Copyright
©The Author(s) 2020.
World J Gastroenterol. Jul 7, 2020; 26(25): 3686-3711
Published online Jul 7, 2020. doi: 10.3748/wjg.v26.i25.3686
Published online Jul 7, 2020. doi: 10.3748/wjg.v26.i25.3686
Ref. | Intervention | Comparator(s) | Study design, “Open” Label / “Blinded” / “Double blinded” | Total sample size | Patient sub-group | Pt sub-group sample size | Sex (% female) | Average age (yr) | Mean/median | Total GI-NET, % | P-NET, % | Functioning /Non-functioning, “function” | Additional information about disease1: “Stage (TNM)” “progressive” “stable”, (“advanced” “metastatic/metastases” “spread”) (“grow” “grade” “differentiated”) |
Zandee et al[58], 2019 | 177Lu-DOTATATE | NA | Retrospective study | 34 | NA | NA | 50 | 59 | Mean | NA | 100 | Functioning (100%) | Grade 1 or 2 tumours with metastases (stage IV). Metastatic disease sites: Liver (97%), bone (21%), lung (6%) |
Ramage et al[54], 2019 | Everolimus | NA | Phase IV, open | 48 | All Patients | 46 | 30 | 64.3 | Median | NR | 100 | NR | Advanced and/or metastatic, well-differentiated, grade 1 and 2 |
Continuing treatment at month 6 | 30 | NR | NR | NR | NR | NR | |||||||
Ballal | 225Ac-DOTATATE | NA | Prospective study, open | 21 | NA | NA | 57 | 54 | Median | 38 | 57 | NR | Metastatic GEP-NETs with stable disease after completing 177Lu-PRRT (57%) or progressive disease on 177Lu-PRRT (43%). Grades 1 (n = 9), 2 (n = 11), and 3 (n = 1). Metastatic disease sites: Liver (86%), lymph node (71%), bone (33%) |
Marinova et al[61], 2019 | 177Lu-DOTATATE | NA | Retrospective study | 70 | NA | NA | 44.3 | 64.2 | Mean | 100 | NR | Functioning (83%), non-functioning (17%) | Metastatic. Grade 1 (50%), grade 2 (35.7%), unknown (14.3%). Morphological or clinical progression prior to 1st cycle PRRT (78.6%) |
Rinke et al[16], 2019 | Long-acting octreotide | Placebo (sodium chloride) | Clinical trial (RCT), Phase IIIb trial, double blind, placebo controlled | 85 | Long-acting octreotide | 42 | 49.4 | 62.4 | Mean | NR | NR | Functioning (39%), non-functioning (61%) | Metastatic, liver metastases (86%) |
Placebo | 43 | 60.3 | Mean | NR | NR | ||||||||
NA | NA | NR | NA | NR | NR | ||||||||
Martini et al[59], 2018 | DOTATATE or 90Y-DOTATOC | General population norms | Retrospective study | 61 | Small intestine NET patients | 37 | 40.5 | 62.8 | Mean | 100 | 0 | NR | No brain metastases; otherwise not defined |
P-NET patients | 24 | 37.5 | 61.0 | Mean | 0 | 100 | |||||||
Lewis et al[3], 2018 | Not defined | Patients with CS vs patients without CS | Prospective study | 50 | Without CS (CS) | 25 | 48.0 | 62.0 | Median | 60.0 | 40.0 | NR | Advanced, well-differentiated, with liver metastases |
With CS (CS) | 25 | 36.0 | 67.0 | Median | 96.0 | 4.0 | NR | ||||||
Strosberg et al[17], 2018 | 177Lu-DOTATATE | High-dose octreotide | Clinical trial (RCT), phase III, open | 231 | 177Lu-DOTATATE | 117 | NR | NR | NR | 100 | NR | NR | Advanced, progressive, low- or intermediate-grade |
octreotide LAR | 114 | NR | NR | NR | 100 | NR | |||||||
Karppinen et al[46], 2018 | NA | Control population | Cross-sectional | 134 | Impaired excretion | 87 | 55 | 66.8 | Mean | 100 | NR | Flushing (31%), diarrhoea (63%) | Locally advanced or metastatic disease (91%), grade 1 (54.1%), grade 2 (45.9%) |
Cella et al[44], 2018 | Telotristat ethyl | Placebo | Clinical trial (RCT), phase III trial, double blind | 135 | NA | 135 | 48.1 | 63.6 | Mean | NR | NR | NR | Well-differentiated, metastatic NETs and CS inadequately controlled by somatostatin analogues (for ≥ 3 mo) |
Durable responders (DR) | 48 | 52.1 | 63.4 | Mean | NR | NR | |||||||
