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Old 05-18-2013, 09:33 PM   #1
Lani
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Join Date: Mar 2006
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Thumbs up ASCO 2013--Stage IVs living longer and longer as treatments improve

Abstract only from upcoming asco--her2 not mentioned, probably because data based on SEER results which probably don't record her2 status


Is the proportion of patients with synchronous stage IV breast cancer surviving > 2 years increasing over time?

Sub-category:
ER+

Category:
Breast Cancer - HER2/ER

Meeting:
2013 ASCO Annual Meeting

Abstract No:
524

Citation:
J Clin Oncol 31, 2013 (suppl; abstr 524)

Publication-only abstracts (abstract number preceded by an "e"), published in conjunction with the 2013 Annual Meeting but not presented at the Meeting, can be found online only.

Author(s): Shaheenah S. Dawood, Benjamin Haaland, Constance T. Albarracin, Ana M. Gonzalez-Angulo, Sudeep Gupta, Javier Cortes, Yoon Sim Yap, Rebecca Dent; Dubai Hospital, Dubai, United Arab Emirates; Duke-National University of Singapore Graduate Medical School, Singapore, Singapore; The University of Texas MD Anderson Cancer Center, Houston, TX; Tata Memorial Centre, Mumbai, India; Vall d'Hebron University Hospital, Barcelona, Spain; National Cancer Centre Singapore, Singapore, Singapore; National Cancer Center Singapore, Duke-National University Singapore, Singapore, Singapore

Abstract Disclosures


Abstract:

Background: Studies have shown a moderate increase in survival over time among pts with stageIV breast cancer. Median survival is approximately 2 yrs. The aim of this study was to evaluate trends over time of pts with synchronous stage IV disease who survive >2 yrs. Methods: Using the SEER registry we identified female pts with synchronous stage IV breast cancer diagnosed between 1990-2007. Pts were divided into 3 groups according to year of diagnosis(1990-1995, 1996-2000, 2001-2007). Probability of surviving more than >2 yrs was computed within each group. A multivariable logistic regression model was then fitted to determine the association between year of diagnosis and the probability of surviving >2 yrs after adjusting for other prognostic factors. Results: 22,492 pts were identified of whom 9,388 (41.7%) had a survival of >2 yrs. The probability of surviving >2 yrs was 36.2%, 40.1%, and 44.2% among pts diagnosed in periods 1990-1995, 1996-2000, and 2001-2007 respectively (p-value < 0.0001). The probability of surviving >2 yrs was 55.3% and 29.3% among pts with ER+ and ER- disease respectively (p-value <0.0001) and was 32.9% and 43.5% among pts of black and white race respectively (p-value <0.0001). In the multivariable model the probability of surviving >2 yrs increased with increasing year of diagnosis (OR 1.04, 95% CI 1.03-1.05, p <0.0001). Other factors significantly associated with an increased probability of surviving >2 yrs included radiation therapy, lower grade, younger age, hormone receptor (HR) positive disease and non-inflammatory disease. Interaction term between race and year of diagnosis was marginally significant, such that black pts had a more slowly increasing probability of surviving >2 yrs compared to whites (OR 0.97, 95% CI 0.96-1.00, p = 0.037). Interaction term between HR status and year of diagnosis was not significant. Conclusions: Our results indicate that among pts with synchronous stage IV breast cancer the probability of surviving >2 yrs has increased over time reflecting the introduction and FDA approval of multiple efficacious chemotherapeutic and endocrine therapeutic options. Of concern, the probability of surviving >2 yrs has increased more slowly among pts of black race.
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Old 05-18-2013, 09:37 PM   #2
Pray
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Re: ASCO 2013--Stage IVs living longer and longer as treatments improve

