Leveque | Pessac | France |
| CH Annecy Genevois | Pringy | France |
| Centre Paul Strauss | Strasbourg | France |
| Hôpital privé | Villeneuve-d'Ascq | France |
| COMPLETED |
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| NOT COMPLETED |
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All the patients enrolled in the study and treated by Regorafenib
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| ID | Title | Description |
|---|---|---|
| BG000 | Regorafenib 160 mg | Regorafenib monotherapy at an initial dose of 160 mg once daily orally (21 days on, 7 days off treatment) |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | years |
| |||||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||||
| Region of Enrollment | Number | participants |
| ||||||||||||||||||
| Koehne Score | Low is for patients with OMS equal to 0 or 1 and with 1 metastatic site Intermediate is for patients with 0MS equal to 0-1 and with more than 1 metastatic site and Phosphatases Alcalines <300 U/L, or patients with OMS >1 and WBC <10.109/L and 1 metastatic site Higi is for patients with OMS 0/1 and with more than 1 metastatic site and with phosphatases alcalines > 300 U/L or patients with OMS > 1 and with more than 1 metastatic site or patients with WBC >10.109 /L | Count of Participants | Participants |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Percentage of Patients With a Tumoral Control Rate at 2 Months | Tumor control rate is defined as the percentage of patients with complete tumor response, partial tumor response, or tumor stability on regorafenib therapy at 2 months after initiation of therapy as determined by the investigator per Response Evaluation Criteria In Solid Tumors Criteria (RECIST V1.1 criteria) for target lesions and assessed by CT-Scan: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Stability : neither complete or partial response nor progression. | Posted | Number | 90% Confidence Interval | Percentage of patients | 2 months after the start of treatment |
|
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| ||||||||||||||||||||||||||
| Secondary | Overall Survival | Overall survival was defined as the time from the date of the patient's inclusion to the patient's death (all causes). For alive patients the date of the latest news wastaken into account. Overall survival was estimated also after the treatment stopped explaining the difference of time frame between this outcome and the adverse events outcome. | All patients included in the study and who have been treated with regorafenib | Posted | Median | 95% Confidence Interval | months | Up to approximatively 1 year after the end of the treatment |
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Up to the end of treatment. Treatement was usually stopped after 70 days of treatments. Overall survival was estimated also after the treatment stopped explaining the difference of time frame between this outcome and the adverse events outcome.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Regorafenib 160 mg | Regorafenib monotherapy at an initial dose of 160 mg once daily orally (21 days on, 7 days off treatment) | 36 | 42 | 17 | 42 | 42 | 42 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Pulmonary embolism | Vascular disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Fall | Injury, poisoning and procedural complications | NCI CTC version 4.0 | Systematic Assessment |
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| Hypertension | Cardiac disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Haematoma | Cardiac disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Tachycardia | Cardiac disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Cerebrovascular ischemia | Nervous system disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Headache | Nervous system disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Neuropathy peripheral | Nervous system disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Fatigue | General disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Diarrhoea | Gastrointestinal disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Deshydratation | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Aspartate aminotransferase increased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Alanine aminotransferase increased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Total Bilirubin increased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Gamma-glutamyltransferase increased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| White blood cell count decreased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Lipase increased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Neutrophils decreased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Lymphocytes decreased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Phosphatases Alcalines increased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Platelets decreased | Investigations | NCI CTC version 4.0 | Systematic Assessment |
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| Hypertension | Cardiac disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Anemia | Blood and lymphatic system disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Dysphonia | Respiratory, thoracic and mediastinal disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Headache | Nervous system disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Dysgueusia | Nervous system disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Fatigue | General disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Pyrexia | General disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Constipation | Gastrointestinal disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Diarrhoea subjects | Gastrointestinal disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Abdominal pain | Gastrointestinal disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Stomatitis | Gastrointestinal disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Nausea | Gastrointestinal disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Proteinuria | Renal and urinary disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Palmar-plantar erythrodysaesthesia syndrome | Skin and subcutaneous tissue disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Arthralgia | Musculoskeletal and connective tissue disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Myalgia | Musculoskeletal and connective tissue disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hypokaliemia | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hypothyroidism | Endocrine disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Anorexia | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hyperkalaemia | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hypoalbuminaemia | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hypocalcaemia | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hypomagnesaemia | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hyponatremia | Musculoskeletal and connective tissue disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Hypophosphataemia | Metabolism and nutrition disorders | NCI CTC version 4.0 | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Karine Le Malicot | Fédération Francophone de Cancérologie Digestive | +33 3 80 39 34 79 | karine.le-malicot@u-bourgogne.fr |
| Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Feb 23, 2017 | Jun 24, 2022 | SAP_001.pdf |
| ID | Term |
|---|---|
| C559147 | regorafenib |
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| Unknown or Not Reported |
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| High |
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