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Raltitrexed-based chemotherapy as second-line treatment in advanced colorectal cancer: a prospective, multi-center, non-intervention registration study

Raltitrexed-based chemotherapy as second-line treatment in advanced colorectal cancer: a prospective, multi-center, non-intervention registration study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016185
Enrollment
Unknown
Registered
2018-05-17
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Interventions

Case series:raltitrexed plus Irinotecan

Sponsors

81th Hospital of PLA, Dongfang Hospital Affiliated to Shanghai Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Above 18 years old male or female; 2. histological and/or cytological confirmation of ACC; 3. Disease progression while on first-line palliative fluoropyrimidine-based chemotherapy or relapse within 6 months after adjuvant chemotherapy or first-line maintenance treatment within 3 months of disease progression; and from the last chemotherapy for more than one month; 4. at least one measurable objective tumor lesion by spiral CT examination, the maximum diameter = 1cm(according to RECIST 1.1); 5. Participants volunteered to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. History of malignancy within 5 years except treated and considered cured cutaneous squamous or basal cell carcinoma, in situ cervical cancer, or in situ breast ductal carcinoma; 2. inflammatory bowel disease or a history of extensive removal of the colon> 50% or extensive small bowel resection with chronic diarrhea; 3. uncontrolled brain metastasis; 4. uncontrolled ascites with clinical intervention; 5. pregnant or lactated women; 6. unsuitable for the study determined by investigator.

Design outcomes

Primary

MeasureTime frame
Progression Free Survival;

Secondary

MeasureTime frame
Overall Survival;Objective Response Rate;Disease Control Rate;Percentage of participants experiencing grade 3-4 adverse events;Quality of Life;

Countries

China

Contacts

Public ContactQin Shukui, Li Jin

81th Hospital of PLA / Oriental Hospital, Shanghai Tonji University

qinsk@csco.org.cn+86 025-80864541

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026