Literature DB >> 28214657

Ipilimumab alone or in combination with nivolumab after progression on anti-PD-1 therapy in advanced melanoma.

Lisa Zimmer1, Susmitha Apuri2, Zeynep Eroglu3, Lisa A Kottschade4, Andrea Forschner5, Ralf Gutzmer6, Max Schlaak7, Lucie Heinzerling8, Angela M Krackhardt9, Carmen Loquai10, Svetomir N Markovic4, Richard W Joseph4, Kelly Markey3, Jochen S Utikal11, Carsten Weishaupt12, Simone M Goldinger13, Vernon K Sondak3, Jonathan S Zager3, Dirk Schadendorf14, Nikhil I Khushalani3.   

Abstract

BACKGROUND: The anti-programmed cell death-1 (PD-1) inhibitors pembrolizumab and nivolumab alone or in combination with ipilimumab have shown improved objective response rates and progression-free survival compared to ipilimumab only in advanced melanoma patients. Anti-PD-1 therapy demonstrated nearly equal clinical efficacy in patients who had progressed after ipilimumab or were treatment-naïve. However, only limited evidence exists regarding the efficacy of ipilimumab alone or in combination with nivolumab after treatment failure to anti-PD-therapy. PATIENTS AND METHODS: A multicenter retrospective study in advanced melanoma patients who were treated with nivolumab (1 or 3 mg/kg) and ipilimumab (1 mg or 3 mg/kg) or ipilimumab (3 mg/kg) alone after treatment failure to anti-PD-1 therapy was performed. Patient, tumour, pre- and post-treatment characteristics were analysed.
RESULTS: In total, 47 patients were treated with ipilimumab (ipi-group) and 37 patients with ipilimumab and nivolumab (combination-group) after treatment failure to anti-PD-1 therapy. Overall response rates for the ipi- and the combination-group were 16% and 21%, respectively. Disease control rate was 42% for the ipi-group and 33% for the combination-group. One-year overall survival rates for the ipi- and the combination-group were 54% and 55%, respectively.
CONCLUSIONS: Ipilimumab should be considered as a viable treatment option for patients with failure to prior anti-PD-1 therapy, including those with progressive disease as best response to prior anti-PD-1. In contrast, the combination of ipilimumab and nivolumab appears significantly less effective in this setting compared to treatment-naïve patients.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anti-PD-1; Disease progression; Efficacy; Ipilimumab; Ipilimumab and nivolumab; Melanoma; Nivolumab; Pembrolizumab; Treatment failure

Mesh:

Substances:

Year:  2017        PMID: 28214657     DOI: 10.1016/j.ejca.2017.01.009

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  52 in total

1.  Utility of ipilimumab in melanoma patients who progress on anti-PD-1 therapy.

Authors:  Cesar E Ochoa; Richard W Joseph
Journal:  Melanoma Manag       Date:  2017-07-26

2.  Anti-PD-1 monotherapy versus anti-PD1 plus anti-CTLA4 in advanced melanoma: how do we decide?

Authors:  Lewis Au; Aine O'Reilly; James Larkin
Journal:  Melanoma Manag       Date:  2017-08-02

Review 3.  Immunotherapy of Melanoma: Facts and Hopes.

Authors:  Sarah A Weiss; Jedd D Wolchok; Mario Sznol
Journal:  Clin Cancer Res       Date:  2019-03-28       Impact factor: 12.531

4.  Predictors of immunotherapy-induced immune-related adverse events.

Authors:  A Kartolo; J Sattar; V Sahai; T Baetz; J M Lakoff
Journal:  Curr Oncol       Date:  2018-10-31       Impact factor: 3.677

5.  Dosing immunotherapy combinations: Analysis of 3,526 patients for toxicity and response patterns.

Authors:  Mina Nikanjam; Harsh Patel; Razelle Kurzrock
Journal:  Oncoimmunology       Date:  2017-06-28       Impact factor: 8.110

6.  Clinical outcomes of advanced stage cancer patients treated with sequential immunotherapy in phase 1 clinical trials.

Authors:  Dylan J Martini; Yuan Liu; Julie M Shabto; Colleen Lewis; Meredith R Kline; Hannah Collins; Mehmet Akce; Haydn T Kissick; Bradley C Carthon; Walid L Shaib; Olatunji B Alese; Rathi N Pillai; Conor E Steuer; Christina S Wu; David H Lawson; Ragini R Kudchadkar; Viraj A Master; Bassel F El-Rayes; Suresh S Ramalingam; Taofeek K Owonikoko; R Donald Harvey; Mehmet Asim Bilen
Journal:  Invest New Drugs       Date:  2019-02-06       Impact factor: 3.850

7.  The next-generation BET inhibitor, PLX51107, delays melanoma growth in a CD8-mediated manner.

Authors:  Dan A Erkes; Conroy O Field; Claudia Capparelli; Manoela Tiago; Timothy J Purwin; Inna Chervoneva; Adam C Berger; Edward J Hartsough; Jessie Villanueva; Andrew E Aplin
Journal:  Pigment Cell Melanoma Res       Date:  2019-05-20       Impact factor: 4.693

Review 8.  Treatment Options for Advanced Melanoma After Anti-PD-1 Therapy.

Authors:  Nalan Akgul Babacan; Zeynep Eroglu
Journal:  Curr Oncol Rep       Date:  2020-03-20       Impact factor: 5.075

9.  Immunotherapy After Immunotherapy: Response Rescue in a Patient With Microsatellite Instability-high Colorectal Cancer Post-Pembrolizumab.

Authors:  Satya Das; Audrey Allen; Jordan Berlin
Journal:  Clin Colorectal Cancer       Date:  2020-02-08       Impact factor: 4.481

10.  Ipilimumab and Radiation in Patients with High-risk Resected or Regionally Advanced Melanoma.

Authors:  April K S Salama; Manisha Palta; Christel N Rushing; M Angelica Selim; Kristen N Linney; Brian G Czito; David S Yoo; Brent A Hanks; Georgia M Beasley; Paul J Mosca; Chelsae Dumbauld; Katelyn N Steadman; John S Yi; Kent J Weinhold; Douglas S Tyler; Walter T Lee; David M Brizel
Journal:  Clin Cancer Res       Date:  2020-11-10       Impact factor: 12.531

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