The Role of Adjuvant Chemotherapy before Osimertinib in Epidermal Growth Factor Receptor Mutant Resected Non-Small Cell Lung Cancer and Communicating It to Patients
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Maione, Paolo
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SG Moscati Hosp, Div Med Oncol, I-83100 Avellino, ItalySG Moscati Hosp, Div Med Oncol, I-83100 Avellino, Italy
Maione, Paolo
[1
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Salvi, Rosario
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SG Moscati Hosp, Div Thorac Surg, I-83100 Avellino, ItalySG Moscati Hosp, Div Med Oncol, I-83100 Avellino, Italy
Salvi, Rosario
[2
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Gridelli, Cesare
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SG Moscati Hosp, Div Med Oncol, I-83100 Avellino, ItalySG Moscati Hosp, Div Med Oncol, I-83100 Avellino, Italy
Gridelli, Cesare
[1
]
机构:
[1] SG Moscati Hosp, Div Med Oncol, I-83100 Avellino, Italy
[2] SG Moscati Hosp, Div Thorac Surg, I-83100 Avellino, Italy
Patients with radically resected stage II and III NSCLC are exposed to a high risk of disease recurrence. Thus, adjuvant cisplatin-based chemotherapy is routinely offered to this patient population, although it results in an absolute increase in 5-year survival rate of only 4%. This modest improvement in survival rate makes it challenging to communicate to our patients about the decision to be treated with adjuvant chemotherapy or not. Nowadays, the decision to administer adjuvant chemotherapy or not in resected NSCLC is almost never completely shared with patients because its role is very difficult to explain. The risk-benefit ratio becomes clearly unfavourable in elderly and unfit patients. Recently, the phase III ADAURA trial demonstrated a clinically significant disease-free survival and overall survival benefit with adjuvant osimertinib (with or without adjuvant chemotherapy) versus a placebo in EGFR-mutated stage IB-IIIA resected NSCLC. In this patient population, the decision to administer chemotherapy or not is much more challenging given the great benefit offered by osimertinib alone. Thus, it is time now to improve our communication tools to explain the role of adjuvant chemotherapy to our patients, especially in the EGFR-mutated population, in order to undertake real shared decision making in a clinical context in which the opportunity to administer toxic chemotherapy is debatable and subjective.
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Pulm & Crit Care Med,Dept Med, 81 Irwon Ro, Seoul 06351, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Pulm & Crit Care Med,Dept Med, 81 Irwon Ro, Seoul 06351, South Korea
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Univ Toronto, Princess Margaret Hosp, Dept Med Oncol & Hematol, Toronto, ON M5G 2M9, CanadaUniv Toronto, Princess Margaret Hosp, Dept Med Oncol & Hematol, Toronto, ON M5G 2M9, Canada
Booth, Christopher M.
Shepherd, Frances A.
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Univ Toronto, Princess Margaret Hosp, Dept Med Oncol & Hematol, Toronto, ON M5G 2M9, CanadaUniv Toronto, Princess Margaret Hosp, Dept Med Oncol & Hematol, Toronto, ON M5G 2M9, Canada
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Stanford Univ, Stanford Canc Ctr, Dept Med Oncol, 875 Blake Wilbur Dr, Stanford, CA 94305 USAStanford Univ, Stanford Canc Ctr, Dept Med Oncol, 875 Blake Wilbur Dr, Stanford, CA 94305 USA
Wakelee, Heather
Chhatwani, Laveena
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Virginia Commonwealth Univ, Dept Pulm Crit Care Med, Richmond, VA USAStanford Univ, Stanford Canc Ctr, Dept Med Oncol, 875 Blake Wilbur Dr, Stanford, CA 94305 USA