Any increase in life span is a good increase! In cancer land a win for some of us is a wi for all of us.
__________________
dx 11/12/09 IDCI
Stage 3a
ER 98% PR 80%
Her2 +3
4/12 nodes
6 rounds TCH
Herceptin 12 months 3weeks
Rad. 30 tx
Tamoxifin 6 months stopped
Arimedex stopped 9/12 (side effects)
Aromasin 10/12
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Old 05-19-2013, 01:25 AM   #3
Bunty
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Re: ASCO 2013--Stage IVs living longer and longer as treatments improve

Thanks Lani - does synchronous stage IV breast cancer mean that a patient is stage iv at initial diagnosis?
Cheers Marie
__________________
dx Dec 2000 dcis 2.5cm clear sentinel node, ER/PR- Her-2+
lumpectomy, 6 cycles AC, 6 weeks rads
October 2007 three x 2.5cm lung mets. 8 months Taxol, started Herceptin and continue. Significant reduction in lung mets.
June 2011 3cm x 4cm liver tumour. Started Abraxane and continue with Herceptin.
November 2011. Finished with Abraxane, continue with just Herceptin. Liver tumour now reduced to 15mm x 12mm. Lung tumour now 10mm x 0.5mm
February 2012. Scans show everything stable, and brain scan clear.
July 2012. PET/CT scans show I'm in remission - no active cancer!
]Dec CT brain cllear, lungs stable, liver tumour has increased to 20mm. PET scans showed active liver met and active lung thinglet, and possible bone met.
Jan 2013 recommence Abraxane, continue with Herceptin.
June 2013 finish Cycle 6 Abraxane, continue with Herceptin. 30% reduction in liver tumour, everything stable.
December 2013. CA15-3 on rise.
February 2014. PET and CT scans show single liver tumour has increased to 35mm. No other activity.
March 2014. Planned for SBRT for liver met, but couldn't have treatment as tumour too close to bowel. Continue Herceptin.
April 2014. Surgeon advises that I am a good candidate for liver resection, so will have operation early May (after camping holiday). Tumour now 44mm x 29mm.
May 7, 2014. Two liver tumours surgically removed. Third of liver removed, and gall bladder. Am I NED?May 2014. Pathology of tumour shows it's now ER+ (95% staining).
June 2014. CA15-3 has decreased to 18 from a pre-surgery reading of 59!
June 2014. Started Femara, continue with Herceptin.
July 2014. Stop Femara due to severe Osteoporosis. Commence Tamoxifen, continue Herceptin. Waiting to hear if I can have Aclasta infusion.
August 2014. CA15-3 has decreased further to 12 - YAY!
October 2014. Aclasta infusion for Osteoporosis. November 2014, CA15-3 decreased to 11. Scans of liver all clear, something new showing up on lung, but just watching at the moment.
November 2015. Started SBRT on solitary lung met.
November 2015. Bone density scan showed very good improvement so back on Femara - yay!
December 2016. 6 treatments of SBRT radiation on lung. Seems to have had some effect.
June 2016. CA15-3 still stable and low at 9.
June 2016. Started subcutaneous Herceptin replacing infusion.
Jan 2017. LVEF dropped to 46%. Stopped Herceptin.
Feb 2017. Started ACE Inhibitor and BETA Blocker. Still off Herceptin.
Aug 2017. Two new mets - Portacaval lymph node and mediastinal lymph node.
Aug 2017. Blood tests show extremely elevated liver enzyme levels. Many tests to investigate.
Sept 2017. Portacaval lymph node blocking liver bile duct causing liver enzyme and Bilirubin problems.
Oct 2017. 8cm stent inserted into liver bile duct. Procedure caused pancreatitis, and hospitalised for 3 days. Liver enzymes improving rapidly.
Nov 2017. Commenced 4 weeks of radiation on Portacaval lymph node. 5 week break before chemo.
Jan 2018. CT scan. 11 new small liver mets, and new superclavical lymph node med.
Jan 2018. Start Kadcyla. CA15-3 426.
Apr 2018. First scans since starting Kadcyla. All tumours reducing. CA15-3 dropped to 30 from 426.
Dec 2019. Still on Kadcyla, but two small brain mets have been treated in the past month with SRS. CA15-3 stable for 12 months at 11.
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Old 05-19-2013, 07:10 AM   #4
'lizbeth
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Re: ASCO 2013--Stage IVs living longer and longer as treatments improve

