Sacituzumab Govitecan in Primary HER2-negative Breast Cancer

Triple Negative Breast Cancer Clinical Trial

— SASCIA  

Official title:

Phase III Postneoadjuvant Study Evaluating Sacituzumab Govitecan, an Antibody Drug Conjugate in Primary HER2-negative Breast Cancer Patients With High Relapse Risk After Standard Neoadjuvant Treatment - SASCIA

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04595565
• Other study ID #: GBG102 - SASCIA
• Status: Recruiting
• Phase: Phase 3
• Start date: October 28, 2020
• Est. completion date: March 30, 2029

Study information

• Verified date: February 2023
• Source: German Breast Group
• Contact: Verena Katzki, Dr.
• Phone: 0049610274800
• Email: SASCIA[@]gbg.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Phase III, prospective, multi-center, randomized, open label, parallel group, study in patients with HER2-negative breast cancer with residual disease after neoadjuvant chemotherapy with 1:1 allocation to: - Arm A: Sacituzumab govitecan (days 1, 8 q3w for eight cycles); - Arm B: treatment of physician´s choice (TPC, defined as capecitabine or platinum-based chemotherapy for eight cycles or observation. Treatment in either arm will be given for eight cycles. In patients with HR-positive breast cancer, endocrine-based therapy, which includes the use of CDK4/6 inhibitors, will be administered according to local guidelines. The start of endocrine therapy will be at the discretion of the investigator; however, it will be encouraged to start after surgery/radiotherapy in patients without additional cytotoxic agents. Adjuvant pembrolizumab can be given until the completion of radiotherapy before randomization. Within the study the use of pembrolizumab in patients with TNBC who received pembrolizumab as neoadjuvant therapy is allowed as monotherapy in the TPC arm, according to the approval of pembrolizumab in this setting.

Description:

Neoadjuvant chemotherapy (NACT) allows monitoring of tumor response to treatment and a pathological complete response (pCR) is associated with superior survival. This association is strongest in the most aggressive subtype, i.e. in patients with triple-negative breast cancer (TNBC). Patients with TNBC not achieving a pCR have a 5-year event free survival rate of about 50%. The association between pCR and prognosis is less pronounced in HR-positive/HER2-negative patients. However, the CPS+EG scoring system for prognosis after neoadjuvant chemotherapy, taking into account clinical stage, post treatment pathological stage, estrogen receptor status and grade, leads to an improved estimate of prognosis allowing to select patients at high risk of relapse for post-neoadjuvant therapy. Patients with TNBC not achieving a pCR as well as those with HR-positive/HER2-negative tumors and a CPS+EG score of 3 or 2/ypN+ are at high risk of relapse, warranting additional experimental therapies after NACT. There is proof of concept, that post-neoadjuvant therapy can significantly improve survival. First data was provided by the CREATE X trial, randomizing patients with residual tumor after neoadjuvant chemotherapy to either capecitabine or observation. CREATE X included HER2-negative patients and demonstrated a significant improvement in disease-free survival (DFS) and overall survival (OS) in the overall population, which was confined to the TNBC subgroup. Recently, the randomized post-neoadjuvant phase III KATHERINE study demonstrated an improved invasive disease-free survival in HER2-positive patients without pCR after trastuzumab +/- pertuzumab treated postoperatively with T-DM1, an antibody-drug-conjugate compared to trastuzumab. Sacituzumab govitecan has demonstrated unprecedented activity in heavily pretreated patients with metastatic triple-negative and HR-positive/HER2-negative breast cancer, even after prior immune-checkpoint inhibitors or CDK4/6 and mTOR inhibitors. Based on the results of the phase I/II study, sacituzumab govitecan was granted a breakthrough therapy designation for the treatment of patients with advanced or metastatic TNBC who have received at least two previous lines of treatment for metastatic disease. The efficacy of sacituzumab govitecan in advanced TNBC was confirmed in the phase III ASCENT trial. Based on this study, sacituzumab govitecan received regular approval. Additionally, the TROPiCS-02 study showed an improvement in progression-free survival and OS over single-agent chemotherapy and a manageable safety profile in patients with heavily pre-treated HR-positive/HER2-negative endocrine-resistant, unresectable locally advanced or metastatic BC.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1332
• Est. completion date: March 30, 2029
• Est. primary completion date: March 30, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 99 Years

Eligibility

Inclusion Criteria:

1. Written informed consent prior to beginning specific protocol procedures, including expected cooperation of the patients for the treatment and follow-up, must be obtained and documented according to the local regulatory requirements.

