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![Page 1: Tubulin Inhibition in Breast Cancer: A Therapeutic Target Critical to Improving Outcomes William J. Gradishar, MD Professor of Medicine Robert H. Lurie.](https://reader035.fdocuments.us/reader035/viewer/2022081518/551b66585503465c7e8b6541/html5/thumbnails/1.jpg)
Tubulin Inhibition in Breast Cancer:A Therapeutic Target Critical to
Improving Outcomes
William J. Gradishar, MDProfessor of Medicine
Robert H. Lurie Comprehensive Cancer Center
Northwestern University Feinberg School of Medicine
Chicago, IL
Clinical Updates
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Role of Microtubule in Cellular Physiology Microtubules, a key component of cell cytoskeleton
• comprise filamentous polymers
• dynamic structures that depolymerize and rearrange to form mitotic spindle which is essential to cell division
Microtubules
• through mitotic spindle, align and separate chromosomes
• transport cellular material
• engage in intracellular signalling
• play integral role in cell growth and mitosis
• re-organized in cell invasion and migration, processes essentialto tumor metastasis
Biological function of microtubules regulated by polymerization dynamics
McIntosh et al, Microtubules. Wiley-Liss: New York 1994; 413–34; Oakley et al, Microtubules. Wiley-Liss: New York 1994; 33–45
Wordeman et al, Microtubules. Wiley-Liss: New York 1994; 287–301
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Structure of a Microtubule
Jordan & Kamath, Curr Cancer Drug Targets 2007; 7: 730–42
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Microtubule Involvement in Mitosis
Jackson et al, Nat Rev Cancer 2007; 7: 107–17Reprinted by permission from Macmillan Publishers Ltd.
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Effects of Tubulin-binding Drugs on Microtubules
Jordan et al, Mol Cancer Ther 2005; 4: 1086–95
Verrills & Kavallaris, Curr Pharm Des 2005; 11: 1719–33
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Taxane-based Therapy
Active against a wide spectrum of malignancies
– Standard component of breast, ovarian, and NSCLC therapy
Limitations with traditional taxanes
– Hydrophobic and require solvents
• Cremophor® with paclitaxel
• Tween 80 with docetaxel
van Zuylen L, et al. Invest New Drugs. 2001;19:125-141; van Tellingen O, et al. Clin Cancer Res. 1999;5:2918-2924; Ellis AG, et al. Cancer Chemother Pharmacol. 1996;38:81-87; LoRusso PM,
Pilat MJ. ONS News. 2004;19:75-76.
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Solvent-based Taxane Toxicities
Reaction Docetaxel Paclitaxel
Hypersensitivity reaction (grade 3/4) 2.6%* 2%
Neutropenia (<500 mm3) 85.9% 52%
Leukopenia (<1000 mm3) 43.7% 17%
Thrombocytopenia (<100,000/mm3) 9.2% 20%
Anemia (<11 g/dL) 93.6% 78%
Peripheral neuropathy (grade 3/4) 5.5% 3%
Arthralgia/myalgia (grade 3/4) 10% 8%
Mucositis 7.4% 31%
Cardiovascular events 8.1% 16%
Adapted from product inserts of paclitaxel (BMS, n=812) and docetaxel (Aventis, n=2045).
*Regardless of premedication.
