Lurbinectedin Combined With Durvalumab in Pre-treated Patients With Extensive Stage Small-cell Lung Cancer

NCT ID: NCT05572476

Last Updated: 2024-06-05

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-10-31
• Study Completion Date: 2024-05-31

Brief Summary

Multicenter, prospective, open-labeled, 2-arm, randomized non-comparative (2:1) phase II trial assessing the efficacy of lurbinectedin in association with durvalumab

Detailed Description

Multicenter, prospective, open-labeled, 2-arm, randomized non-comparative (2:1) phase II trial assessing the efficacy of lurbinectedin in association with durvalumab in pre-treated patients with platinum sensitive extensive stage small-cell lung cancer (SCLC) which failed one prior platinum-containing regimen.

Conditions

Small Cell Lung Cancer; Platinum-Sensitive Lung Small Cell Carcinoma; Extensive-stage Small-cell Lung Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Experimental Arm A: treatment by lurbinectedin and durvalumab

Patients with with platinum sensitive extensive stage small-cell lung cancer (SCLC) which failed one prior platinum-containing regimen will be treated by the association of lurbinectedin and durvalumab

Group Type: EXPERIMENTAL

Association of lurbinectedin and durvalumab

Intervention Type: DRUG

A treatment cycles consists of 3 weeks (i.e. 21 days). Lurbinectedin will be administered by intravenous infusion on Day 1 every 3 weeks.

Durvalumab will be administered by intravenous infusion on Day 1 every 3 weeks.

Standard Arm B: treatment by carboplatin and etoposide

Patients with with platinum sensitive extensive stage small-cell lung cancer (SCLC) which failed one prior platinum-containing regimen will be treated by the association of carboplatin and etoposide

Group Type: OTHER

Association of carboplatin and etoposide

Intervention Type: DRUG

Treatment will be administered on a 21-days cycle basis up to a maximum of 6 cycles.

Carboplatin will be administered by intravenous infusion on Day 1 every 3 weeks.

Etoposide will be administered by intravenous infusion on Day 1-3 every 3 weeks

Interventions

Association of lurbinectedin and durvalumab

A treatment cycles consists of 3 weeks (i.e. 21 days). Lurbinectedin will be administered by intravenous infusion on Day 1 every 3 weeks.

Durvalumab will be administered by intravenous infusion on Day 1 every 3 weeks.

Intervention Type: DRUG

Association of carboplatin and etoposide

Treatment will be administered on a 21-days cycle basis up to a maximum of 6 cycles.

Carboplatin will be administered by intravenous infusion on Day 1 every 3 weeks.

Etoposide will be administered by intravenous infusion on Day 1-3 every 3 weeks

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Histology: confirmed diagnosis of extensive stage SCLC which failed one prior platinum-containing regimen,

2. Recurrent and platinum-sensitive SCLC: defined as those patients with SCLC recurrence at least 90 days from the last dose of platinum-based chemotherapy. Definition of platinum-sensitive disease is patient with at least 90 days of progression-free duration after finishing first-line platinum-based chemotherapy

3. Patients must have received as first line a combo with platinum+ etoposide + PD_L1 inhibitor

4. Metastatic or unresectable locally advanced disease, not ammenable to curative therapy,

5. Age ≥ 18 years,

6. Eastern Cooperative Oncology Group ≤ 1,

7. Life expectancy > 3 months,

8. Patients must have measurable disease as per RECIST v1.1.

9. Documented disease progression according to RECIST v1.1 before study entry,

10. At least three weeks since last chemotherapy, immunotherapy or any other pharmacological treatment for neoplastic disease and/or radiotherapy,

11. Adequate hematological, renal, metabolic and hepatic function

12. Women of childbearing potential must have a negative serum pregnancy test within 72 hours prior to receiving the first dose of trial medication. Both women and men must agree to use a highly effective method of contraception ,

13. No prior or concurrent malignant disease diagnosed or treated in the last 2 years except for adequately treated in situ carcinoma of the cervix, concomitant endometrial carcinoma stage IA grade 1, basal or squamous skin cell carcinoma, or in situ transitional bladder cell carcinoma,

14. Recovery to grade ≤ 1 from any adverse event derived from previous treatment (excluding alopecia of any grade and non-painful peripheral neuropathy grade ≤ 2) according to the NCI-CTCAE, version 5,

15. Body weight >30kg

16. Voluntarily signed and dated written informed consent prior to any study specific procedure,

17. Patients with a social security in compliance with the French law.

Exclusion Criteria

1. Previous treatment with lurbinectedin,

2. Current or prior use of immunosuppressive medication including any use of oral glucocorticoids, within 14 days before the first dose of durvalumab,

3. Active or prior documented inflammatory bowel disease,

4. Has an active autoimmune disease requiring systemic treatment within the past 2 years,

5. Has evidence of active non-infectious pneumonitis,

6. Has an active or ongoing infection requiring systemic therapy,

7. Currently active bacterial or fungus infection, HIV1, HIV2, hepatitis A or hepatitis B or hepatitis C infections,

8. Symptomatic untreated, or steroid-requiring, or progressing central nervous system malignancy is excluded.

9. Men or women of childbearing potential who are not using an effective method of contraception as previously described; women who are pregnant or breast feeding,

10. Previous enrolment in the present study,

11. Patient unable to follow and comply with the study procedures because of any geographical, social or psychological reasons,

12. Has received a live vaccine within 30 days prior to the first dose of trial treatment,

13. Known hypersensitivity to any involved study drug or any of its formulation components,

14. Tumors not accessible for biopsy,

15. Active infection including tuberculosis,

16. Person under judicial protection or deprived of liberty,

17. Concomitant use of strong inhibitors or inductors of cytochrome CYP3A4 taken within 21 days prior to the first dose of study drug,

18. Uncontrolled symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia, myocardial infarction, clinically significant valvular heart disease,

19. Intermittent or continuous oxygen requirement,

20. Presence of any external drainage,

21. Known myopathy,

22. Concomitant administration of any other antineoplastic therapy, other investigational agents, immunosuppressive therapies, Aprepitan or any other NK-1 antagonist,

23. Major surgical procedure within 28 days prior to the first dose of durvalumab.

24. History of allogenic organ transplantation,

25. History of leptomeningeal carcinomatosis,

26. QT interval corrected for heart rate using Fridericia's formula ≥470 ms

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

AstraZeneca

INDUSTRY

Sponsor Role: collaborator

PharmaMar

INDUSTRY

Sponsor Role: collaborator

Institut Bergonié

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Institut Bergonié

Bordeaux, , France

Countries

France

Other Identifiers

2022-001114-19

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

IB 2022-01

Identifier Type: -

Identifier Source: org_study_id