2. Age at diagnosis at least 18 years.

3. Willingness and ability to provide archived formalin fixed paraffin embedded tissue (FFPE) block from surgery after neoadjuvant chemotherapy and from core biopsy before start of neoadjuvant chemotherapy, which will be used for centralized prospective confirmation of HR status, HER2 status, Ki-67 and tumor-infiltrating lymphocytes (TILs) and for retrospective exploratory correlation between genes, proteins, and mRNAs relevant to sensitivity/resistance to the investigational agents. For patients with bilateral carcinoma, FFPE blocks from both sides have to be provided for central testing.

4. Histologically confirmed unilateral or bilateral primary invasive carcinoma of the breast, confirmed histologically by core biopsy. The lead tumor has to be defined by the investigator based on the inclusion criteria for the respective subtype and on the risk status.

5. Centrally confirmed HER2-negative (IHC score 0-1 or FISH negative according to ASCO/CAP guideline) and either

• HR-positive (=1% positive stained cells) disease or
• HR-negative (<1% positive stained cells) assessed preferably on tissue from postneoadjuvant residual invasive disease of the breast, or if not possible, of residual nodal invasion. If not evaluable, core of diagnostic biopsy will be used. In case of bilateral breast cancer, HER2-negative status has to be confirmed for both sides.

6. Patients with residual invasive disease after neoadjuvant chemotherapy at high risk of

recurrence defined by either:

• For HR-negative: any residual invasive disease > ypT1mi and/or ypN1>1mm
• For HR-positive disease: a CPS+EG score = 3 or CPS+EG score 2 and ypN+ using local ER and grade assessed on core biopsies taken before start of neoadjuvant treatment.

7. Adequate surgical treatment including resection of clinically evident disease and ipsilateral axillary lymph node dissection. SNB before NACT is discouraged. Axillary dissection before NACT is not permitted. Axillary dissection, including Targeted Axillary Dissection (TAD) should be performed according to guidelines. Histologic complete resection (R0) of all invasive and in situ tumors is required.

8. Patients must have received neoadjuvant taxane-based chemotherapy for 16 weeks (anthracyclines are permitted). This period must include 6 weeks of a taxane containing neoadjuvant chemotherapy (exception: for patients with progressive disease that occurred after at least 6 weeks of taxane-containing neoadjuvant chemotherapy, a total treatment period of less than 16 weeks is also eligible).

9. No clinical evidence for locoregional or distant relapse during or after preoperative chemotherapy. Local progression during chemotherapy is not an exclusion criterion if adequate local control could be obtained.

10. In case of local progression during neoadjuvant therapy, distant metastases must be excluded by adequate imaging (CT/MRI recommend) prior to entering the trial.

11. Immune checkpoint inhibitor / immunotherapy during (neo)adjuvant therapy is allowed until the completion of radiotherapy.

12. Patients with known gBRCA1/2 mutation without indication to adjuvant olaparib therapy are allowed to participate in the trial.

13. An interval of less than 16 weeks since the date of final surgery or less than 10 weeks from completing radiotherapy (whichever occurs last) and the date of randomization is required.

14. Radiotherapy should be delivered before the start of study treatment. Radiotherapy to the breast is indicated in all patients with breast conserving surgery and to the chest wall and lymph nodes according to local guidelines as well as in all patients with cT3/4 or ypN+ disease treated by mastectomy.

15. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.

16. Resolution of all acute toxic effects of prior anti-cancer therapy or surgical procedure or radiotherapy to NCI CTCAE v 5.0 grade = 1 (except alopecia or other toxicities not considered a safety risk for the patients at the investigator´s discretion).

17. Estimated life expectancy of at least 5 years irrespective of the diagnosis of breast cancer.

18. The patient must be accessible for scheduled visits, treatment and follow-up.

19. Normal cardiac function after neoadjuvant chemotherapy must be confirmed according to local guidelines. Results for LVEF must be above the normal limit of the institution.

20. Laboratory requirements:

Hematology

• Absolute neutrophil count (ANC) =1.5 x 109 / L
• Platelets =100 x 109 / L
• Hemoglobin =10 g/dL (=6.2 mmol/L) Hepatic function
• Total bilirubin <1.25x UNL
• AST and ALT =1.5x UNL
• Alkaline phosphatase =2.5x UNL Renal Function
• <1.25x ULN creatinine or creatinine clearance =30 ml/min (according to Cockroft-Gault, if creatinine is above UNL).

