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E-Poster Display

832P - GEICO1601-ROLANDO trial: A multicentric single arm phase II clinical trial to evaluate the combination of olaparib and pegylated liposomal doxorubicin for platinum-resistant ovarian cancer

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Ovarian Cancer

Presenters

Jose Alejandro Perez Fidalgo

Citation

Annals of Oncology (2020) 31 (suppl_4): S551-S589. 10.1016/annonc/annonc276

Authors

J.A. Perez Fidalgo1, A. Cortés2, Y. García3, M. Iglesias4, U. Bohn Sarmiento5, E. Calvo García6, L. Manso Sánchez7, A. Santaballa8, A. Oaknin9, A. Redondo10, M.J. Rubio11, A. González Martín12

Author affiliations

  • 1 Dept. Medical Oncology, Hospital Clinico Universitario de Valencia, 46010 - Valencia/ES
  • 2 Medical Oncology, Hospital Universitario Ramón y Cajal, 28034 - Madrid/ES
  • 3 Medical Oncology, Hospital de Sabadell, 08208 - Sabadell/ES
  • 4 Medical Oncology, Hospital Son Llatzer, 07198 - Palma de Mallorca/ES
  • 5 Medical Oncology, Hospital Universitario de Gran Canaria Doctor Negrín, 35012 - Las Palmas de Gran Canaria/ES
  • 6 Medical Oncology, Hospital Universitario Virgen del Rocío, 41013 - Sevilla/ES
  • 7 Medical Oncology, Hospital Universitario 12 de Octubre, 28041 - Madrid/ES
  • 8 Medical Oncology, Hospital Universitari i Politècnic La Fe, 46026 - Valencia/ES
  • 9 Medical Oncology, Vall d'Hebron University Hospital, 8035 - Barcelona/ES
  • 10 Dept. Oncologia Medica, Hospital Universitario La Paz, 28046 - Madrid/ES
  • 11 Medical Oncology, University Hospital Reina Sofia, 14004 - Cordoba/ES
  • 12 Medical Oncology Department, Clinica Universidad de Navarra, 28027 - Madrid/ES

Resources

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Abstract 832P

Background

The benefit of olaparib (OLA) in platinum-resistant ovarian cancer (PROC) patients (pts) with BRCA wild-type tumors is scarce. The combination with DNA-damaging chemotherapy may be synergistic and improve the activity of OLA.

Methods

Patients with high-grade serous or endometrioid and one previous PROC (between 28 days-6 months after last platinum) were eligible regardless of BRCA status. Pts had received ≤ 4 previous lines (up to 5 in BRCA-mut pts), and primary PROC was only allowed in the presence of BRCA-mut otherwise at least one previous platinum-sensitive relapse was required. Pts received 6 cycles of OLA 300 mg b.i.d + pegylated liposomal doxorubicin (PLD) 40 mg/m2 (PLD40) intravenously q28d followed by OLA 300 mg b.i.d. until progression or toxicity. Due to high toxicity a protocol amendment was performed to reduce PLD to 30 mg/m2 (PLD30). The primary endpoint was progression-free survival at 6 months (6mPFS) by RECIST 1.1 and the threshold for futility was 40% 6mPFS.

Results

31 pts (ITT cohort) received at least 1 cycle, but only 20 pts were in the per protocol cohort (PP). ITT median age was 58,03 years, ECOG 0/1: 32.3/67.7%, serous subtype 84%. PP median age was 60 y.o., ECOG 0/1: 25%/75%, serous subtype: 85% and BRCA status was WT/mut/unk: 75%/20%/5%. Median of prior lines was 2 (1-4). Median number of cycles was 4.2 (0.9-19.5) for OLA and 4 (2-6) for PLD. After a median follow-up of 9.29 (0.9-21.3) mo, the 6mPFS in the ITT population was 44.2% (95%CI 28.7-68.1%) and median PFS 5.32 mo. In the PP cohort 6mPFS was 46.1% (95%CI 27.2-78.3) with a median PFS of 5.42 mo (4-12). 65% pts achieved stable disease and 25% partial response (overall control rate 90%). 74% of ITT pts had a Grade ≥3 adverse event (AE), being the most frequent neutropenia/anemia/febrile neutropenia: 39%/19%/10%. SAEs were less frequent in PLD30 (N=14) than in PLD40 (n=17): 21%/47%, as well as PLD delays 30/40: 30%/45% and reductions 30/40: 10%/25%.

Conclusions

OLA+PLD combination has shown clear activity with 46% 6mPFS rate in PROC regardless of BRCA status. PLD at 30 mg/m2 was better tolerated in the combination.

Clinical trial identification

EudraCT: 2016-004850-14; NCT03161132.