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Appropriate Clinical Utilization of Novel Taxane Formulations
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Improved Taxane Formulations
Rationale
– Decrease hypersensitivity reactions
– Avoid solvent toxicities
– Improve side effect profiles
– Favorable PK
– Decrease infusion times
Agents
– nab paclitaxel
– Paclitaxel poliglumex
– Milataxel
– DHA-paclitaxel
– Paclitaxel tocopherol-based emulsion formulation
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Nanoparticle Albumin Bound (nab) Platform
TopicalTopical
OralOral
InhalationalInhalational
IV/IAIV/IAProtein
Insoluble drug
Stable nanoparticles~0.1-0.2 µm, negatively charged
Proprietary process
Albumin
Human albumin
Active drug
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Endothelial cell
(EC)
Tumor cell
EC membrane
Caveolae and vesicles
Leaky junctionTumor interstitium
(B) Receptor mediated
(C) Tumor uptake
Mechanisms of Transport of nab Paclitaxel to Tumors
Tumor cell
Lumen of tumor
microvessel
(A) Enhanced permeation and retention (EPR) effect
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nab Paclitaxel
First clinical application of albumin-bound nanoparticle (nab) technology (FDA approved: Jan 2005)
Paclitaxel bound to albumin in a nanoparticle
– Increases drug selectivity for tumor cells (albumin intake mechanisms)
No routine steroid or antihistamine premedication required, no toxic solvents
In a phase III trial, demonstrated superior efficacy vs paclitaxel in MBC
– RR doubled
– Prolonged TTP
– Improved grade 4 neutropenia/sensory neuropathy
Gradishar WJ, et al, J Clin Oncol. 2005;23:7794-7803.
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Phase III Trial of nab Paclitaxel in MBC
Gradishar et al. J Clin Oncol. 2005;23:7794-7803.
Nab paclitaxel 260 mg/m2
i.v. over 30 min q 3 wk
No standard premedication
Cremophor paclitaxel 175 mg/m2
i.v. over 3 hours q 3 wk
Standard premedication with dexamethasone and antihistamines
or
• Women with measurable stage IV breast cancer
• No prior taxane therapy
• N = 460
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Phase III TrialAlbumin-Bound Paclitaxel vs. Paclitaxel in MBC
Albumin-Bound Paclitaxel
N=229
Paclitaxel
N=225P-Value
Overall Response Rate 33% 19% .001
Time to Progression 23.0 wk 16.9 wk .006
Grade 4 Neutropenia 9% 22% <.001
Grade 3 Sensory Neuropathy 10%* 2% <.001
Albumin-bound paclitaxel: 260 mg/m2 q3w; Paclitaxel:175 mg/m2 q3w
* Median time to improvement: 22 days
Gradishar et al. JCO 23: 7794; 2005
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Phase III Every 3w Hematologic Toxicities
Hematologic toxicity
nab Paclitaxel
n=229
Paclitaxel
n=225
P-Value*Grade 3 Grade 4 Grade 3 Grade 4
Neutropenia 25% 9% 31% 22% <0.001
Thrombocytopenia <1% 0% <1% 0% 0.387
Anemia <1% <1% 0% 0% 0.192
Febrile neutropenia <1% <1% <1% 0% 0.491
Septic deaths 0 0 --
*Cochran-Mantel-Haenszel test based upon all grades.
Gradishar et al. JCO 23: 7794; 2005
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Randomized Study Comparing nab-Paclitaxel with Solvent-based Paclitaxel in Chinese Patients with
Metastatic Breast Cancer
Zhong-Zhen Guan, M.D.1; Fengyi Feng, M.D.2, Qing Li Li, M.D.3, Zefei Jiang, M.D.4, Zhenzhou Shen, M.D.5, Shiying Yu, M.D.6, Jifeng Fen, M.D.7, Jianjin
Huang, M.D.8, Zhiwen Yao, M.D.9, Michael. J. Hawkins, M.D.9
1Sun Yat Sen University Cancer Centre, Guangdong, China; 2Cancer Center of CAMS, Beijing, China; 3Tianjin Tumor Hospital, Tianjin, China; 4PLA 307 Hospital, Beijing, China;
5Fudan University Cancer Center, Shanghai, China; 6Tonghi Hospital, Wuhan, China; 7Jiansu Tumor Hospital, Jiansu, China, 8No. 2 Hospital of Medical College, Zhejiang
University, Hangzhou, China, 9Abraxis BioScience, Inc., Los Angeles, CA.
