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Expert Interviews
Lung Cancer, Immunotherapy CE/CME accredited

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Experts answer questions with in-depth advice on the current clinical landscape and how new therapies and guidance might impact regional clinical practice. Useful tips below will show how to navigate the activity. Close

Immunotherapy for early-stage, resectable NSCLC: From clinical trial data to guidelines

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Heather Wakelee is professor of medicine and chief of the Division of Oncology at Stanford University and deputy director of the Stanford Cancer Institute. read more

She is past president of the International Association for the Study of Lung Cancer (IASLC) and a Fellow of the American Society of Clinical Oncology (FASCO). 

Prof. Wakelee has authored or co-authored more than 300 medical articles on lung cancer and thymic malignancies and she is involved in dozens of clinical trials on adjuvant therapy, immunotherapy (particularly the use of immunotherapy in the perioperative setting for non-small cell lung cancer) and anti-angiogenesis agents. Additionally, her research focuses on specific lung cancer subtypes defined by genetic mutations such as EGFR, ALK, ROS1, RET and BRAF, as well as broad translational efforts. 

Prof. Heather Wakelee discloses: Advisory Board or panel fees from BeiGene (relationship terminated), IOBiotech, OncoC4, Mirati (relationship terminated). Consultancy fees from AstraZeneca, BMS (relationship terminated), Genentech/Roche, Merck. Grants/research support fees from AstraZeneca/Medimmune, Bayer, BMS, Genentech/Roche, Helsinn, Merck, SeaGen, Xcovery.

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Heather Wakelee is professor of medicine and chief of the Division of Oncology at Stanford University and deputy director of the Stanford Cancer Institute. read more

She is past president of the International Association for the Study of Lung Cancer (IASLC) and a Fellow of the American Society of Clinical Oncology (FASCO). 

Prof. Wakelee has authored or co-authored more than 300 medical articles on lung cancer and thymic malignancies and she is involved in dozens of clinical trials on adjuvant therapy, immunotherapy (particularly the use of immunotherapy in the perioperative setting for non-small cell lung cancer) and anti-angiogenesis agents. Additionally, her research focuses on specific lung cancer subtypes defined by genetic mutations such as EGFR, ALK, ROS1, RET and BRAF, as well as broad translational efforts. 

Prof. Heather Wakelee discloses: Advisory Board or panel fees from BeiGene (relationship terminated), IOBiotech, OncoC4, Mirati (relationship terminated). Consultancy fees from AstraZeneca, BMS (relationship terminated), Genentech/Roche, Merck. Grants/research support fees from AstraZeneca/Medimmune, Bayer, BMS, Genentech/Roche, Helsinn, Merck, SeaGen, Xcovery.

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Heather Wakelee is professor of medicine and chief of the Division of Oncology at Stanford University and deputy director of the Stanford Cancer Institute. read more

She is past president of the International Association for the Study of Lung Cancer (IASLC) and a Fellow of the American Society of Clinical Oncology (FASCO). 

Prof. Wakelee has authored or co-authored more than 300 medical articles on lung cancer and thymic malignancies and she is involved in dozens of clinical trials on adjuvant therapy, immunotherapy (particularly the use of immunotherapy in the perioperative setting for non-small cell lung cancer) and anti-angiogenesis agents. Additionally, her research focuses on specific lung cancer subtypes defined by genetic mutations such as EGFR, ALK, ROS1, RET and BRAF, as well as broad translational efforts. 

Prof. Heather Wakelee discloses: Advisory Board or panel fees from BeiGene (relationship terminated), IOBiotech, OncoC4, Mirati (relationship terminated). Consultancy fees from AstraZeneca, BMS (relationship terminated), Genentech/Roche, Merck. Grants/research support fees from AstraZeneca/Medimmune, Bayer, BMS, Genentech/Roche, Helsinn, Merck, SeaGen, Xcovery.

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  • Select in the video player controls bar to choose subtitle language. Subtitles available in English, French, German, Spanish.
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Learning Objectives

After watching this activity, participants should be better able to:

  • Recall the recent advances in immunotherapy for early-stage NSCLC in the neoadjuvant/adjuvant settings
  • Describe how immunotherapy fits in the treatment algorithm for early-stage NSCLC
  • Summarize the key eligibility criteria for neoadjuvant/adjuvant immunotherapy, including clinical characteristics and biomarkers
Overview

In this activity, Prof. Heather Wakelee, a leading expert in the management of non-small cell lung cancer (NSCLC), discusses the use of immunotherapy in the treatment of early-stage, resectable NSCLC. She reviews pivotal clinical trials and recent data from ASCO 2024, focusing on their implication for clinical practice. read more

Target Audience

This activity has been designed to meet the educational needs of medical and clinical oncologists (including lung cancer specialists), pulmonologists and oncology nurses involved in the management of patients with NSCLC.

