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editorial
. 2013 Oct 14;19(38):6315–6318. doi: 10.3748/wjg.v19.i38.6315

Table 1.

Mainly clinical trial and target therapies

Study Design Median PFS (mo) Median OS (mo) Toxicity (grade 3/4) Genetic analyses Response rate
PACCE trial[18] PMAB + Bev/Ox-CT 10 19.4 Skin rash, diarrhea, infections and pulmonary embolism KRAS status was determined in 82% tumor samples. Mutations were found in 40% 46%
+
PMAB + Bev/Iri-CT
Bev/Ox-CT 11.4 24.5 48%
+
Bev/Iri-CT
Peeters et al[22] Panitumumab-FOLFIRI (in the WT KRAS subpopulation) 5.9 14.51 Toxicities associated with anti-EGFR therapy KRAS status was available for 91% of patients: 597 (55%) with wild-type KRAS tumors, and 486 (45%) with mutant KRAS tumors Improved to 35% vs 10% with the addition of panitumumab
FOLFIRI (in the WT KRAS subpopulation) 3.9 12.51
PRIME study[28] Wild-type KRAS stratum Panitumumab + 9.6 23.91 Toxicities associated with anti-EGFR therapy KRAS results were available for 1100 ( 93%)patients 55%
FOLFOX (4)
FOLFOX(4) 8.0 19.71
Mutant KRAS stratum 48%
Panitumumab + 7.3 15.51 40%
FOLFOX (4)
FOLFOX (4) 8.8 19.31 40%
COIN trial[29] Ox and 5FU (arm A) in KRAS wild-type tumours 8.61 17.91 NA 565 (43%) had KRAS mutations 57%
Ox and 5FU plus cetuximab (arm B) in KRAS wild-type tumours 8.61 17.01 Skin rash and gastrointestinal toxic effects 64%
NORDIC-VII[20] Standard Nordic FLOX (arm A) 7.91 20.41 The regimens were well tolerated KRAS and BRAF mutation analyses were obtained in 498 (88%) and 457 patients (81%) respectively 41%
Cetuximab and FLOX (arm B) 8.31 19.71 49%
Cetuximab combined with intermittent FLOX (arm C) 7.31 20.31 47%
1

Without statistical significance. PFS: Progression-free survival; OS: Overall survival; PMAB: Panitumumab; Bev: Bevacizumab; Ox:CT: Oxaliplatin:based chemotherapy; Iri-CT: Irinotecan-based chemotherapy; 5FU: 5-fluorouracil; FOLFOX/FLOX: Fluorouracil, leucovorin and oxaliplatin; FOLFIRI: Fluorouracil, leucovorin and irinotecan; NA: Not applicable.