I would infer synchronous with stage IV from initial diagnosis from reading this:

http://annonc.oxfordjournals.org/con...nc.mdq301.full

Data from the Surveillance, Epidemiology, and End Results (SEER) program and the European Concerted Action on survival and Care of Cancer Patients (EUROCARE) project indicate that ∼6% of women newly diagnosed with breast cancer have stage IV disease, representing ∼12 600 new cases per year in the United States in 2005 [1, 2]. The 5-year overall survival (OS) rate among such patients rarely exceeds 20% [3]. Survival can be improved by endocrine therapy, chemotherapy, and biological therapy [4, 5]. Local treatment is often recommended to prevent or relieve symptoms but is traditionally considered to have no noteworthy impact on survival [4, 5]. However, several recent observational studies have shown that 35%–60% of breast cancer patients with stage IV disease at diagnosis receive treatment of the primary tumor and that this treatment is associated with a survival advantage [618]. The impact of treatments targeting regional lymphatics is unclear, and the patient subgroups most likely to benefit from treatment of the primary tumor remain to be identified. Two prospective studies are currently examining the benefits of locoregional therapy compared with systemic therapy alone in this setting. The main objective of this review is to highlight current issues regarding treatment of the primary tumor in breast cancer patients with synchronous metastases in order to highlight clinicians in their therapeutic decision.
__________________
Diagnosed 2007
Stage IIb Invasive Ductal Carcinoma, Pagets, 3 of 15 positive nodes

Traditional Treatment: Mastectomy and Axillary Node Dissection followed by Taxotere, 6 treatments and 1 year of Herceptin, no radiation
Former Chemo Ninja "Takizi Zukuchiri"

Additional treatments:
GP2 vaccine, San Antonio Med Ctr
Prescriptive Exercise for Cancer Patients
ENERGY Study, UCSD La Jolla

Reconstruction: TRAM flap, partial loss, Revision

The content of my posts are meant for informational purposes only. The medical information is intended for general information only and should not be used in any way to diagnose, treat, cure, or prevent disease
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Old 05-19-2013, 10:32 AM   #5
Lani
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Re: ASCO 2013--Stage IVs living longer and longer as treatments improve

Citation:
J Clin Oncol 31, 2013 (suppl; abstr e12003)
Publication-only abstracts (abstract number preceded by an "e"), published in conjunction with the 2013 Annual
Meeting but not presented at the Meeting, can be found online only.
Author(s): Pengyu Chen, Skye H Hong-Chun Cheng; Koo Foundation Sun Yat-Sen Cancer Center, Taipei
City, Taiwan
Abstract Disclosures
Abstract:
Background: Breast cancer has three major subtypes, including luminal-like (hormone receptor positive, no
HER2 overexpression), HER2-rich (HER2 overexpression), and triple negative (hormone receptor negative
and no HER2 overexpression). This study is to analyze the prognosis in each subtype of stage IV breast
cancer patients. Methods: We reviewed 246 patients with de novo stage IV breast cancer treated at our
hospital between 1990 and 2009. Multivariable Cox analysis was used to determine the survival associated
the subtypes and clinicopathologic factors. Results: Patients with luminal-like subtype are mostly
premonopausal (66.9%, P=0.0002), with abnormal CA 15-3 level at initial diagnosis (58.7%, P=0.01), with
higher rate of bone mets (78.1%, P=0.02), and less rate of liver mets (23.1%, P<0.0001). Patients with HER2-
rich and triple negative had higher rate of nuclear grade III of primary breast tumor, up to 35% and 40%,
respectively (P=0.01). There is no difference in the systemic chemotherapy (82.2~95%, P=0.09) and
locoregional treatment (40.0~51.2%, P=0.23) among three groups. The median overall survival of 246
patients was 23.1 months. The median overall survival in patients with luminal-like, HER2-rich, and triple
negative subtype were 39.6, 17.9, and 13.3 months, respectively (P<0.0001). In multivariate analysis,
hormone receptor and HER2 status were significant independent factors associated with survival (P<0.0001).
Other significant factors associated with survival included liver mets (Hazard Ratio 2.3, P<0.0001), lung mets
(Hazard Ratio 1.7, P=0.0004), and brain mets (Hazard Ratio 1.5, P=0.03). In subgroup analysis, locoregional
treatment to primary breast tumor had significant survival benefit in patients with luminal-like (P=0.0001)
and HER2-rich(P=0.0012) subtype. In triple negative subtype, local treatment did not improve outcome
(P=0.9575). Conclusions: Hormone receptors and HER2 status are the most important factors affecting
survival for these patients. Locoregional treatment to primary breast tumor may provide better outcome,
especially those with luminal-like or HER2-rich subtype.
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Old 05-19-2013, 10:33 AM   #6
Lani
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Join Date: Mar 2006
Posts: 4,778
Re: ASCO 2013--Stage IVs living longer and longer as treatments improve

