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Tomohide Sugiyama



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    EP1.01 - Advanced NSCLC (ID 150)

    • Event: WCLC 2019
    • Type: E-Poster Viewing in the Exhibit Hall
    • Track: Advanced NSCLC
    • Presentations: 1
    • Now Available
    • Moderators:
    • Coordinates: 9/08/2019, 08:00 - 18:00, Exhibit Hall
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      EP1.01-83 - Efficacy and Safety of EGFR-TKI Rechallenge Treatment in Elderly Patients with Advanced NSCLC Harboring Sensitive EGFR Mutations (Now Available) (ID 81)

      08:00 - 18:00  |  Author(s): Tomohide Sugiyama

      • Abstract
      • Slides

      Background

      Epidermal growth factor receptor–tyrosine kinase inhibitor (EGFR–TKI) is effective as first-line chemotherapy for patients with advanced non-small-cell lung cancer (NSCLC) harboring sensitive EGFR mutations. However, whether the efficacy of second-line EGFR–TKI treatment after first-line EGFR–TKI treatment was poorly studied in elderly patients aged ≥ 75 years harboring sensitive EGFR mutations. Therefore, we aimed to investigate the efficacy and safety of EGFR-TKI re-administration after first-line EGFR–TKI treatment in elderly patients with NSCLC harboring sensitive EGFR mutations.

      Method

      Between October 2002 and December 2015, 22 elderly patients with advanced NSCLC harboring sensitive EGFR mutations who were initiated on EGFR–TKI Rechallenge at four Japanese institutions were included in this study.

      The eligibility criteria were histologically or cytologically confirmed NSCLC, unresectable stage III/IV disease, and a drug-sensitive EGFR mutation (exon 19 deletion or exon 21 L858R).

      All patients were initially treated with gefitinib (250 mg/day) or erlotinib (150 mg/day) and after recurrence, re-administration of EGFR-TKIs (gefitinib, erlotinib, afatinib) was performed as a secondary chemotherapy

      Result

      Ultimately, 22 cases of this study were studied. The median age was 77.5 years (range 75-87 years).

      Although it was a retrospective analysis, even with re-administration of EGFR-TKI rechallenge, the response rate was 23%, PFS 5.26 months, OS (after EGFR-TKI rechallenge) 14.4 months (the administration lines were 2, 3 and 4 lines ).

      Conclusion

      Until now it was said that EGFR-TKI rechallenge does not contribute to OS in LUX-LUNG 1 and so on.

      On the other hand, there are also reports on the usefulness of EGFR-TKI rechallenge.

      From the results of this study it can be said that it can be one of the options among the limited treatment options for elderly EGFR positive lung cancer.

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    P1.04 - Immuno-oncology (ID 164)

    • Event: WCLC 2019
    • Type: Poster Viewing in the Exhibit Hall
    • Track: Immuno-oncology
    • Presentations: 1
    • Moderators:
    • Coordinates: 9/08/2019, 09:45 - 18:00, Exhibit Hall
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      P1.04-34 - Efficacy and Safety of First-Line Pembrolizumab Monotherapy in Elderly Patients (Aged ≥ 75 years) with Non-Small Cell Lung Cancer (ID 265)

      09:45 - 18:00  |  Presenting Author(s): Tomohide Sugiyama

      • Abstract
      • Slides

      Background

      Pembrolizumab is effective as first-line treatment for advanced non-small cell lung cancer (NSCLC) patients expressing high programmed death-ligand 1 (PD-L1). However, it is unclear whether the efficacy of first-line pembrolizumab treatment in elderly patients (aged ≥75 years) is similar to that in non-elderly patients expressing high PD-L1. Therefore, we aimed to investigate the efficacy and safety of first-line pembrolizumab monotherapy in elderly patients with NSCLC expressing high PD-L1.

      Method

      Between February 2017 and February 2018, 128 patients (comprising 47 elderly) with advanced NSCLC expressing high PD-L1 received first-line pembrolizumab monotherapy at 10 Japanese institutions. Baseline characteristics, efficacy of pembrolizumab treatment, and adverse events were recorded.