USF Accreditation

Disclosures

USF Health adheres to the Standards for Integrity and Independence in Accredited Continuing Education. All individuals in a position to influence content have disclosed to USF Health any financial relationship with an ineligible organization. USF Health has reviewed and mitigated all relevant financial relationships related to the content of the activity. The relevant relationships are listed below. All individuals not listed have no relevant financial relationships.

Faculty

Prof. Heather Wakelee discloses: Advisory Board or panel fees from BeiGene (relationship terminated), IOBiotech, OncoC4, Mirati (relationship terminated). Consultancy fees from AstraZeneca, BMS (relationship terminated), Genentech/Roche, Merck. Grants/research support fees from AstraZeneca/Medimmune, Bayer, BMS, Genentech/Roche, Helsinn, Merck, SeaGen, Xcovery.

Content reviewer

Carolina Leon BSN, MSN, ARNP-BC has no financial interests/relationships or affiliations in relation to this activity.

Touch Medical Contributors

Adriano Boasso has no financial interests/relationships or affiliations in relation to this activity.

USF Health Office of Continuing Professional Development and touchIME staff have no financial interests/relationships or affiliations in relation to this activity.

Requirements for Successful Completion

In order to receive credit for this activity, participants must review the content and complete the post-test and evaluation form. Statements of credit are awarded upon successful completion of the post-test and evaluation form.

If you have questions regarding credit please contact cpdsupport@usf.edu 

Accreditations

Physicians

This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through a joint providership of USF Health and touchIME. USF Health is accredited by the ACCME to provide continuing medical education for physicians.

USF Health designates this enduring material for a maximum of 0.75 AMA PRA Category 1 CreditsTM.  Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Advanced Practice Providers

Physician Assistants may claim a maximum of 0.75 Category 1 credits for completing this activity. NCCPA accepts AMA PRA Category 1 CreditTM from organizations accredited by ACCME or a recognized state medical society.

The AANPCP accepts certificates of participation for educational activities approved for AMA PRA Category 1 CreditTM by ACCME-accredited providers. APRNs who participate will receive a certificate of completion commensurate with the extent of their participation.

Nurses

USF Health is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center’s Commission on Accreditation.

A maximum of 0.75 contact hour may be earned by learners who successfully complete this  continuing professional development activity. USF Health, the accredited provider, acknowledges touchIME as the joint provider in the planning and execution of this CNE activity.

Date of original release: 11 July 2024. Date credits expire: 11 July 2025.

If you have any questions regarding credit, please contact cpdsupport@usf.edu

 

This activity is CE/CME accredited

To obtain the CE/CME credit(s) from this activity, please complete this post-activity test.

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Topics covered in this activity

Lung Cancer / Immunotherapy
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touchEXPERT OPINIONS
Immunotherapy for early-stage, resectable NSCLC: From clinical trial data to guidelines
0.75 CE/CME credit

Question 1/5
The PEARLS/KEYNOTE-091 and IMpower010 phase III clinical trials assessed pembrolizumab and atezolizumab, respectively, in the adjuvant setting in patients with early-stage NSCLC. What was observed in these trials?

DFS, disease-free survival; NSCLC, non-small cell lung cancer.

In the PEARLS/KEYNOTE-091 trial, adjuvant pembrolizumab substantially improved DFS vs placebo in the subgroup of patients with stage IB, II, or IIIA NSCLC who received adjuvant platinum-based chemotherapy following complete resection.1 The IMpower010 trial showed a DFS benefit with atezolizumab vs best supportive care after adjuvant chemotherapy in patients with resected stage II–IIIA NSCLC, with pronounced benefit in the subgroup of patients whose tumour PD-L1 expression was 1% or more.2

Abbreviations

DFS, disease-free survival; NSCLC, non-small cell lung cancer; PD-L1, programmed death-ligand 1.

References

  1. Oselin K, et al. J Clin Oncol 2023;41;8520.
  2. Felip E, et al. Lancet. 2021;398:1344–57
Question 2/5
As part of a tumour review board you are assessing the eligibility of a 65-year-old male patient with stage IB NSCLC for adjuvant immunotherapy. When reviewing biomarker test results, which profile do you consider most appropriate for your patient to start therapy?

NSCLC, non-small cell lung cancer; PD-L1, programmed death-ligand 1.

The current NCCN guidelines recommend atezolizumab as an adjuvant therapy option for eligible patients with PD-L1 levels of 1% or more who are also negative for certain biomarkers (EGFR exon 19 deletions, EGFR exon 21 L858R mutations, and ALK rearrangements) and who have previously received adjuvant chemotherapy based on clinical trial data and FDA approval. 