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• For time to progression, 51% of events have occurred
• For progression-free survival, 52% of events have occurred
Response Rate, Time To Progression, Progression-free Survival, and Overall Survival
nab-paclitaxel
(n =104)
SB-paclitaxel
(n = 106)
P-value
Overall Response Rate
(Complete Response + Partial Response)56 (54%) 31 (29%) <0.001*
Median Time To Progression (months) 7.6 6.2 0.078**
95% CI 6.7 to 8.6 4.7 to 8.0
Median Progression-free Survival (months) 7.6 6.2 0.118**
95% CI 6.7 to 8.5 4.7 to 8.0
P-value based on CMH test stratified by study site and line of therapy ** P-value based on log rank test
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Overall Response Rate By Line of Metastatic Study Drug Therapy and By Prior Anthracycline Therapy
0
10
20
30
40
50
60
70
80
90
100
Ove
rall
Res
pons
e R
ate
(%)
P = .132
P = .001P< .001
Prior Adjuvant or Metastatic Anthracycline Therapy
Line of Metastatic Therapy
Yes1st Line No>1st Line
P = .181
P-value based on CMH test stratified by study site and line of therapy
nab-Paclitaxel 61 43 60 44
SB-paclitaxel 64 42 72 34
N
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Comparison of nab Paclitaxel and Docetaxel
Arm A: nab paclitaxel 300 mg/m2 q3w1st line MBC patients
(N=300)
Comparisons
• nab paclitaxel vs docetaxel (A, B, C vs D)
• Weekly vs every-3-weeks nab paclitaxel (B, C vs A)
• Low vs high dose weekly nab paclitaxel (B vs C)
Arm B: nab paclitaxel 100 mg/m2
weekly 3 out of 4
Arm C: nab paclitaxel 150 mg/m2
weekly 3 out of 4
Arm D: docetaxel 100 mg/m2 q3w
R
A
N
D
O
M
I
Z
E
Gradishar W, et al. ASCO 2007. Abstract 1032.
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Response Rates for nab Paclitaxel vs. Docetaxel
Gradishar W, et al. ASCO 2007. Abstract 1032.
Res
pons
e ra
te (
%)
300 mg/m2 100 mg/m2 150 mg/m2 Docetaxelq3w qw 3/4 qw 3/4 100 mg/m2 q3w
(A: n=76) (B: n=76) (C: n=74) (D: n=74)
nab paclitaxel
43%
62%
70%
38%
0%
10%
20%
30%
40%
50%
60%
70%
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Comparison of Investigator and Independent Radiology Review Response Assessments
Res
pons
e R
ate
(%)
300 mg/m2 100 mg/m2 150 mg/m2 docetaxelq3w qw 3/4 qw 3/4 100 mg/m2 q3w
(A: n = 76) (B: n = 76) (C: n = 74) (D: n = 74)
nab paclitaxel
Pearson Correlation Coefficient (Investigator vs. IRR) = 0.507
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Neutropenia (Based Upon Central Laboratory Data)
Treatment arm
Grade (%)
Febrile
neutropenia
(%)P vs
docetaxel P vs (B)I II III IV
nab paclitaxel
300 mg/m2 q3w (A)20 29 39 5 1 <0.001 0.007
nab paclitaxel
100 mg/m2 weekly (B)
24 32 20 5 1 <0.001
nab paclitaxel
150 mg/m2 weekly (C)
15 34 34 9 1 <0.001 0.004
Docetaxel
100 mg/m2 q3w (D)3 3 19 75 7
P-values by Cochran-Mantel-Haenszel; includes all grades of toxicity.
Gradishar W, et al. ASCO 2007. Abstract 1032.
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Treatment-related Adverse Events Peripheral Neuropathy
Treatment arm
Grade (%)
I II III IVP vs
docetaxel P vs (B)
nab paclitaxel
300 mg/m2 q3w (A)34 21 17 0.140 0.006
nab paclitaxel
100 mg/m2 weekly (B)33 11 9 0.190
nab paclitaxel
150 mg/m2 weekly (C)30 20 16 0.345 0.027
Docetaxel
100 mg/m2 q3w (D)32 19 11
Gradishar W, et al. ASCO 2007. Abstract 1032.
