Cost of & Access to Molecularly Targeted Therapies as Barriers to Optimal Care H. Jack West, MD Swedish Cancer Institute Seattle, WA Global Resource for.

Slides:



Advertisements
Similar presentations
Oncologic Drugs Advisory Committee
Advertisements

James R. Rigas Comprehensive Thoracic Oncology Program
Strategies to overcome resistance in NSCLC with driver mutations
William J. Gradishar MD, FACP Betsy Bramsen Professor of Breast Oncology Director, Maggie Daley Center For Women's Cancer Care Robert H. Lurie Comprehensive.
1 Sitemap Storyflow Title slideOverview slide13.6 months PFSSymptom controlQoL OS across 7 trials3 months OS > 12 month OS Summary slide.
Using Non-targeted Therapies in Targeted Lung Cancer Populations Nathan Pennell, M.D., Ph.D. September 6, 2014.
Randomized Phase II Trial of Erlotinib (E) Alone or in Combination with Carboplatin/Paclitaxel (CP) in Never or Light Former Smokers with Advanced Lung.
Acquired Resistance Patient Forum September 6, 2014 | Boston In ALK, ROS1 & EGFR Lung Cancers Life After Erlotinib: What Next? Jared Weiss Vice President,
©American Society of Clinical Oncology All rights reserved - American Society of Clinical Oncology Provisional.
Network Experience of TKI inhibitors as 1 st line use in advanced NSCLC Dr Jill Gardiner and Mr Steve Williamson April 2012.
First-Line TKI Use in EGFR Mutation-Positive NSCLC
New Developments in Cancer Treatment Dulcinea Quintana, MD.
1 SNDA Gemzar plus Carboplatin Treatment of Late Relapsing Ovarian Cancer.
Treatment Regimens of HER2+ Adjuvant Patients (Actuals) Source: Genentech ASCO 2005 (data release) Nov 2006 (Approval)
 Angiogenesis Signaling Cascades EGFR PI3K MAPK Nucleus Gene Activation Cell Cycle Progression M G1G1 S G2G2 Fos P P MAPK = mitogen-activated protein.
Adam Heathfield, PhD Senior Director, Worldwide Policy, Pfizer Inc. September 25, 2013 Personalised Medicine – an industry perspective.
CI-1 Tarceva ® (erlotinib) Tablets in Combination with Gemcitabine as a 1st-line Treatment of Pancreatic Cancer Presentation to the Oncologic Drugs Advisory.
Activity and Tolerability of Afatinib (BIBW 2992) and Cetuximab in NSCLC Patients with Acquired Resistance to Erlotinib or Gefitinib Janjigian YY et al.
Please note, these are the actual video-recorded proceedings from the live CME event and may include the use of trade names and other raw, unedited content.
Medical Oncology Department University Hospital Perugia, Italy
Professor Martin Schuler MD West German Cancer Center Essen, Germany
Treatment of advanced NSCLC:
Final Efficacy Results from OAM4558g, a Randomized Phase II Study Evaluating MetMAb or Placebo in Combination with Erlotinib in Advanced NSCLC Spigel DR.
Overall survival in NSCLC
The highlight of resistance mechanism of targeted therapy on clinical therapy Zuhua Chen Dep. of GI oncology.
CB-1 Background of Pancreatic Cancer & NCIC CTG PA.3 Study Design Malcolm Moore, MD Professor of Medicine and Pharmacology Princess Margaret Hospital Chair,
until tumour progression until tumour progression
Sumitra Thongprasert, MD
01 Reporting & Interpreting Statistics in Clinical Research Robert Pirker, MD Medical University of Vienna Vienna, Austria.
Biomarker analyses from a phase III, randomized, open-label, first-line study of gefitinib (G) versus carboplatin/paclitaxel (C/P)
