Publication: Pertuzumab, trastuzumab and taxane-based treatment for visceral organ metastatic, trastuzumab-naïve breast cancer: real-life practice outcomes
dc.contributor.buuauthor | Evrensel, Türkkan | |
dc.contributor.buuauthor | Yılmaz, Hatice | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Tıbbi Onkoloji Ana Bilim Dalı | |
dc.contributor.orcid | 0000-0002-9732-5340 | |
dc.contributor.researcherid | AAJ-1027-2021 | |
dc.contributor.scopusid | 6603942124 | |
dc.contributor.scopusid | 57202594040 | |
dc.date.accessioned | 2024-01-15T06:17:49Z | |
dc.date.available | 2024-01-15T06:17:49Z | |
dc.date.issued | 2018-10-25 | |
dc.description | Çalışmada 34 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır. | |
dc.description.abstract | PurposeIn this study, we aimed to describe the real-life practice outcomes of pertuzumab-trastuzumab-taxane (PTT) combination in visceral organ metastatic, trastuzumab-naive breast cancer (BC) patients.MethodsThis study was conducted by Turkish Oncology Group and included 317 patients' data from 36 centers.ResultsMedian age was 51 (22-82). Median PFS was 28.5months, while median OS was 40.3months. Patients with brain metastases (n: 13, 4.1%) had worse PFS (16.8m vs. 28.5m; p=0.002) and OS (26.7m vs. 40.3m; p=0.009). Patients older than 65years of age (n: 42, 13.2%) had significantly lower OS results (19.8m vs. 40.3m; p=0.01). Two hundred sixty-eight patients (86.7%) received docetaxel while 37 patients (11.7%) received paclitaxel. PFS and OS were similar between taxane groups. In eight patients (2.5%), 5-40% ejection fraction decrement from baseline was detected without any clinical sign of heart failure.ConclusionsOur RLP trial included only visceral metastatic, trastuzumab-naive BC patients including cases with brain involvement who received PTT combination in the first-line treatment. Regardless of negative prognostic characteristics, our results are in parallel with pivotal trial. Further strategies for brain metastasis should be developed to improve outcomes despite encouraging results with PTT treatment. Taxane selection can be personalized and endocrine maintenance may further improve outcomes after taxanes were discontinued. To our knowledge, this is the largest scale real-life clinical practice study of pertuzumab-trastuzumab-taxane therapy to date. | |
dc.identifier.citation | Evrensel, T. vd. (2018). "Pertuzumab, trastuzumab and taxane-based treatment for visceral organ metastatic, trastuzumab-naïve breast cancer: real-life practice outcomes". Cancer Chemotherapy and Pharmacology, 83(1), 131-143. | |
dc.identifier.endpage | 143 | |
dc.identifier.issn | 0344-5704 | |
dc.identifier.issn | 1432-0843 | |
dc.identifier.issue | 1 | |
dc.identifier.pubmed | 30377778 | |
dc.identifier.scopus | 2-s2.0-85056003618 | |
dc.identifier.startpage | 131 | |
dc.identifier.uri | https://doi.org/10.1007/s00280-018-3712-7 | |
dc.identifier.uri | https://link.springer.com/article/10.1007/s00280-018-3712-7 | |
dc.identifier.uri | https://hdl.handle.net/11452/39005 | |
dc.identifier.volume | 83 | |
dc.identifier.wos | 000458407200014 | |
dc.indexed.wos | SCIE | |
dc.language.iso | en | |
dc.publisher | Springer | |
dc.relation.journal | Cancer Chemotherapy and Pharmacology | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Oncology | |
dc.subject | Pharmacology & pharmacy | |
dc.subject | AntiHER2 | |
dc.subject | Visceral metastasis | |
dc.subject | Brain metastasis | |
dc.subject | Trastuzumab | |
dc.subject | Pertuzumab | |
dc.subject | Clinical-outcomes | |
dc.subject | Older patients | |
dc.subject | Therapy | |
dc.subject | Docetaxel | |
dc.subject | Cleopatra | |
dc.subject | Trial | |
dc.subject | Paclitaxel | |
dc.subject | Survival | |
dc.subject | Chemotherapy | |
dc.subject | Plus | |
dc.subject | Oncology | |
dc.subject | Pharmacology & pharmacy | |
dc.subject.emtree | Adult | |
dc.subject.emtree | Aged | |