P-values by Cochran-Mantel-Haenszel; includes all grades of toxicity.
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Treatment-related Adverse Events Fatigue
Treatment Arm
Grade (%)
I II III IVP vs
docetaxel P vs (B)
nab paclitaxel
300 mg/m2 q3w (A)7 24 4 0.131 0.018
nab paclitaxel
100 mg/m2 weekly (B)18 13
nab paclitaxel
150 mg/m2 weekly (C)20 19 3 0.103 0.015
Docetaxel
100 mg/m2q3w (D)22 15 19
P-values by Cochran-Mantel-Haenszel; includes all grades of toxicity.Gradishar W, et al. ASCO 2007. Abstract 1032.
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nab Paclitaxel vs Docetaxel in Taxane-naïve MBC
Gradishar W, et al. ASCO 2007. Abstract 1032.
Higher overall response rates with weekly nab paclitaxel 100 mg/m2 and 150 mg/m2 compared with docetaxel
nab paclitaxel 150 mg/m2 weekly and 300 mg/m2 every 3 weeks increased PFS compared to docetaxel with an improved safety profile
nab paclitaxel 100 mg/m2 weekly was well tolerated and resulted in PFS comparable to docetaxel
nab paclitaxel 150 mg/m2 weekly produced a longer PFS than nab paclitaxel 100 mg/m2 weekly
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Clinical Response to nab Paclitaxel + Capecitabine
More than 50% of patients achieved at least a partial response
Patient Best ResponseEvaluable Patients
(n = 34)
Complete 3 (9%)
Partial 15 (44%)
Stable disease 11 (32%)
Disease progression 5 (15%)
Schwartzberg LS, et al. SABCS 2006. Abstract 1096.
Conclusion: First-line therapy with weekly nanoparticle albumin-bound paclitaxel plus daily capecitabine is active and well tolerated
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nab Paclitaxel + Capecitabine Time to Progression (TTP)
Schwartzberg LS, et al. SABCS 2006. Abstract 1096.
• Preliminary data demonstrates prolonged TTP with this combination
Product limited estimate curve
Censored observations
25% Quartile for Time to Progression: 133 days Progression-free Survival
0
0.25
0.5
0.75
1
0 50 100 150 200 250 300 350
Days from first chemo date
Sur
viva
l dis
trib
utio
n fu
nctio
n
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Case #1
A 42-year old woman was diagnosed with stage II, left sided breast cancer in 2005.
Initial therapy included BCS. T= 3 cm; SLNB-negative; ER, PR, HER2- negative.
Adjuvant therapy was TC x 4 (docetaxel, cyclophosphamide) and radiation therapy.
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Case #1 (cont.)
3 ½ years later she presents with left rib pain. PE reveals a 1 cm left supraclavicular node.
Restaging demonstrates multiple lytic bone lesions and several small lung nodules.
FNA of SCN is positive for adenocarcinoma and appears similar to the original breast cancer.
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Case #1 (cont.)
Paclitaxel / Bevacizumab
Capecitabine
Paclitaxel / Gemcitabine
nab-Paclitaxel
Doxorubicin
Which systemic therapy would you recommend in addition to bisphosphonate (BP) therapy?
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Paclitaxel / Bevacizumab
Capecitabine
Paclitaxel / Gemcitabine
nab-Paclitaxel
Doxorubicin
Case 1 (cont.)
Which systemic therapy would you recommend in addition to bisphosphonate (BP) therapy?
Recommended Approach:All options are reasonable.