21. Negative pregnancy test (urine or serum) within 14 days prior to randomization for all women of childbearing potential. A woman is considered to be of childbearing potential

if she is not postmenopausal. Postmenopausal is defined as:

• Age =60 years
• Age <60 years and =12 continuous months of amenorrhea with no identified cause other than menopause
• Surgical sterilization (bilateral oophorectomy and/or hysterectomy).

22. For women of childbearing potential and males with partners of childbearing potential:

agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods that result in a failure rate of < 1% per year during the treatment period and for at least 6 months after the last dose of sacituzumab govitecan for female patients and for at least 3 months for male patients; for at least 6 months after the last dose of capecitabine or carboplatin/cisplatin for female patients and for at least 3 months after the last dose of capecitabine or 6 months after the last dose of carboplatin/cisplatin for male patients. Examples of non-hormonal contraceptive methods with a failure rate of < 1% per year include: bilateral tubal ligation; male partner sterilization; intrauterine devices.

23. Complete staging work-up prior to the initiation of neoadjuvant chemotherapy. Missing staging investigations must be performed prior to randomization.

Exclusion Criteria:

1. Known hypersensitivity reaction to one of the compounds or substances used in this protocol.

2. Patients with definitive clinical or radiologic evidence of stage IV cancer (metastatic disease) are not eligible.

3. Patients with known gBRCA1/2 mutation and indicated or planned adjuvant olaparib therapy if available.

4. Patients with a history of any malignancy are ineligible with the following

exceptions:

• Patient has been disease-free for at least 5 years and is at low risk for recurrence of that malignancy
• CIS of the cervix, basal cell and squamous cell carcinomas of the skin.

5. Female patients: pregnancy or lactation at the time of randomization or intention to become pregnant during the study and up to 6 months after sacituzumab govitecan and up to 6 months after treatment with capecitabine or carboplatin/cisplatin.

6. Severe and relevant co-morbidity that would interact with the application of cytotoxic agents or the participation in the study, including Gilbert´s disease, Crigler-Najjar-Syndrome, known hepatitis B, hepatitis C, known HIV positivity or known autoimmune disease other than diabetes, vitiligo, or stable thyroid disease, vitiligo, or other autoimmune skin disease with dermatologic manifestations only are permitted

provided all of the following conditions are met:

• Rash must cover < 10% of body surface area
• Disease is well controlled at baseline and requires only low-potency topical corticosteroids
• No occurrence of acute exacerbations of the underlying condition requiring psoralen plus ultraviolet A radiation (PUVA), methotrexate, retinoids, biologic agents, oral calcineurin inhibitors, or high-potency or oral corticosteroids within the previous 12 months.

7. Any condition that interferes with the safe administration of the treatment of physician´s choice in case the patient is randomized into the TPC arm.

8. Known or suspected congestive heart failure (>NYHA I) and/or coronary heart disease, angina pectoris requiring antianginal medication, previous history of myocardial infarction, evidence of prior infarction on ECG, uncontrolled or poorly controlled arterial hypertension (i.e. BP >150/90 mmHg under treatment with at maximum three antihypertensive drugs), rhythm abnormalities requiring permanent treatment (excluding chronic atrial fibrillation not requiring a pacemaker), clinically significant valvular heart disease, supraventricular and nodal arrhythmias requiring a pacemaker or not controlled with medication;conduction abnormality requiring a pacemaker.

9. History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g. bronchiolitis obliterans), drug-induced pneumonitis, idiopathic pneumonitis or active pneumonitis on chest CT scan.

10. Receipt of live attenuated vaccination within 30 days prior to study entry or within 30 days of receiving chemotherapy.

11. History of significant neurological or psychiatric disorders including psychotic disorders, dementia or seizures that would prohibit the understanding and giving of informed consent.

12. Any condition that, in the opinion of the investigator, would interfere with evaluation of study treatment or interpretation of patient safety or study results.

13. Known allergic reactions to irinotecan.

14. Concurrent treatment with:

• Chronic corticosteroids prior to study entry with the exceptions of intranasal and inhaled corticosteroids or systemic corticosteroids at physiological doses, which are not to exceed 10 mg/day of prednisone, or equivalent corticosteroid.

