000 | 04563nam a22005897a 4500 | ||
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008 | 171110s20172017 xxu||||| |||| 00| 0 eng d | ||
022 | _a0732-183X | ||
040 | _aOvid MEDLINE(R) | ||
099 | _a29072977 | ||
245 | _aLong-Term Follow-Up of Cardiac Function and Quality of Life for Patients in NSABP Protocol B-31/NRG Oncology: A Randomized Trial Comparing the Safety and Efficacy of Doxorubicin and Cyclophosphamide (AC) Followed by Paclitaxel With AC Followed by Paclitaxel and Trastuzumab in Patients With Node-Positive Breast Cancer With Tumors Overexpressing Human Epidermal Growth Factor Receptor 2. | ||
251 | _aJournal of Clinical Oncology. 35(35):3942-3948, 2017 Dec 10 | ||
252 | _aJ Clin Oncol. 35(35):3942-3948, 2017 Dec 10 | ||
253 | _aJournal of clinical oncology : official journal of the American Society of Clinical Oncology | ||
260 | _c2017 | ||
260 | _fFY2018 | ||
266 | _d2017-11-10 | ||
501 | _aAvailable online from MWHC library: 1999 - present, Available in print through MWHC library: 1999 - 2008 | ||
520 | _aPurpose Early cardiac toxicity is a risk associated with adjuvant chemotherapy plus trastuzumab. However, objective measures of cardiac function and health-related quality of life are lacking in long-term follow-up of patients who remain cancer free after completion of adjuvant treatment. Patients and Methods Patients in NSABP Protocol B-31 received anthracycline and taxane chemotherapy with or without trastuzumab for adjuvant treatment of node-positive, human epidermal growth factor receptor 2-positive early-stage breast cancer. A long-term follow-up assessment was undertaken for patients who were alive and disease free, which included measurement of left ventricular ejection fraction by multigated acquisition scan along with patient-reported outcomes using the Duke Activity Status Index (DASI), the Medical Outcomes Study questionnaire, and a review of current medications and comorbid conditions. Results At a median follow-up of 8.8 years among eligible participants, five (4.5%) of 110 in the control group and 10 (3.4%) of 297 in the trastuzumab group had a > 10% decline in left ventricular ejection fraction from baseline to a value < 50%. Lower DASI scores correlated with age and use of medications for hypertension, cardiac conditions, diabetes, and hyperlipidemia, but not with whether patients had received trastuzumab. Conclusion In patients without underlying cardiac disease at baseline, the addition of trastuzumab to adjuvant anthracycline and taxane-based chemotherapy does not result in long-term worsening of cardiac function, cardiac symptoms, or health-related quality of life. The DASI questionnaire may provide a simple and useful tool for monitoring patient-reported changes that reflect cardiac function. | ||
546 | _aEnglish | ||
650 | _a*Antineoplastic Combined Chemotherapy Protocols/ad [Administration & Dosage] | ||
650 | _a*Breast Neoplasms/dt [Drug Therapy] | ||
650 | _a*Breast Neoplasms/pp [Physiopathology] | ||
650 | _a*Cardiovascular System/pp [Physiopathology] | ||
650 | _a*Receptor, ErbB-2/bi [Biosynthesis] | ||
650 | _aAntineoplastic Combined Chemotherapy Protocols/ae [Adverse Effects] | ||
650 | _aBreast Neoplasms/en [Enzymology] | ||
650 | _aBreast Neoplasms/pa [Pathology] | ||
650 | _aChemotherapy, Adjuvant | ||
650 | _aCohort Studies | ||
650 | _aCyclophosphamide/ad [Administration & Dosage] | ||
650 | _aCyclophosphamide/ae [Adverse Effects] | ||
650 | _aDoxorubicin/ad [Administration & Dosage] | ||
650 | _aDoxorubicin/ae [Adverse Effects] | ||
650 | _aFemale | ||
650 | _aFollow-Up Studies | ||
650 | _aHumans | ||
650 | _aLymphatic Metastasis | ||
650 | _aMiddle Aged | ||
650 | _aPaclitaxel/ad [Administration & Dosage] | ||
650 | _aPaclitaxel/ae [Adverse Effects] | ||
650 | _aQuality of Life | ||
650 | _aTrastuzumab/ad [Administration & Dosage] | ||
650 | _aTrastuzumab/ae [Adverse Effects] | ||
650 | _aVentricular Dysfunction, Left/pp [Physiopathology] | ||
651 | _aWashington Cancer Institute | ||
657 | _aJournal Article | ||
700 | _aSwain, Sandra M | ||
700 | _aZapas, John L | ||
790 | _aAtkins JN, Biggs DD, Brufsky AM, Cecchini RS, Fehrenbacher L, Flynn PJ, Ganz PA, Geyer CE Jr, Gross HM, Jeong JH, Mamounas EP, Polikoff J, Rastogi P, Romond EH, Seay TE, Swain SM, Wade JL 3rd, Wahl TA, Wolmark N, Zapas JL | ||
856 |
_uhttps://dx.doi.org/10.1200/JCO.2017.74.1165 _zhttps://dx.doi.org/10.1200/JCO.2017.74.1165 |
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942 |
_cART _dArticle |
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999 |
_c3020 _d3020 |