Table 3.
Patient | Tumor type | Prior lines ofchemotherapy | Best overall response | Best responseby RECIST, % | Treatmentduration, days | Reason for discontinuing study | Molecular testing |
---|---|---|---|---|---|---|---|
1 | Oropharynx | 5 | SD | −6 | 222 | Disease progression | ASXL1; DNMT3B; ATR; EP300; MLL3; PIK3R1 |
2 | Anal | 1 | SD | 6 | 59 | Withdrawal of consenta | Not performed |
3 | Cervix | 3 | SD | 8 | 39 | Toxicity(anemia) | PIK3CA; SOX2; EIF4A2; TP63; BLM; FBXW7; FGFR1; GRIN2A; MGA; MLL2; NUP93; PAK7; RAD51C; RPTOR; SMO; SUFU; TSC2 |
4 | Anal | 2 | POD | 39 | 27 | Disease progression | TP63; CTNNB1 |
5 | Anal | 2 | SD | −1 | 55 | Progression (nontarget lesion) | PIK3CA; B2M; BRAF; CRKL; EP300; ERG; KDM6A; LATS2; MLL3; PIK3C3; RYBP; STAG2; TETI |
6b | Oropharynx | 3 | – | – | 27 | Clinical decline (pain) | ERBB2; TP63; DICER1; MDC1; NOTCH1; ATR |
7b | Anal | 6 | SD | 1 | 27 | Withdrawal of consenta | PIK3CA |
8 | Anal | 2 | SD | 3 | 173 | Disease progression | PIK3CA, GNA11; TGFBR2; ANKRD11; DICER1; DIS3; SPEN; KDM6A |
9 | Cervix | 3 | POD | 0 | 19 | Progression (nontarget lesion) | Not performed |
10 | Oropharynx | 4 | POD | 5 | 29 | Disease progression | GSK3B |
11b | Oropharynx | 5 | – | – | 19 | Withdrawal of consenta | PIK3CA; FBXW7; FOXA1; PTEN |
12 | Cervix | 2 | POD | −1 | 41 | Progression (nontarget lesion) | Not performed |
POD, progression of disease; RECIST, Response Evaluation Criteria in Solid Tumors; SD, stable disease.
Reasons for consent withdrawal: Patient 2: rectal bleeding; Patient 7: radiographic progression not meeting RECIST criteria; Patient 11: clinical decline.
Inevaluable for response: Patients 6 and 11: no interval imaging was performed; Patient 7: radiographic progression not meeting RECIST criteria, incomplete cycle.