N Lynn Henry1, Mark R Somerfield2, Vandana G Abramson3, Nofisat Ismaila2, Kimberly H Allison4, Carey K Anders5, Diana T Chingos6, Andrea Eisen7, Bruno L Ferrari8, Thomas H Openshaw9, Patricia A Spears5, Praveen Vikas10, Vered Stearns11. 1. 1University of Utah Huntsman Cancer Institute, Salt Lake City, UT. 2. 2American Society of Clinical Oncology, Alexandria, VA. 3. 3Vanderbilt-Ingram Cancer Center, Nashville, TN. 4. 4Stanford University Medical Center, Stanford, CA. 5. 5University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC. 6. 6Patient Advocate in Research, Los Angeles, CA. 7. 7Sunnybrook Odette Cancer Centre, Cancer Care Ontario, Toronto, Canada. 8. 8Oncoclinicas Group, São Paulo, Brazil. 9. 9Northern Light Cancer Institute, Brewer, ME. 10. 10University of Iowa Holden Comprehensive Cancer Center, Iowa City, IA. 11. 11Kimmel Cancer Center at Johns Hopkins, Baltimore, MD.
Abstract
PURPOSE: To update the American Society of Clinical Oncology endorsement of the Cancer Care Ontario recommendations on the Role of Patient and Disease Factors in Adjuvant Systemic Therapy Decision Making for Early-Stage, Operable Breast Cancer. METHODS: Two phase III trials-the Trial Assigning Individualized Options for Treatment (TAILORx) in women with hormone receptor-positive, node-negative tumors and the Microarray in Node-Negative and 1 to 3 Positive Lymph Node Disease May Avoid Chemotherapy (MINDACT) trial-provided the evidence for this update. UPDATED RECOMMENDATIONS: Shared decision making between clinicians and patients is appropriate for adjuvant systemic therapy for breast cancer. For patients older than age 50 years and whose tumors have Oncotype DX recurrence scores less than 26, and for patients age 50 years or younger whose tumors have Oncotype DX recurrence scores less than 16, there is little to no benefit from chemotherapy. Clinicians may offer endocrine therapy alone for these patients. For patients age 50 years or younger with recurrence scores of 16 to 25, clinicians may offer chemoendocrine therapy. Patients with recurrence scores greater than 30 should be considered candidates for chemoendocrine therapy. Based on informal consensus, the Panel recommends that oncologists may offer chemoendocrine therapy to patients with Oncotype DX scores of 26 to 30.The MammaPrint assay could be used to guide decisions on withholding adjuvant systemic chemotherapy in patients with hormone receptor-positive lymph node-negative breast cancer and in select patients with lymph node-positive cancers. In both patients with node-positive and node-negative disease, evidence of clinical utility of the MammaPrint assay was only apparent in those determined to be at high clinical risk; the Panel thus did not recommend use of MammaPrint assay in patients determined to be at low clinical risk. Remaining recommendations from the 2016 ASCO guideline endorsement are unchanged.Additional information is available at www.asco.org/breast-cancer-guidelines.
PURPOSE: To update the American Society of Clinical Oncology endorsement of the Cancer Care Ontario recommendations on the Role of Patient and Disease Factors in Adjuvant Systemic Therapy Decision Making for Early-Stage, Operable Breast Cancer. METHODS: Two phase III trials-the Trial Assigning Individualized Options for Treatment (TAILORx) in women with hormone receptor-positive, node-negative tumors and the Microarray in Node-Negative and 1 to 3 Positive Lymph Node Disease May Avoid Chemotherapy (MINDACT) trial-provided the evidence for this update. UPDATED RECOMMENDATIONS: Shared decision making between clinicians and patients is appropriate for adjuvant systemic therapy for breast cancer. For patients older than age 50 years and whose tumors have Oncotype DX recurrence scores less than 26, and for patients age 50 years or younger whose tumors have Oncotype DX recurrence scores less than 16, there is little to no benefit from chemotherapy. Clinicians may offer endocrine therapy alone for these patients. For patients age 50 years or younger with recurrence scores of 16 to 25, clinicians may offer chemoendocrine therapy. Patients with recurrence scores greater than 30 should be considered candidates for chemoendocrine therapy. Based on informal consensus, the Panel recommends that oncologists may offer chemoendocrine therapy to patients with Oncotype DX scores of 26 to 30.The MammaPrint assay could be used to guide decisions on withholding adjuvant systemic chemotherapy in patients with hormone receptor-positive lymph node-negative breast cancer and in select patients with lymph node-positive cancers. In both patients with node-positive and node-negative disease, evidence of clinical utility of the MammaPrint assay was only apparent in those determined to be at high clinical risk; the Panel thus did not recommend use of MammaPrint assay in patients determined to be at low clinical risk. Remaining recommendations from the 2016 ASCO guideline endorsement are unchanged.Additional information is available at www.asco.org/breast-cancer-guidelines.
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Authors: Suzanne C O'Neill; Susan T Vadaparampil; Richard L Street; Tanina Foster Moore; Claudine Isaacs; Hyo S Han; Bianca Augusto; Jennifer Garcia; Katherine Lopez; Matilda Brilleman; Jinani Jayasekera; Susan Eggly Journal: Patient Educ Couns Date: 2020-09-03
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Authors: Sun Young Chae; Seol Hoon Park; Hyo Sang Lee; Jin-Hee Ahn; Sung-Bae Kim; Kyung Hae Jung; Jeong Eun Kim; Sei Hyun Ahn; Byung Ho Son; Jong Won Lee; Beom Seok Ko; Hee Jeong Kim; Gyungyub Gong; Jungsu S Oh; Seo Young Park; Dae Hyuk Moon Journal: Sci Rep Date: 2022-05-12 Impact factor: 4.996
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Authors: Gagan Gupta; Caroline Dasom Lee; Mary L Guye; Robert E Van Sciver; Michael P Lee; Alex C Lafever; Anthony Pang; Angela M Tang-Tan; Janet S Winston; Billur Samli; Rick J Jansen; Richard A Hoefer; Amy H Tang Journal: Ann Breast Cancer Ther Date: 2020-05-02