Patient Profiles

Could the patients below be eligible for Optune Lua?

Explore patient profiles

David
55 years old

Example patient case; 
actor portrayal. 

  • 25% PD-L1, stage IVa squamous cell NSCLC
  • Durable response to IO + platinum-based chemo, now with slow progression
Laura
73 years old

Example patient case;

actor portrayal.

  • PD-L1 negative, stage IVb squamous cell NSCLC
  • Motivated patient with rapidly progressing multiple new lesions
Susan
60 years old

Example patient case;

actor portrayal.

  • 75% PD-L1, stage IVa nonsquamous NSCLC
  • Avoided 1L IO due to autoimmune comorbidity

Key Clinical Characteristics from LUNAR1

  • Stage: IV
  • Line: 2L+
  • ECOG: 0-2
  • Adult patients
  • Not pregnant, trying to get pregnant, might be pregnant, or breastfeeding
  • Does not have a known sensitivity to gel used with Optune Lua
  • Progression on or after platinum-based chemotherapy
  • No implantable electronic medical devices in the upper torso (eg, pacemaker) or active CNS metastases

Based on the broad study population, Optune Lua may be appropriate regardless of:

  • Histology
  • PD-L1 status2
  • Driver mutations
  • Smoking status
  • Site of metastases

Patient Motivation and Goals

  • Patients who want more control over their therapy (ie, want to be active participants) 
  • Chemo-averse patients who reject/resist chemo overall or don’t want it again after 1L 
  • Patients who are motivated to extend survival 
  • Patients looking for the latest treatment options
David

55 years old

25% PD-L1, stage IVa squamous cell NSCLC Durable response to IO + platinum-based chemo, now with slow progression 

“I’ve already completed chemotherapy and prefer not to do it again.*”

Patient History 

  • Divorced, 3 school-aged children, teacher  
  • Current smoking history: 30 pack-years 
  • Coronary artery disease, hypertension  
  • ECOG PS 0 

History of Present Illness

  • Stage IVa NSCLC: 5-cm mass and a 1.5-cm nodule in the right lung, with mediastinal and supraclavicular lymphadenopathy  
  • Squamous cell carcinoma with no targetable driver mutations  
  • 25% PD-L1 expression 

Treatment History 

  • Pembrolizumab + carboplatin-paclitaxel Q3W for 4 cycles, with continuation of pembrolizumab Q3W for 25 cycles 

Current Disease Status 

  • Demonstrated slow progression in the right lung after 20 months on pembrolizumab. Pembrolizumab was continued with expectant observation  
  • Four months later, right lung continues to progress 
  • Now with a nodule close to 1 cm in size and mild pleural-based progression, but remaining mostly asymptomatic
View the results from the Optune Lua + PD-1/PD-L1 inhibitor subgroup 
Laura

73 years old

PD-L1 negative, stage IVb squamous cell NSCLC
Motivated patient with rapidly progressing multiple new lesions

“I’m willing to try whatever treatment option my doctor recommends.*”

Patient History 

  • Married, adult children, retired  
  • Person with smoking history 
  • Coronary artery disease, hypertension, type 2 diabetes  
  • ECOG PS 1

History of Present Illness

  • Stage IVb NSCLC: multiple small, bilateral lung nodules and a liver lesion   
  • Squamous cell carcinoma with no targetable driver mutations  
  • PD-L1 negative

Treatment History 

  • Nivolumab + ipilimumab + carboplatin-paclitaxel for 2 cycles, followed by nivolumab + ipilimumab for 6 cycles 

Current Disease Status 

  • Five months after initiating treatment, the patient experienced progressive disease with new bone lesions in the lower spine and a few small liver lesions 
View the results from the Optune Lua + docetaxel subgroup 
Susan

60 years old

75% PD-L1, stage IVa nonsquamous NSCLC

Avoided 1L IO due to autoimmune comorbidity    

“I am exploring treatment options that will extend my survival.*”

Patient History 

  • Widowed with a caregiver, adult children. First grandchild due in 6 months  
  • Never smoker  
  • On active treatment for her autoimmune comorbidity 
  • ECOG PS 1 

History of Present Illness

  • Stage IVa NSCLC: referred from rheumatologist. Single lung mass of 6 cm in diameter, with a 1.3-cm liver lesion  
  • Nonsquamous cell carcinoma with no targetable driver mutations
  • 75% PD-L1 expression 

Treatment History 

  • Carboplatin/pemetrexed for 4 cycles with continued pemetrexed. IO was avoided given the history of her autoimmune comorbidity

Current Disease Status 

  • Radiologic assessment showed stable disease for 3 months, but she now has progressive disease in the lung and liver
View the results from the Optune Lua + PD-1/PD-L1 inhibitor subgroup 

Review guidelines for managing skin-related adverse reactions

Learn more

1L, first line; 2L+, second line or after; CNS, central nervous system; ECOG PS, Eastern Cooperative Oncology Group performance status; IO, immuno-oncology agent; mNSCLC, metastatic non–small cell lung cancer; NSCLC, non–small cell lung cancer; OS, overall survival; PD-1/PD-L1, programmed cell death 1 protein/programmed cell death 1 ligand 1; Q3W, every 3 weeks.