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Overcoming Breast Cancer Resistance to Taxanes
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New Strategies for Resistant Breast Cancer
Taxanes, alone or in combination with anthracyclines, form the mainstay of adjuvant and metastatic breast cancer therapy
Taxane pre-treated recurrent breast cancer is an increasingly important clinical issue
A number of complex mechanisms may generate resistance to established chemotherapies, including taxanes
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New Strategies for Resistant Breast Cancer
Clinically, taxane cross-resistance and an absence of guidance regarding re-treatment increases the need for novel chemotherapies with differing mechanisms of action
Randomized controlled data demonstrating the activity of the epothilone, ixabepilone, in taxane-resistant and pre-treated patients supports its use in clinical practice
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Taxane Re-treatment Following Previous Taxane Therapy for MBC
Modest clinical efficacy when taxanes re-introduced in taxane-pre-treated / resistant MBC
- Single-agent taxane, ORR varies between 17- 44%
Disease-free interval believed important
Nishimura et al, Chemotherapy 2005; 51: 126–31 Taguchi et al, Breast J 2004; 10: 509–13
Perez et al, J Clin Oncol 2001; 19: 4216–23
In studies, there is significant variability in DFI criteria and little correlation between interval and observed response rate
Valero et al, J Clin Oncol 1998; 16: 3362–8 Seidman et al, J Clin Oncol 1996; 14: 1877–84 Yonemori et al, Breast Cancer Res Treat 2005; 89: 237–41Sawaki et al, Tumori 2004; 90: 36–9
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Response Rates: MBC Re-exposure to Single-agent Taxanes
Nishimura et al, Chemotherapy 2005; 51: 126–31 Taguchi et al, Breast J 2004; 10: 509–13
Perez et al, J Clin Oncol 2001; 19: 4216–23
Valero et al, J Clin Oncol 1998; 16: 3362–8Seidman et al, J Clin Oncol 1996; 14: 1877–84 Yonemori et al, Breast Cancer Res Treat 2005; 89: 237–41Sawaki et al, Tumori 2004; 90: 36–9
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Time to Progression: MBC Re-exposure to Single-agent Taxanes
Valero et al, J Clin Oncol 1998; 16: 3362–8Seidman et al, J Clin Oncol 1996; 14: 1877–84Yonemori et al, Breast Cancer Res Treat 2005; 89: 237–41Sawaki et al, Tumori 2004; 90: 36–9
Nishimura et al, Chemotherapy 2005; 51: 126–31 Taguchi et al, Breast J 2004; 10: 509–13
Perez et al, J Clin Oncol 2001; 19: 4216–23
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Epothilones as Anticancer Agents
Epothilones are tubulin-binding agents
Ixabepilone is currently the only FDA-approved epothilone
• in combination with capecitabine for the treatment of patients with metastatic or locally advanced breast cancer resistant to treatment with an anthracycline and a taxane
• as monotherapy for the treatment of metastatic or locally advanced breast cancer in patients whose tumors are resistant or refractory to anthracyclines,taxanes, and capecitabine
www.fda.gov
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Phase II Study of Ixabepilone in Taxane-refractory MBC
Thomas et al, J Clin Oncol 2007; 25: 3399–406
*5/6 responders had not responded to prior taxane therapy
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Phase II Study of Ixabepilone in Taxane Pre-treated Locally Advanced or MBC
Low et al, J Clin Oncol 2005; 23: 2726–34
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Ixabepilone Efficacy in Heavily Pre-treated MBC Study Design
Perez et al, J Clin Oncol 2007; 25: 3407–14
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Ixabepilone in Heavily Pre-treated MBC Response
Perez et al, J Clin Oncol 2007; 25: 3407–14
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Ixabepilone in Heavily Pre-treated MBC Survival
Perez et al, J Clin Oncol 2007; 25: 3407–14
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Capecitabine ± Ixabepilone in Anthracycline- and Taxane-resistant, Locally Advanced or MBC
Response
Thomas et al, J Clin Oncol 2007; 25: 5210–7
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Capecitabine ± Ixabepilone in Anthracycline- and Taxane-resistant, Locally Advanced or MBC
Grade 3/4 Adverse Events
Thomas et al, J Clin Oncol 2007; 25: 5210–7
*70/79 treated cases resolved after treatment discontinuation, median time to event resolution 6 weeks
Most common grade 3/4 events
