Copyright
©The Author(s) 2016.
World J Gastroenterol. Mar 21, 2016; 22(11): 3127-3149
Published online Mar 21, 2016. doi: 10.3748/wjg.v22.i11.3127
Published online Mar 21, 2016. doi: 10.3748/wjg.v22.i11.3127
Table 1 Chemotherapy for advanced or metastatic disease (NCCN and ESMO guidelines)
| Options for | Options for therapy | Options for therapy |
| Initial therapy | After first progression | After second progression |
| FOLFOX +/- bmab or cetux/pmab1 | Irinotecan +/- bmab or aflib or cmab/pmab1 | Irinotecan + cmab or pmab1 |
| CAPOX +/- bmab or cmab/pmab1 | FOLFIRI +/- bmab or aflib or cmab/pmab1 | Regorafenib |
| Clinical trial | ||
| Best supportive care | ||
| FOLFIRI +/- bmab or cmab/pmab1 | FOLFOX +/- bmab | CAPOX |
| CAPOX +/- bmab | FOLFOX | |
| Irinotecan + cmab/pmab1 | Irinotecan + cmab/pmab1 | |
| Regorafenib | ||
| Clinical trial | ||
| Best supportive care | ||
| Bmab + 5-FU/LV or Cape or FOLFOXIRI | Bmab + FOLFOX/FOLFIRI/Irinotecan/CAPOX | Irinotecan + cmab/pmab1 |
| Bmab + Irinotecan + Oxaliplatin | FOLFOX | |
| Aflib + FOLFIRI/Irinotecan | CAPOX | |
| Irinotecan + cmab/pmab1 | Regorafenib | |
| Regorafenib |
Table 2 Highlights of ongoing clinical trials (National Cancer Institute) regarding systemic treatment for metastatic colorectal cancer
| Protocol ID | Principle investigator | Phase, purpose, and relevance |
| NCT02149108 | Boehringer Ingelheim | Phase III study of salvage nindetanib |
| NCT02305758 | AbbVie | Phase IIstudy of first-line veliparib (PARP inhibitor) added to FOLFIRI +/- bmab |
| NCT02060188 | Bristol-Myers Squibb | Phase II study of nivolumab (anti-PD1 antibody) +/- Ipilimumab in recurrent and microsatellite high (MSI-H) colon cancer |
| NCT02119676 | Incyte | Phase II study of salvage ruxolitinib (a JAK1 and JAK2 inhibitor) in combination with regorafenib |
| NCT02260440 | University of Pittsburgh | Phase II study of salvage pembrolizumab (anti-PD1) in combination with azacitidine |
| NCT01661972 | Duke University Medical Center | Phase I/II study of capecitabine plus aflibercept (“X-TRAP study”) |
| NCT02168777 | Bayer | Phase I/II study of remafetinib with regorafenib |
| NCT02079740 | National Cancer Institute, United States | Phase Ib/II study of trametinib (a MEK inhibitor) and navitoclax (BCL-2 Family Inhibitor) in KRAS mutant advanced tumors |
| NCT00940316 | Genentech, OSI Pharmaceuticals, Amgen | Phase I/II study of dual epidermal growth factor receptor inhibition With Erlotinib and Panitumumab with or without chemotherapy |
| NCT01985763 | Mt. Sinai School of Medicine, New York City | Phase I/II study of first line genistein (a soy derivative that interrupts Wnt signaling) in addition to standard regimens |
| NCT01471353 | University of Florida | Phase II study of salvage sorafenib plus capecitabine (SorCape) |
| NCT01750918 | GlaxoSmithKline | Phase I/II study of trametinib and dabrafenib in combination with panitumumab in BRAF-mutation V600E colorectal cancer and in patients with resistance to prior anti-EGFR therapy |
Table 3 Highlights of radiofrequency ablation literature for colorectal liver metastases
| Ref. | Level of evidence | Year | Study details | 1 yr OS% | 3 yr OS% | 5 yr OS% | 7 yr OS% | 10 yr OS% | Median OS (mo) | Procedure-related complications |
| 1Gillams et al[53] | II-2 | 2004 | Prospective, 167 patients | 91 | 28 | 25 | 38 | < 1% (1/167) | ||
