Table 5.
Combining response rate with PFS in evaluating chemotherapy.
| Year | Chemotherapy regimen | RR (%) | PFS | OS |
|---|---|---|---|---|
| Category A: both RR and PFS above average (n=9) | ||||
| 2006 | gemcitabine + epirubicin13 | 43.3 | 8 | |
| 2008 | pegylated liposomal doxorubicin (biweekly)24 | 40 | 4.1 | 16.5 |
| 2008 | gemcitabine + pegylated liposomal doxorubicin14 | 37.5 | 6.9 | 18.2 |
| 2009 | gemcitabine + oxaliplatin17 | 37 | 4.6 | 11.4 |
| 2007 | gemcitabine + cisplatin (biweekly)19 | 31.5 | 4.9 | 13.2 |
| 2006 | topotecan + pegylated liposomal doxorubicin26 | 28 | 7.5 | 10.3 |
| 2006 | pegylated liposomal doxorubicin25 | 23.1 | 5.4 | 13.8 |
| 2005 | docetaxel + irinotecan69 | 20 | 5 | 11 |
| 2006 | gemcitabine + cisplatin20 | 16 | 5.4 | 14.9 |
| Category B: RR above average but PFS below average (n=4) | ||||
| 2006 | gemcitabine + pegylated liposomal doxorubicin15 | 33.3 | 3.8 | 15.8 |
| 2005 | gemcitabine + pegylated liposomal doxorubicin16 | 22 | 2.7 | 8.4 |
| 2009 | pemetrexed55 | 21 | 2.9 | 11.4 |
| 2008 | gemcitabine + topotecan21 | 17 | 3 | 12.6 |
| Category C: RR below average but PFS above average (n=6) | ||||
| 2007 | bevacizumab50 | 15.9 | 4.4 | 10.7 |
| 2005 | canfosfamide 70 | 15 | 7.2 | 14.1 |
| 2010 | ixabepilone53 | 14.3 | 4.4 | 14.8 |
| 2006 | LY355703 (cryptophycin analog)57 | 12.5 | 5.1 | |
| 2007 | gemcitabine + oxaliplatin18 | 9.5 | 5 | 9.2 |
| 2005 | sabarubicin73 | 5.3 | 4.2 | 2.1 |
| Category D: both RR and PFS below average (n=10) | ||||
| 2005 | 9-aminocamptothecin54 | 14 | 2.9 | 10 |
| 2009 | pemetrexed56 | 9.9 | 2.8 | 11.1 |
| 2008 | topotecan + pegylated liposomal doxorubicin27 | 9.1 | 2 | 10.5 |
| 2007 | pegylated liposomal doxorubicin†,12 | 8.3 | 3.1 | 13.5 |
| 2007 | gemcitabine†,12 | 6.1 | 3.6 | 12.7 |
| 2009 | canfosfamide74 | 4.3 | 2.3 | 13.5 |
| 2009 | capecitabine75 | 3.1 | 2.3 | |
| 2007 | tamoxifen + gefitinib60 | 0 | 1.9 | 8.4 |
| 2007 | docetaxel (weekly)44 | 0 | 3.1 | 12.3 |
| 2007 | matuzumab79 | 0 | 1.8 | 13.3 |
Total 29 clinical trials that both response rate and PFS were available were classified into 4 groups based on the cutoff values of overall response rate (16%) and PFS (4.1 months) among clinical trials.
Abbreviations: RR, response rate; PFS, median progression-free survival (months); and OS, median overall survival (months).