Non-durable responders (DR) | 87 | 46 | 63.6 | Mean | NR | NR | |||||||
Meng et al[28], 2017 | Somatostatin analogue lanreotide | Placebo | Clinical trial (RCT), phase III trial, double blind | 204 | Lanreotide | 101 | 48 | 62.1 | Mean | NR | NR | Non-functioning | Advanced, well-differentiated or moderately differentiated, somatostatin receptor-positive NETs of grade 1 or 2 |
Placebo | 103 | NR | NR | ||||||||||
Overall | 204 | NR | NR | ||||||||||
Vinik et al[35], 2016 | Sunitinib plus best supportive care | Placebo plus best supportive care | Clinical trial (RCT), phase III trial, double blind | 171 | NA | NA | NR | NR | NR | NA | 100 | NR | Advanced and/or metastatic, pathologically confirmed, well-differentiated P-NETs with disease progression as assessed by RECIST |
Haugland et al[9], 2016 | None | None | Cross-sectional | 196 | None | NA | 50.5 | 65.0 | Mean | 100.0 | 0.0 | NR | NR |
Pavel et al[56], 2016 | Everolimus | NA | Clinical trial, Phase IIIb, open, expanded access study | 246 | P-NET | 126 | 46 | 61 | Median | NR | 100 | Functioning (n = 38), non-functioning (n = 88) | Metastatic, well differentiated (n = 81), moderately differentiated (n = 26), poorly differentiated (n = 1), unknown (n = 16), missing (n = 2) |
Non P-NET | 120 | 50.8 | 66 | Median | NR | 0 | Functioning (n = 66), non-functioning (n = 55) | Metastatic, well differentiated (n = 65), moderately differentiated (n = 34), poorly differentiated (n = 2), unknown (n = 19) | |||||
Delpassand et al[66], 2014 | 177Lu-DOTATATE | NA | Clinical trial, phase II, open | 37 | Patients with available data participated in quality of life questionnaire | 27 | 56.8 | 63.4 | Mean | 43.2 | 37.8 | NR | Grade 1 and grade 2, disseminated, progressive, somatostatin receptor-positive. Multiple metastases in the liver: grade 2 (n = 4), grade 3 (n = 26), grade 4 (n = 7). Metastatic disease sites: Liver (n = 34), lymph nodes (n = 16), bone (n = 11), pancreas (n = 8), lung (n = 3) |
Ducreux et al[41], 2014 | Bevacizumab combined with 5-FU/ streptozocin (Mitry et al[40] 2014) | Capecitabine plus bevacizumab | Clinical trial, phase II, open | 34 | NA | NA | 35 | 55 | Median | NR | 100 | Functioning (n = 7): CS (n = 3), Zollinger–Ellison syndrome (n = 1), other (n = 3) | Progressive, metastatic disease. Metastatic disease sites: Liver (n = 33), lymph node (n = 14), peritoneum (n = 2), lung (n = 3), bone (n = 2), other (n = 2) |
Mitry et al[40], 2014 | Bevacizumab combined with 5-FU/ streptozocin (reported in a companion paper focusing on P-NET patients (Ducreux et al[41], 2014) | Capecitabine plus bevacizumab | Clinical trial, phase II, open | 49 | NA | NA | 47 | 60 | Median | 100 | NA | NR | Progressive, metastatic well-differentiated. Metastatic disease sites: Liver (n = 46), lymph node (n = 24), peritoneum (n = 23), lung (n = 7), bone (n = 7), other (n = 5) |
Meyer et al[42], 2014 | Capecitabine and streptozocin plus cisplatin (stratified) | Capecitabine and streptozocin (stratified) | Clinical trial (RCT), Phase II | 86 | Capecitabine and streptozocin | 44 | 39 | 57 | Median | 21 | 46.0 | Functioning (n = 31; 36%) | Advanced and/or metastatic. Metastatic disease sites: Local/regional (n = 2), distant (n = 42), liver (included in distant; n = 41) |
Capecitabine and streptozocin plus cisplatin | 42 | 45 | 59 | Median | 19 | 50.0 | |||||||
