| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000001312 |
| Receipt No. | R000001593 |
| Official scientific title of the study | Safety and efficacy of Alternating mFOLFOX6 plus bevacizumab and FOLFIRI plus bevacizumab every 4cycles as First line Therapy in Advanced colorectal Cancer |
| Date of disclosure of the study information | 2008/08/12 |
| Last modified on | 2017/01/13 (Ver. 13) |
| Basic information | ||
| Official scientific title of the study | Safety and efficacy of Alternating mFOLFOX6 plus bevacizumab and FOLFIRI plus bevacizumab every 4cycles as First line Therapy in Advanced colorectal Cancer | |
| Title of the study (Brief title) | Safety and efficacy of Alternating mFOLFOX6 plus bevacizumab and FOLFIRI plus bevacizumab every 4cycles as First line Therapy in Advanced colorectal Cancer(KSCC0801) | |
| Region |
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| Condition | ||||||
| Condition | Unresectable advanced/recurrent colorectal cancer | |||||
| Classification by specialty |
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| Classification by malignancy | Malignancy | |||||
| Genomic information | NO | |||||
| Objectives | |
| Narrative objectives1 | Safety and efficacy of Alternating mFOLFOX6 plus bevacizumab and FOLFIRI plus bevacizumab every 4cycles as First line Therapy in Advanced colorectal Cancer |
| Basic objectives2 | Safety,Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | Phase II |
| Assessment | |
| Primary outcomes | PFS |
| Key secondary outcomes | Response rate,
Safety, OS |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Single arm |
| Randomization | Non-randomized |
| Randomization unit | |
| Blinding | Open -no one is blinded |
| Control | Uncontrolled |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | ||
| No. of arms | 1 | |
| Purpose of intervention | Treatment | |
| Type of intervention |
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| Interventions/Control_1 | Alternating mFOLFOX6 plus bevacizumab and FOLFIRI plus bevacizumab every 4cycles. | |
| Interventions/Control_2 | ||
| Interventions/Control_3 | ||
| Interventions/Control_4 | ||
| Interventions/Control_5 | ||
| Interventions/Control_6 | ||
| Interventions/Control_7 | ||
| Interventions/Control_8 | ||
| Interventions/Control_9 | ||
| Interventions/Control_10 | ||
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1.colorectal cancer, cytologically and/or histrogically
2.Unresectable advanced/recurrent colorectal cancer 3.no prior chemotherapy 4.no prior radiotherapy 5.age: 20-75 years old 6. Performance Status(ECOG):0-2 7.with measurable lesions 8.CT/MRI within 28 days 9.Life expectancy estimated >= 3 months 10.no bleeding tendency 11.Sufficient organ functions 12.witten informed consents |
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| Key exclusion criteria | 1. Administering antithrobotic drug within 7 days
2. Serious complications (renal failure or hepatic failure) 3. Serious drug hypersensitivity or a history of drug allergy 4. Peripheral neuropathy 5. Active concomitant malignancy 6. Active infections 7. High blood pressure and diabetic that cannot be controlled 8. symptomatic or asymptomatic but treated heart disease 9. interstitial pnumonitis, pulmonary fibrosis or high-grade pulmonary emphysema 10. histry of mental disturbances or cerebrovascular attach 11. Fresh hemorrhage from digestive tube, intestines tube paralysis, intestinal obstruction and peptic ulcer 12. Current or previous (within one year) history of GI perforation 13. Plerral effusion, peritoneal fluid and pericardial fluid 14. Symptomatic brain metastasis 15. Water solubility diarrhea, in case of the patient who has a colostomy, diarrhea impairs daily life activity 16. Need to treatment with atazanavir sulfate 17. under coutinuous steroid therapy 18. Any surgical treatments including skin-open biopsy, trauma surgery and other more intensive surgery within 4 weeks or aspiration biopsy within one week 19. CV-port procedure within one week 20. Anti-platelets therapy (including aspirin and NSAIDS) 21. history of organ transplantation 22. Traumatic gracture of unrecovery 23. Bevacizumab used previous chemotherapy 24. Pregnant women, possibly pregnant women, wishing to become pregnant, and nursing mothers 25. Other conditions not suitable for this study |
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| Target sample size | 51 | |||
| Research contact person | |
| Name of lead principal investigator | Maehara Yoshihiko |
| Organization | Kyushu University |
| Division name | Dpt. of surgery and science |
| Address | Maidashi 3-1-1, Higashi-ku, Fukuoka, 812-8582 |
| TEL | 092-631-2920 |
| info2@cres-kyushu.or.jp | |
| Public contact | |
| Name of contact person | KSCC |
| Organization | CReS |
| Division name | KSCC |
| Address | Maidashi 3-1-1, Higashi-ku, Fukuoka, 812-8582 |
| TEL | 092-631-2920 |
| Homepage URL | |
| kscc2@cres-kyushu.or.jp | |
| Sponsor | |
| Institute | KSCC |
| Institute | |
| Department | |
| Funding Source | |
| Organization | CReS |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
| Institutions | 九州大学(福岡県)
国立病院機構九州医療センター(福岡県) 公立学校共済組合九州中央病院(福岡県) 済生会福岡総合病院(福岡県) 福岡歯科大学医科歯科総合病院(福岡県) 済生会八幡総合病院(福岡県) 新日鐵八幡記念病院(福岡県) 社会保険田川病院(福岡県) 社会保険仲原病院(福岡県) 久留米大学(福岡県) 久留米大学医療センター(福岡県) 社会保険久留米第一病院(福岡県) 聖マリア病院(福岡県) 公立八女総合病院(福岡県) 大牟田市立総合病院(福岡県) 福岡県済生会大牟田病院(福岡県) 麻生飯塚病院(福岡県) 福岡市民病院(福岡県) 有田共立病院(佐賀県) 佐世保市立総合病院(長崎県) 長崎大学(長崎県) 光晴会病院(長崎県) 国立病院機構長崎医療センター(長崎県) 済生会熊本病院(熊本県) 熊本大学(熊本県) 健康保険人吉総合病院(熊本県) 大分県立病院(大分県) 大分赤十字病院(大分県) 国立病院機構大分医療センター(大分県) 国立病院機構別府医療センター(大分県) 中津市立中津市民病院(大分県) 大分県済生会日田病院(大分県) 小林市立病院(宮崎県) 宮崎県立延岡病院(宮崎県) 社会保険宮崎江南病院(宮崎県) 国立病院機構南九州病院(鹿児島県) 今給黎総合病院(鹿児島県) 潤愛会 鮫島病院(鹿児島県) 鹿児島大学(鹿児島県) 鹿児島厚生連病院(鹿児島県) 済生会川内病院(鹿児島県) 県民健康プラザ鹿屋医療センター(鹿児島県) 鹿児島県立薩南病院(鹿児島県) 浦添総合病院(沖縄県) 中頭病院(沖縄県) ハートライフ病院(沖縄県) 琉球大学(沖縄県) 北部地区医師会病院(沖縄県) 広島赤十字・原爆病院(広島県) 松山赤十字病院(愛媛県) 防府消化器病センター 防府胃腸病院(山口県) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | Completed | ||||||
| Date of protocol fixation |
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| Anticipated trial start date |
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| Date analysis concluded | |||||||
| Related information | |
| URL releasing protocol | |
| Publication of results | Published |
| URL releasing results | http://www.ncbi.nlm.nih.gov/pubmed/26037783 |
| Results | |
| Other related information | |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001593 |