Editorial acknowledgement

Legal entity responsible for the study

Grupo Español de Investigación en Cáncer de Ovario (GEICO).

Funding

AstraZeneca.

Disclosure

J.A. Perez Fidalgo: Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: AstraZeneca; Advisory/Consultancy: Ability Pharma; Advisory/Consultancy: Clovis; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: GSK. A. Cortés: Speaker Bureau/Expert testimony, Research grant/Funding (self), Research grant/Funding (institution): Pfizer; Speaker Bureau/Expert testimony: Roche; Research grant/Funding (institution): Roche-Genentech; Speaker Bureau/Expert testimony, Research grant/Funding (institution): AstraZeneca; Speaker Bureau/Expert testimony, Research grant/Funding (institution): Eisai; Advisory/Consultancy, Research grant/Funding (institution): Lilly; Advisory/Consultancy: Ferrer; Research grant/Funding (institution): Novartis; Research grant/Funding (institution): Corcept Therapeutics; Research grant/Funding (institution): Seattle Genetics. Y. García: Advisory/Consultancy: Clovis; Advisory/Consultancy, Travel/Accommodation/Expenses: GSK/Tesaro; Advisory/Consultancy: AstraZeneca; Advisory/Consultancy, Travel/Accommodation/Expenses: Roche. A. Oaknin: Honoraria (self): AbbVie, Inc.; Honoraria (self), Honoraria (institution): Amgen, S.A; Honoraria (self): AstraZeneca; Honoraria (self), Honoraria (institution): Clovis Oncology; Honoraria (self), Honoraria (institution): F. Hoffman - La Roche Ltd; Honoraria (self): Genmab; Honoraria (self): GlaxoSmithKline SA; Honoraria (self), Honoraria (institution): ImmunoGen; Honoraria (self): Merck Sharp & Dohme; Honoraria (self), Honoraria (institution): Pharma Mar, SA; Honoraria (self): prIME; Honoraria (self), Honoraria (institution): Tesaro; Honoraria (institution): AbbVie Deutschland; Honoraria (institution): Ability Pharmaceuticals; Honoraria (institution): Advaxis Inc.; Honoraria (institution): Aeterna Zentaris; Honoraria (institution): Aprea Therapeutics AB; Honoraria (institution): EISAI limited LTD; Honoraria (institution): Regeneron Pharmaceuticals; Honoraria (institution): Merck Sharp & Dohme de España SA; Honoraria (institution): Millennium Pharmaceuticals Inc; Honoraria (institution): BMS; Leadership role: GEICO; Leadership role: GCIG Phase II Committee and Cervix Cancer Committee Representative on behalf of GEICO; Leadership role: ESMO Faculty Member Gynaecological for ESMO 2018 and Chair of Gynaecological Tack for ESMO 2019; Non-remunerated activity/ies: ESMO; Non-remunerated activity/ies: ASCO; Non-remunerated activity/ies: GCIG; Non-remunerated activity/ies: SEOM; Non-remunerated activity/ies: GOG. A. Redondo: Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (institution): Roche; Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (institution): PharmaMar; Advisory/Consultancy, Speaker Bureau/Expert testimony: AstraZeneca; Advisory/Consultancy, Speaker Bureau/Expert testimony: GSK; Advisory/Consultancy, Speaker Bureau/Expert testimony: Clovis; Speaker Bureau/Expert testimony: Novartis; Advisory/Consultancy: Amgem; Research grant/Funding (institution): Eisai; Non-remunerated activity/ies, PI of phase II Cecilia study (carboplatin-paclitaxel and bevacizumab in advanced cervical cancer), sponsored by Roche: Roche; Leadership role, Member of Executive Board and Secretary of Spanish Group of Ovarian Cancer Research: GEICO. A. González Martín: Advisory/Consultancy, Speaker Bureau/Expert testimony: Roche; Advisory/Consultancy, Speaker Bureau/Expert testimony: AstraZeneca; Advisory/Consultancy, Speaker Bureau/Expert testimony: Tesaro; Advisory/Consultancy: Clovis; Advisory/Consultancy: Pfizer/Merck; Advisory/Consultancy: ImmunoGen; Advisory/Consultancy, Speaker Bureau/Expert testimony: PharmaMar; Advisory/Consultancy: MSD; Advisory/Consultancy: Genmab; Advisory/Consultancy: Oncoinvent; Honoraria (institution), Financial support for ANITA/GEICO trial: Roche; Honoraria (institution), Financial support for ANITA/GEICO trial: Tesaro; Non-remunerated activity/ies, Principal Investigator of PRIMA study sponsored by Tesaro: Tesaro; Leadership role, Chairman: GEICO; Leadership role, Chairman: ENGOT. All other authors have declared no conflicts of interest.

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