Yadegarfar et al[33], 2013 | Somatostatin analogues or interferon therapy (88 patients) | Peptide-receptor radiotherapy (102 patients), chemotherapy (23 patients), surgery (20 patients) or ablative/ other therapies (20 patients) | Phase IV, open | 253 | P-NET | 70 | NR | NR | NR | NR | NR | Functioning: Secreting 5-hydroxy-indoloacetic acid (n = 111), gastrin (n = 4), glucagon (n = 3), insulin (n = 5), vasoactive intestinal peptide (n = 1). Non-functioning (secreting only chromogranin-A; n = 124) | Any gut-primary with metastases, lung-primary with liver/abdominal metastases and pancreas with/without metastases |
Casciano et al[36], 2012 | Everolimus (Afinitor) | Sunitinib (Sutent) | Economic analysis of phase III studies | NA | NA | NA | NA | NA | NA | NA | NA | NR | Advanced, progressive |
Kvols et al[29], 2012 | Pasireotide | Octreotide | Prospective study, phase II, open | 44 | Pasireotide responders | 12 (Baseline), 12 (Month 1), 10 (Month 2), 11 (Month 3) | 44 | 61 | Mean | NR | NR | NR | Advanced, metastatic (symptoms refractory or resistant to octreotide LAR therapy). Metastatic disease sites: Liver (87%), lymph node (n = 16), peritoneum (n = 8), lung (n = 5), bone (n = 3), abdomen (n = 3), pleura (n = 3), retroperitoneal (n = 2), pancreas (n = 2), kidney (n = 1) |
Pasireotide non responders | 13 (Baseline), 13 (Month 1), 13 (Month 2), 13 (Month 3) | NR | NR | ||||||||||
Patients who discontinued treatment before 3 mo | 19 (Baseline), 15 (Month 1), 8 (Month 2) | NR | NR | ||||||||||
Raymond et al[34], 2011 | Sunitinib plus Best Supportive Care | Placebo plus Best Supportive Care | Clinical trial (RCT), phase III, double blind | 171 | sunitinib | 86 | 51 | 56 | Median | NR | 100 | Sunitinib Arm: Functioning: Gastrinoma (n = 9), glucagonoma (n = 3), insulinoma (n = 2), somatostatinoma (n = 1), other, multisecretory, or unknown (n = 10). Non-functioning (n = 42) | Advanced and/or metastatic, progressive, well-differentiated |
Placebo | 85 | 53 | 57 | Median | NR | 100 | Placebo Arm: Functioning: Gastrinoma (n = 10), glucagonoma (n = 2), insulinoma (n = 2), vasoactive intestinal peptide–secreting tumour (n = 2), other, multisecretory, or unknown (n = 5). Non-functioning (n = 44) | ||||||
Pezzilli et al[49], 2009 | NA | NA | Prospective study | 51 | NA | NA | 58.8 | 61 | Mean | NR | 100 | NR | Advanced disease (lymph node involvement/liver metastases) (n = 22) |
Rinke et al[27], 2009 | Octreotide LAR | Placebo | Clinical trial (RCT), phase IIIb, double blind | 85 | Octreotide LAR | 42 | 52.4 | 63.5 | Median | 100 | NR | Octreotide LAR arm: Functioning: CS (n = 17) 40.5% | Well-differentiated, metastatic. Metastatic disease sites: Liver (n = 73), regional lymph node involvement (n = 6) |
Placebo | 43 | 46.5 | 61 | Median | 100 | NR | Placebo arm: Functioning: CS (n = 16) 37.2% | ||||||
Korse et al[30], 2009 | Long-acting sandostatin LAR | Short-acting Sandostatin | Clinical trial, phase II | 39 | NA | NA | 51.3 | 61 | Mean | 51.3 | NR | Functioning: CS (n = 39) | Metastatic: Liver metastases (n = 35) |
van der Horst-Schrivers et al[67] , 2009 | NA | NA | Prospective study | 43 | NA | NA | 37.2 | 60.6 | Mean | NR | NR | NR | Metastatic midgut carcinoid tumours: Liver metastases (n = 37) |
Haugland et al[47], 2009 | NA | NA | Cross-sectional | 5341 | NET patients | 189 | 50 | 65 | Mean | 100 | NR | NR | GI-NET patients (excluded radical surgery that may have been curative), otherwise undefined |
General population | 5152 | 48.8 | NR | NR | NA | NA | |||||||
Larsson and Janson[50], 2008 | Erythropoietin | None | Pilot study | 18 | None | NA | 50.0 | 63.0 | Mean | 100 | NR | NR | NR |
Kulke et al[55], 2008 | Sunitinib | NA | Clinical trial, phase II, open | 107 | NA | NA | 40.2 | Carcinoid tumour = 58, P-NET= 56 | Median | 37.3 | 61.7 | P-NET: Functioning: Gastrinoma n = 5 (7.6%), insulinoma n = 3 (4.5%), VIPoma n = 2 (3.0%), glucagonoma n = 4 (6.1%), other n = 5 (7.6%). Non-functioning n = 46 (69.7%) | Advanced carcinoid or P-NET |
