Table 2.

Pathologic response to chemo-radiation according to EGFR mutation

GroupingThe leading mutationMPRpCRMean residual tumor cells (%)
Driver mutationsEGFR N = 133/13 (23%)0/13 (0%)43.4% (SD35)
BRAF N = 10/1 (0%)0/1 (0%)45%
RET N = 10/1 (0%)0/1 (0%)50%
ROS N = 10/1 (0%)0/1 (0%)50%
No driver mutationsFGFR N = 22/2 (100%)2/2 (100%)0% (SD 0)
KRAS N = 108/10 (80%)4/10 (40%)13.7% (SD 23)
ERBB4 N = 11/1 (100%)0/1 (100%)5%
AKT amplification N = 11/1 (100%)0/1 (100%)9%
Negative for mutation N = 1711/17 (64.7%)3/17 (17.6%)19.9% (SD24)
Biomarker groupingMPR (n, %)p-valuepCR (n, %)p-valueMRTC (%, SD)p-value
Driver mutations N = 163/16 (19%)0.00010/16 (0%)0.00444.4% (SD 31)0.001
EGFR only mutations N = 133/13 (23%)0.0030/13 (0%)0.0243.4% (SD 35)0.009
No driver mutations N = 3122/31 (71%)reference8/31 (26%)reference15.8% (SD 22.4)reference
GroupingThe leading mutationMPRpCRMean residual tumor cells (%)
Driver mutationsEGFR N = 133/13 (23%)0/13 (0%)43.4% (SD35)
BRAF N = 10/1 (0%)0/1 (0%)45%
RET N = 10/1 (0%)0/1 (0%)50%
ROS N = 10/1 (0%)0/1 (0%)50%
No driver mutationsFGFR N = 22/2 (100%)2/2 (100%)0% (SD 0)
KRAS N = 108/10 (80%)4/10 (40%)13.7% (SD 23)
ERBB4 N = 11/1 (100%)0/1 (100%)5%
AKT amplification N = 11/1 (100%)0/1 (100%)9%
Negative for mutation N = 1711/17 (64.7%)3/17 (17.6%)19.9% (SD24)
Biomarker groupingMPR (n, %)p-valuepCR (n, %)p-valueMRTC (%, SD)p-value
Driver mutations N = 163/16 (19%)0.00010/16 (0%)0.00444.4% (SD 31)0.001
EGFR only mutations N = 133/13 (23%)0.0030/13 (0%)0.0243.4% (SD 35)0.009
No driver mutations N = 3122/31 (71%)reference8/31 (26%)reference15.8% (SD 22.4)reference

Abbreviations: Epidermal growth factor receptor (EGFR), Major pathologic response (MPR), Mean residual tumor cells (MRTC) Pathologic complete response (pCR). The driver mutations group include EGFR, RET, ROS1 and BRAF. The EGFR only group excluded RET, ROS and BRAF from the analysis. P values are for comparison of no- driver mutations to driver mutations and EGFR only mutations.

Table 2.

Pathologic response to chemo-radiation according to EGFR mutation

GroupingThe leading mutationMPRpCRMean residual tumor cells (%)
Driver mutationsEGFR N = 133/13 (23%)0/13 (0%)43.4% (SD35)
BRAF N = 10/1 (0%)0/1 (0%)45%
RET N = 10/1 (0%)0/1 (0%)50%
ROS N = 10/1 (0%)0/1 (0%)50%
No driver mutationsFGFR N = 22/2 (100%)2/2 (100%)0% (SD 0)
KRAS N = 108/10 (80%)4/10 (40%)13.7% (SD 23)
ERBB4 N = 11/1 (100%)0/1 (100%)5%
AKT amplification N = 11/1 (100%)0/1 (100%)9%
Negative for mutation N = 1711/17 (64.7%)3/17 (17.6%)19.9% (SD24)
Biomarker groupingMPR (n, %)p-valuepCR (n, %)p-valueMRTC (%, SD)p-value
Driver mutations N = 163/16 (19%)0.00010/16 (0%)0.00444.4% (SD 31)0.001
EGFR only mutations N = 133/13 (23%)0.0030/13 (0%)0.0243.4% (SD 35)0.009
No driver mutations N = 3122/31 (71%)reference8/31 (26%)reference15.8% (SD 22.4)reference
GroupingThe leading mutationMPRpCRMean residual tumor cells (%)
Driver mutationsEGFR N = 133/13 (23%)0/13 (0%)43.4% (SD35)
BRAF N = 10/1 (0%)0/1 (0%)45%
RET N = 10/1 (0%)0/1 (0%)50%
ROS N = 10/1 (0%)0/1 (0%)50%
No driver mutationsFGFR N = 22/2 (100%)2/2 (100%)0% (SD 0)
KRAS N = 108/10 (80%)4/10 (40%)13.7% (SD 23)
ERBB4 N = 11/1 (100%)0/1 (100%)5%
AKT amplification N = 11/1 (100%)0/1 (100%)9%
Negative for mutation N = 1711/17 (64.7%)3/17 (17.6%)19.9% (SD24)
Biomarker groupingMPR (n, %)p-valuepCR (n, %)p-valueMRTC (%, SD)p-value
Driver mutations N = 163/16 (19%)0.00010/16 (0%)0.00444.4% (SD 31)0.001
EGFR only mutations N = 133/13 (23%)0.0030/13 (0%)0.0243.4% (SD 35)0.009
No driver mutations N = 3122/31 (71%)reference8/31 (26%)reference15.8% (SD 22.4)reference

Abbreviations: Epidermal growth factor receptor (EGFR), Major pathologic response (MPR), Mean residual tumor cells (MRTC) Pathologic complete response (pCR). The driver mutations group include EGFR, RET, ROS1 and BRAF. The EGFR only group excluded RET, ROS and BRAF from the analysis. P values are for comparison of no- driver mutations to driver mutations and EGFR only mutations.

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