A Study of Etirinotecan Pegol (NKTR-102) Versus Treatment of Physician's Choice (TPC) in Patients With Metastatic Breast Cancer Who Have Stable Brain Metastases and Have Been Previously Treated With an Anthracycline, a Taxane, and Capecitabine

Breast Cancer Clinical Trial

— ATTAIN  

Official title:

A Phase 3 Open-Label, Randomized, Multicenter Study of NKTR-102 Versus Treatment of Physician's Choice (TPC) in Patients With Metastatic Breast Cancer Who Have Stable Brain Metastases and Have Been Previously Treated With an Anthracycline, a Taxane, and Capecitabine

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02915744
• Other study ID #: 15-102-14
• Status: Completed
• Phase: Phase 3
• Start date: November 2016
• Est. completion date: July 2020

Study information

• Verified date: April 2023
• Source: Nektar Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label, randomized, active comparator, multicenter, international Phase 3 study of NKTR-102 versus TPC in patients with metastatic breast cancer who have stable brain metastases and have been previously treated with an anthracycline, a taxane, and capecitabine in either the adjuvant or metastatic setting (prior anthracycline may be omitted if medically appropriate or contraindicated for the patient).

Description:

This is an open-label, randomized, active comparator, multicenter, international Phase 3 study of NKTR-102 versus TPC in patients with metastatic breast cancer who have stable brain metastases and have been previously treated with an anthracycline, a taxane, and capecitabine in either the adjuvant or metastatic setting (prior anthracycline may be omitted if medically appropriate or contraindicated for the patient).

In Group A, NKTR-102 will be administered at a dose level of 145 mg/m2 on a q21d schedule as a 90-minute intravenous (IV) infusion on Day 1 of each treatment cycle. In Group B, TPC will be administered per standard of care. Patients randomized to TPC will receive single-agent IV chemotherapy, limited to choice of one of the following 7 agents: eribulin, ixabepilone, vinorelbine, gemcitabine, paclitaxel, docetaxel, or nab-paclitaxel.

This study will randomize approximately 220 patients using a 1:1 randomization ratio and stratification based on geographic region, tumor receptor status, and Eastern Cooperative Oncology Group (ECOG) status. At Screening, the Investigator must determine which TPC will be offered to the patient.

Data will be collected on subsequent anticancer therapies in both treatment groups from the time patients come off the study treatment until the time of primary data analysis for Overall Survival (OS).

An independent data monitoring committee (DMC) will assess interim safety and efficacy data and determine final number of death events needed to provide 80% conditional power based on the zone adaptive design.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 178
• Est. completion date: July 2020
• Est. primary completion date: July 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Female or male, age = 18 years.

• Histologically-confirmed carcinoma of the breast (either the primary or metastatic lesions) for whom single-agent cytotoxic chemotherapy is indicated. Patients may have either measurable or non-measurable disease according to RECIST version 1.1.

• Patients must have a history of brain metastases that are non-progressing.

• For triple-negative breast cancer, a minimum of 1 prior cytotoxic chemotherapy regimen must have been administered for the indication of metastatic disease.Depending on receptor status, 1 or 2 prior cytotoxic regimens are required prior to enrollment in this trial; hormonal and/or human epidermal growth factor receptor 2 (HER2) -targeted agents may be required.

• Have had prior therapy (administered in the neoadjuvant, adjuvant, and/or metastatic setting) with an anthracycline, a taxane, and capecitabine (prior anthracycline can be omitted if not medically appropriate or contraindicated for the patient).

• Last dose of anticancer therapy must have been administered within 6 months of the date of randomization into this study.

• All anticancer- and radiation therapy-related toxicities must be completely resolved or downgraded to Grade 1 or less (neuropathy may be Grade 2 or less).

• Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

• Demonstrate adequate organ function obtained within 14 days prior to randomization and analyzed by the central laboratory.

• Women of childbearing potential (WCBP) must agree to use highly effective methods of birth control throughout the duration of the study until 6 months following the last dose of study drug.

• Males with female partners of child-bearing potential must agree to use a barrier contraception (e.g., condom with spermicidal foam/gel/film/cream/suppository) throughout the duration of the study until 6 months following the last dose of study drug; in addition to their female partner using either an intrauterine device or hormonal contraception and continuing until 6 months following the last dose of study drug. Male patients should not donate sperm until 6 months following the last dose of study drug.

