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ePoster Display

603P - Objective computerized cognitive assessment in men with metastatic castrate-resistant prostate cancer (mCRPC) randomly receiving darolutamide or enzalutamide in the ODENZA trial

Date

16 Sep 2021

Session

ePoster Display

Topics

Tumour Site

Prostate Cancer

Presenters

Emeline Colomba

Citation

Annals of Oncology (2021) 32 (suppl_5): S626-S677. 10.1016/annonc/annonc702

Authors

E. Colomba1, S.F. Jonas2, J. Eymard3, R. Delva4, P.E. Brachet5, Y. Neuzillet6, N. Penel7, G. Roubaud8, E. Bompas9, H. Mahammedi10, R. Longo11, C. Helissey12, P. Barthelemy13, D. Borchiellini14, A. Hasbini15, F. Priou16, C. Saldana17, E. Voog18, S. Foulon19, K. Fizazi20

Author affiliations

  • 1 Medical Oncology Department, Institut Gustave Roussy, 94805 - Villejuif/FR
  • 2 Department Of Biostatistics, Institut Gustave Roussy, 94805 - Villejuif/FR
  • 3 Medical Oncology Department, Institut Jean Godinot, 51056 - Reims/FR
  • 4 Medical Oncology, Institut de Cancerologie de l’Ouest, 49055 - Angers/FR
  • 5 Medical Oncology Department, Centre Francois Baclesse, 14076 - Caen/FR
  • 6 Urology Department, Hopital Foch, 92151 - Suresnes/FR
  • 7 General Oncology Department, Centre Oscar Lambret, 59020 - Lille/FR
  • 8 Medical Oncology, Institute Bergonié, 33000 - Bordeaux/FR
  • 9 Oncology, ICO Institut de Cancerologie de l'Ouest René Gauducheau, 44805 - Saint-Herblain/FR
  • 10 5department Of Medical Oncology, Centre de Lutte Contre le Centre Jean Perrin, Clermont-Ferrand/FR
  • 11 Medical Oncology Department, Hopital de Mercy-CHR Metz-Thionville, 57085 - Metz-Tessy/FR
  • 12 Val De Marne, Bégin Military Teaching Hospital, 94160 - Saint-Mandé/FR
  • 13 Medical Oncology Department, ICANS - Institut de Cancérologie Strasbourg Europe, 67200 - Strasbourg/FR
  • 14 Medical Oncology Department, Centre Anticancer Antoine Lacassagne, 06189 - Nice/FR
  • 15 Medical Oncology Department, Clinique Pasteur Lanroze, 29200 - Brest/FR
  • 16 Medical Oncology Department, CHD Vendee - Hopital Les Oudairies, 85925 - La Roche-sur-Yon/FR
  • 17 Medical Oncology Department, Centre Hospitalier Universitaire Henri-Mondor AP-HP, 94010 - Creteil/FR
  • 18 Medical Oncology Department, Clinique Victor Hugo Le Mans, 72015 - Le Mans/FR
  • 19 Biostatistics And Epidemiology Office, Gustave Roussy - Cancer Campus, 94805 - Villejuif/FR
  • 20 Cancer Medicine Department, Institut Gustave Roussy, 94805 - Villejuif/FR

Resources

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Abstract 603P

Background

Darolutamide (Daro) and enzalutamide (Enza) are next generation androgen receptor inhibitors. Daro does not significantly penetrate the blood-brain barrier, which may reduce cognitive impairment. ODENZA is a prospective, cross-over, preference, randomized phase II trial of Daro and Enza in patients (pts) with mCRPC. Pts (n=249) were randomized 1/1 to receive Daro 1200 mg/d for 12 weeks followed by Enza 160 mg/d for 12 weeks or the reverse sequence. Numerically more pts with early mCRPC preferred Daro over Enza, although the difference did not reach significance (Colomba et al, ASCO 2021).

Methods

Cognitive assessment using computerized cognitive tests (COGSTATE) was a key secondary endpoint of ODENZA. Changes from baseline were described by assessing each 12 weeks period. Individual tests (Detection Test: psychomotor function, Identification Test: visual attention, One Back Test: working memory, International Shopping List Test (ISL): verbal learning, International Shopping list Test Delayed Recall (ISRL): verbal memory, Groton Maze Learning: executive function) were used and three composite scores (eg ISL/ISRL for episodic memory) were created. Treatment effects were analyzed using Mixed-Effects Model Repeated Measures. Effect sizes were classified as clinically meaningful when greater than or equal to 0.5.

