14
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      nab-Paclitaxel plus carboplatin or gemcitabine versus gemcitabine plus carboplatin as first-line treatment of patients with triple-negative metastatic breast cancer: results from the tnAcity trial

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Metastatic triple-negative breast cancer (mTNBC) has a poor prognosis and aggressive clinical course. tnAcity evaluated the efficacy and safety of first-line nab-paclitaxel plus carboplatin ( nab-P/C), nab-paclitaxel plus gemcitabine ( nab-P/G), and gemcitabine plus carboplatin (G/C) in patients with mTNBC.

          Patients and methods

          Patients with pathologically confirmed mTNBC and no prior chemotherapy for metastatic BC received (1 : 1 : 1) nab-P 125 mg/m 2 plus C AUC 2, nab-P 125 mg/m 2 plus G 1000 mg/m 2, or G 1000 mg/m 2 plus C AUC 2, all on days 1, 8 q3w. Phase II primary end point: investigator-assessed progression-free survival (PFS); secondary end points included overall response rate (ORR), overall survival (OS), percentage of patients initiating cycle 6 with doublet therapy, and safety.

          Results

          In total, 191 patients were enrolled ( nab-P/C, n = 64; nab-P/G, n = 61; G/C, n = 66). PFS was significantly longer with nab-P/C versus nab-P/G [median, 8.3 versus 5.5 months; hazard ratio (HR), 0.59 [95% CI, 0.38–0.92]; P = 0.02] or G/C (median, 8.3 versus 6.0 months; HR, 0.58 [95% CI, 0.37–0.90]; P = 0.02). OS was numerically longer with nab-P/C versus nab-P/G (median, 16.8 versus 12.1 months; HR, 0.73 [95% CI, 0.47–1.13]; P = 0.16) or G/C (median, 16.8 versus 12.6 months; HR, 0.80 [95% CI, 0.52–1.22]; P = 0.29). ORR was 73%, 39%, and 44%, respectively. In the nab-P/C, nab-P/G, and G/C groups, 64%, 56%, and 50% of patients initiated cycle 6 with a doublet. Grade ≥3 adverse events were mainly hematologic.

          Conclusions

          First-line nab-P/C was active in mTNBC and resulted in a significantly longer PFS and improved risk/benefit profile versus nab-P/G or G/C.

          Related collections

          Most cited references14

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Current approaches in treatment of triple-negative breast cancer

          Triple-negative breast cancer (TNBC) is diagnosed more frequently in younger and premenopausal women and is highly prevalent in African American women. TNBC is a term derived from tumors that are characterized by the absence of ER, PgR, and HER2. So patients with TNBC do not benefit from hormonal or trastuzumab-based therapies. TNBCs are biologically aggressive, although some reports suggest that they respond to chemotherapy better than other types of breast cancer, prognosis remains poor. This is due to: shortened disease-free interval in the adjuvant and neoadjuvant setting and a more aggressive course in the metastatic setting.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Iniparib plus chemotherapy in metastatic triple-negative breast cancer.

            Triple-negative breast cancers have inherent defects in DNA repair, making this cancer a rational target for therapy based on poly(adenosine diphosphate-ribose) polymerase (PARP) inhibition. We conducted an open-label, phase 2 study to compare the efficacy and safety of gemcitabine and carboplatin with or without iniparib, a small molecule with PARP-inhibitory activity, in patients with metastatic triple-negative breast cancer. A total of 123 patients were randomly assigned to receive gemcitabine (1000 mg per square meter of body-surface area) and carboplatin (at a dose equivalent to an area under the concentration-time curve of 2) on days 1 and 8--with or without iniparib (at a dose of 5.6 mg per kilogram of body weight) on days 1, 4, 8, and 11--every 21 days. Primary end points were the rate of clinical benefit (i.e., the rate of objective response [complete or partial response] plus the rate of stable disease for ≥6 months) and safety. Additional end points included the rate of objective response, progression-free survival, and overall survival. The addition of iniparib to gemcitabine and carboplatin improved the rate of clinical benefit from 34% to 56% (P=0.01) and the rate of overall response from 32% to 52% (P=0.02). The addition of iniparib also prolonged the median progression-free survival from 3.6 months to 5.9 months (hazard ratio for progression, 0.59; P=0.01) and the median overall survival from 7.7 months to 12.3 months (hazard ratio for death, 0.57; P=0.01). The most frequent grade 3 or 4 adverse events in either treatment group included neutropenia, thrombocytopenia, anemia, fatigue or asthenia, leukopenia, and increased alanine aminotransferase level. No significant difference was seen between the two groups in the rate of adverse events. The addition of iniparib to chemotherapy improved the clinical benefit and survival of patients with metastatic triple-negative breast cancer without significantly increased toxic effects. On the basis of these results, a phase 3 trial adequately powered to evaluate overall survival and progression-free survival is being conducted. (Funded by BiPar Sciences [now owned by Sanofi-Aventis]; ClinicalTrials.gov number, NCT00540358.).
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Cisplatin plus gemcitabine versus paclitaxel plus gemcitabine as first-line therapy for metastatic triple-negative breast cancer (CBCSG006): a randomised, open-label, multicentre, phase 3 trial.