| Percutaneous (ValleyLab) | ||||||||||
| Mean 4 lesions | ||||||||||
| Mean 4 cm max diameter | ||||||||||
| Hildebrand et al[108] | II-2 | 2006 | Prospective, 88 pts/420 lesions | 92 | 42 | 28 | 3.4% (3/88) | |||
| Percutaneous (RITA/ValleyLab) | ||||||||||
| Mean 3.5 lesions | ||||||||||
| Median 2.7 cm max diameter | ||||||||||
| Siperstein et al[109] | II-2 | 2007 | Prospective, 234 patients | 20.2 | 18.4 | 24 | Not reported | |||
| Laparoscopic | ||||||||||
| Mean 3 lesions | ||||||||||
| Median 4 cm max diameter | ||||||||||
| Berber et al[110] | II-2 | 2008 | Prospective, 68 pts/68 lesions | 20.6 | 30 | 20.5 | 2.9% (2/68) | |||
| Laparoscopic | ||||||||||
| All solitary lesions | ||||||||||
| Median 3.7 cm max diameter | ||||||||||
| Veltri et al[111] | II-2 | 2008 | Retrospective, 122 pts/199 lesions | 79 | 38 | 22 | 31.5 | 1% (2/199) | ||
| Percutaneous (RITA/ValleyLab /LeVeen) | ||||||||||
| Mean 1.6 lesions | ||||||||||
| Median 3 cm max diameter | ||||||||||
| Gleisner et al[112] | II-2 | 2008 | Prospective, 66 patients | 92.3 | 51.1 | 28.3 | 38.1 | Not reported | ||
| Intraoperative (RITA) | ||||||||||
| Median 2 lesions | ||||||||||
| Median 3 cm max diameter | ||||||||||
| 1Gillams and Lees[113] | II-2 | 2009 | Prospective, 309 pts/617 lesions | 49 | 24 | 36 | 3.7% (23/617) | |||
| Percutaneous (Covidien/RITA) | ||||||||||
| Mean 4 lesions | ||||||||||
| Median 2.3 cm max diameter | ||||||||||
| Sofocleous et al[114] | II-2 | 2011 | Prospective, 56 pts/71 lesions | 91 | 41 | 31 | 4% (2/56) | |||
| Percutaneous (LeVeen/Valleylab/RITA) | ||||||||||
| Mean 1.4 lesions | ||||||||||
| Median 1.9 cm max diameter | ||||||||||
| Solbiati et al[115] | II-2 | 2012 | Retrospective, 99 pts/202 lesions | 98 | 69.3 | 47.8 | 25 | 18 | 53.2 | 1.3% (2/156) |
| Percutaneous (Covidien) | ||||||||||
| Mean 2 lesions | ||||||||||
| Mean 2.1 cm diameter +/- 0.75 cm std deviation | ||||||||||
| Bale et al[52] | II-2 | 2012 | Retrospective, 63 pts/189 lesions | 87 | 44 | 27 | 27 mo for unresectable patients, | 17% (17/98) | ||
| Percutaneous (Covidien) with Treon Navigation | 58 mo for resectable patients | |||||||||
| Mean 2 lesions | (P = 0.002) | |||||||||
| Mean 2 cm diameter | ||||||||||
| Hamada et al[116] | II-2 | 2012 | Retrospective 84 pts/141 lesions | 90.6 | 44.9 | 20.8 | 34.9 | 2.2% (3/138) | ||
| Percutaneous (Valleylab) | ||||||||||
| Mean 1.7 lesions | ||||||||||
| Mean 2.3 cm max diameter +/- 1.4 cm |
Table 4 Highlights of cryoablation literature for colorectal liver metastases
| Ref. | Level of evidence | Year | Study details | 1 yr OS% | 3 yr OS% | 5 yr OS% | Median OS (mo) | Procedure-related Complications |
| Rivoire et al[117] | II-2 | 2002 | Retrospective, 24 patients, 69 lesions | 92 | 58 | 39 | 21% (5/24) had iceball fracture, successfully treated with suture (all cryoablation performed at laparotomy) | |
| Laparotomy (Erbokryo CS-6) | ||||||||
| 10-15 min freeze, 5 min thaw, 5-10 min freeze, occasionally with Pringle maneuver | ||||||||
| Mean 3 lesions | ||||||||
| Mean 4.5 cm max diameter | ||||||||
| Yan et al[118] | II-2 | 2003 | Prospective, 172 pts/420 lesions Laparotomy (L.C.S. 3000/Erbe) 1 cm margin, freeze-partial thaw-freeze Mean 4 lesions | 89 | 41 | 19 | 28 | 28% (48/172) (all cryoablation performed at laparotomy, not percutaneously) |