 

References: 1. Optune Lua for Non-Small Cell Lung Cancer (NSCLC). Physician Instructions for Use. Novocure; 2024. 2. Novocure Data on File GLB-DOF-0020.

Important Safety Information 

Contraindications 

Do not use Optune Lua® in patients with an electrical implant. Use of Optune Lua together with electrical implants has not been tested and may lead to malfunctioning of the implanted device. 

 

Do not use Optune Lua in patients known to be sensitive to conductive hydrogels. In this case, skin contact with the gel used with Optune Lua may commonly cause increased redness and itching, and rarely may even lead to severe allergic reactions, such as a fall in blood pressure and breathing difficulty.

Warnings and Precautions 

Optune Lua can only be prescribed by a healthcare provider that has completed the required certification training provided by Novocure® (the device manufacturer). 

 

Do not prescribe Optune Lua for patients who are pregnant, whom you think might be pregnant, or who are trying to get pregnant, as the safety and effectiveness of Optune Lua in these populations have not been established. 

 

The most common (≥10%) adverse events involving Optune Lua concurrent with PD-1/PD-L1 inhibitors or docetaxel were dermatitis, musculoskeletal pain, fatigue, anemia, dyspnea, nausea, cough, diarrhea, anorexia, pruritus, leukopenia, pneumonia, respiratory tract infection, localized edema, rash, pain, constipation, skin ulcers, and hypokalemia. 

 

Other potential adverse effects associated with the use of Optune Lua include treatment related skin toxicity, allergic reaction to the adhesive or to the gel, overheating of the array leading to pain and/or local skin burns, infections at the site where the arrays make contact with the skin, local warmth and tingling sensation beneath the arrays, medical device site reaction, muscle twitching, and skin breakdown or skin ulcer. 

 

If the patient has an underlying serious skin condition on the chest, evaluate whether this may prevent or temporarily interfere with Optune Lua treatment.

 

Indication For Use

Optune Lua is intended as a treatment concurrent with PD-1/PD-L1 inhibitors or docetaxel for adult patients with metastatic non-small cell lung cancer who have progressed on or after a platinum-based regimen. 

 


Please see full Instructions For Use (IFU) and Patient Information and Operation Manual (PIOM) for Optune Lua®.

Important Safety Information 

Contraindications 

Do not use Optune Lua® in patients with an electrical implant. Use of Optune Lua together with electrical implants has not been tested and may lead to malfunctioning of the implanted device. 

 

Do not use Optune Lua in patients known to be sensitive to conductive hydrogels. In this case, skin contact with the gel used with Optune Lua may commonly cause increased redness and itching, and rarely may even lead to severe allergic reactions, such as a fall in blood pressure and breathing difficulty.

Warnings and Precautions 

Optune Lua can only be prescribed by a healthcare provider that has completed the required certification training provided by Novocure® (the device manufacturer). 

 

Do not prescribe Optune Lua for patients who are pregnant, whom you think might be pregnant, or who are trying to get pregnant, as the safety and effectiveness of Optune Lua in these populations have not been established. 

 

The most common (≥10%) adverse events involving Optune Lua concurrent with PD-1/PD-L1 inhibitors or docetaxel were dermatitis, musculoskeletal pain, fatigue, anemia, dyspnea, nausea, cough, diarrhea, anorexia, pruritus, leukopenia, pneumonia, respiratory tract infection, localized edema, rash, pain, constipation, skin ulcers, and hypokalemia. 

 

Other potential adverse effects associated with the use of Optune Lua include treatment related skin toxicity, allergic reaction to the adhesive or to the gel, overheating of the array leading to pain and/or local skin burns, infections at the site where the arrays make contact with the skin, local warmth and tingling sensation beneath the arrays, medical device site reaction, muscle twitching, and skin breakdown or skin ulcer. 

 

If the patient has an underlying serious skin condition on the chest, evaluate whether this may prevent or temporarily interfere with Optune Lua treatment.

 

Indication For Use

Optune Lua is intended as a treatment concurrent with PD-1/PD-L1 inhibitors or docetaxel for adult patients with metastatic non-small cell lung cancer who have progressed on or after a platinum-based regimen. 

 


Please see full Instructions For Use (IFU) and Patient Information and Operation Manual (PIOM) for Optune Lua®.

Novocure Websites

This website is intended for US healthcare professionals seeking information on Optune Lua.

 

 

 

 


External links

OptuneGioHCP.com
OptuneLuaHCP.com/MPM
Novocuretrials.com


©2024 Novocure GmbH. All Rights Reserved. 

Optune Lua, MyNovocure, MyLink, and Novocure are trademarks of Novocure GmbH.

US-OPL-00070 v1.0 November 2024