      Result

      Overall, 47 patients (40 men and 7 women) (median age, 79 [range, 75–88] years) were included in our analysis. In these patients who received first-line pembrolizumab monotherapy, the overall response, disease control rates, median progression-free survival (PFS), and overall survival (OS) were 53.1%, 74.4%, 7.0 months, and not reached, respectively. Common adverse events included anorexia, fatigue, skin rash, and hypothyroidism. Two treatment-related deaths due to pneumonitis and infection were noted. First-line pembrolizumab monotherapy with non-progressive disease (PD) was associated with better PFS. Pembrolizumab monotherapy with good performance status and non-PD was also linked to better OS.

      Conclusion

      First-line pembrolizumab monotherapy among elderly patients with NSCLC expressing high PD-L1 was effective and safe and showed outcomes equivalent to those in non-elderly patients. First-line pembrolizumab monotherapy without PD, and with good performance status and non-PD, might be associated with better PFS and OS, respectively.

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    P2.08 - Oligometastatic NSCLC (ID 172)

    • Event: WCLC 2019
    • Type: Poster Viewing in the Exhibit Hall
    • Track: Oligometastatic NSCLC
    • Presentations: 1
    • Moderators:
    • Coordinates: 9/09/2019, 10:15 - 18:15, Exhibit Hall
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      P2.08-05 - The Role of Surgical Treatment for Patients with NSCLC Demonstrating Limited Pleural Dissemination (ID 701)

      10:15 - 18:15  |  Author(s): Tomohide Sugiyama

      • Abstract

      Background

      Pleural dissemination or malignant pleural effusion confirmed during surgery generally indicates incurable disease and is a contraindication for lung resection. However, recent studies suggested that complete removal of the disseminated nodule in combination with lung resection is associated with long-term survival when dissemination is limited.

      This study investigated whether there is a curable subgroup of patients with NSCLC exhibiting limited malignant pleural disease (MPD).

      Method

      Among 1966 patients who underwent lung surgery for primary lung cancer at our institution between 1986 and 2015, 61 patients were diagnosed with MPD during the operation. Excluding 3 patients who had other active malignancies and 2 patients who were lost to follow-up, we analyzed 59 patients, including 33 who had signs of MPD on preoperative CT. The type of surgery was biopsy only for 26, extrapleural pneumonectomy (EPP) for 17, lobectomy for 13, and wedge resection for 3. Macroscopic complete resection (MCR) was carried out for 24 patients. All but one patient were followed until December 2018 or death, and the follow-up period for surviving patients ranged from 48 to 361 months (median 158 months).

      Result
      Overall and progression-free survival
      Patients group Type of surgery Number of patients 5yOS/PFS(%) 10yOS/PFS(%) 15yOS/PFS(%)
      All patients 59 28.1/10.1 18.1/6.7 13.8/6.7
      MCR 24 37.5/25.0 25.0/16.7 20.8/16.7
      EPP 17 41.2/29.4 35.3/23.5 29.4/23.5
      No sigh of MPD preoperatively 26 34.6/15.4 19.8/11.5 19.8/11.5
      MCR 11 45.5/36.4 27.3/27.3 27.3/27.3
      EPP 5 60/60 60/60 60/60
      Any sign of MPD preoperatively 33 23.1/6.0 13.2/3.0 9.9/3.0
      MCR 13 30.8/15.3 23.1/7.6 15.4/7.6
      EPP 12 33.0/16.6 25.0/8.3 16.7/8.3

      Among the 59 patients, 4 patients survived without recurrence for more than 10 years. Furthermore, 3 out of the 4 patients were still alive at 361 months, 300 months, and 211 months, respectively. Among the 4 patients, 3 patients did not exhibit signs of malignant pleural disease preoperatively, and all 4 patients underwent EPP. The overall and progression-free survival rates at 5, 10, and 15 years for all 59 patients, the 26 not exhibiting signs of MPD preoperatively, and the 33 patients with signs of MPD according to the type of surgery are presented in the Table. Prognostic factors significantly associated with longer progression-free survival were early clinical stage, adenocarcinoma histology, absence of pathological mediastinal nodal metastasis, MCR, and EPP.

      Conclusion

      A curable subgroup may exist among patients diagnosed with malignant pleural disease during surgery, especially among those without signs of pleural disease preoperatively treated by EPP.