Exclusion Criteria:

• Last dose of anticancer therapy (including HER2-targeted therapy) within 14 days prior to randomization.

• High-dose chemotherapy followed by stem cell transplantation (autologous or allogeneic).

• Major surgery within 28 days prior to randomization.

• Concomitant use of any anticancer therapy or use of any investigational agent(s).

• Received prior treatment for cancer with a camptothecin-derived agent.

• Lesions on imaging, by cerebrospinal fluid or with neurological findings that are consistent with leptomeningeal disease or meningeal carcinomatosis.

• Chronic or acute GI disorders resulting in diarrhea of any severity grade.

• Patients who are pregnant or lactating, plan to get pregnant, or have a positive serum pregnancy test prior to randomization.

• Enzyme-inducing anti-epileptic drugs (EIAEDs) within 14 days of randomization.

• Hepatitis B or C, tuberculosis, or HIV.

• Cirrhosis.

• Prior malignancy (other than breast cancer) unless diagnosed and definitively treated more than 5 years prior to randomization.

• Daily use of oxygen supplementation.

• Significant known cardiovascular impairment.

• Prior treatment with NKTR-102.

• Psychiatric illness, social situation, or geographical situation that preclude informed consent or limit compliance.

• Known intolerance or hypersensitivity to any of the products used in this study or their excipients.

• For patients selecting vinorelbine or gemcitabine as the TPC agent, patients may not receive yellow fever vaccine in the 28 days prior to randomization.

Related Conditions & MeSH terms

• Brain Neoplasms
• Breast Cancer
• Breast Neoplasms
• Metastasis
• Neoplasm Metastasis

Intervention

Drug:
• NKTR-102

• Eribulin

• Ixabepilone

• Vinorelbine

• Gemcitabine

• Paclitaxel

• Docetaxel

• Nab-paclitaxel

Locations

Country	Name	City	State
Australia	Investigatory Site - Albury	Albury	New South Wales
Australia	Investigator Site - Box Hill	Box Hill
Australia	Investigator Site - Darlinghurst	Darlinghurst	New South Wales
Australia	Investigator Site - Nedlands	Nedlands
Australia	Investigator Site - Subiaco	Subiaco	Western Australia
Australia	Investigator Site - Wollongong	Wollongong	New South Wales
Belgium	Investigator Site - Brussels	Brussels
Belgium	Investigator Site - Brussels	Brussels
Belgium	Investigator Site - Brussels	Brussels
Belgium	Investigator Site - Charleroi	Charleroi
Belgium	Investigator Site - Edegem	Edegem
Belgium	Investigator Site - Liege	Liège
Belgium	Investigator Site - Woluwe- Saint-Lambert	Woluwe-Saint-Lambert
Canada	Investigator Site - Montreal	Montréal	Quebec
France	Investigator Site - Le Mans	Le Mans
France	Investigator Site - Nimes	Nîmes
France	Investigator Site - Paris	Paris
France	Investigator Site - Rennes	Rennes
France	Investigator Site - Rouen	Rouen
France	Investigator Site - Strasbourg	Strasbourg
Israel	Investigator Site - Beersheba	Beersheba
Israel	Investigator Site - Haifa	Haifa
Israel	Investigator Site - Tel Aviv	Tel Aviv
Italy	Investigator Site - Milan	Milan
Italy	Investigator Site - Milano	Milano
Italy	Investigator Site - Napoli	Napoli
Italy	Investigator Site - Roma	Roma
Portugal	Investigator Site - Lisboa	Lisboa
Portugal	Investigator Site - Porto	Porto
Spain	Investigator Site - Barcelona	Barcelona
Spain	Investigator Site - Barcelona	Barcelona
Spain	Investigator Site - Madrid	Madrid
Spain	Investigator Site - Santa Cruz de Tenerife	Santa Cruz de Tenerife
Spain	Investigator Site - Sevilla	Sevilla
United Kingdom	Investigator Site - Bradford	Bradford
United Kingdom	Investigator Site - Manchester	Manchester
United Kingdom	Investigator Site - Nottingham	Nottingham
United States	Investigator Site - Athens	Athens	Georgia
United States	Investigator Site - Baltimore	Baltimore	Maryland
United States	Investigator Site - Boston	Boston	Massachusetts
United States	Investigator Site - Chapel Hill	Chapel Hill	North Carolina
United States	Investigator Site - Columbus	Columbus	Ohio
United States	Investigator Site - Fort Worth	Fort Worth	Texas
United States	Investigator Site - Germantown	Germantown	Tennessee
United States	Investigator Site - Houston	Houston	Texas
United States	Investigator Site - Miami	Miami	Florida
United States	Investigator Site - Minneapolis	Minneapolis	Minnesota
United States	Investigator Site - New York	New York	New York
United States	Investigator Site - Orange	Orange	California
United States	Investigator Site - Plantation	Plantation	Florida
United States	Investigator Site - Saint Louis	Saint Louis	Missouri
United States	Investigator Site - Salt Lake City	Salt Lake City	Utah
United States	Investigator Site - San Francisco	San Francisco	California
United States	Investigator Site - Seattle	Seattle	Washington
United States	Investigator Site - Tucson	Tucson	Arizona
United States	Investigator Site - West Palm Beach	West Palm Beach	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Nektar Therapeutics

