slide1 n.
Skip this Video
Loading SlideShow in 5 Seconds..
INTRODUCTION PowerPoint Presentation
Download Presentation

Loading in 2 Seconds...

play fullscreen
1 / 19

INTRODUCTION - PowerPoint PPT Presentation

Download Presentation
An Image/Link below is provided (as is) to download presentation

Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.

- - - - - - - - - - - - - - - - - - - - - - - - - - - E N D - - - - - - - - - - - - - - - - - - - - - - - - - - -
Presentation Transcript

  1. American Society of Clinical Oncology Clinical Practice Guideline Updateon Adjuvant Endocrine Therapy for Women with Hormone-Receptor Positive Breast Cancer 

  2. INTRODUCTION • ASCO initially published its first technology assessment for the use of aromatase inhibitors (AIs) in the adjuvant setting for women with hormone receptor-positive breast cancer in 2002 • ASCO guidelines are updated at intervals by an Update Committee of the original Expert Panel; the last update was in 2004 • For the 2010 update, the Update Committee reviewed literature published since May 2007

  3. Guideline Methodology: Systematic Review • The Update Committee completed a systematic review and analysis of the medical literature, using the Cancer Care Ontario systematic review of literature through May 2007, and ASCO’s searches of literature from May 2007 to February 2009 • Medline • Pre-Medline • Cochrane Collaboration Library • ASCO and San Antonio Breast Cancer Symposium abstracts from 2007 - 2009

  4. Limitations of the literature • Timing of randomization – patient populations in sequential, extended, and primary therapy trials may all differ from one another • Longest median follow-up data available is 8 years, most studies less • Median time to event yet to be achieved • Modest # of events, including for subgroups • Different definitions of study endpoints

  5. Clinical Questions 1a. What adjuvant endocrine treatments should be offered to postmenopausal women with hormone receptor-positive breast cancer? 1b. What is the appropriate duration of adjuvant endocrine therapy? 1c. If tamoxifen is administered first, how long should it be continued before the switch to an AI? 2. Are there specific patient populations that derive differing degrees of benefit from an aromatase inhibitor in comparison to tamoxifen?

  6. Clinical Questions, cont’d 3. What are the toxicities and risks of adjuvant endocrine therapy? 4. Are aromatase inhibitors effective adjuvant therapy for women who are premenopausal at the time of diagnosis? 5. Can the third-generation aromatase inhibitors be used interchangeably?

  7. Recommendations Recommendation 1a. The Update Committee recommends, based on data from randomized controlled trials, that most postmenopausal women consider taking an aromatase inhibitor during the course of adjuvant treatment to lower recurrence risk, either as primary therapy or after two to three years of tamoxifen, strategies that yield equivalent outcomes in prospective studies. Duration of aromatase inhibitor therapy should not exceed five years.

  8. Recommendations Recommendation 1b. Therapy with an aromatase inhibitor should not extend beyond five years in either the primary or extended adjuvant settings, outside of the clinical trials setting. In the sequential setting, the Update Committee recommends, based on available evidence from randomized controlled trials, that patients receive an AI after two or three years of tamoxifen for a total of five years of adjuvant endocrine therapy. The Update Committee recommends that patients who are initially treated with an AI but discontinue treatment before five years of therapy consider taking tamoxifen for a total of five years of adjuvant endocrine therapy.

  9. Recommendations Recommendation 1c. The Update Committee recommends that, based on available evidence from randomized controlled trials, patients who initially receive tamoxifen as adjuvant therapy may be offered an AI after two to three years (sequential) or after five years (extended) of therapy. The time to switch from an AI to tamoxifen (or the converse) that maximally improves outcomes is not known from available direct evidence. The Update Committee recommends switching at two to three years based on data from sequential trials that employed this strategy. Switching at five years is also a strategy supported by the extended adjuvant randomized trials.

  10. Strategies: (P)-primary; (S)-sequential; (E)-extended

  11. Recommendations • Recommendation 2. Direct evidence from randomized trials does not identify a specific marker or clinical subset that predicted which adjuvant treatment strategy, tamoxifen or AI monotherapy or sequential therapy, would maximally improve outcomes for a given patient. • Among men with breast cancer, tamoxifen remains the standard adjuvant endocrine treatment. • The Update Committee recommends against using CYP2D6 genotype to select adjuvant endocrine therapy. The Committee encouraged caution with concurrent use of CYP2D6 inhibitors (such as bupropion, paroxetine, fluoxetine) and tamoxifen because of the known drug-drug interactions.

  12. Recommendations Recommendation 3. The Update Committee recommends that clinicians consider side effect profiles, patient preferences, and pre-existing conditions when recommending an adjuvant endocrine strategy for postmenopausal women. Clinicians should discuss side effect profiles when presenting available treatment options to patients. The Update Committee suggests that clinicians consider recommending that patients change treatment if side effects are intolerable or patients are persistently non-compliant with therapy.

  13. Recommendations • Recommendation 4. The Update Committee recommends that women who are pre- or perimenopausal at the time of breast cancer diagnosis be treated with five years of tamoxifen. • Additional considerations. The Update Committee recommends that clinicians use caution in evaluating menopausal status of patients who were pre- or perimenopausal at diagnosis. Unequivocal determination of menopausal status may be challenging to prove. Even among women who have not experienced menses for over one year, laboratory testing is inadequate as patients may recover ovarian function. This particularly applies to those patients who experience chemotherapy- or tamoxifen-induced amenorrhea.

  14. Recommendations Recommendation 5. In the absence of direct comparisons, the Update Committee interprets available data as suggesting that benefits of AI therapy represent a “class effect.” Meaningful clinical differences between the commercially available third-generation aromatase inhibitors have not been demonstrated to date. In the clinical opinion of the Committee (rather thandirect evidence from randomized trials), postmenopausal patients intolerant of one AI but who are still candidates for adjuvant endocrine therapy may be advised to consider tamoxifen or a different AI.

  15. Side-effects Comparison Please note: √ represents higher risk of side-effect in column of that particular agent.. *BMD-bone mineral density

  16. Guideline Methodology: Panel Members

  17. Guideline Methodology: Panel Members, cont’d

  18. Additional ASCO Resources • The full text of the guideline, an abridged version of the guideline, a Journal of Oncology Practice Summary, this slide set, and additional clinical tools and resources can be found at: • A patient guide, “What to Know” about this guideline, is available at:

  19. ASCO Guidelines