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Hong Kwan Kim



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    MA08 - Pawing the Way to Improve Outcomes in Stage III NSCLC (ID 127)

    • Event: WCLC 2019
    • Type: Mini Oral Session
    • Track: Treatment of Locoregional Disease - NSCLC
    • Presentations: 1
    • Now Available
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      MA08.03 - Adjuvant Pembrolizumab in N2 Positive NSCLC Treated with Concurrent Chemoradiotherapy Followed by Surgery: Phase II, Prospective Study (Now Available) (ID 1744)

      15:15 - 16:45  |  Author(s): Hong Kwan Kim

      • Abstract
      • Presentation
      • Slides

      Background

      The standard treatment option for stage IIIA-N2 subgroup is still under discussion with controversies. We hypothesize that immune checkpoint inhibitor consolidation therapy could have an additional role in prolongation of the disease-free survival (DFS) for stage IIIA-N2 NSCLC treated with tri-modalities therapy.

      Method

      This is a phase 2 study evaluating the clinical efficacy of pembrolizumab treatment after CCRT with curative resection in stage IIIA-N2 NSCLC pts (NCT03053856). Pathologically confirmed pts were treated with five cycles of CCRT, weekly paclitaxel (50mg/m2) and cisplatin (25mg/m2) combined with radiotherapy (total of 44Gy over 22 fractions) followed by curative resection. Adjuvant Pembrolizumab (200mg fixed dose) is applied every three weeks up to 2 years or until disease recurrence. The primary objective is disease-free survival of more than 20 months. The first patient was recruited in October 2017, and the data for this abstract was locked at 20th of January, 2019.

      Result

      Total of 40 pts were screened, and 37 pts received treatment. Median age was 64 years (range 39-74), and twenty-three pts were male (62.2%). As a curative surgery, pts received lobectomy (n=34), bi-lobectomy (n=2), or pneumonectomy (n=1). Adenocarcinoma was predominant (n=27, 73.0%). After the neoadjuvant CCRT, down-staging were observed in nine pts (24.3%). The median follow-up duration was 10.6 months (range 3.1-17.2), and pts received a median of 11 cycles (range 1-22) of adjuvant pembrolizumab. DFS is not reached. Fourteen patients discontinued treatment due to disease progression (n=9), adverse events (n=4) and withdraw consent (n=1). There was a case of grade 4 pneumonitis and a case of grade 3 autoimmune hepatitis which lead to discontinuation of the treatment. Otherwise, grade 1-2 hypothyroidism (n=6), pneumonitis (n=5), skin rash (n=3) were observed. Patients with severe immune-related adverse event showed a significantly high percentage of Ki-67 + cells among CD8 T-cells in peripheral blood.

      Conclusion

      This study is the first study to demonstrate the feasibility of adjuvant pembrolizumab monotherapy in stage IIIA-N2 patients. Updated clinical outcome will be presented at the conference.

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    OA10 - Sophisticated TNM Staging System for Lung Cancer (ID 136)

    • Event: WCLC 2019
    • Type: Oral Session
    • Track: Staging
    • Presentations: 1
    • Now Available
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      OA10.02 - Recommended Change for N Descriptor Proposed by the IASLC: A Validation Study from a Single-Center Experience (Now Available) (ID 2117)

      14:00 - 15:30  |  Author(s): Hong Kwan Kim

      • Abstract
      • Presentation
      • Slides

      Background

      The International Association for the Study of Lung Cancer (IASLC) recently proposed changes for N descriptor based on the location and number of involved lymph node stations. The aim of our study was to evaluate the discriminatory ability and prognostic performance of the proposed N descriptor in a large independent non-small cell lung cancer (NSCLC) cohort.

      Method

      IASLC proposals include: a classification of N descriptor by combining the present nodal categories and number of involved lymph node stations into: N0; single-station N1 (N1a); multiple-stations N1 (N1b); single-station N2 without N1 involvement (N2a1); single-station N2 with N1 involvement (N2a2); multiple-stations N2 (N2b) and N3. A total of 1128 patients who underwent major pulmonary resection for pathologic N1 or N2 NSCLC between 2004 and 2014 were analyzed in this study. survival analysis was performed using Cox proportional hazard model to assess the prognostic significance of the N descriptor.

      Result

      From 2004 to 2014, 7437 patients were operated on for non-small-cell lung carcinoma (NSCLC). Among those, patients who underwent preoperative treatment for stage IIIA-N2 NSCLC were excluded (N=-698, 9.4%). Patients who were confirmed as pathologic N1 (N=676) or N2 (N=452) after surgery were included in this study. Invasive mediastinal staging (EBUS or mediastinoscopy) was done in 614 patients (54.4%). After surgery, adjuvant treatments were performed in 901 patients (81.7%). The mean total number of dissected lymph node was 25.7 ± 11.0, and the mean number of involved (metastatic) lymph node was 3.0 ± 3.2. The 5-year overall survival rate was 64.7 % in N1a, 57.1% in N1b, 68.0% in N2a1, 50.1% in N2a2, and 46.7% in N2b. Based on our study about the overall survival and recurrence-free survival, N2a1 is not clearly divided into N1a and N1b is not clearly divided with N2a2.

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      Conclusion

      Based on the proposed N stage classification by combining the LN station number with the proposed anatomic location in IASLC, all 5 groups were not clearly identified. According to our analysis, it would be better to classify similar prognostic group as 3 or 4 group to divide the group. The new N classifications should be considered for future revisions of TNM staging system for lung cancer.