              Platinum chemotherapy has a role in the treatment of metastatic triple-negative breast cancer but its full potential has probably not yet been reached. We assessed whether a cisplatin plus gemcitabine regimen was non-inferior to or superior to paclitaxel plus gemcitabine as first-line therapy for patients with metastatic triple-negative breast cancer.
                Bookmark

                Author and article information

                Journal
                Ann Oncol
                Ann. Oncol
                annonc
                Annals of Oncology
                Oxford University Press
                0923-7534
                1569-8041
                August 2018
                06 June 2018
                06 June 2018
                : 29
                : 8
                : 1763-1770
                Affiliations
                [1 ]Sarah Cannon Research Institute and Tennessee Oncology PLLC, Medical Oncology, Nashville, USA
                [2 ]Department of Oncology and Metabolism, Weston Park Hospital, University of Sheffield, Sheffield, UK
                [3 ]Department of Surgery, Oncology and Gastroenterology, University of Padova and Medical Oncology 2, Istituto Oncologico Veneto, Padova, Italy
                [4 ]Medical Oncology, Ramon y Cajal University Hospital, Madrid; Vall d'Hebron Institute of Oncology, Barcelona, Spain
                [5 ]Hematology/Oncology, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, USA
                [6 ]Medical Oncology, Ironwood Physicians, PC, Chandler, USA
                [7 ]Medical Oncology, The Center for Cancer and Blood Disorders, Fort Worth, USA
                [8 ]Medical Oncology, Misericordia General Hospital, Grosseto, Italy
                [9 ]Medical Oncology, Henry Ford Health System, Detroit, USA
                [10 ]Hematology and Oncology, Florida Cancer Specialists, Sarasota, USA
                [11 ]Gynecology and Medical Oncology, Heidelberg University Hospital, Heidelberg, Germany
                [12 ]Clinical Oncology, Hospital Universitario Virgen Macarena, Seville, Spain
                [13 ]Hematology and Medical Oncology, Texas Oncology, San Antonio, USA
                [14 ]Hematology, Medical Oncology, Baylor Sammons Cancer Center, Texas Oncology, US Oncology, Dallas, USA
                [15 ]GMA Early Assets, Celgene Corporation, Summit, USA
                [16 ]Department of Biostatistics, Celgene Corporation, Summit, USA
                [17 ]Clinical Research and Development, Hematology/Oncology, Celgene Corporation, Summit, USA
                [18 ]Breast Cancer Center, University of Munich, Munich, Germany
                Author notes
                Correspondence to: Dr Denise A. Yardley, Tennessee Oncology, 250 25th Avenue North, Suite 100, Nashville, TN 37203, USA. Tel: +1-615-329-7272; Fax: +1-615-320-1225; E-mail: dyardley@ 123456tnonc.com
                Article
                mdy201
                10.1093/annonc/mdy201
                6096741
                29878040
                dd63a123-0acf-4479-b0c3-ef7d42fe079f
                © The Author(s) 2018. Published by Oxford University Press on behalf of the European Society for Medical Oncology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                Page count
                Pages: 8
                Categories
                Original Articles
                Breast Tumors

                Oncology & Radiotherapy
                chemotherapy,triple-negative breast cancer,nab-paclitaxel,gemcitabine
                Oncology & Radiotherapy
                chemotherapy, triple-negative breast cancer, nab-paclitaxel, gemcitabine

                Comments

                Comment on this article