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Phase II Study of Ixabepilone in Taxane-naïve, Second-line MBC
Denduluri et al, J Clin Oncol 2007; 25: 3421–7
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Ixabepilone as First-line Therapy in MBC Patients Following Adjuvant Anthracyclines
Study Design
Roché et al, J Clin Oncol 2007; 25: 3415–20
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Ixabepilone as First-line Therapy in MBC Patients Following Adjuvant Anthracyclines
Efficacy
Roché et al, J Clin Oncol 2007; 25: 3415–20
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Ixabepilone Studies in Taxane-naïve or Pre-treated MBC
Response Rate
3Roché et al, ASCO 2002; Abstract 223
Denduluri et al, J Clin Oncol 2007; 25: 3421–74Roché et al, J Clin Oncol 2007; 25: 3415–20
Moulder et al, SABCS 2007; Abstract 152
1Thomas et al, J Clin Oncol 2007; 25: 3399–406Low et al, J Clin Oncol 2005; 23: 2726–34 Perez et al, J Clin Oncol 2007; 25: 3407–142Thomas et al, J Clin Oncol 2007; 25: 5210–7
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Ixabepilone Efficacy by Disease Stageand Degree of Resistance
Adapted from, Fumoleau et al, ECCO 2007; Abstract 2119
A/T=anthracycline- / taxane-resistant, Multi=multi-resistant, T=taxane-resistant, T-naïve=taxane-naïve
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Case #2
47-year old female presents with recurrent metastatic BC involving the liver (3 lesions) and bone. Bx confirmed IDC – (ER, PR, HER2-negative)
2 years earlier the patient was diagnosed with Stage II IDC of the right breast (T = 3 cm; N = 3 of 12 positive axillary nodes); ER, PR, HER2-negative
Treatment included BCS followed by RT and dose-dense AC followed by T
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Case #2 (cont.)
At this time what systemic treatment would you recommend? Paclitaxel and bevacizumab
Capecitabine
Capecitabine and docetaxel
Gemcitabine and paclitaxel
nab-paclitaxel
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Case #2 (cont.)
At this time what systemic treatment would you recommend?
Paclitaxel and bevacizumab
Capecitabine
Capecitabine and docetaxel
Gemcitabine and paclitaxel
nab-paclitaxel
Recommended Approach:The use of Capecitabine as a single agent is a reasonable option.
• Most patients tolerate the drug well.• It has become very useful as an oral medication
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• The patient receives capecitabine as a single agent
• Repeat scans after 3 cycles confirm a partial response in the liver and stable bone lesions
• Capecitabine is continued for 7 months at which time disease progression is documented in the liver
• PS-1, LFT remain normal
Case #2 (cont.)
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Case #2 (cont.)
At this time you would recommend: Docetaxel and bevacizumab
Paclitaxel and bevacizumab
Ixabepilone
Gemcitabine
Navelbine
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Case #2 (cont.)
At this time you would recommend: Docetaxel and bevacizumab
Paclitaxel and bevacizumab
Ixabepilone
Gemcitabine
Navelbine
Recommended Approach: Eliminate Gemcitabine and Navelbine as first choices.
Clinical data supports Docetaxel + Bevacizumab, Paclitaxel + Bevacizumab and Ixabepilone
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Conclusions
The tolerability profiles of classic solvent-based taxanes are not optimal, warranting the advent of new tubulin inhibitor formulations
nab paclitaxel has demonstrated favorable efficacy versus solvent-based taxanes, while decreasing the severity of neutropenia and shortening the resolution of neuropathy
Many patients with progressive MBC, following prior treatment with anthracyclines and taxanes ( and capecitabine), remain good candidates for additional systemic therapy
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Conclusions (cont.)
Identifying optimal treatment choices in this population is a challenge
Ixabepilone represents the first FDA-approved epothilone for treatment of advanced breast cancer
Ixabepilone has significant antitumor activity in heavily pretreated patients with a manageable toxicity profile
Ongoing clinical trials will establish the role of ixabepilone in chemo-naïve patients and in combination with biologic agents
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Tubulin Inhibition in Breast Cancer:A Therapeutic Target Critical to
Improving Outcomes
Clinical Updates