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    P1.18 - Treatment of Locoregional Disease - NSCLC (ID 190)

    • Event: WCLC 2019
    • Type: Poster Viewing in the Exhibit Hall
    • Track: Treatment of Locoregional Disease - NSCLC
    • Presentations: 1
    • Moderators:
    • Coordinates: 9/08/2019, 09:45 - 18:00, Exhibit Hall
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      P1.18-24 - Neoadjuvant Therapy versus Upfront Surgery for NSCLC Patients with Clinically Suspected Subaortic or Paraaortic Lymph Nodes (ID 2568)

      09:45 - 18:00  |  Author(s): Hong Kwan Kim

      • Abstract

      Background

      Subaortic lymph nodes (#LN5) and para-aortic lymph nodes (#LN6) cannot be accessed by routine mediastinoscopy and E(B)US-FNA but need additional invasive surgical staging methods such as VATS or anterior mediastinotomy. Therefore, a considerable number of patients with suspected #LN5 or #LN6 receive multimodal treatment or, upfront surgery based on imaging staging only. We investigated survival outcomes of each therapeutic strategy.

      Method

      An institutional lung cancer database of consecutive patients between 2007 and 2016 (N=134) was reviewed retrospectively. Eligible patients had pathologically confirmed non-small cell lung cancer with clinically suspected #LN5 or #LN6 involvement by CT or PET-CT without clinical or pathological evidence of other N2 station involvement. Excluded are those with involvement of other N2 stations, unexpected N2, low grade malignancy, and prior history of cancer. Patients in group 1 received neoadjuvant therapy followed by surgery (n=68) and those in group 2 underwent upfront surgery (n=66).

      Result

      Group 1 consisted of patients with clinically suspected (n=39, 57%), and biopsy-proven #LN5 or #LN6 (n=29, 43%) by VATS (n=19), anterior mediastinotomy (n=6), or EUS-FNA (n=4). They received preoperative chemoradiation (n=62, 91%) and the rest received chemotherapy (n=6, 9%). Nodal down-staging was occurred in 36 (53%) patients whereas persistent N2 in 32 (47%). On the contrary, group 2 consisted of patients with clinically suspected #LN5 or 6 (n=66). After surgery, 30 (45%) patients were confirmed to have pathologic N0 or N1. The rest 36 (55%) patients were confirmed pathologic N2, and 29 (81%) of them received adjuvant therapy: chemoradiation in 23, and chemotherapy in 6. Overall survival rate at 5-year (5YOS) were 50.5% in group 1 versus 58.9% in group 2 (p=0.55); recurrence-free survival at 5-year (5YRFS) was 42.2% versus 46.7% (p=0.98), respectively. In subgroup, the 5YOS were 44.6% in pathologic N2 in group 2, which were similar to persistent N2 (52.8%, p=0.6), down-staged (49.2%, p=0.89), or biopsy-proven N2 (57.8%, p=0.54) in group 1. The 5YRFS were 26.7% in pathologic N2 in group 2, which were similar to persistent N2 (30.3%, p=0.89) and biopsy-proven N2 (43.9%, p=0.15), but lower than down-staged (53%, p=0.03) in group 1.

      Conclusion

      Upfront surgery or omission of invasive mediastinal staging for #LN5 or 6 may not compromise survival outcomes. Each therapeutic strategy is effective in terms of oncologic outcomes.

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    P2.05 - Interventional Diagnostic/Pulmonology (ID 168)

    • Event: WCLC 2019
    • Type: Poster Viewing in the Exhibit Hall
    • Track: Interventional Diagnostics/Pulmonology
    • Presentations: 1
    • Moderators:
    • Coordinates: 9/09/2019, 10:15 - 18:15, Exhibit Hall
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      P2.05-13 - Impact of Diffusing Capacity for Postoperative Pulmonary Complications in Patients Without Obstructive Pulmonary Disease (ID 2314)

      10:15 - 18:15  |  Author(s): Hong Kwan Kim

      • Abstract

      Background

      This study evaluated the impact of diffusing capacity of the lungs for carbon monoxide (DLco) on postoperative pulmonary complications (PPCs) after lung resection in patients without obstructive pulmonary disease

      Method

      We retrospectively reviewed non-small cell lung cancer patients undergoing anatomical lung resection without induction treatment between 2015 and 2016. Of these, 1233 patients without obstructive pulmonary disease were included in the study. We considered the following PPCs as study outcomes: pneumonia, acute respiratory distress syndrome (ARDS), significant atelectasis, empyema, bronchopleural fistula, prolonged air leakage and pneumothorax. The independent effects of DLco on PPCs were evaluated using multivariate logistic regression. Models were adjusted for age, sex, smoking status, comorbidity, histology and type of surgery.

      Result

      Twenty three percentage of patients showed the decrement of pred % of DLco less than 80. A total of 104 patients (8.4%) developed at least one PPC. More PPCs were occurred in the patients with impaired DLco (6.2% vs 15.7%, p<0.001). In multivariable-adjusted analyses, risk of PPC in patients with impaired DLco was more than 2 times [the adjusted odds ratio (aOR)=2.44 (1.58,3.77)] compared to those in patients with preserved DLco. Also, with every 10% decreasing in % pred DLco, the risk of developing PPC was gradually increased. [DLco ≥ 80 vs. 70≤DLco<80, aOR=2.07 (1.22, 3.49); 60≤DLco<70, aOR=2.79 (1.45, 5.36); DLco<60, aOR=4.69 (1.72, 12.75), p<0.001]

      Conclusion

      Patients with impaired DLco had more risk of PPCs after lung resection even without airflow obstruction. Assessment of DLco is necessary for the prediction of PPCs in lung resection surgery for NSCLC.