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ctDNA guiding adjuvant immunotherapy in urothelial carcinoma

Author

Listed:
  • Thomas Powles

    (Queen Mary University of London ECMC, Barts Health)

  • Zoe June Assaf

    (Roche/Genentech)

  • Nicole Davarpanah

    (Roche/Genentech)

  • Romain Banchereau

    (Roche/Genentech)

  • Bernadett E. Szabados

    (Queen Mary University of London)

  • Kobe C. Yuen

    (Roche/Genentech)

  • Petros Grivas

    (University of Washington
    Seattle Cancer Care Alliance
    Fred Hutchinson Cancer Research Center)

  • Maha Hussain

    (Northwestern University)

  • Stephane Oudard

    (University of Paris)

  • Jürgen E. Gschwend

    (Technical University Munich)

  • Peter Albers

    (University Hospital Düsseldorf)

  • Daniel Castellano

    (University Hospital 12 de Octubre, Medical Oncology Department CIBER-ONC)

  • Hiroyuki Nishiyama

    (Faculty of Medicine University of Tsukuba)

  • Siamak Daneshmand

    (USC Norris Comprehensive Cancer Center)

  • Shruti Sharma

    (Natera, Inc)

  • Bernhard G. Zimmermann

    (Natera, Inc)

  • Himanshu Sethi

    (Natera, Inc)

  • Alexey Aleshin

    (Natera, Inc)

  • Maurizio Perdicchio

    (F. Hoffmann-La Roche Ltd)

  • Jingbin Zhang

    (Hoffmann-La Roche Ltd, Mississauga)

  • David S. Shames

    (Roche/Genentech)

  • Viraj Degaonkar

    (Roche/Genentech)

  • Xiaodong Shen

    (Roche/Genentech)

  • Corey Carter

    (Roche/Genentech)

  • Carlos Bais

    (Roche/Genentech)

  • Joaquim Bellmunt

    (Harvard Medical School)

  • Sanjeev Mariathasan

    (Roche/Genentech)

Abstract

Minimally invasive approaches to detect residual disease after surgery are needed to identify patients with cancer who are at risk for metastatic relapse. Circulating tumour DNA (ctDNA) holds promise as a biomarker for molecular residual disease and relapse1. We evaluated outcomes in 581 patients who had undergone surgery and were evaluable for ctDNA from a randomized phase III trial of adjuvant atezolizumab versus observation in operable urothelial cancer. This trial did not reach its efficacy end point in the intention-to-treat population. Here we show that ctDNA testing at the start of therapy (cycle 1 day 1) identified 214 (37%) patients who were positive for ctDNA and who had poor prognosis (observation arm hazard ratio = 6.3 (95% confidence interval: 4.45–8.92); P

Suggested Citation

  • Thomas Powles & Zoe June Assaf & Nicole Davarpanah & Romain Banchereau & Bernadett E. Szabados & Kobe C. Yuen & Petros Grivas & Maha Hussain & Stephane Oudard & Jürgen E. Gschwend & Peter Albers & Dan, 2021. "ctDNA guiding adjuvant immunotherapy in urothelial carcinoma," Nature, Nature, vol. 595(7867), pages 432-437, July.
  • Handle: RePEc:nat:nature:v:595:y:2021:i:7867:d:10.1038_s41586-021-03642-9
    DOI: 10.1038/s41586-021-03642-9
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    Cited by:

    1. Xu Hua & Hui Zhou & Hui-Chen Wu & Julia Furnari & Corina P. Kotidis & Raul Rabadan & Jeanine M. Genkinger & Jeffrey N. Bruce & Peter Canoll & Regina M. Santella & Zhiguo Zhang, 2024. "Tumor detection by analysis of both symmetric- and hemi-methylation of plasma cell-free DNA," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    2. A. Gordon Robertson & Khyati Meghani & Lauren Folgosa Cooley & Kimberly A. McLaughlin & Leigh Ann Fall & Yanni Yu & Mauro A. A. Castro & Clarice S. Groeneveld & Aurélien Reyniès & Vadim I. Nazarov & V, 2023. "Expression-based subtypes define pathologic response to neoadjuvant immune-checkpoint inhibitors in muscle-invasive bladder cancer," Nature Communications, Nature, vol. 14(1), pages 1-19, December.

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