Related Conditions & MeSH terms

• Breast Neoplasms
• HER2-negative Breast Cancer
• Triple Negative Breast Cancer
• Triple Negative Breast Neoplasms

Intervention

Drug:
• Capecitabine
2000 mg/m² day 1-14 q21 day cycle for eight cycles
• Carboplatin
AUC 5 q3w or AUC 1.5 weekly for eight 3 weekly cycles
• Cisplatin
25mg/m3 weekly or 75 mg/m3 q3w
• Sacituzumab govitecan
10 mg/kg body weight on days 1, 8 q3w

Locations

Country	Name	City	State
Austria	MUG - Univ.-Klinik f. Frauenheilkunde u. Geburtshilfe Graz	Graz
Austria	MUG - Univ.-Klinik f. Innere Medizin Graz	Graz
Austria	MUI - Univ. Klinik f. Frauenheilkunde Innsbruck	Innsbruck
Austria	Universitätsklinikum Krems	Krems
Austria	LKH Hochsteiermark Leoben	Leoben
Austria	Ordensklinikum Linz GmbH - BHS	Linz
Austria	TumorZentrum Kepler Uniklinikum Linz	Linz
Austria	LKH Salzburg - PMU	Salzburg
Austria	Universitätsklinikum St. Pölten	St. Pölten
Austria	Salzkammergut-Klinikum Vöcklabruck	Vöcklabruck
Austria	Klinikum Wels-Grieskirchen GmbH	Wels
Austria	Klinik Hietzing	Wien
Austria	MUW - AKH Wien	Wien
Austria	MUW - Med. Univ.-Klinik AKH Wien	Wien
Austria	Landesklinikum Wr. Neustadt	Wiener Neustadt
Belgium	AZ KLINA	Brasschaat
Belgium	Institut Jules Bordet	Brussels
Belgium	CHR de la Citadelle	Liège
Belgium	CHU UCL Namur/Site Sainte Elisabeth	Namur
France	Institut de cancérologie de l'ouest (Angers)	Angers
France	Institut Sainte Catherine	Avignon
France	Clinique Tivoli Ducos	Bordeaux
France	Institut Bergonié	Bordeaux
France	Polyclinique Bordeaux Nord Aquitaine	Bordeaux
France	CH Fleyriat	Bourg En Bresse
France	Centre François Baclesse	Caen
France	Centre Jean Perrin 5	Clermont Ferrand
France	Centre Georges François Leclerc	Dijon
France	Centre Oscar Lambret	Lille
France	CHU de Limoges	Limoges
France	GHBS hôpital du Scorff	Lorient
France	Centre Leon Berard	Lyon
France	Institut Paoli-Calmettes	Marseille
France	Institut régional du Cancer de Montpellier - ICM Val d'Aurelle	Montpellier
France	Hôpital privé du Confluent	Nantes
France	Centre Antoine Lacassagne	Nice
France	Groupe Hospitalier Diaconesses Croix Saint Simon	Paris
France	Institut Curie (Paris)	Paris
France	Centre Hospitalier de Pau	Pau
France	Hôpital Privé Des Côtes d'Armor- Centre CARIO-HPCA	Plérin
France	Institut Godinot	Reims
France	Centre Eugène Marquis	Rennes
France	Centre Henri Becquerel	Rouen
France	Gcs Rissa	Sarcelles
France	Institut de Cancérologie Strasbourg Europe-ICANS	Strasbourg
France	Institut Claudius Regaud IUCTO	Toulouse
France	CHU Bretonneau	Tours
France	Institut de Cancérologie de Lorraine	Vandoeuvre-lès-Nancy
France	Gustave Roussy Cancer Campus	Villejuif
Germany	Universitätsklinikum Aachen	Aachen	Nordrhein-Westfalen
Germany	Gemeinschaftspraxis Dres. Heinrich / Bangerter	Augsburg	Bayern
Germany	Hochwaldkrankenhaus, Gesundheitszentrum Wetterau gGmbH	Bad Nauheim	Hessen
Germany	Sozialstiftung Bamberg, Klinik am Bruderwald	Bamberg	Bayern
Germany	Charité Universitätsmedizin Campus Charité Mitte	Berlin	Brandenburg
Germany	MediOnko-Institut GbR	Berlin
Germany	Onkologische Schwerpunktpraxis, Studiengesellschaft Onkologie Bielefeld GbR	Bielefeld	Nordrhein-Wastfalen
Germany	Kreiskliniken Böblingen gGmbH	Böblingen	Baden-Württemberg
Germany	Marienhospital Bottrop gGmbH	Bottrop	Nordrhein-Westfalen
Germany	Studien GbR Braunschweig	Braunschweig	Niedersachsen
Germany	Hämato-Onkologie im Medicum	Bremen
Germany	Klinikum Chemnitz	Chemnitz	Sachsen
Germany	DONAUISAR Klinikum Deggendorf	Deggendorf
