Combined Use of Raltitrexed and S-1 as Treatment for Patients With Metastasizing Colorectal Cancer

NCT02618356 | Unknown Phase 2 DMC

• 1 other identifier: guoweijian-2015-RS
• Study Type: interventional
• Target: 82
• Locations: 1 country
• Sites: 1

Brief Summary

The primary endpoint is to evaluate the Median disease progression free survival (mPFS).

Conditions

Metastatic Colon Cancer

Outcome Measures

Primary Outcomes (1)

• Median disease progression free survival (mPFS) of Raltitrexed combined with S-1

  at least 24 months

Study Arms (1)

combined use Raltitrexed and S-1

EXPERIMENTAL

Raltitrexed 3mg/m2 intravenously guttae, d1 and S-1,bid,po,d1-d14,every three weeks for a cycle. BSA(body surface area) S-1 dosage \<1.25 m2 80 mg/d * 1.25m2 - \<1.5 m2 100 mg/d * 1.5 m2 120 mg/d

Drug: Raltitrexed and S-1

Interventions

Raltitrexed and S-1 DRUG

Raltitrexed 3mg/m2 intravenously guttae, d1 and S-1,bid,po,d1-d14,every three weeks for a cycle. BSA (body surface area) S-1 dosage \<1.25 m2 80 mg/d * 1.25m2 - \<1.5 m2 100 mg/d * 1.5 m2 120 mg/d

Also known as: Tomudex, Gimeracil and oteracil porassium

combined use Raltitrexed and S-1

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• ≥18 years of age
• Histologically or cytologically confirmed adenocarcinoma of the colon or rectum 3. No systemic chemotherapy for metastatic tumors
• \. ECOG (Eastern Cooperative Oncology Group) 0-1 and expected survival period for 3 months or more 5. At least one measurable objective tumor lesions according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 6. ANC≥1.5\*109/L；PLT≥80\*109/L；HB≥90g/L；Total bilirubin ≤ 1.5 x the upper limit of normal (ULN) ; Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 x ULN (≤ 5 x ULN for subjects with liver involvement of their cancer)；ALB ≥ 30g/L; Serum creatinine ≤1.5(ULN) or glomerular filtration rate (GFR) ≥60 ml/min screening within 7 days 7. Progression during or within 3 months following the last administration of approved standard therapies which must include a fluoropyrimidine, oxaliplatin and irinotecan. Subjects treated with oxaliplatin in an adjuvant setting should have progressed during or within 6 months of completion of adjuvant therapy. Subjects who progress more than 6 months after completion of oxaliplatin containing adjuvant treatment must be retreated with oxaliplatin-based therapy to be eligible. Subjects who have withdrawn from standard treatment due to unacceptable toxicity warranting discontinuation of treatment and precluding retreatment with the same agent prior to progression of disease will also be allowed into the study. Subjects may have received prior treatment with Avastin (bevacizumab) and/or Erbitux (cetuximab)/Vectibix (panitumumab) (if KRAS WT) 8. Signed informed consent obtained before any study specific procedures. Subjects must be able to understand and willing to sign a written informed consent.

You may not qualify if:

• Prior treatment with raltitrexed and gimeracil and oteracil potassium
• Systemic anticancer therapy including cytotoxic therapy, signal transduction inhibitors, immunotherapy and hormonal therapy during this trial or within 4 weeks (or 6 weeks for mitomycin C) before starting to receive study medication.
• Alcohol or drug addictions
• Previous or concurrent cancer that is distinct in primary site or histology from colorectal cancer within 5 years prior to randomization EXCEPT for curatively treated cervical cancer in situ, non-melanoma skin cancer and superficial bladder tumors \[Ta (non-invasive tumor), Tis (carcinoma in situ) and T1 (tumor invades lamina propria)\]
• Any history of or currently known brain metastases
• Multiple primary colorectal carcinoma
• Concomitant participation or participation within the last 30 days in another clinical trial
• There is an important organ failure or other serious diseases, including coronary artery disease, symptomatic cardiovascular disease or myocardial infarction within 12 months; serious neurological or psychiatric history; severe infection; actively disseminated vascula blood coagulation.
• Extended field radiotherapy within 4 weeks or limited field radiotherapy within 2 weeks prior to randomization. Subjects must have recovered from all therapy-related toxicities. The site of previous radiotherapy should have evidence of progressive disease if this is the only site of disease.
• Pregnant or breast-feeding subjects. Women of childbearing potential must have a pregnancy test performed a maximum of 7 days before start of treatment, and a negative result must be documented before start of treatment.
• Pleural effusion or ascites that causes respiratory compromise (≥Common Terminology Criteria for Adverse Events \[CTCAE\]) Grade 2 dyspnea)
• Subjects unable to swallow oral medications
• Known history of human immunodeficiency virus (HIV) infection

Sponsors & Collaborators

• Fudan University: lead

Study Sites (1)

Fudan University Cancer Hospital

Shanghai, Shanghai Municipality, 200032, China

RECRUITING

Related Publications (1)

• Huang M, Yang Y, Zhu X, Chen Z, Zhang W, Wang C, Zhang X, Qiu L, Zhang Z, Zhao X, Li W, Wang Y, Guo W. A prospective phase II study of raltitrexed combined with S-1 as salvage treatment for patients with refractory metastatic colorectal cancer. Asia Pac J Clin Oncol. 2021 Dec;17(6):513-521. doi: 10.1111/ajco.13511. Epub 2021 Feb 10.

  PMID: 33567129 DERIVED

MeSH Terms

Conditions

Colonic Neoplasms

Interventions

raltitrexed; S 1 (combination); gimeracil

Condition Hierarchy (Ancestors)

Colorectal Neoplasms; Intestinal Neoplasms; Gastrointestinal Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Colonic Diseases; Intestinal Diseases

Study Officials

• Wei Jian Guo, doctor

  Fudan University

  STUDY CHAIR

Central Study Contacts

Wei Jian Guo, doctor

CONTACT

13816066360; mingzhuhuang0718@163.com

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: professor

Study Record Dates

• First Submitted: November 17, 2015
• First Posted: December 1, 2015
• Study Start: December 25, 2015
• Primary Completion: November 1, 2017
• Study Completion: November 1, 2017
• Last Updated: October 2, 2017

Record last verified: 2017-09

Locations

CN (1)