ENDOMETRIAL CARCINOMA UPDATES Dr Marco Matos Gold Coast Cancer Care, Gold Coast University Hospital and Pacific Private Oncology Group.
Personalized medicine in lung cancer R4 김승민. Personalized Medicine in Lung Cancer patients with specific types and stages of cancer should be treated.
Mok TS, Wu SL, Thongprasert S, et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma. N Engl J Med. 2009;361: Gefitinib Superior.
Erlotinib plus Gemcitabine Compared with Gemcitabine Alone in Patients with Advanced Pancreatic Cancer: A Phase III Trial of the National Cancer Institute.
Empowering induction therapy for locally advanced head and neck cancer A. Argiris1* & M. V. Karamouzis2 1Division of Hematology–Oncology, Department of.
Lancet Oncol 2012; 13: 528–38 Vincent A Miller, Vera Hirsh, Jacques Cadranel, Yuh-Min Chen, Keunchil Park, Sang-We Kim, Caicun Zhou, Wu-Chou Su, Mengzhao.
1 LUX-Lung 3 clinical trial ECOG=Eastern Cooperative Oncology Group. Sequist LV et al. J Clin Oncol. 2013;31(27): Treatment-naïve Advanced NSCLC.
Recent Advances in NSCLC Treatment
Belani CP et al. ASCO 2009; Abstract CRA8000. (Oral Presentation)
CHEMO-IMMUNO-TARGET THERAPIES
LUX-Lung 6 clinical trial
LUX-Lung 3 clinical trial
Rosell R et al. Proc ASCO 2011;Abstract 7503.
Unità Clinica di Diagnostica Istopatologica e Molecolare
Strategies for the Management of EGFR TKI Resistance in Advanced NSCLC
Acquired EGFR TKI resistance: What are the current therapeutic strategies? Gregory J. Riely.
until tumour progression until tumour progression
Assessing the Impact: New Data in T790+ NSCLC
Progression After Cancer Immunotherapy in Advanced NSCLC
The Nurse View: Best Practices in Advanced Non-Small Cell Lung Cancer
Updates in Lung Cancer: Insights From Vienna
Proof-of-concept clinical studies validating AZD9291 as a mutant-selective EGFR kinase T790M inhibitor. Proof-of-concept clinical studies validating AZD9291.
Meta-analysis of randomised phase III clinical trials comparing EGFR tyrosine kinase inhibitor (TKI) shows that male patients with non-small cell lung.
Aligning Patients and Clinicians: Optimizing Outcomes in Metastatic NSCLC.
Baselga J et al. SABCS 2009;Abstract 45.
Moving Care Forward in Advanced NSCLC
EGFR-Mutated NSCLC and CNS Involvement: the Conundrum
Beyond Erlotinib: Better EGFR Inhibitors?
University of British Columbia British Columbia Cancer Agency
Defining Patient-Centered Care: Spotlight on Advanced Non-Small Cell Lung Cancer.
All for One: Multidisciplinary Management in EGFR-Mutated NSCLC
Meta-Analysis of First-Line Therapies in Advanced Non–Small-Cell Lung Cancer Harboring EGFR-Activating Mutations  Benjamin Haaland, PhD, Pui San Tan,
Quality Improvement and Molecular Profiling in Advanced Non-Small Cell Lung Cancer.
Risk of Treatment-Related Toxicities from EGFR Tyrosine Kinase Inhibitors: A Meta- analysis of Clinical Trials of Gefitinib, Erlotinib, and Afatinib in.
Checkpoint Inhibitors in First-Line Advanced NSCLC
Third-Generation EGFR TKIs
Thoracic Oncology Division, IEO, Milan, Italy
What's on the Horizon in the Management of EGFR-Mutated Lung Cancer?
Location of common clinically relevant mutations in EGFR
Updates in Best Practices in Non-Small Cell Lung Cancer
Presentation transcript:

Cost of & Access to Molecularly Targeted Therapies as Barriers to Optimal Care H. Jack West, MD Swedish Cancer Institute Seattle, WA Global Resource for Advancing Cancer Education (GRACE)

Cost of Cancer Drugs is Rising Rapidly and Unsustainably

This is Leading to Controversy as We Try to Balance Obligation to Patients and to the Rest of Society

Ceritinib: New Treatment Option for ALK-Positive NSCLC Cost: $13,500/mo FDA Approved April, 2014

LUX Lung-3, LUX Lung-6 EGFR Mut’n Pos Advanced NSCLC No Prior Rx N= 345 Global RANDRAND Afatinib 40 mg PO daily until progression Cisplatin/Alimta up to 6 cycles Primary endpoint: PFS Afatinib 40 mg PO daily until progression Cisplatin/Gemcitabine up to 6 cycles Wu, Lancet 2014 EGFR Mut’n Pos Advanced NSCLC No Prior Rx N= 364 Asia LUX Lung-6 2:1 LUX Lung-3 RANDRAND Primary endpoint: PFS Sequist, JCO 2013

Treatment after Progression on First Line Therapy (Del 19 and L858R only) LUX-Lung 3LUX-Lung 6 Afatinib (n=203) Pem/Cis (n=104) Afatinib (n=216) Gem/Cis (n=108) Discontinued treatment, n (%)184 (100)104 (100)194 (100)108 (100) Subsequent systemic therapy, n (%) † 144 (78)88 (85)123 (63)70 (65) Chemotherapy, n (%)131 (71)49 (47)114 (59)29 (27) EGFR TKI therapy, n (%) Erlotinib Gefitinib Afatinib AZD9291 Dacomitinib Icotinib EGFR TKI combinations 81 (44) 61 (33) 28 (15) 2 (1) – 5 (3) 78 (75) 46 (42) 44 (42) 7 (7) 1 (1) – 9 (9) 50 (26) 21 (11) 19 (10) – 11 (6) 5 (3) 61 (56) 22 (20) 39 (36) – 3 (3) Other systemic therapy ±, n (%)5 (3)2 (2)3 (2)4 (4) Radiotherapy, n (%)32 (17)21 (20)4 (2)0 (0) † Collection of data on subsequent therapies still ongoing. ± include investigational agents, monoclonal antibodies, non-EGFR targeting protein kinase inhibitors etc Yang, ASCO 2014, A#8004

Treatment after Progression on First Line by Country’s Reimbursement* Countries with universal reimbursement policies** Countries without universal reimbursement policies*** Afatinib (n=144) Chemo (n=75) Afatinib (n=275) Chemo (n=137) Discontinued treatment, n (%)127 (100)75 (100)251 (100)137 (100) Subsequent systemic therapy, n (%)112 (88)69 (92)158 (63)89 (65) Chemotherapy, n (%)103 (81)35 (47)142 (57)43 (31) EGFR TKI, n (%)76 (60)68 (91)55 (22)71 (52) Other, n (%)5 (4)2 (3)3 (1)4 (3) Radiotherapy, n (%)27 (22)18 (24)9 (4)3 (2) *Determined by presence or absence of a national reimbursement policy in effect throughout the period of trial conduct: **Main countries contributing : Japan, Taiwan, Korea, Germany, France, Australia, UK, Belgium ***Main countries contributing : China, Thailand, Russia, the Philippines, Malaysia Yang, ASCO 2014, A#8004

Avastin/Tarceva vs. Tarceva Alone for Advanced EGFR Mutation-Positive NSCLC Adv NSCLC EGFR Mut’n (exon 19/21) Treatment-naïve N = 154 Tarceva daily + Avastin IV once every 3 weeks until progression or prohibitive toxicity Primary endpoint: PFS Tarceva daily until progression or prohibitive toxicity RANDRAND Kato, ASCO 2014, A#8005

Cost Considerations with Tarceva/Avastin Combination Addition of Avastin increases cost of first line treatment by ~$120,000 for 16 treatments (acquisition cost alone) Cost/ Month ($USD) Tarceva Tarceva/ Avastin

In 2014, Cost/Value of Therapy is a Factor in Cancer Care Cost matters, especially as new drugs have eclipsed the prior $10,000/mo barrier With limited societal resources, treatment benefits need to be clinically significant and have some semblance of value Appropriate to address it openly and not just have it bias our clinical judgment Cost is limiting our ability to deliver best treatment Optimal Rx ($$$$) Cost/practical limits Drug delivery to needy patients

How Do You See Drug Costs Affecting Cancer Treatment? Are people unable to get needed agents? Psychological or financial stress? How do you see the cost debate? How much does cost limit access to trials? Is it more an issue of interest in research? Education?