Germany	St, Johannes Hospital	Dortmund	Nordrhein-Westfalen
Germany	Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden	Dresden	Sachsen
Germany	Heinrich-Heine-Universität Düsseldorf	Düsseldorf	Nordrhein-Westfalen
Germany	Praxis Dr. B. Adhami	Erkelenz	Nordrhein-Westfalen
Germany	Universitätsklinik Erlangen	Erlangen	Bayern
Germany	Kliniken Essen-Mitte Evang. Huyssens-Stiftung/Knappschaft GmbH	Essen	Nordrhein-Westfalen
Germany	Universitätsklinikum Essen	Essen	Nordrhein-Westfalen
Germany	Klinikum Esslingen GmbH	Esslingen	Baden-Württember
Germany	Klinikum Esslingen GmbH	Esslingen am Neckar	Baden-Württemberg
Germany	AGAPLESION Markus Krankenhaus	Frankfurt	Hessen
Germany	Centrum für Hämatologie und Onkologie am Bethanien-Krankenhaus	Frankfurt	Hessen
Germany	Klinikum der J. W. Goethe Universität	Frankfurt	Hessen
Germany	Universitätsklinikum Freiburg	Freiburg	Baden- Württemberg
Germany	Schwerpunktpraxis der Gynäkologie und Onkologie	Fürstenwalde	Brandenburg
Germany	MVZ II der Niels Stensen Kliniken	Georgsmarienhütte	Niedersachsen
Germany	SRH Wald-Klinikum Gera gGmbH, Brustzentrum Ostthüringen	Gera	Thüringen
Germany	Universitäsklinik Halle/Saale	Halle	Sachsen-Anhalt
Germany	Mammazentrum Hamburg	Hamburg
Germany	Klinikum Stadt Hanau	Hanau	Hessen
Germany	DIAKOVERE Henriettenstift Gynäkologie	Hannover	Niedersachsen
Germany	Städtisches Klinikum Karlsruhe	Karlsruhe	Baden-Württemberg
Germany	ViDia Christliche Kliniken Karlsruhe	Karlsruhe	Baden-Württemberg
Germany	Elisabeth Krankenhaus	Kassel	Hessen
Germany	Klinikum Kassel GmbH, Gynäkologische Ambulanz	Kassel	Hessen
Germany	Praxisklinik für Hämatologie und Onkologie	Koblenz	Rheinland-Pfalz
Germany	Kliniken der Stadt Köln	Köln	Nordrhein-Westfalen
Germany	St. Elisabeth-Krankenhaus, Brustzentrum Köln-Hohenlind	Köln	Nordrhein-Westfalen
Germany	Klinikum Landshur GmbH	Landshut	Bayern
Germany	Klinikum der Otto-v.-Guericke-Universität	Magdeburg	Sachsen-Anhalt
Germany	Uniklinikum, Klinik für Geburtshilfe und Gynäkologie	Mainz	Rheinland-Pfalz
Germany	Universitätsklinikum Mannheim, Frauenklinik	Mannheim	Baden-Württemberg
Germany	Institut für Versorgungsforschung	Mayen	Rheinland-Pfalz
Germany	Rotkreuzklinikum München	München
Germany	Universitätsklinikum Münster	Münster	Nordrhein-Westfalen
Germany	Ruppiner Kliniken	Neuruppin	Brandenburg
Germany	MVZ Nordhausen gGmbH im Südharz Krankenhaus	Nordhausen	Thüringen
Germany	medius Kliniken gGmbH Nürtingen	Nürtingen	Baden-Württemberg
Germany	Sana Klinikum Offenbach	Offenbach	Hessen
Germany	Klinikum Oldenburg AöR	Oldenburg	Niedersachsen
Germany	Studienzentrum Onkologie Ravensburg	Ravensburg
Germany	Oncologianova GmbH	Recklinghausen	Nordrhein-Westfalen
Germany	Klinikum am Steinenberg	Reutlingen	Baden-Württemberg
Germany	Klinikum Obergöltzsch Rodewisch	Rodewisch	Sachsen
Germany	Klinikum Südstadt	Rostock	Mecklenburg-Vorpommern
Germany	Caritasklinik St. Theresia	Saarbrücken	Saarland
Germany	Onkologische Schwerpunkt- Praxis Speyer	Speyer	Rheinland-Pfalz
Germany	MVZ in der Klinik Dr. Hancken	Stade	Niedersachsen
Germany	ohanniter Krankenhaus Genthin-Stendal	Stendal	Sachsen-Anhalt
Germany	SRH Zentralklinikum Suhl	Suhl	Thüringen
Germany	Kreiskrankenhaus Torgau	Torgau	Sachsen
Germany	Gemeinschaftspraxis Dr. U. Kronawitter/ Dr. C. Jung	Traunstein	Bayern
Germany	Universitätsklinikum Ulm	Ulm	Baden-Württemberg
Germany	Schwarzwald-Baar-Klinikum	Villingen-Schwenningen	Baden-Württemberg
Germany	Helios Klinik Wiesbaden	Wiesbaden	Hessen