| Median 3.6 cm max diameter | Gelfoam packed into every tract | |||||||
| Brooks et al[119] | II-2 | 2005 | Prospective, 93 patients | 85 | 43 | 19 | 33 | Cryoablation-related complications not specifically reported |
| Laparotomy (L.C.S. 3000/Erbe) | ||||||||
| Median 2 lesions | ||||||||
| Niu et al[120] | II-2 | 2007 | Prospective, 124 pts/124 lesions | 84 | 43 | 24 | 29 | Not reported |
| Laparotomy (L.C.S. 3000/Erbe) | Gelfoam was packed into every tract | |||||||
| 1 cm margin, freeze-partial thaw-freeze | ||||||||
| For lesions > 3 cm, two probes always used | ||||||||
| Mean 4 lesions | ||||||||
| Mean 4 cm max diameter | ||||||||
| Paganini et al[121] | II-2 | 2007 | Retrospective, 49 pts | 87 | 43 | 23 | 31 | 22% (11/49) |
| Laparotomy (CMS AccuProbe/Erbe) | ||||||||
| Mean 5 lesions | ||||||||
| Median 3 cm max diameter | ||||||||
| Ng et al[122] | II-2 | 2012 | Retrospective, 211 pts | 87 | 21 | 12 | 27 | Cryoablation-related complications not specifically reported |
| (Part 1) | Laparotomy (L.C.S. 3000/Erbe) | |||||||
| Single-freeze thaw performed except for “smaller” lesions where partial double freeze-thaw performed | ||||||||
| Mean 4.4 lesions | ||||||||
| II-2 | 2012 | Mean size 4 cm | 87 | 31 | 17 | 34 | Cryoablation-related complications not specifically reported | |
| Ng et al[122] | Retrospective, 93 pts | |||||||
| (Part 2) | Laparotomy-assisted cryoablation of inadequate resection margins as determined by operator; (L.C.S. 3000/Erbe) | |||||||
| Shyn et al[123] | II-2 | 2014 | Mean 2.2 lesions | Local progression at a mean interval of 30.3 mo (range 13-72 mo) was seen in 14/54 patients (26%). Survival not reported | Not reported | |||
| Mean lesion size 5.7 cm | ||||||||
| Retrospective, 39 patients, 54 lesions | ||||||||
| Percutaneous (Galil) | ||||||||
| Median 4 probes (range 1-7) each 17 Gauge, 15 min freeze, 10 min passive thaw, 15 min freeze cycle | ||||||||
| Mean 1.4 lesions | ||||||||
| Mean lesion size 3 cm | ||||||||
Table 5 Highlights of microwave ablation literature for colorectal liver metastases
| Ref. | Level of evidence | Year | Study details | 1 yr OS% | 3 yr OS% | 5 yr OS% | Median OS (mo) | Procedure-related complications |
| Shibata et al[59] | II-1 | 2000 | Prospective, randomized, 14 pts, 58 lesions | 71 | 14 | 27 | 14% (2/14) - one biliary fistula and one hepatic abscess | |
| Laparotomy (Azwell HSD-20M) | ||||||||
| Mean 4 lesions | ||||||||
| Mean 2.7 cm | ||||||||
| Liang et al[124] | II-2 | 2003 | Retrospective, 74 patients, 149 lesions | 91.4 | 46.4 | 29 | 20.5 | 4% (3/74) skin burns (in patients with tumors with extracapsular extension) |
| Laparotomy (Microtaze AZM-520) | ||||||||
| Mean 2 lesions | ||||||||
| Mean 0.8 cm max diameter | ||||||||
| Tanaka et al[125] | II-2 | 2006 | Retrospective, 16 patients, 35 lesions | 80 | 51 | 17 | 28 | 19% (3/16) Bleeding, biliary fistula, wound infection. (all patients underwent MWA via laparotomy, none percutaneous) |
| Laparotomy (Microtaze AZM-520) | ||||||||
| Mean 2 lesions | ||||||||
| Mean 0.8 cm max diameter |
Table 6 Highlights of chemoembolization literature for colorectal liver metastases
| Ref. | Level of evidence | Year | Study details | Response rate (SD, CR, PR) | PFS/TTP (mo) | 1 yr OS | 2 yr OS | Median OS (mo) |