ALong those lines they have just shown that her2+s benefit more than others from removal of the primary tumor

Citation:
J Clin Oncol 31, 2013 (suppl; abstr e12003)
Publication-only abstracts (abstract number preceded by an "e"), published in conjunction with the 2013 Annual
Meeting but not presented at the Meeting, can be found online only.
Author(s): Pengyu Chen, Skye H Hong-Chun Cheng; Koo Foundation Sun Yat-Sen Cancer Center, Taipei
City, Taiwan
Abstract Disclosures
Abstract:
Background: Breast cancer has three major subtypes, including luminal-like (hormone receptor positive, no
HER2 overexpression), HER2-rich (HER2 overexpression), and triple negative (hormone receptor negative
and no HER2 overexpression). This study is to analyze the prognosis in each subtype of stage IV breast
cancer patients. Methods: We reviewed 246 patients with de novo stage IV breast cancer treated at our
hospital between 1990 and 2009. Multivariable Cox analysis was used to determine the survival associated
the subtypes and clinicopathologic factors. Results: Patients with luminal-like subtype are mostly
premonopausal (66.9%, P=0.0002), with abnormal CA 15-3 level at initial diagnosis (58.7%, P=0.01), with
higher rate of bone mets (78.1%, P=0.02), and less rate of liver mets (23.1%, P<0.0001). Patients with HER2-
rich and triple negative had higher rate of nuclear grade III of primary breast tumor, up to 35% and 40%,
respectively (P=0.01). There is no difference in the systemic chemotherapy (82.2~95%, P=0.09) and
locoregional treatment (40.0~51.2%, P=0.23) among three groups. The median overall survival of 246
patients was 23.1 months. The median overall survival in patients with luminal-like, HER2-rich, and triple
negative subtype were 39.6, 17.9, and 13.3 months, respectively (P<0.0001). In multivariate analysis,
hormone receptor and HER2 status were significant independent factors associated with survival (P<0.0001).
Other significant factors associated with survival included liver mets (Hazard Ratio 2.3, P<0.0001), lung mets
(Hazard Ratio 1.7, P=0.0004), and brain mets (Hazard Ratio 1.5, P=0.03). In subgroup analysis, locoregional
treatment to primary breast tumor had significant survival benefit in patients with luminal-like (P=0.0001)
and HER2-rich(P=0.0012) subtype. In triple negative subtype, local treatment did not improve outcome
(P=0.9575). Conclusions: Hormone receptors and HER2 status are the most important factors affecting
survival for these patients. Locoregional treatment to primary breast tumor may provide better outcome,
especially those with luminal-like or HER2-rich subtype.
Other
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