Pemetrexed, Cisplatin With Soft Tissue Sarcoma

Sarcoma,Soft Tissue Clinical Trial

— ALBATROSS  

Official title:

A Single-Arm, Multicenter, Open-Label, Phase 2 Study of Pemetrexed/Cisplatin Chemotherapy for Patients With Metastatic/Recurrent Soft Tissue Sarcoma in 4- Independent Histologic Subtypes

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04605770
• Other study ID #: 4-2019-0923
• Status: Recruiting
• Phase: Phase 2
• Start date: December 22, 2020
• Est. completion date: November 1, 2022

Study information

• Verified date: April 2021
• Source: Yonsei University
• Contact: Hyo Song Kim, MD, Ph.D
• Phone: 82-2-2228-8124
• Email: hyosong77[@]yuhs.ac
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Soft tissue sarcoma (STS) is rare malignancy of mesodermal origin, representing less than 1% of all malignant neoplasms. They are a group of diseases encompassing diverse histological subtypes with very different biomorphologies, prognoses, and responses to treatments. At advanced stages of STS, anticancer treatments are less effective and the prognosis is poor with a median survival of 8 to 18 months. Doxorubicin and ifosfamide given each alone or in their combination have represented the mainstream of anticancer treatments in metastatic STS. However, salvage treatments for patients with progression after doxorubicin/ifosfamide-based treatment are limited and anticancer agents such as gemcitabine/docetaxel, pazopanib, eribulin and trabectedin are currently used as a standard of care (SOC).

For metastatic sarcoma, a study of pemetrexed alone in patients with refractory STS who have progressed after doxorubicin and/or ifosfamide-based anticancer treatment was conducted. In this study including 48 patients, most of whom had relatively poor course of disease with disease progression after the 2nd- and/or 3rd-line treatment, pemetrexed was well tolerated and associated with 5% of response rate and 33% of 3-month progression-free rates suggesting potential antitumor efficacy with good tolerability profile with refractory STS.

However, as conventional agents have showed different efficacy depending on various subtypes of STS, a confirmatory study to see clinical utilities of a given regimen by subtype is required also for pemetrexed/cisplatin. Therefore, the investigators intend to proceed this phase 2 clinical trial to evaluate the efficacy and safety of pemetrexed/cisplatin combination therapy in patients with advanced/metastatic STS who received up to two-lines of prior palliative anticancer treatments with histological subtype-specific cohorts (leiomyosarcoma, synovial sarcoma, malignant peripheral nerve sheath tumor, and others) in order to provide a basis for a subsequent phase 3 study by selecting histological subtype(s) in which the efficacy of study regimen is to be proven.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 164
• Est. completion date: November 1, 2022
• Est. primary completion date: November 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

• histologically confirmed, advanced/metastatic STS

• Is = 19 years of age

• Eastern Cooperative Oncology Group performance status of 0 or 1

• measurable disease per Response Evaluation Criteria in Solid Tumors Version 1.1

• laboratory values indicating adequate organ function

• a documented postmenopausal woman, or is a premenopausal woman with negative urine or serum pregnancy test

• life expectancy = 12 weeks

Exclusion Criteria:

• previously received more than 2 regimens of cytotoxic chemotherapy

• received chemotherapy, surgery to major organ, or radiotherapy within the last 2 weeks

• ongoing toxicity (= CTCAE grade 2) from previous anticancer therapy

• central nervous system (CNS) metastases requiring active treatment

• diagnosis of second malignancy or has a history of active malignancy within the past 3 years

• other medical conditions where the study treatment is intolerable

• history of active infection

• hypersensitivity to pemetrexed or any of its excipients

• Co-administration with yellow fever vaccine

• pregnancy

Related Conditions & MeSH terms

• Sarcoma
• Sarcoma,Soft Tissue

Intervention

Drug:
• pemetrexed+cisplatin
Pemetrexed 500 mg/m2 (Day 1) and cisplatin 75 mg/m2 (Day 1) will be given via intravenous (IV) infusion. Each cycle consists of 21 days, and this combination therapy will be continued until Cycle 6. Starting from Cycle 7, pemetrexed alone will be administered every 3 weeks (Q3W) as IV infusion until disease progression. Vitamin B12 1000 mcg intramuscular (IM) injection will be given within 14 days prior to the first dose of pemetrexed, every 9 weeks (on the same day as study treatment) thereafter, and then 21 days after the last dose of pemetrexed. Folic acid 1 mg will be administered daily starting from 14 days before the first dose of pemetrexed and continued until 21 days after the last dose of pemetrexed. Study treatment will be continued until PD, unacceptable AE, or decision to discontinue by subject or physician.

Locations

Country	Name	City	State
Korea, Republic of	Severance Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free survival (PFS) rate	Progression-free survival rate at Week 12 (PFR 12) based on RECIST 1.1	at 12 weeks
Secondary	overall response rate		every 6 weeks, up to 52 weeks