Nivolumab (nivo) ± ipilimumab (ipi) in advanced small-cell lung cancer (SCLC): First report of a randomized expansion cohort from CheckMate 032.

Author:

Hellmann Matthew David1,Ott Patrick Alexander2,Zugazagoitia Jon3,Ready Neal E.4,Hann Christine L.5,De Braud Filippo G.6,Antonia Scott Joseph7,Ascierto Paolo Antonio8,Moreno Victor9,Atmaca Akin10,Salvagni Stefania11,Taylor Matthew H.12,Amin Asim13,Camidge D. Ross14,Horn Leora15,Calvo Emiliano16,Cai Weiguo17,Fairchild Justin P.17,Callahan Margaret K.1,Spigel David R.18

Affiliation:

1. Memorial Sloan Kettering Cancer Center, New York, NY;

2. Dana-Farber Cancer Institute, Boston, MA;

3. Hospital Universitario 12 de Octubre, Madrid, Spain;

4. Duke University, Durham, NC;

5. The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, MD;

6. Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy;

7. H. Lee Moffitt Cancer Canter and Research Institute, Tampa, FL;

8. Istituto Nazionale Tumori “Fondazione G.Pascale”- IRCCS, Naples, Italy;

9. START Madrid-FJD, Hospital Fundación Jiménez Díaz, Madrid, Spain;

10. Krankenhaus Nordwest GmbH Institut für Klinisch-Onkologische Forschung, Frankfurt, Germany;

11. Policlinico Sant’Orsola – Malpighi University Hospital, Bologna, Italy;

12. Oregon Health & Science University, Portland, OR;

13. Levine Cancer Institute, Carolinas Medical Center, Charlotte, NC;

14. University of Colorado Comprehensive Cancer Center, Aurora, CO;

15. Vanderbilt University Ingram Cancer Center, Nashville, TN;

16. START Madrid, Centro Integral Oncológico Clara Campal, Madrid, Spain;

17. Bristol-Myers Squibb, Princeton, NJ;

18. Sarah Cannon Research Institute and Tennessee Oncology, PLLC, Nashville, TN;

Abstract

8503 Background: Patients (pts) with advanced SCLC after first-line platinum-based chemotherapy (PLT-CT) have a poor prognosis and limited treatment options. CheckMate 032 is a phase I/II trial evaluating multiple regimens of nivo ± ipi in solid tumors, including advanced SCLC. Tolerability and efficacy of nivo ± ipi were demonstrated in early results from the initial treatment arms (Antonia, Lancet Oncol 2016), prompting long-term follow-up and the addition of a randomized expansion cohort to further evaluate nivo ± ipi in advanced SCLC. Methods: In the initial treatment arms, pts with advanced SCLC and disease progression after prior PLT-CT were assigned to nivo (3 mg/kg Q2W; n = 98) or nivo 1 + ipi 3 (1 mg/kg and 3 mg/kg Q3W x 4, then nivo 3 Q2W; n = 61); safety/efficacy was assessed with a follow-up of ~18 mo. In the subsequent SCLC expansion cohort, pts were randomized 3:2 to nivo vs nivo 1 + ipi 3 and stratified by number of prior therapies. The primary endpoint was objective response rate (ORR). Results: Updated efficacy/safety results from the initial (non-randomized) nivo and nivo 1 + ipi 3 arms are summarized in the table. Responses were durable and occurred regardless of PD-L1 expression or PLT-sensitivity; safety was consistent with prior nivo ± ipi studies. In the expansion cohort, 247 pts were randomized to nivo or nivo 1 + ipi 3. The presentation will contain the first report of efficacy/safety results and subgroup analyses from this randomized expansion cohort. Conclusions: Durable responses are observed with nivo and nivo + ipi in pts with previously treated SCLC. The expansion cohort represents the first randomized evaluation of combined immune checkpoint blockade in SCLC. Clinical trial information: NCT01928394. [Table: see text]

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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