Status:
UNKNOWN
Anlotinib and Irinotecan for Ewing Sarcoma
Lead Sponsor:
Peking University People's Hospital
Conditions:
Ewing's Tumor Metastatic
Eligibility:
All Genders
5-65 years
Phase:
PHASE1
PHASE2
Brief Summary
The investigators explored the activity of anlotinib combined with irinotecan in patients with relapsed and metastatic Ewing Sarcoma.
Detailed Description
After standard multimodal therapy, the prognosis of relapsed and metastatic Ewing Sarcoma is dismal and unchanged over the last decades.Thus, the investigators explored the activity of anlotinib combi...
Eligibility Criteria
Inclusion
- Histologically confirmed Ewing sarcoma.
- Evidence of Ewing sarcoma translocation by fluorescence in situ hybridization (FISH) or real-time polymerase chain reaction (RT-PCT).
- Recurrent or refractory tumors with no known curative treatment options according to the judgment of the investigator.
- Prior treatment consisted of standard Ewing Sarcoma chemotherapy agents including doxorubicin, vincristine, cyclophosphamide, ifosfamide and etoposide; metastatic relapsed and unresectable progressive disease (PD);
- Life expectancy of ≥ 3 months.
- Eastern Cooperative Oncology Group performance status 0-1
- Measurable disease on CT or MRI by RECIST 1.1.
- Adequate organ function.
- Time elapsed from previous therapy must be ≥ 3 weeks for systemic therapy, ≥ 2 weeks for radiation therapy or major surgery.
- Patients who have undergone autologous hematopoietic stem cell transplantation are eligible once they have recovered from all toxicities from therapy.
- Patients who have received allogeneic hematopoietic stem cell transplantation will be eligible 6 months after the procedure provided there is no evidence of active graft-versus-host disease and immunosuppressive treatment has been discontinued for at least 30 days.
- Patients with central nervous system disease are eligible for enrollment if they have received prior radiotherapy or surgery to sites of central nervous system metastatic disease, have been off glucocorticoids for at least 4 weeks, have no overt evidence of neurological deficit and are ≥ 6 weeks from completion of brain irradiation.
- Females of childbearing potential as well as males and their partners must agree to use an effective form of contraception during the study and for 6 months following the last dose of study medication.
Exclusion
- Clinically significant unrelated illness which would, in the judgment of the treating physician, compromise the patient's ability to tolerate the investigational agent or be likely to interfere with the study procedures or results.
- Prior treatment consisted of anlotinib, any other antiangiogenic TKIs, or irinotecan.
- Patients with baseline corrected QT interval(QTc) \> 480 msec.
- Known hypersensitivity reaction to anlotinib or any of its components, and irinotecan or any of its components.
- Concomitant use of any other investigational or anticancer agent(s).
- Pregnant patients or patients who are breast feeding. Subjects capable of pregnancy (post menarche and not post-menopausal, defined as over 12 months since final menstrual period) must have a negative pregnancy test within 7 days prior to first dose.
- Inability to swallow capsules or water.
- Other clinically significant malignant disease diagnosed within the previous 5 years, excluding intra-epithelial cervical neoplasia or non-melanoma skin cancer.
- Known persistent (\> 4 weeks) ≥ Grade 2 neutropenia, ≥ Grade 2 thrombocytopenia or \> Grade 3 anemia from prior cancer therapy.
- Other kinds of malignant tumors at the same time.
Key Trial Info
Start Date :
January 22 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2020
Estimated Enrollment :
47 Patients enrolled
Trial Details
Trial ID
NCT03416517
Start Date
January 22 2018
End Date
December 1 2020
Last Update
February 15 2019
Active Locations (5)
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1
Peking University First Hospital
Beijing, China, 100034
2
Peking University People's Hospital
Beijing, China, 100044
3
Peking University Shougang Hospital
Beijing, China, 100144
4
Peking University Third Hospital
Beijing, China, 100191