Results

Cognitive data were available in 193 pts. Performance on verbal learning (ISL) was significantly better with Daro at each of the post-baseline assessments, within both periods and when averaged over periods. Effects were clinically meaningful at the second period (-0.62, p=0.0001) and overall (-0.54, p<0.0001). Performance on verbal memory (ISRL) was significantly better with Daro at the second period and when averaged over periods, although the effect sizes were less meaningful (second period: -0.4, p=0.01 and overall: -0.29, p=0.0075). No difference in other tests was found. The composite scores reported a moderate benefit in episodic memory after treatment with Daro compared to Enza.

Conclusions

In early mCRPC, Daro was associated with a statistically significant benefit in verbal learning and verbal memory compared to Enza.

Clinical trial identification

NCT03314324.

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Bayer.

Disclosure

E. Colomba: Financial Interests, Personal, Invited Speaker: Ipsen; Financial Interests, Institutional, Invited Speaker: MSD; Financial Interests, Institutional, Advisory Board: GSK; Financial Interests, Institutional, Advisory Board: BMS; Financial Interests, Personal, Advisory Board: Pfizer; Financial Interests, Personal, Invited Speaker: Tesaro. Y. Neuzillet: Financial Interests, Personal, Advisory Board: BMS; Financial Interests, Personal, Advisory Board: Ipsen; Financial Interests, Personal, Advisory Board: Janssen; Financial Interests, Personal, Invited Speaker: Sanofi. G. Roubaud: Financial Interests, Personal, Invited Speaker: Ipsen; Financial Interests, Personal, Advisory Board: Janssen; Financial Interests, Personal, Advisory Board: Sanofi; Financial Interests, Personal, Invited Speaker: Astellas. C. Helissey: Financial Interests, Personal, Invited Speaker: Ipsen; Financial Interests, Personal, Advisory Board: Sanofi; Financial Interests, Personal, Invited Speaker: Astellas; Financial Interests, Personal, Invited Speaker: Janssen. P. Barthelemy: Financial Interests, Personal, Invited Speaker: Ipsen; Financial Interests, Personal, Invited Speaker: BMS; Financial Interests, Personal, Invited Speaker: Sanofi; Financial Interests, Personal, Invited Speaker: Astellas; Financial Interests, Personal, Invited Speaker: Pfizer. D. Borchiellini: Financial Interests, Personal, Invited Speaker: BMS; Financial Interests, Personal, Invited Speaker: Pfizer; Financial Interests, Personal, Invited Speaker: Ipsen. C. Saldana: Financial Interests, Personal, Advisory Board: Pfizer; Financial Interests, Personal, Invited Speaker: Sanofi; Financial Interests, Personal, Advisory Board: Ipsen; Financial Interests, Personal, Advisory Board: BMS. K. Fizazi: Financial Interests, Institutional, Advisory Board: AAA; Financial Interests, Institutional, Invited Speaker: Astellas; Financial Interests, Institutional, Invited Speaker: Orion; Financial Interests, Institutional, Invited Speaker: Janssen; Financial Interests, Institutional, Advisory Board: Janssen; Financial Interests, Personal, Advisory Board: Curevas; Financial Interests, Institutional, Advisory Board: Astellas; Financial Interests, Institutional, Advisory Board: AstraZeneca; Financial Interests, Institutional, Invited Speaker: AstraZeneca; Financial Interests, Institutional, Invited Speaker: Bayer; Financial Interests, Institutional, Advisory Board: Bayer; Financial Interests, Institutional, Invited Speaker: MSD; Financial Interests, Institutional, Advisory Board: MSD; Financial Interests, Institutional, Invited Speaker: Sanofi; Financial Interests, Institutional, Research Grant: Bayer; Financial Interests, Institutional, Research Grant: BMS; Financial Interests, Institutional, Research Grant: Janssen; Financial Interests, Institutional, Research Grant: MSD; Financial Interests, Institutional, Research Grant: Orion; Financial Interests, Institutional, Research Grant: Pfizer. All other authors have declared no conflicts of interest.

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