Abbreviations

NCCN, National Comprehensive Cancer Network; PD-L1, programmed death-ligand 1.

Reference

NCCN. Clinical Practice Guidelines in Oncology 2024. Non-small cell lung cancer. Version 6.2024. Available at: www.nccn.org/professionals/physician_gls/pdf/nscl.pdf (accessed 20 June 2024).

Question 3/5
Based on current NCCN guidelines, in which circumstances would you use neoadjuvant immunotherapy?

NCCN, National Comprehensive Cancer Network; NSCLC, non-small cell lung cancer.

The NCCN guidelines recommend that all patients should be evaluated for neoadjuvant immunotherapy with strong consideration for those with node-positive disease or tumour diameter of 4 cm or more and no contraindications for immune checkpoint inhibitors. However, neoadjuvant therapy should not be used to attempt to induce resectability in patients who do not already meet criteria for resectability on initial evaluation.

Abbreviation

NCCN, National Comprehensive Cancer Network.

Reference

NCCN. Clinical Practice Guidelines in Oncology 2024. Non-small cell lung cancer. Version 6.2024. Available at: www.nccn.org/professionals/physician_gls/pdf/nscl.pdf (accessed 20 June 2024).

Question 4/5
Your patient has completely resected, high-risk stage IIA NSCLC; their tumour is PD-L1 positive (45%) and negative for EGFR aberrations and ALK rearrangements. According to the current NCCN guideline recommendations, which adjuvant immunotherapy option do you choose for this patient?

NCCN, National Comprehensive Cancer Network; NSCLC, non-small cell lung cancer; PD-L1, programmed death-ligand 1.

The NCCN guidelines recommend atezolizumab as an adjuvant therapy option for eligible patients with completely resected stage IIB to IIIA, stage IIIB (only T3, N2), or high-risk stage IIA NSCLC and with PD-L1 expression of 1% or more, who are negative for EGFR aberrations and ALK rearrangements, and who have previously received adjuvant chemotherapy.  

Abbreviations

NCCN, National Comprehensive Cancer Network; NSCLC, non-small cell lung cancer; PD-L1, programmed death-ligand 1.

Reference

NCCN. Clinical Practice Guidelines in Oncology 2024. Non-small cell lung cancer. Version 6.2024. Available at: www.nccn.org/professionals/physician_gls/pdf/nscl.pdf (accessed 20 June 2024).

Question 5/5
When considering perioperative immunotherapy for your patient with early-stage NSCLC, what would be the best course of action while waiting for PD-L1 and molecular biomarker test results?

NSCLC, non-small cell lung cancer; PD-L1, programmed death-ligand 1.

The phase III AEGEAN trial assessed perioperative durvalumab + neoadjuvant chemotherapy, vs neoadjuvant chemotherapy alone. Patients with known EGFR/ALK aberrations were excluded from the efficacy analyses in the modified intent-to-treat population.1 An exploratory analysis of patients with EGFR-mutated resectable NSCLC showed minimal benefit of neoadjuvant durvalumab in this population: the unstratified EFS HR was 0.86 (95% CI, 0.35–2.19; vs modified intent-to-treat population: stratified HR, 0.68; 95% CI, 0.53–0.88; p=0.003902). PCR and MPR of the EGFR-mutated subgroup were 3.8% and 7.7%  vs 17.2% and 33.3% in the modified intent-to-treat population.1 The CheckMate 77T trial also excluded patients with EGFR mutations or known ALK translocations.2 Molecular testing was not mandated in the KEYNOTE-671 trial, and very few patients with EGFR mutations or ALK translocations were identified, a situation that limited any insights in these subgroups.3

NCCN guidelines recommend testing for PD-L1 status, EGFR mutations and ALK rearrangements for patients with stages IB–IIIA, IIIB [T3,N2], and exclusion of EGFR mutations and ALK rearrangements is recommended prior to consideration for neoadjuvant nivolumab plus chemotherapy.4 

Abbreviations

CI, confidence interval; EFS, event-free survival; HR, hazard ratio; MPR, major pathological response; NSCLC, non-small cell lung cancer; PCR, pathological complete response.

References

  1. He J, et al. J Thorac Oncol. 2023;18(Suppl. 11):S72–3.
  2. Cascone T, et al. N Engl J Med. 2024;390:1756–69.
  3. Wakelee H, et al. N Engl J Med. 2023;389:491–503.
  4. NCCN. Clinical Practice Guidelines in Oncology 2024. Non-small cell lung cancer. Version 6.2024. Available at: www.nccn.org/professionals/physician_gls/pdf/nscl.pdf (accessed 20 June 2024).
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