Germany	Gemeinschaftspraxis Dallacker / Eilers	Wolfenbüttel	Niedersachsen
Germany	Klinikum Worms	Worms	Rheinland-Pfalz
Germany	Helios Universitätsklinikum Wuppertal	Wuppertal	Nordrhein-Westfalen
Ireland	Cork University Hospital	Cork
Ireland	Beaumont Hospital	Dublin
Ireland	Mater Misericordiae University Hospital	Dublin
Ireland	St James's Hospital	Dublin
Ireland	St Vincent's University Hospital	Dublin
Ireland	University Hospital Limerick	Limerick
Ireland	University Hospital Waterford	Waterford
Italy	Centro di Riferimento Oncologico (CRO) - IRCCS	Aviano
Italy	Oncologia Medica Ospedale di Bolzano	Bolzano
Italy	IRCCS AOU San Martino-IST	Genova
Italy	Istituto Europeo di Oncologia	Milano
Italy	Università del Piemonte Orientale	Novara
Italy	Istituti Clinici Scientifici Maugeri SpA-SB	Pavia
Italy	Ospedale Di Trento- Presidio Ospedaliero S.Chiara	Trento
Spain	COMPLEJO HOSPITALARIO UNIVERSITARIO A CORUÑA-Hospital Teresa Herrera (CHUAC)	A Coruña
Spain	Complejo Hospitalario Universitario de Albacete	Albacete
Spain	Hospital Virgen de Los Lirios	Alcoy
Spain	Hospital General Universitario de Alicante	Alicante
Spain	Hospital Universitario de Cruces	Barakaldo	Bizkaia
Spain	Consorci Sanitari de Terrassa	Barcelona
Spain	Corporació Sanitária Parc Taulí	Barcelona
Spain	Hospital de La Santa Creu I Sant Pau	Barcelona
Spain	Hospital de Mataró	Barcelona
Spain	Ico de Badalona (Hospital Universitari Germans Trias I Pujol)	Barcelona
Spain	Hospital San Pedro de Alcántara	Cáceres
Spain	Consorcio Hospitalario Provincial de Castellón	Castellón De La Plana
Spain	Hospital Galdakao-Usansolo	Galdakao
Spain	Complejo Hospitalario de Jaén	Jaen
Spain	Clinica Universidad de Navarra	Madrid
Spain	Hospital Universitario 12 de Octubre	Madrid
Spain	Hospital Universitario de Fuenlabrada	Madrid
Spain	Hospital Universitario Fundación Alcorcón	Madrid
Spain	Hospital Universitario La Paz	Madrid
Spain	Hospital Universitario Quirónsalud Madrid	Madrid
Spain	Hospital Universitario Ramón Y Cajal	Madrid
Spain	Hospital Universitario Severo Ochoa	Madrid
Spain	Hospital Clinico Universitario Virgen de la Victoria	Málaga
Spain	Hospital Clínico Universitario Virgen de La Arrixaca	Murcia
Spain	Hospital General Universitario Morales Meseguer	Murcia
Spain	Complejo Hospitalario Universitario de Orense-Hospital Santa Maria Nai	Ourense
Spain	Hospital Universitari Son Espases	Palma de Mallorca
Spain	Hospital Universitari Son Llátzer	Palma de Mallorca
Spain	Clinica Universidad de Navarra	Pamplona
Spain	Hospital Universitari Sant Joan de Reus	Reus
Spain	Hospital Universitario de Salamanca	Salamanca
Spain	Hospital Universitario de Canarias	Santa Cruz de Tenerife
Spain	Hospital Universitario Ntra.Sra. de Candelaria	Santa Cruz de Tenerife
Spain	Complejo Hospitalario Universitario de Santiago (Chus)	Santiago De Compostela
Spain	Hospital Quirónsalud Sagrado Corazón	Sevilla
Spain	Hospital Universitario Virgen de La Macarena	Sevilla
Spain	Consorci Hospital General Universitari de Valencia	Valencia
Spain	Fundación Instituto Valenciano de Oncología	Valencia
Spain	Hospital Clinico Universitario de Valencia	València
Spain	Hospital Clínico Universitario de Valladolid	Valladolid
Spain	Hospital Universitario Araba-Txagorritxu	Vitoria
Switzerland	Cancer Care Center	Basel
Switzerland	Kantonsspital Graubünden	Chur
Switzerland	Breast Center KSSG	St. Gallen
Switzerland	Kantonsspital Winterthur	Winterthur
Switzerland	Brust-Zentrum Zürich	Zürich