dc.subject.emtree | Arthralgia | |
dc.subject.emtree | Article | |
dc.subject.emtree | Blood transfusion reaction | |
dc.subject.emtree | Brain metastasis | |
dc.subject.emtree | Cancer combination chemotherapy | |
dc.subject.emtree | Cancer prognosis | |
dc.subject.emtree | Cancer survival | |
dc.subject.emtree | Clinical outcome | |
dc.subject.emtree | Diarrhea | |
dc.subject.emtree | Fatigue | |
dc.subject.emtree | Heart left ventricle ejection fraction | |
dc.subject.emtree | Human | |
dc.subject.emtree | Human epidermal growth factor receptor 2 positive breast cancer | |
dc.subject.emtree | Hyperbilirubinemia | |
dc.subject.emtree | Hypertransaminasemia | |
dc.subject.emtree | Hypokalemia | |
dc.subject.emtree | Liver metastasis | |
dc.subject.emtree | Loading drug dose | |
dc.subject.emtree | Lung metastasis | |
dc.subject.emtree | Major clinical study | |
dc.subject.emtree | Mucosa inflammation | |
dc.subject.emtree | Multiple cycle treatment | |
dc.subject.emtree | Myalgia | |
dc.subject.emtree | Neutropenia | |
dc.subject.emtree | Overall survival | |
dc.subject.emtree | Peripheral neuropathy | |
dc.subject.emtree | Priority journal | |
dc.subject.emtree | Progression free survival | |
dc.subject.emtree | Rash | |
dc.subject.emtree | Retrospective study | |
dc.subject.emtree | Side effect | |
dc.subject.emtree | Thrombocytopenia | |
dc.subject.emtree | Transthoracic echocardiography | |
dc.subject.emtree | Visceral metastasis | |
dc.subject.emtree | Vomiting | |
dc.subject.emtree | Breast tumor | |
dc.subject.emtree | Clinical practice | |
dc.subject.emtree | Female | |
dc.subject.emtree | Follow up | |
dc.subject.emtree | Lobular carcinoma | |
dc.subject.emtree | Metastasis | |
dc.subject.emtree | Middle aged | |
dc.subject.emtree | Mortality | |
dc.subject.emtree | Paget nipple disease | |
dc.subject.emtree | Pathology | |
dc.subject.emtree | Prognosis | |
dc.subject.emtree | Survival rate | |
dc.subject.emtree | Tumor invasion | |
dc.subject.emtree | Very elderly | |
dc.subject.emtree | Young adult | |
dc.subject.emtree | Docetaxel | |
dc.subject.emtree | Epidermal growth factor receptor 2 | |
dc.subject.emtree | Paclitaxel | |
dc.subject.emtree | Pertuzumab | |
dc.subject.emtree | Trastuzumab | |
dc.subject.emtree | Antineoplastic agent | |
dc.subject.emtree | Docetaxel | |
dc.subject.emtree | Monoclonal antibody | |
dc.subject.emtree | Paclitaxel | |
dc.subject.emtree | Pertuzumab | |
dc.subject.emtree | Trastuzumab | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Aged, 80 and over | |
dc.subject.mesh | Antibodies, monoclonal, humanized | |
dc.subject.mesh | Antineoplastic combined chemotherapy protocols | |
dc.subject.mesh | Breast neoplasms | |
dc.subject.mesh | Carcinoma, ductal, breast | |
dc.subject.mesh | Carcinoma, lobular | |
dc.subject.mesh | Docetaxel | |
dc.subject.mesh | Female | |
dc.subject.mesh | Follow-up studies | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Middle aged | |
dc.subject.mesh | Neoplasm invasiveness | |
dc.subject.mesh | Neoplasm metastasis | |
dc.subject.mesh | Paclitaxel | |
dc.subject.mesh | Practice patterns, physicians' | |
dc.subject.mesh | Prognosis | |
dc.subject.mesh | Retrospective studies | |
dc.subject.mesh | Survival rate | |
dc.subject.mesh | Trastuzumab | |
dc.subject.mesh | Young adult | |
dc.subject.scopus | Breast Neoplasms; Trastuzumab Emtansine; Neratinib | |
dc.subject.wos | Oncology | |
dc.subject.wos | Pharmacology & pharmacy | |
dc.title | Pertuzumab, trastuzumab and taxane-based treatment for visceral organ metastatic, trastuzumab-naïve breast cancer: real-life practice outcomes | |
dc.type | Article | |
dc.wos.quartile | Q2 | |
dc.wos.quartile | Q3 | |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/Tıbbi Onkoloji Ana Bilim Dalı | |
local.indexed.at | WOS | |
local.indexed.at | Scopus |
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