Countries where clinical trial is conducted

United States,  Australia,  Belgium,  Canada,  France,  Israel,  Italy,  Portugal,  Spain,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Survival (OS) of Patients	To compare Overall Survival (OS) of patients who receive 145 mg/m2 NKTR-102 given once every 21 days (q21d) with OS of patients who receive Treatment of Physician's Choice (TPC). Overall survival is defined as the time from the date of randomization to the date of death from any cause. Patients will be followed until their date of death or until final database closure. Patients who are lost-to-follow-up or are alive at the time of analysis will be censored at the time they were last known to be alive or at the date of event cut-off for OS analysis.	Within 3 years from study start
Secondary	Progression-Free Survival (Outside the Central Nervous System)	Progression-Free Survival (PFS) is defined as the time from the date of randomization to the earliest evidence of documented Progressive Disease (PD) or of death from any cause. The date of global deterioration or symptomatic deterioration will not be used as the date of PD. The assessment of PFS outside the CNS will utilize RECIST criteria v1.1.	Through study completion, an expected average of 1 year
Secondary	Progression-Free Survival in Brain Metastasis (PFS-BM)	Progression-Free Survival in Brain Metastasis (PFS-BM) is defined as the time from the date of randomization to the earliest evidence of documented Progressive Disease (PD) per Response Assessment in Neuro-Oncology-Brain Metastases (RANO-BM) in brain metastases or death from any cause. The PD will also be determined by the investigator's assessments. Progressive Disease (PD) is defined as at least a 20% increase in the sum of longest diameters of CNS target lesions, taking as reference the smallest sum on study. This included the baseline sum if that was the smallest on study. In addition to the relative increase of 20%, at least 1 lesion had to increase by an absolute value of 5 mm or more to be considered progression.	Through study completion, an expected average of 1 year
Secondary	Progression-Free Survival (Overall)	Progression-free survival (CNS and peripheral) is defined as the time from the date of randomization to the earliest evidence of documented PD in either the CNS or peripheral (using RANO-BM) or death from any cause. The PD will be determined by both the investigator's and the central imaging facility assessments. The same statistical methods that were used for PFS and PFS-BM will be used for PFS (Overall). Progressive Disease (PD) is defined as at least a 20% increase in the sum of longest diameters of CNS target lesions, taking as reference the smallest sum on study. This included the baseline sum if that was the smallest on study. In addition to the relative increase of 20%, at least 1 lesion had to increase by an absolute value of 5 mm or more to be considered progression.	Through study completion, an expected average of 1 year
Secondary	Objective Response Rates (ORR) of the NKTR-102 Treatment and the Treatment of Physician's Choice (TPC)	RECIST criteria for lesions outside the Central Nervous System (CNS); RANO-BM criteria for CNS lesions) based upon the best response as assessed by the central imaging facility. CR is defined as disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) had to have reduction in short axis to < 10 mm. PR is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. ORR is calculated as the sum of CR and PR. Progressive Disease (PD) is defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this included the baseline sum if that was the smallest on study). Stable Disease (SD) is defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum diameters while on study.	Through study completion, an expected average of 1 year
