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      Average duration of prior treatment lines predicts clinical benefit to eribulin chemotherapy in patients with metastatic breast cancer

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          Abstract

          Purpose

          The aim of this study was to identify factors associated with progression-free survival (PFS) and overall survival (OS) in patients with metastatic breast cancer (MBC) treated with eribulin in a real-world setting, to improve information provision in those considering treatment.

          Methods

          Patients treated with eribulin for MBC at The Christie NHS Foundation Trust, Manchester, UK, between August 2011 and December 2018 were included ( n = 439). Data were collected by retrospective review of medical records and electronic prescribing systems. Factors such as biological subtype, distant recurrence-free interval, previous lines of chemotherapy and the ‘average duration of previous treatment lines’ (ADPT) (calculated as: (date of initiation of eribulin–date of MBC) / the number of previous treatment lines in the metastatic setting) were evaluated for prognostic impact using Cox proportional hazards regression.

          Results

          In the full cohort, the median PFS and OS were 4.1 months (95% CI 3.7–4.4) and 8.6 months (95% CI 7.4–9.8), respectively. Outcomes were significantly inferior for those with triple-negative breast cancer (TNBC) ( n = 92); PFS TNBC: 2.4 months (95% CI 2.1–3.0), p =  < 0.001 and OS TNBC: 5.4 months (95% CI 4.6–6.6), p =  < 0.001. ADPT was the only factor other than subtype significantly associated with PFS and OS. Longer ADPT was also significantly associated with PFS and OS in those with TNBC. For example, women in the lowest ADPT tertile (< 5.0 months) achieved a median OS of only 4.3 months, whereas those in the upper ADPT tertile (> 8.7 months) had a median OS of 12.1 months ( p = 0.004).

          Conclusion

          Our results indicate that the ADPT lines is an important factor when predicting the outcome with eribulin chemotherapy in a palliative setting and that quantitative guidance on the likely PFS and OS with treatment can be provided using ADPT. Validation in additional cohorts is warranted.

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          Most cited references16

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          Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries

          This article provides a status report on the global burden of cancer worldwide using the GLOBOCAN 2018 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer, with a focus on geographic variability across 20 world regions. There will be an estimated 18.1 million new cancer cases (17.0 million excluding nonmelanoma skin cancer) and 9.6 million cancer deaths (9.5 million excluding nonmelanoma skin cancer) in 2018. In both sexes combined, lung cancer is the most commonly diagnosed cancer (11.6% of the total cases) and the leading cause of cancer death (18.4% of the total cancer deaths), closely followed by female breast cancer (11.6%), prostate cancer (7.1%), and colorectal cancer (6.1%) for incidence and colorectal cancer (9.2%), stomach cancer (8.2%), and liver cancer (8.2%) for mortality. Lung cancer is the most frequent cancer and the leading cause of cancer death among males, followed by prostate and colorectal cancer (for incidence) and liver and stomach cancer (for mortality). Among females, breast cancer is the most commonly diagnosed cancer and the leading cause of cancer death, followed by colorectal and lung cancer (for incidence), and vice versa (for mortality); cervical cancer ranks fourth for both incidence and mortality. The most frequently diagnosed cancer and the leading cause of cancer death, however, substantially vary across countries and within each country depending on the degree of economic development and associated social and life style factors. It is noteworthy that high-quality cancer registry data, the basis for planning and implementing evidence-based cancer control programs, are not available in most low- and middle-income countries. The Global Initiative for Cancer Registry Development is an international partnership that supports better estimation, as well as the collection and use of local data, to prioritize and evaluate national cancer control efforts. CA: A Cancer Journal for Clinicians 2018;0:1-31. © 2018 American Cancer Society.
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            5th ESO-ESMO international consensus guidelines for advanced breast cancer (ABC 5) †

            Highlights • This ESO-ESMO ABC 5 Clinical Practice Guideline provides key recommendations for managing advanced breast cancer patients • It provides updates on the management of patients with all breast cancer subtypes, LABC, follow-up, palliative and supportive care • Updated diagnostic and treatment algorithms are also provided • All recommendations were compiled by a multidisciplinary group of international experts • Recommendations are based on available clinical evidence and the collective expert opinion of the authors
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              Pertuzumab, trastuzumab, and docetaxel for HER2-positive metastatic breast cancer (CLEOPATRA): end-of-study results from a double-blind, randomised, placebo-controlled, phase 3 study

              CLEOPATRA was a phase 3 study comparing the efficacy and safety of pertuzumab, trastuzumab, and docetaxel with placebo, trastuzumab, and docetaxel in patients with HER2-positive metastatic breast cancer. In the primary analysis and subsequent reports, progression-free and overall survival were significantly improved in the pertuzumab group compared with the placebo group. Here, we report the end-of-study analysis of CLEOPATRA.
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                Author and article information

                Contributors
                maria.ekholm@rjl.se
                Journal
                Breast Cancer Res Treat
                Breast Cancer Res Treat
                Breast Cancer Research and Treatment
                Springer US (New York )
                0167-6806
                1573-7217
                29 November 2021
                29 November 2021
                2022
                : 191
                : 3
                : 535-543
                Affiliations
                [1 ]GRID grid.412917.8, ISNI 0000 0004 0430 9259, Department of Pharmacy, , The Christie NHS Foundation Trust, ; Manchester, UK
                [2 ]GRID grid.412917.8, ISNI 0000 0004 0430 9259, Department of Clinical Oncology, , The Christie NHS Foundation Trust, ; Manchester, UK
                [3 ]GRID grid.412917.8, ISNI 0000 0004 0430 9259, Department of Medical Oncology, , The Christie NHS Foundation Trust, ; Manchester, UK
                [4 ]GRID grid.412917.8, ISNI 0000 0004 0430 9259, Department of Analytics and Statistics, Digital Services, , The Christie NHS Foundation Trust, ; Manchester, UK
                [5 ]GRID grid.413253.2, Department of Oncology, , Ryhov Hospital, ; Jönköping, Sweden
                [6 ]GRID grid.8761.8, ISNI 0000 0000 9919 9582, Institute of Biomedicine, Department of Laboratory Medicine, , Sahlgrenska Center for Cancer Research, Sahlgrenska Academy at University of Gothenburg, ; Gothenburg, Sweden
                Author information
                http://orcid.org/0000-0002-5553-5323
                Article
                6438
                10.1007/s10549-021-06438-7
                8831340
                34843027
                b6bceab3-8219-4784-9216-73668eada1cc
                © The Author(s) 2021

                Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 3 September 2021
                : 25 October 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100010772, Percy Falks Stiftelse för Forskning Beträffande Prostata- och Bröstcancer;
                Funded by: Bröstcancerförbundet
                Funded by: FundRef http://dx.doi.org/10.13039/501100009752, Futurum - Akademin för Hälsa och Vård, Region Jönköpings läns;
                Funded by: FundRef http://dx.doi.org/10.13039/501100007687, Svenska Läkaresällskapet;
                Funded by: Fonden för Klinisk Cancerforskning i Jönköping
                Funded by: Manchester NIHR Biomedical Research Centre
                Funded by: University of Gothenburg
                Categories
                Clinical Trial
                Custom metadata
                © Springer Science+Business Media, LLC, part of Springer Nature 2022

                Oncology & Radiotherapy
                metastatic breast cancer,eribulin,real world,subtypes,chemotherapy,palliative
                Oncology & Radiotherapy
                metastatic breast cancer, eribulin, real world, subtypes, chemotherapy, palliative

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