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Fumihiro Tanaka
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P1.03 - Chemotherapy/Targeted Therapy (ID 689)
- Event: WCLC 2017
- Type: Poster Session with Presenters Present
- Track: Chemotherapy/Targeted Therapy
- Presentations: 1
- Moderators:
- Coordinates: 10/16/2017, 09:30 - 16:00, Exhibit Hall (Hall B + C)
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P1.03-027 - Randomized Phase 2 Study Comparing CBDCA+PTX+BEV and CDDP+PEM+BEV in Treatment-Naïve Advanced Non-Sq NSCLC (CLEAR Study) (ID 8490)
09:30 - 09:30 | Author(s): Fumihiro Tanaka
- Abstract
Background:
The study objective was to compare efficacy and safety of CBDCA+PTX+BEV and CDDP+PEM+BEV in non-squamous (non-Sq) NSCLC patients.
Method:
Treatment-naïve patients aged 20-74 with advanced or recurrent EGFR/ALK-negative non-Sq NSCLC were randomly assigned at 1:2 ratio to either treatment A (4 cycles of CBDCA [AUC 6] + PTX [200mg/m[2]] + BEV [15mg/kg] q3wk, and maintenance therapy with BEV q3wk until progression) or treatment B (4 cycles of CDDP [75mg/m[2]] + PEM [500mg/m[2]] + BEV q3wk, and maintenance therapy with PEM + BEV until progression). The primary endpoint was PFS by central review. The secondary endpoints included OS and safety profile. Target enrollment number was 210.
Result:
A total of 55 sites across Japan enrolled 199 patients: 67/132 (A/B). The median age was 67/66 years, 70%/74% were male, 54%/52% were PS 0, 75%/73% were stage IV and 93%/98% had adenocarcinomas. As of April 14, 2017, patients had completed a median of 7/8 treatment cycles, while 94%/80% had discontinued treatment. The most common ≥G3 adverse events were neutropenia (75%/24%), and hyponatraemia (6%/10%). The most common BEV-related adverse events (≥G1) were hypertension (44%/58%), proteinuria (52%/43%) and epistaxis (26%/14%). Dose reduction was necessary due to an adverse event in 31%/22% patients. Treatment-related death (pulmonary infection) was reported in 1 patient receiving treatment B.
Conclusion:
CBDCA+PTX+BEV and CDDP+PEM+BEV had different safety profiles. Efficacy results including the primary endpoints will be presented in 2018.
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P1.07 - Immunology and Immunotherapy (ID 693)
- Event: WCLC 2017
- Type: Poster Session with Presenters Present
- Track: Immunology and Immunotherapy
- Presentations: 1
- Moderators:
- Coordinates: 10/16/2017, 09:30 - 16:00, Exhibit Hall (Hall B + C)
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P1.07-030 - Prognostic Impact of PD-L1 Expression in Correlation with HLA Class I Expression Status in Adenocarcinoma of the Lung (ID 9975)
09:30 - 09:30 | Author(s): Fumihiro Tanaka
- Abstract
Background:
Programmed death-ligand 1 (PD-L1) and human leukocyte antigen (HLA) class I, expressed on tumor cells are important roles in cancer immunity. The current study was conducted to assess prognostic impact of PD-L1 status in correlation with HLA class I status in lung adenocarcinoma.
Method:
A total of 166 patients with completely resected lung adenocarcinoma were retrospectively reviewed. PD-L1 expression on tumor cells was evaluated with immunohistochemistry, in correlation with several clinicopathological and molecular features including HLA class I expression on tumor cells.
Result:
Twenty-one patients (12.7%) had tumor with positive PD-L1 expression (percentage of tumor cells expressing PD-L1, ≥ 5%), and the incidence was higher in smokers with higher smoking index and in poorly differentiated tumor. There was no significant correlation between HLA class I expression and PD-L1 expression. PD-L1 positivity provided no prognostic impact for all patients, but seemed to be correlated with a poor prognosis among patients with normal HLA class I expression (p=0.145). When only p-stage I patients were analyzed, PD-L1 positivity was a significant factor to predict a poor survival (5-year survival rate, 66.7% versus 85.9%; P=0.049), which was enhanced in tumor with normal HLA class-I expression (P=0.029) but was not evident in tumor with reduced HLA class I expression (P=0.552)
Conclusion:
The prognostic impact of PD-L1 expression on tumor cells in resectable lung adenocarcinoma was distinct according to HLA class I expression on tumor cells.
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SH 04 - WCLC 2017 Highlights of the Previous Day (ID 754)
- Event: WCLC 2017
- Type: Scientific Highlights
- Track: Biology/Pathology
- Presentations: 1
- Moderators:
- Coordinates: 10/18/2017, 07:00 - 08:00, F203 + F204 (Annex Hall)
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SH 04.02 - Locally Advanced NSCLC & Radiotherapy (ID 10933)
07:20 - 07:40 | Presenting Author(s): Fumihiro Tanaka
- Abstract
- Presentation
Abstract not provided
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