Table 1.
Upper gastrointestinal cancers: indications for chemotherapy, levels, and sources of evidence.
| Outcome number | Clinical scenario | Treatment indicated | Level of evidencea | Reference(s) | Proportion of all patients with that cancer |
|---|---|---|---|---|---|
| Oesophageal cancer | |||||
| 3 | Oesophageal cancer, recurrence, good PS | Palliative chemotherapy | II | NCCN [18] NCI PDQ [23] BCCA [27] SIGN [32] |
0.23 |
| 5 | Oesophageal cancer, localised, unresectable, good PS | Radical chemoradiation | I | NCCN [18] NCI PDQ [23] BCCA [27] |
0.29 |
| 6 | Oesophageal cancer, metastatic, good PS | Palliative chemotherapy | II | NCCN [18] NCI PDQ [23] BCCA [27] SIGN [32] |
0.27 |
| Total proportion of patients with oesophageal cancer in whom chemotherapy is recommended | 0.79 | ||||
|
| |||||
| Gastric cancer | |||||
| 7 | Gastric cancer, resected stage 1A, recurrence, good PS | Palliative chemotherapy | I | NCCN [21] NCI PDQ [22] BCCA [27] CCO [35] |
<0.01 |
| 9 | Gastric cancer, locoregional, resectable, higher than stage 1A, good PS |
Postoperative chemoradiation or perioperative chemotherapy |
II | NCCN [21] NCI PDQ [22] BCCA [27] SIGN [32] |
0.42 |
| 10 | Gastric cancer, locoregional disease, unresectable | Palliative chemotherapy | I | NCCN [21] NCI PDQ [22] BCCA [27] SIGN [32] |
0.15 |
| 11 | Gastric cancer, metastatic, good PS | Palliative chemotherapy | I | NCCN [21] NCI PDQ [22] BCCA [27] SIGN [32] |
0.26 |
| Total proportion of patients with gastric cancer in whom chemotherapy is recommended | 0.83 | ||||
|
| |||||
| Pancreatic cancer | |||||
| 1 | Pancreatic cancer, localised, operable | Palliative chemotherapy | I | NCCN [19] NCI PDQ [24] BCCA [35] CCO [28] |
0.08 |
| 2 | Pancreatic cancer, localised, inoperable, good PS | Palliative chemotherapy | II | NCCN [19] NCI PDQ [24] BCCA [35] CCO [28] |
0.12 |
| 4 | Pancreatic cancer, metastatic, good PS | Palliative chemotherapy | II | NCCN [19] NCI PDQ [24] BCCA [35] CCO [28] |
0.15 |
| Total proportion of patients with pancreatic cancer in whom chemotherapy is recommended | 0.35 | ||||
|
| |||||
| Hepatocellular cancer | |||||
| 6 | Liver cancer, localised, unresectable, good PS | Chemoembolization | I | NCCN [20] NCI PDQ [25] BCCA [27] |
0.20 |
| 8 | Liver cancer, localised, resected, intrahepatic recurrence, good PS |
Chemoembolization | IV | NCI PDQ [25] | 0.07 |
| Total proportion of patients with hepatocellular cancer in whom chemotherapy is recommended | 0.27 | ||||
|
| |||||
| Gallbladder cancer | |||||
| 17 | Gallbladder cancer, locoregional, recurrence, good PS |
Palliative chemotherapy | III | NCCN [20] NCI PDQ [26] BCCA [27] CCO [31] |
0.47 |
| 18 | Gallbladder cancer, metastatic, good PS | Palliative chemotherapy | III | NCCN [20] NCI PDQ [26] BCCA [27] CCO [31] |
0.33 |
| Total proportion of patients with gallbladder cancer in whom chemotherapy is recommended | 0.80 | ||||
PS: performance status, NCCN: National Comprehensive Cancer Network, NCI PDQ: National Cancer Institute Physicians Data Query, BCCA: British Columbia Cancer Agency, CCO: Cancer Care Ontario, and SIGN: Scottish Intercollegiate Guidelines Network.
aLevels of evidence: level I: evidence obtained from a systematic review of all relevant randomised controlled trials; level II: evidence obtained from at least one properly designed randomised controlled trial; level III: evidence obtained from well-designed controlled trials without randomisation (these include trials with “pseudorandomisation” where a flawed randomisation method was used (e.g., alternate allocation of treatments) or comparative studies with either comparative or historical controls); level IV: evidence obtained from case series. Taken from the National Health and Medical Research Council (NHMRC) hierarchy of levels of evidence [33].