Table 1.
Martini Melamed criteria10 | ACCP guidelines11 | TNM staging system (8th edition)12 |
sMPLCs: 1. Tumors physically distinct and separate 2. Histology: A. Different histological types B. Same histological type, but in different segments, lobes, if origin from carcinoma in situ And no carcinoma in lymphatics common to both And no extrapulmonary metastases |
sMPLCs: 1. Different histology 2. Different molecular genetic characteristics 3. Arising from a separate focus of carcinoma in situ 4. Same histology, if: Tumors in different lobes And no N2, N3 involvement And no systemic metastases |
Clinical Criteria for sMPLCs: 1. Different histological types on biopsy 2. Arguments favoring sMPLCs: Different radiographic appearance or metabolic uptake Different growth rates Different biomarker pattern Absence of lymphatic or systemic metastases |
mMPLCs: 1. Different histological types 2. Same histological type, if: Free interval between cancers ≥2 years Or origin from carcinoma in situ Or second cancer in different lobes and no carcinoma in common lymphatics and extrapulmonary sites |
mMPLCs: 1. Different histology 2. Different molecular genetic characteristics 3. Arising from a separate focus of carcinoma in situ 4. Same histology, temporarily separated, if: Free interval between cancers ≥4 years And no systemic metastases |
Pathologic criteria for sMPLCs (e.g., after resection): 1. Different histological types 2. Clearly different comprehensive histologic assessment 3. Squamous carcinomas arising from carcinoma in situ. 4. Arguments favoring sMPLCs: Different biomarker pattern Free of lymphatic or systemic metastases. |
Abbreviations: ACCP, American College of Chest Physicians; sMPLCs, synchronous multiple primary lung cancers; mMPLCs, metachronous multiple primary lung cancers.