Sponsors (7)

Lead Sponsor	Collaborator
German Breast Group	Austrian Breast & Colorectal Cancer Study Group, Cancer Trials Ireland, ETOP IBCSG Partners Foundation, Gilead Sciences, Spanish Breast Cancer Research Group (GEICAM), UNICANCER

Countries where clinical trial is conducted

Austria,  Belgium,  France,  Germany,  Ireland,  Italy,  Spain,  Switzerland, 

References & Publications (1)

Marmé F, Hanusch C, Furlanetto J, et al. Safety interim analysis (SIA) of the phase III postneoadjuvant SASCIA study evaluating sacituzumab govitecan (SG) in patients with primary HER2-negative breast cancer (BC) at high relapse risk after neoadjuvant tre

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Invasive disease free survival (iDFS) between patients treated with sacituzumab govitecan vs. treatment of physician's choice.	iDFS is defined as time from randomization until first iDFS event: local invasive recurrence following mastectomy, local invasive recurrence in the ipsilateral breast following lumpectomy, regional recurrence, distant recurrence, contralateral invasive breast cancer, second non-breast primary cancer (excluding squamous or basal cell carcinoma of the skin), or death from any cause. (according to Hudis (J Clin Oncol 2007) ); There will be one interim analysis for efficacy after 2/3 of the events to allow for early stopping of the trial due to overwhelming efficacy.	Assuming 3.25 years of recruitment with 12 months ramp-up and 42 patients per month at peak and 3 years of follow-up after the last patient in, 396 events will be needed and final analysis is expected 75 months after study start.
Secondary	To compare overall survival (OS) between patients treated with sacituzumab govitecan vs. treatment of physician's choice.	OS is defined as the time from randomization until death from any cause.; One interim analysis of the key secondary endpoint OS will be performed at the time of the final analysis of the iDFS.	Assuming 3.25 years of recruitment 398 events will be needed with a power of 80% and final analysis is expected after 99 months (8.3 years after first patient in, 2 years after final analysis of iDFS).
Secondary	Distant disease-free survival (DDFS) between patients treated with sacituzumab govitecan vs. treatment of physician's choice.	DDFS is defined as the time from randomization until distant recurrence of disease, second primary invasive cancer (non-breast, excluding squamous or basal cell carcinoma of the skin), and death due to any cause.	DDFS will be analyzed at the time of the final iDFS analysis (is expected 75 months after study start)
Secondary	To compare the invasive breast cancer-free survival (iBCFS) between both groups.	iBCFS is defined as the time from randomization until first iDFS event excluding any second non-breast primary cancer.	iBCFS will be analyzed at the time of the final iDFS analysis (is expected 75 months after study start)
Secondary	Locoregional recurrences-free interval between patients treated with sacituzumab govitecan vs. treatment of physician's choice.	LRRFI is defined as the time from randomization until any loco-regional (ipsilateral breast (invasive), chest wall, local/regional lymph nodes) recurrence of disease or any invasive contralateral breast cancer whichever occurs first. Distant recurrence, secondary malignancy and death are considered as competing risks and will be accounted for in the analysis.	Time-to-Event Outcome Measure up to 75 month after study start.
Secondary	iDFS in stratified subgroups.	HR-negative vs. HR-positive ypN+ vs. ypN0.	Will be analyzed at the time of the final iDFS analysis (is expected 75 months after study start)
Secondary	OS in stratified subgroups.	HR-negative vs. HR-positive ypN+ vs. ypN0.	Will be analyzed after 99 months (8.3 years after first patient in, 2 years after final analysis of iDFS)
Secondary	iDFS in exploratory subgroups.	Prior platinum therapy (TNBC); Prior immune-checkpoint inhibitor therapy (TNBC); Experimental arm vs. active TPC in TNBC, overall and in subgroups of different active TPC; low vs. high TROP2-expression	Will be analyzed at the time of the final iDFS analysis (is expected 75 months after study start)
