Author(s) | Study design | Years of data collection | Patient (N) | Case selection | Type of treatment | QoL measure | QoL measured at: baseline | 3 months | 6 months | 1 year | > 2 years | Recurrence | QAa |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
EPP | |||||||||||||
O (prospective; multi-center) | 2000–2003 | 45 | Clinical T1-T3, N0–2; M0, any histology | Neo-adjuvant chemo (pre-op; n = 45/61), EPP, radiotherapy (post-op; n = 36/45) | Rotterdam Symptoms checklist; SEIQoL | y (pre-op) | 1, 3 | y | y |  | Median 13.5 months | 10/12 | |
O (prospective; single-center) | 1997–2007 | 29 | NR | EPP, adjuvant chemotherapy and radiotherapy (post-op) | SF 36, St George, symptoms, lung function, 6 min walk, cardiac EF, Karnovsky | y (pre-op) | y | y | y | 2, 3 | Median 19.5 months | 8/12 | |
 ALVAREZ [33] | O (prospective; single-center) | 2004–2007 | 16 (18 no EPP) | stage I, II, epithelioid, age < 70 years | EPP, chemotherapy, radiotherapy (post-op) | ECOG, Karnofsky | ECOG 0 |  | y | y |  | 18% at 6 months | 8/12 |
 TREASURE [34] | RCT (multi-center) | 2005–2008 | 12 (19 no EPP) | T1–3, N0–1, M0, any histology | Chemotherapy (pre-op), EPP, Radiotherapy (post-op) | EORTC C30; LC 13 | y (pre-op) | 6 weeks, 3 months | 6, 9 | 12, 18 months | y | 75% at 6 months | NA |
P/D | |||||||||||||
O (prospective; single- center) | 2010–2011 | 36 | Epithelioid, biphasic WHO PS 0–2 | EPD (some talc, neoadjuvant chemotherapy (n = 3), adjuvant chemotherapy (n = 30) | EORTC C30, lung function | y (pre-op) | 4 | 5, 7, 8 |  |  | NA | 9/12 | |
 SAUTER [37] | O (prospective; single-center | 1988–1992 | 20 | NR | Partial P (some chemotherapy, some radiation; post-op) | dyspnea, pain | y |  | y |  |  | Median 10 months | 9/12 |
 SOYSAL [38] | O (retrospective; single-center) | 1974–1992 | 100 | NR | 56 P/D; 44 Partial P, chemotherapy (n = 24/100; post-op), radiotherapy (n = 31/100; post-op), chemo + radio (n = 20/100; post-op) | dyspnea, pain, cough |  | y | y |  |  | Median survival 17 months | 4/10 |
 MARTIN-UCAR [39] | O (prospective; single-center) | 1997–2001 | 51 | Exclude early stage | P/D palliative | symptoms | y (pre-op) | 6 weeks, 3 months | y | y |  | 53% at 6 months | 9/12 |
 BOLUKBAS [40] | O (prospective; single-center) | 2010 | 16 | NR | radical P, chemotherapy, radiation (post-op) | lung function | y (pre-op) | 2 months |  |  |  | NA | 9/12 |
 RINTOUL [41] | RCT (multi-center) | 2003–2012 | 73 | NR | 73 Partial P, 78 talc, some chemotherapy, radiotherapy (post-op) | EORTC C30, LC 13, Euro 5, lung function | y (pre-op) | 1, 3 | y | y |  | Median survival 13 months | NA |
 TANAKA [42] | O (prospective; single-center) | 2013–2015 | 22 | NR | P/D, some chemotherapy (pre-op) | SF-36, lung function | y (pre-op) |  |  |  |  | NA | 8/11 |
 VIGNESWARAN [43] | O (prospective; single-center) | 2008–2015 | 114 | NR | 28 chemotherapy before P/D | EORTC C30 | y (pre-op) | 1 | 4–5, 7–8 | 10–11 |  | Median survival 15.21 months | 9/12 |
EPP VS P/D | |||||||||||||
 RENA [44] | O (prospective; single-center) | 1998–2009 | 77 | Stage I and II | 40 EPP (n = 7 adjuvant chemotherapy; n = 33 neoadjuvant); 37 P/D (n = 6 adjuvant chemotherapy; n = 31 neoadjuvant) | EORTC C30 | y (pre-op) |  | y | y | Median survival 14 and 11 months | 8/12 | |
 PLOENES [45] | O (retrospective; single-center) | NR | 48 | NR | 25 EPP; 23 P/D (intraoperative chemotherapy; n = 6) | lung function | y (pre-op) |  | y | y | Median survival 22 and 29 months | 10/12 | |
TOTAL CASES | Â | Â | 659 | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |