Clinical and Pharmacokinetic Study of Lurbinectedin in Combination with Irinotecan in Patients with Advanced Solid Tumors
- Conditions
- Selected Advanced Solid TumorsMedDRA version: 21.1Level: LLTClassification code 10065147Term: Malignant solid tumorSystem Organ Class: 100000004864Therapeutic area: Diseases [C] - Cancer [C04]
- Registration Number
- EUCTR2015-003602-16-DE
- Lead Sponsor
- Pharma Mar S.A.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 320
1)Voluntarily signed and dated written informed consent prior to any specific-study procedure
2)Age =18years
3)ECOG performance status =1
4)Life expectancy =3 months
5)Histologically or cytologically confirmed diagnosis of advanced disease of any of the following tumor types:
- Lurbinectedin Escalation Group and Irinotecan Escalation Group:
a)Glioblastoma
b)Soft-tissue sarcoma (excluding GIST)
c)Endometrial carcinoma
d)Epithelial ovarian carcinoma (including primary peritoneal disease and/or fallopian tube carcinomas and/or endometrial adenocarcinomas) regardless of platinum sensitivity
e)Mesothelioma
f)GEP-NET
g)SCLC
h)Pancreatic adenocarcinoma
i)Gastric carcinoma
j)CRC
- Intermediate Escalation Group:
a)Endometrial carcinoma
b)SCLC
c)Other solid tumors may be included, if appropriate, after discussion between the Investigators and the Sponsor
For the Phase II expansion stage:
a)Glioblastoma
b)Soft tissue sarcoma (including synovial sarcoma)
c)Endometrial carcinoma
d)SCLC
e)Neuroendocrine tumors
- Group 1: Poorly differentiated grade 3 NEC (Ki-67 >20%) according to the 2019 WHO classification of tumors of the digestive system, of gastroenteropancreatic origin
or unknown primary site (lung primary tumors will be excluded)
- Group 2: Well differentiated grade 2 (Ki-67 3-20%) or grade 3 (Ki-67 21-55%) GEP-NETs according to the 2019 WHO classification of tumors of the
digestive system
6)The number of prior lines of therapy allowed per patient will be as follows:
-Phase I Escalation Stage: No more than 2 prior lines of cytotoxic-containing chemotherapy regimens for advanced disease
-Phase II Lurbinectedin Expansion Stage:
•For SCLC, 1 prior line of platinum-containing chemotherapy with/without antibodies against PD-1 or PD-L1
•For NENs, in Group 1 (patients with poorly differentaited NEC of gastroenteropancreatic origin or unknown primary site, excluding lung primary tumors), one prior line of platinum-based chemotherapy; and in Group 2 (patients with well differentiated GEP-NETs), no more than 3 prior lines of systemic therapy
(that may include somatostatin analogues, chemotherapy, everolimus and/or sunitinib)
•For all other tumor types, no more than 2 prior lines of cytotoxic-containing chemotherapy regimens for advanced disease
There is no limit for prior targeted therapy, hormonal therapy and immunotherapy (such as nivolumab)
7)Phase II expansion stage: Tumor-specific cohort(s) at the RD:
a)Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST)v1.1. For patients with glioblastoma: Measurable disease according to RECISTv.1.1 and Response Assessment in Neuro-Oncology (RANO) criteria
b)Documented disease progression per RECISTv.1.1 during or immediately after last therapy according to any of the aforementioned criteria. For patients with glioblastoma: Documented disease progression per RECISTv.1.1 and RANO criteria
8)At least 3 weeks since the last anticancer therapy (including immunotherapy, investigational drugs and radiotherapy), and at least 6 weeks since nitrosoureas and mitomycin C (systemic). For biological/investigational anticancer therapies given orally, the aforementioned period of at least 3 weeks could be changed for one of at least 5 half-lives (whichever occurred first), provided that the therapy is given as single agent and not combined with other drugs. If this is not the case, this exception will not be acceptable. For patients with glioblastoma
1)Concomitant diseases/conditions:
a)History or presence of unstable angina, myocardial infarction, congestive heart failure, or clinically significant valvular heart disease within the previous year
b)Symptomatic arrhythmia or any uncontrolled arrhythmia requiring ongoing treatment
c) Myopathy or any clinical situation that causes significant and persistent elevation of CPK (> 2.5 × ULN in two different determinations performed one week apart)
d) Ongoing chronic alcohol consumption or cirrhosis with Child-Pugh score B or C. Known Gilbert disease
e) Active uncontrolled infection
f) Known human immunodeficiency virus (HIV) or known hepatitis C virus (HCV) infection or active hepatitis B
g) Any past or present chronic inflammatory colon and/or liver disease, past intestinal obstruction, pseudo or subocclusion or paralysis
h) Evident symptomatic pulmonary fibrosis or interstitialpneumonitis, pleural or cardiac effusion rapidly increasing and/or necessitating prompt local treatment within seven days
i) Any other major illness that, in the Investigator's judgment, will substantially increase the risk associated with the patient's participation in this study.
j) Active COVID-19 disease
k) Hypersensitivity to any of the study drugs or their excipients.
2) Prior treatment with lurbinectedin, trabectedin (Yondelis®) or topoisomerase I inhibitors (irinotecan, topotecan, etc.). Prior topoisomerase inhibitors (e.g., irinotecan) are only allowed in patients with colorectal carcinoma or NENs
3) Prior bone marrow or stem cell transplantation, or radiation therapy in more than 35% of bone marrow
4) Known brain metastases or leptomeningeal disease involvement. Glioblastoma lesions (primary or locally advanced) are eligible. Exception: patients with brain metastases are eligible provided they are radiologically stable, i.e. without evidence of progression for at least 4 weeks by repeat imaging (note that the repeat imaging should be performed during study screening), clinically stable and without requirement of steroid treatment (patients taking steroids in the process of already being tapered within two weeks prior to screening are allowed). Brain CT-scan or MRI results must be provided at baseline.
5) Women who are pregnant or breast feeding and fertile patients (men and women) who are not using an effective method of contraception *
6) Limitation of the patient's ability to comply with the treatment or follow-up protocol
* Women of childbearing potential (WOCBP) must agree to use an effective contraception method to avoid pregnancy during the course of the trial (and for at least six months after the last infusion). Fertile male patients must agree to refrain from fathering a child or donating sperm during the trial and for four months after the last infusion
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method