| Lang and Brown[126] | II-2 | 1993 | TACE, Doxorubicin | 63 | 65% | 22% | ||
| Prospective cohort, 46 patients | ||||||||
| Hong et al[127] | II-2 | 2009 | TACE, cisplatin + doxorubicin + mitomycin C | 43% | 10% | 7.7 | ||
| Retrospective cohort, 21 patients | ||||||||
| Vogl et al[82] | II-2 | 2009 | TACE, mitomycin C alone or with gemcitabine vs irinotecan | 63 | 62% | 28% | 14 | |
| Prospective cohort, 463 patients | ||||||||
| Albert et al[77] | II-2 | 2011 | TACE, cisplatin, doxorubicin, mitomycin C | 43 | 3 | 36% | 13% | 9 |
| Retrospective cohort, 121 patients | ||||||||
| Martin et al[128] | II-2 | 2011 | DEB-TACE (DEBIRI) | 75% | 19 | |||
| Prospective cohort, 55 patients | ||||||||
| Fiorentini et al[79] | I | 2012 | DEB-TACE (DEBIRI) | 80 | 7 | 56% | 15 | |
| Randomized Controlled Trial, 74 patients, DEBIRI vs FOLFIRI | ||||||||
| Narayanan et al[129] | II-2 | 2013 | DEB-TACE (DEBIRI) | 68.6 | 3 | 13.3 | ||
| Retrospective cohort, 28 patients | ||||||||
| Iezzi et al[83] | II-1 | 2015 | DEB-TACE (DEBIRI) + Capecitabine | 60 | 4 | 7.3 | ||
| Prospective Phase II Trial, 20 patients |
Table 7 Highlights of yttrium-90 radioembolization literature for colorectal liver metastases
| Ref. | Level of evidence | Year | Study details | Median OS | Median PFS |
| (mo) | (mo) | ||||
| Kennedy et al[86] | II-2 | 2006 | Phase II Prospective study | 10.5 | |
| 208 patients | |||||
| Sharma et al[130] | II-2 | 2007 | Phase I, 20 patients | 9.3 | |
| No prior chemotherapy SIRT + FOLFOX4 | (14.2 if had only liver-confined disease) | ||||
| SIR-Spheres only | |||||
| Benson et al[131] | II-2 | 2013 | Phase II Prospective study | 8.8 | 2.9 |
| 151 patients (61 colorectal) | |||||
| Theraspheres only | |||||
| Lewandowski et al[132] | II-2 | 2014 | Phase II Prospective study | 10.6 | |
| 214 patients | |||||
| Theraspheres only | |||||
| Sofocleous et al[133] | II-2 | 2014 | Phase I, 19 patients | 14.9 | 5.2 |
| Prior hepatic arterial and peripheral chemotherapy | |||||
| SIR-Spheres only | |||||
| Gray et al[87] | I | 2001 | Phase III Randomized controlled trial | 17 vs 15.9 | 15.9 vs 9.7 |
| 74 patients | (P = 0.18) | (P = 0.001) | |||
| First-line SIRT +/- Regional chemotherapy | Liver PFS | ||||
| 46 patients | |||||
| Van Hazel et al[90] | I | 2004 | Phase II Randomized Controlled trial | 29.4 vs 11.8 | 11.5 vs 4.6 |
| 21 patients | (P = 0.008) | (P < 0.004) | |||
| First-line SIRT +/- 5-FU/LV | |||||
| Hendlisz et al[134] | I | 2010 | Phase III Randomized controlled trial | 10 vs 7.3 | 5.5 vs 2.1 (P = 0.001) |
| First-Line SIRT +/- 5-FU | (P = 0.8) | ||||
| SIRFLOX[135] | I | Ongoing | Phase III Randomized controlled trial | ||
| Primary Endpoint: Progression free survival | |||||
| Size: 532 patients | |||||
| FOXFIRE[136] | I | Ongoing | Phase III Randomized controlled trial | ||
| Primary Endpoint: Overall survival | |||||
| Size: 490 patients | |||||
| EPOCH[137] | I | Ongoing | Phase III Randomized controlled trial | ||
| Primary Endpoint: Progression free survival |
- Citation: Sag AA, Selcukbiricik F, Mandel NM. Evidence-based medical oncology and interventional radiology paradigms for liver-dominant colorectal cancer metastases. World J Gastroenterol 2016; 22(11): 3127-3149
- URL: https://www.wjgnet.com/1007-9327/full/v22/i11/3127.htm
- DOI: https://dx.doi.org/10.3748/wjg.v22.i11.3127
