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Poster session 04

946P - Non-examination of lymph nodes (LN) in early-stage non-small cell lung cancer (eNSCLC) is associated with wedge resections and underutilization of adjuvant (adv) chemotherapy

Date

10 Sep 2022

Session

Poster session 04

Topics

Cancer Intelligence (eHealth, Telehealth Technology, BIG Data);  Staging Procedures;  Cancer Epidemiology

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Jay Lee

Citation

Annals of Oncology (2022) 33 (suppl_7): S427-S437. 10.1016/annonc/annonc1062

Authors

J.M. Lee1, C.S. Meyer2, T.M. To2, C. Lin2, S. Wang3, M. Kent3, A. Johnson4, J.S. Lee2

Author affiliations

  • 1 Thoracic Surgery, UCLA - David Geffen School of Medicine, 90095 - Los Angeles/US
  • 2 Evidence For Access (e4a), Genentech, Inc., 94080 - South San Francisco/US
  • 3 Rwe Analytics, Genesis Research, 07030 - Hoboken/US
  • 4 United States Medical Affairs, Genentech, Inc., 94080 - South San Francisco/US

Resources

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Abstract 946P

Background

LN examination among eNSCLC patients (pts) is critical in fulfilling the IASLC complete resection criteria and in perioperative chemotherapy decisions. Previous studies have shown that LN non-examination is associated with overall survival rates similar to pts with LN metastasis, presumably due to inadequate adv treatment (tx). This study evaluated the prevalence of LN exam and adv tx in US Medicare eNSCLC pts.

Methods

This retrospective observational study identified pts with stage IA-IIIB NSCLC (AJCC 7th ed) from SEER data linked with Medicare claims. Pts were ≥65 years at diagnosis between January 2010 and December 2017, had surgery within 1 month prior or 12 months after diagnosis and were continuously enrolled in Medicare Parts A and B ≥6 months before diagnosis. Additional continuous enrollment criteria of Medicare Parts A, B and D ≥6 months post-surgery or up to date of death was required for adv tx outcomes. Pts were grouped by LN exam status: none (pNX), no LN metastasis after LN exam (pN0) or LN metastasis after exam (pN1/2). Adv tx was identified within 6 months or up to death post-surgery. Descriptive statistics were used to summarize results.

Results

A total of 14,684 pts were included; 1596 (11%) were pNX, 9943 (68%) were pN0 and 3145 (21%) were pN1/2. The proportion of pNX pts decreased from 14% in 2010 to 8% in 2017. A mean (SD) of 11 (9) LNs were examined (median, 9; IQR, 5-15). Adv chemotherapy was identified in 21% (pNX), 13% (pN0) and 63% (pN1/2) of pts. Wedge resections were performed in 47% (pNX), 18% (pN0) and 11% (pN1/2) of pts.

Conclusions

LN examination in Medicare pts with eNSCLC has improved over time with a sufficient number of excised LNs at resection. However, many resections continue to lack LN evaluation and pNX was associated with lower adv chemotherapy utilization rates than pN1/2, which further supports that pNX may negatively impact adv tx decisions. Table: 946P

Variable, n (%) pNX n=1596 pN0 n=9943 pN1/2 n=3145
Extent of lung cancer resection
Pneumonectomy 17 (1) 150 (2) 218 (7)
Bilobectomy <11 103 (1) 71 (2)
Lobectomy 255 (16) 6149 (62) 1985 (63)
Wedge resection 746 (47) 1795 (18) 347 (11)
Segmentectomy 134 (8) 873 (9) 147 (5)
Other surgery 237 (15) 141(1) 71 (2)
Surgery
Robotic-assisted thoracic surgery 31 (2) 307 (3) 74 (2)
Video-assisted thoracic surgery 12 (<1) <11 <11
Thoracotomy 192 (12) 502 (5) 216 (7)
Sternotomy 19 (1) 21 (<1) 32 (1)
pNX n=996 pN0 n=6476 pN1/2 n=1999
Received adj tx
Chemotherapy 211 (21) 846 (13) 1255 (63)
Immunotherapy <11 <11 21 (1)
Targeted therapy 25 (3) 43 (1) 48 (2)
Chemoradiation 118 (12) 197 (3) 494 (25)
Radiation 245 (25) 510 (8) 652 (33)

Clinical trial identification

Editorial acknowledgement

Support for third-party writing assistance for this abstract, furnished by Jeff Frimpter, MPH, of Health Interactions Inc, was provided Genentech Inc.

Legal entity responsible for the study

Genentech, Inc.

Funding

Genentech, Inc.

Disclosure

J.M. Lee: Financial Interests, Personal, Advisory Role: Bistol Meyers Squibb; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Advisory Board, Advisory Board and Steering Committee: Genentech/Roche, Novartis; Financial Interests, Personal, Other, Consultant: Genetech/Roche, Novartis; Financial Interests, Institutional, Research Grant: Merck. C.S. Meyer: Financial Interests, Personal, Full or part-time Employment: Genentech, Inc.; Financial Interests, Personal, Stocks/Shares: Genentech, Inc. T.M. To: Financial Interests, Personal, Full or part-time Employment: Genentech, Inc.; Financial Interests, Personal, Stocks/Shares: Genentech, Inc. C. Lin: Financial Interests, Personal, Full or part-time Employment: Genentech, Inc.; Financial Interests, Personal, Stocks/Shares: Genentech, Inc. A. Johnson: Financial Interests, Personal, Full or part-time Employment: Genentech, Inc.; Financial Interests, Personal, Stocks/Shares: Genentech, Inc. J.S. Lee: Financial Interests, Personal, Full or part-time Employment: Genentech, Inc.; Financial Interests, Personal, Stocks/Shares: Genentech, Inc. All other authors have declared no conflicts of interest.

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