Recommendation | Level of evidence | Quality of evidence | Grade of recommendation |
1.1) Time-to-progression is an intermediate marker for overall survival in advanced NSCLC treated with first-line chemotherapy | MA | 3 | Fs |
1.2) Progression-free survival is a potential intermediate marker for survival in the setting of docetaxel or vinca-alcaloids first-line based regimens | MA | 2 | Fw |
2.1) Objective response is an intermediate criterion for overall survival in advanced NSCLC treated with first-line or salvage chemotherapy | MA/RT | 4 | Fs |
2.2) Objective response is an intermediate criterion for overall survival in extensive disease SCLC treated with first-line chemotherapy | MA/ReS | 2 | Fw |
2.3) Objective response is a potential intermediate criterion for overall survival in operable NSCLC treated with induction chemotherapy and in locoregionally advanced NSCLC treated by chemotherapy and radiotherapy | ReS | 2 | Fw |
3.1) Although commonly used, conventional criteria for response assessment of primary lung tumour treated by (chemo)radiotherapy cannot be used as intermediate criteria for survival | ReS | 1 | Aw |
3.2) Local control, for which the definition has to be clarified, may be a possible intermediate criterion for overall survival | ReS | 1 | Fw |
4) Response at the QoL level cannot be recommended as an intermediate criterion for overall survival due to a lack of robust data | ReS | 1 | Aw |
5) Although not strictly demonstrated, there are numerous arguments from subgroup analyses of randomised trials and retrospective studies that mediastinal downstaging and, to a lesser extent, TN downstaging are associated with better survival in locally advanced NSCLC treated by induction chemotherapy or chemoradiotherapy before surgery | ReS | 2 | Fw |
6.1) Complete resection is a prognostic factor for survival in resected NSCLC and can be used as an intermediate criterion for overall survival | Cohort/ReS | 3 | Fs |
6.2) Pathological TNM is a prognostic factor for survival in resected NSCLC and can be used as an intermediate criterion for overall survival | Cohort | 3 | Fs |
7) Metabolic response assessed by PET scan should not be used for the routine assessment of response to treatment in lung cancer patients in place of morphological criteria | ReS/CS | 1 | Aw |
8) Tissue biological markers have not to be used for evaluation of treatment efficacy and are not adequate intermediate criteria for overall survival in lung cancer patients | CS | 1 | Aw |
9.1) It is suggested that some circulating markers (CEA, Cyfra 21-1 and pro-GRP, and to a lesser extent NSE, CA-125 and CA19-9), used as single criterion to assess overall survival, could be adequate intermediate criteria for survival in lung cancer patients | ReS | 2 | Fw |
9.2) The persistence of circulating tumour cells in NSCLC may have a prognostic impact on further survival | Cohort | 1 | Fw |
NSCLC: nonsmall cell lung cancer; SCLC: small cell lung cancer; QoL: quality of life; PET: positron emission tomography; CEA: carcinoembryonic antigen; pro-GRP: pro-gastrin releasing peptide; NSE: neurone-specific enolase; MA: meta-analysis; RT: randomised trial; ReS: retrospective studies; CS: case series; Fs: strong recommendation for using an intervention; Fw: weak recommendation for using an intervention; Aw: weak recommendation against using an intervention.