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. 2021 Nov 18;126(4):576–585. doi: 10.1038/s41416-021-01632-2

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© The Authors 2021, corrected publication 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a Duration of treatment. b Best percentage change from baseline in target lesions. Symbols > in (a) and + in (b) denote the seven patients who continued pamiparib after closure of the study. BID twice a day, BRCA breast cancer susceptibility gene, CR complete response, EOC epithelial ovarian cancer, HRD homologous recombination deficiency, MU mutated, NA not applicable, NE not estimable, PD progressive disease, PR partial response, QD once a day, SD stable disease, UN unknown, WT wild-type.