Secondary	Clinical Benefit Rate (CBR)	Clinical Benefit Rate will be defined as the proportion of patients having a Complete Response (CR), Partial Response (PR), or Stable Disease (SD) for at least 4 months (= 120 days). CR is defined as disappearance of all target lesions for at least 4 weeks with no new lesions, not use of corticosteroids, and patient was stable or improved clinically. PR is defined as at least a 30% decrease in the sum of longest diameters sustained for at least 4 weeks, no new lesions; stable to decreased corticosteroid dose; stable or improved clinically. Progressive Disease (PD) is defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this included the baseline sum if that was the smallest on study). Stable Disease (SD) is defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum diameters while on study.	For at least 4 months, with an expected average of 1 year
Secondary	Duration of Response (DoR)	Duration of response (DoR) outside the CNS will be defined as the time from first documented CR or PR until the earliest evidence of disease progression per RECIST v1.1 or death from any cause. CR is defined as disappearance of all target lesions for at least 4 weeks with no new lesions, not use of corticosteroids, and patient was stable or improved clinically. PR is defined as at least a 30% decrease in the sum of longest diameters sustained for at least 4 weeks, no new lesions; stable to decreased corticosteroid dose; stable or improved clinically. Progressive Disease (PD) is defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this included the baseline sum if that was the smallest on study). Stable Disease (SD) is defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum diameters while on study.	Through study completion, an expected average of 1 year
Secondary	Compare Health-Related Quality of Life (HRQoL) Using the European Organisation for Treatment of Cancer (EORTC) Quality of Life Core 30 (QLQ-C30) Module With the Brain Neoplasms 20-question (BN-20) Subscale.	The EORTC QLQ-BN20 Scale has a series of 20 questions each of which involve reporting a scale from 1-4. It is an increasing scale where a score of one indicates "not at all" while a score of four indicates "very much". The minimum score is 20 and the maximum score is 80. The higher the score the worse the outcome.	Baseline (prior to first dose of study treatment in Cycle 1 [cycle length = 21 for NKTR-102 or 28 days for TPC] and end of Cycle 44.
Secondary	Compare Health-Related Quality of Life (HRQoL) Using the the EuroQoL 5D (EQ-5D-5L™)	The EQ-5D-5L scale is used to measure health by having a patient answer a series of questions. There are a series of 5 questions each of which is scaled from a score of 4-20 in increasing increments of 4. The scale is numbered from 0 to 100 where 100 means the beast health you can imagine and 0 means the worst health.	Baseline (prior to first dose of study treatment in Cycle 1 [cycle length = 21 for NKTR-102 or 28 days for TPC] and end of Cycle 44
Secondary	Compare Health-Related Quality of Life (HRQoL) Using the Brief Fatigue Inventory (BFI)	The Brief Fatigue Inventory scale utilizes a series of 4 questions. The first three are scored with a scale from 1-10. The fourth question has 6 six sub components each of which are scored with a scale of 1-10. For every scale, a score of 0 indicates no fatigue/interference where a score of 10 indicates as bad as you can imagine. A patient's score can range from 0 to 100 where 0 indicates the best outcome and 100 indicates the worst.	Baseline (prior to first dose of study treatment in Cycle 1 [cycle length = 21 for NKTR-102 or 28 days for TPC] and end of Cycle 44
Secondary	Magnitude of Clinical Benefit Assessed by ESMO-MCBS Derived From Overall Survival	The magnitude of clinical benefit of NKTR-102 is assessed by the European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS) (v1.0). The scale is graded 5, 4, 3, 2, 1, where grades 5 and 4 represent a high level of proven clinical benefit, and grade 1 represents no clinical benefit. To determine the magnitude of clinical benefit when the median OS with the standard of treatment is = 1 year, the score is derived from the Hazard Ratio (HR) of Overall Survival, overall survival gain, and QoL improvement between two treatment arms. Values reported in the data table are Overall Survival values.	Through study completion, within 3 years from study start
Secondary	Number of Participants With Adverse Events as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) v4.3	The number of participants with adverse events as assessed by Common Terminology Criteria for Adverse Events (CTCAE) v4.3	Through study completion, an expected average of 1 year