Secondary	OS in exploratory subgroups.	Prior platinum therapy (TNBC); Prior immune-checkpoint inhibitor therapy (TNBC); Experimental arm vs. active TPC in TNBC, overall and in subgroups of different active TPC; low vs. high TROP2-expression	Will be analyzed after 99 months (8.3 years after first patient in, 2 years after final analysis of iDFS)
Secondary	Safety - To compare safety between patients treated with sacituzumab govitecan vs. treatment of physician's choice.	Frequency and severity of adverse events graded according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.; One interim analysis for safety will be performed after first 50 patients completed 4 cycles of treatment.	Final safety analysis will take place when interim analysis of the primary endpoint is performed (all patients will have completed treatment, estimated 54 months from study start)
Secondary	Compliance - To compare dose-density, dose reductions, dose delays, treatment interruptions and treatment discontinuation rates between patients treated with sacituzumab govitecan vs. treatment of physician's choice.	Safety, tolerability, and treatment compliance: the number and percentage of patients whose treatment had to be reduced, delayed or permanently stopped will be summarized for each treatment arm, reasons for dose modification, delay and premature termination will be categorized according to the main reason and will be presented in frequency tables. Treatment arms will be compared regarding the occurrence of any adverse events (AE) (grade 1-5), low grade AE (grade 1-2), and high grade AE (grade 3-5) using Fisher's exact test. Those tests are descriptive in nature and no adjustments for multiple comparisons will be made.	Analysis with final safety analysis expected 54 months after study start.
Secondary	Patient reported outcome: Functional Assessment of Cancer Therapy - Breast Cancer (FACT-B)	For each treatment group and at each time point, the number and percentage of patients who completed the instrument will be summarized, as well as the reasons for non-completion of these questionnaires, if known.; For each of the FACT-B scales (37 items; 5 point Likert-typ scale; scale from 0-148; the higher the score, the better the QOL) the results will be summarized using descriptive statistics for each treatment group at each time point. Results based on the observed values as well as changes from baseline (including both within group and between group differences) will be displayed.	Through study completion and until 12 months after End of treatment of single patients.
Secondary	Patient reported outcome: Functional Assessment of Cancer Therapy - Cognitive function issues (FACT-Cog)	For each treatment group and at each time point, the number and percentage of patients who completed the instrument will be summarized, as well as the reasons for non-completion of these questionnaires, if known.; For each of the FACT-cog scales (37 items; 5 point Likert-type scale; scale from 0-126; the higher the score, the better the QOL) the results will be summarized using descriptive statistics for each treatment group at each time point. Results based on the observed values as well as changes from baseline (including both within group and between group differences) will be displayed.	Through study completion and until 12 months after End of treatment of single patients.
Secondary	Patient reported outcome: Health Questionnaire 5-Level EQ-5D (EQ-5D-5L)	For each treatment group and at each time point, the number and percentage of patients who completed the instrument will be summarized, as well as the reasons for non-completion of the questionnair, if known.; For the EQ-5D-5L instrument (6 items; 5 times 5 point Likert-type scale; 1-digit number that expresses the level selected for the item; 1 visual analogue scale (0-100mm); the higher the score, the better the QOL) the results will be summarized using descriptive statistics for each treatment group at each time point. Results based on the observed values as well as changes from baseline (including both within group and between group differences) will be displayed.	Through study completion and until 12 months after End of treatment of single patients.

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