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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

2633 - Applicability of Lung-molGPA Index in Non-Small Cell Lung Cancer Patients with Various Gene Alterations and Brain Metastases

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Presenters

Kaiyan Chen

Citation

Annals of Oncology (2018) 29 (suppl_8): viii493-viii547. 10.1093/annonc/mdy292

Authors

K. Chen1, Y. Fan2, Z. Huang2, Y. Xu2, X. Yu1, H. Wang1

Author affiliations

  • 1 Chemotherapy Department, ZHEJIANG CANCER HOSPITAL, 210000 - Hangzhou/CN
  • 2 Key Laboratory On Diagnosis And Treatment Technology On Thoracic Cancer, Zhejiang cancer hospital, 310022 - Hangzhou/CN

Resources

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Abstract 2633

Background

The Lung-molGPA index is based on the original Diagnosis-Specific Graded Prognostic Assessment (DS-GPA) by incorporating recently reported gene alteration data for non-small cell lung cancer (NSCLC) patients with brain metastases (BM). However, the prognostic prediction value of DS-GPA and Lung-molGPA models remains undetermined, especially in patients with different molecule types.

Methods

A total of 1184 NSCLC patients with BM analyses for clinical factors and outcomes were identified at Zhejiang Cancer Hospital, China. All prognostic factors were weighted for significance by hazard ratios. The applicability of DS-GPA and Lung-molGPA were reappraised in NSCLC patients with BM and various genetic profiles. Additionally, a modified Lung-molGPA, was newly developed for mutant NSCLC patients.

Results

The NSCLC patients in the present study had a median survival of 14.0 months from the time of BM diagnosis. Both DS-GPA and Lung-molGPA models could predict the outcomes (P < 0.001), while Lung-molGPA model appeared to exhibit better accurate prediction. Furthermore, Lung-molGPA scores exhibited a discrimination capability in patients with gene variations (3.5-4.0 vs 2.5-3.0 vs 1.5-2.0 vs 0-1.0=62.0 vs 32.0 vs 17.7 vs 3.2 months, P < 0.001). However, no significant difference was reached in wild-type patients (P = 0.133). Regarding the oncogene-positive NSCLC patients with BM, a modified Lung-molGPA index had been established derived from the prognostic factors with the C-index of 0.73 (95% CI: 0.73-0.80) to accurately calculate the survival probability (P < 0.001).

Conclusions

In an era of precision medicine, the Lung-molGPA could precisely predict the prognosis of mutant NSCLC patients with BM, while not working in wild-type patients.

Clinical trial identification

Legal entity responsible for the study

Yun Fan.

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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