Fröjd et al[37] , 2007 | Various included | None | Longitudinal, prospective, comparative study | 59 | T1-T4 successful | 36 | 47.0 | 60.0 | Mean | NR | NR | NR | Metastatic (70% metastatic at start; 78% metastatic at end) |
Davies et al[68], 2006 | NA | NA | Cross-sectional, open | 50 | Patients | 35 | 42.9 | 60 | Mean | NR | NR | NR | Metastatic |
Healthcare workers | 15 | NR | NR | NR | NA | NA | |||||||
Frilling et al[48], 2006 | 90Y-DOTATOC then 177Lu-DOTATOC | NA | Prospective study | 20 | Excluding pt (no 3) with Paraganglioma-neck | 19 | 30 | 53.8 | Median | NR | NR | NR | Advanced, progressive, and metastatic |
Arnold et al[31], 2005 | Octreotide plus interferon alpha | Octreotide monotherapy | Clinical trial (RCT), open | 114 | Octreotide monotherapy | 51 | 47.1 | 58 | Median | NR | NR | Octreotide: Functioning (n = 23), non-functioning (n = 28). Octreotide plus Interferon-alpha: functioning (n = 24), non-functioning (n = 30) | Metastatic or locally advanced disease without curative therapeutic option |
Octreotide plus interferon alpha | 54 | 44.4 | 57 | Median | NR | NR | |||||||
Nonrandomised | 9 | 33.3 | 60 | Median | NR | NR | |||||||
Teunissen et al[62], 2004 | 177Lu-DOTATOC | None | Clinical trial | 50 | None | NA | 56.0 | 58.3 | Mean | NR | 26.0 | NR | Metastatic |
Pasieka et al[43], 2004 | I-MIBG | NA | Clinical trial, open | 19 | I-MIBG | 10 | 40 | 59 | Mean | 90 | 10 | NR | Progressive |
Octreotide | 9 | 55.6 | 55.6 | Mean | 66.6 | 33.3 | |||||||
Kwekkeboom et al[60], 2003 | Somatostatin analogue 177Lu-DOTATOC | NA | Clinical trial, open | 35 | None | NA | 60 | 54 | Mean | NR | NR | NR | Metastatic |
Larsson et al[25], 2001 | Interferon, somatostatin analogue, interferon, and a somatostatin | None | Prospective study | 24 | None | NA | 42.0 | 62.0 | Median | 100 | NR | NR | NR |
O'Toole et al[32], 2000 | Octreotide followed by lanreotide | Lanreotide followed by octreotide | Clinical trial (RTC), double blind | 33 | Patients received octreotide followed by Lanreotide | 16 | 50 | 63 | NR | 62.5 | 0 | ||
Patients received lanreotide followed by octreotide | 17 | 53 | 64 | NR | 76 | 5.9 | NR | NR | |||||
Wymenga et al[57], 1999 | Lanreotide prolonged release | NA | Clinical trial, phase II, open | 55 | NA | NA | 49.1 | 59.7 | Mean | NR | 5.5 | NR | Advanced (Stage IV), metastatic. Metastatic disease sites: Lymph nodes (n = 39), distant organs (n = 44) |
Larsson et al[26], 1999 | Ongoing treatment: interferon and octreotide, other | NA | Cross-sectional | 119 | Patients with carcinoid tumours | 64 | 43.7 | 64 | Median | 53.8 | NA | NR | NR |
Patients with EPT | 55 | 37.5 | 54 | Median | NR | 46.20 | |||||||
Overall | 119 | 43.7 | 61 | Median | 53.8 | 46.20 | |||||||
Larsson et al[38] , 1999 | Interferon and/or a somatostatin analogue | NA | Clinical trial | 99 | NA | NA | 39.4 | 59 | Mean | NR | NR | NR | Stage = not terminal, no other status provided. |
HADS Anxiety (cases) | 19 | NR | NR | NR | NR | NR | |||||||
HADS Depression (cases) | 13 | NR | NR | NR | NR | NR | |||||||
Larsson et al[69], 1998 | Interferon and/or a somatostatin analogue | NA | Cross-sectional | 17 | NA | NA | 47 | 58 | Mean | NR | NR | NR | NR |
- Citation: Watson C, Tallentire CW, Ramage JK, Srirajaskanthan R, Leeuwenkamp OR, Fountain D. Quality of life in patients with gastroenteropancreatic tumours: A systematic literature review. World J Gastroenterol 2020; 26(25): 3686-3711
- URL: https://www.wjgnet.com/1007-9327/full/v26/i25/3686.htm
- DOI: https://dx.doi.org/10.3748/wjg.v26.i25.3686