Synchronous, Metachronous or Metastases?


Abstract views: 129 / PDF downloads: 49

Authors

  • Celalettin İbrahim Kocatürk Department of Thoracic Surgery, Yedikule Chest Diseases and Thoracic Surgery Training and Research Hospital, İstanbul, Turkey

DOI:

https://doi.org/10.5152/EurJTher.2018.1010

Keywords:

Multiple primary lung cancer, non-small cell lung cancer, metachronous lung cancers, satellits tumors

Abstract

Multiple primer lung cancer (MPAK) satellite tumors (accessory tumor of the same type with the same tumor in the same lobe) synchronous tumors (at the time of diagnosis, or at the same site within 3 months or with other tumors in the opposite lung) and metachronous tumors (a newly developed tumor in a patient with a definitively treated tumor). Satellite tumors are synchronous tumors also. It may be difficult to understand whether MPAC is primer tumors originating from different areas of the lung, or whether they are metastases from each other. If the histopathological types of the tumors are different from each other, it can be said that they are generally MPAK. However, if histopathological types are the same, histopathological, molecular, genetic and clinical data are needed. It is useful to demonstrate histopathologically that the detailed analysis of tumors (subtype, dominant type, especially in adenocarcinomas) and carcioma insitu background. Genetic and molecular tests are still a matter of debate. It is both very expensive and can be performed in a small number of centers, and not at the expected activity. Because the cancer cells are very complex and constantly undergoing mutation and change. The clinical criteria, especially the Martini-Melamed criteria have been used for a long time. It is still valid. If the histopathological types are different for metachronous tumors, there is no problem, but if they are the same, the second tumor is defined according to the development time. However, it may be more accurate to evaluate these patients independently from time to time. The best survival data is obtained with surgery even if it is second cancer or local recurrence or metachronous cancer Therefore, if patients with synchronous or metachronous cancer are considered to have no distant metastasis or mediastinal involvement, surgical treatment should be the priority.

Metrics

Metrics Loading ...

References

Shen KR, Meyers BF, Larner JM, Jones DR; American College of Chest Physicians. Special treatment issues in lung cancer: ACCP evidence-based clinical practice guidelines. Chest 2007; 132: 290-305.

Deslauriers J, Brisson J, Cartier R, Fournier M, Gagnon D, Piraux M, et al. Carcinoma of the lung. Evaluation of satellite nodules as a factor influencing prognosis after resection. J Thorac Cardiovasc Surg 1989; 97: 504-12.

Shimizu N, Ando A, Date H, Teramoto S. Prognosis of undetected intrapulmonary metastases in resected lung cancer. Cancer 1993; 71: 3868-72.

Trousse D, D’Journo XB, Avaro JP, Doddoli C, Giudicelli R, Fuentes PA, et al. Multifocal T4 non-small cell lung cancer: a subset with improved prognosis. Eur J Cardiothorac Surg 2008; 33: 99-103.

Keogan MT, Tung KT, Kaplan DK, Goldstraw PJ, Hansell DM. The significance of pulmonary nodules detected on CT staging for lung cancer. Clin Radiol 1993; 48: 94-6.

Oliaro A, Filosso PL, Cavallo A, Giobbe R, Mossetti C, Lyberis P, et al. The significance of intrapulmonary metastasis in non-small cell lung cancer: upstaging or downstaging? A re-appraisal for the next TNM staging system. Eur J Cardiothorac Surg 2008; 34: 438-43.

Port JL, Korst RJ, Lee PC, Kansler AL, Kerem Y, Altorki NK. Surgical resection for multifocal (T4) non-small cell lung cancer: is the T4 designation valid? Ann Thorac Surg 2007; 83: 397-400.

Detterbeck FC, Boffa DJ, Tanoue LT. The new lung cancer staging system. Chest 2009; 136: 260-71.

Detterbeck FC, Jones DR, Kernstine KH, Naunheim KS; American College of Physicians. Lung Cancer. Special treatment issues. Chest 2003; 123: 244-58.

Martini N, Melamed MR. Multiple primary lung cancers. J Thorac Cardiovasc Surg 1975; 70: 606-12.

Antakli T, Schaefer RF, Rutherford JE, Read RC. Second primary lung cancer. Ann Thorac Surg 1995; 59: 863-7.

Kim HL, Puymon MR, Qin M, Guru K, Mohler JL. NCCN clinical practice guidelines in oncologyTM 2009.

Kocaturk CI, Gunluoglu MZ, Cansever L, Dincer IS, Bedirhan MA. Prognosis in patients with non-small cell lung cancer and satellite tumors. Thorac Cardiovasc Surg 2011; 59: 360-3.

Beyreuther H. Multiplicität von Carcinomen bei einem fall von sog.”Schneeberger” lungenkrebs mit tuberkulose. Virchows Arch Pathol Anat Physiol Klin Med 1924; 250: 230-43.

De Leyn P, Moons J, Vansteenkiste J, Verbeken E, Van Raemdonck D, Nafteux P, et al. Survival after resection of synchronous bilateral lung cancer. Eur J Cardio-Thoracic Surg 2008; 34: 1215-22.

Aziz TM, Saad RA, Glasser J, Jilaihawi AN, Prakash D. The management of second primary lung cancers. A single centre experience in 15 years. Eur J Cardio-Thoracic Surg 2002; 21: 527-33.

Detterbeck FC, Jones DR, Funkhouser WK. Satellite nodules and multiple primary cancers. Diagnosis and treatment of lung cancer: an evidence-based guide for the practicing clinician. WB Saunders, Philadelphia, PA; 2001:437-49.

Howe HL. A review of the definition for multiple primary cancers in the United States. NAACCR. Proceedings from 2002 December 4-6; Princeton, New Jersey.

Yang D. Build prognostic nomograms for risk assessment using SAS. Proceedings from 2013; SAS

Tanvetyanon T, Finley DJ, Fabian T, Riquet M, Voltolini L, Kocaturk C, et al. Prognostic nomogram to predict survival after surgery for synchronous multiple lung cancers in multiple lobes. J Thorac Oncol 2015; 10: 338-45.

Tanvetyanon T, Finley DJ, Fabian T, Riquet M, Voltolini L, Kocaturk C, et al. Prognostic factors for survival after complete resections of synchronous lung cancers in multiple lobes: pooled analysis based on individual patient data. Ann Oncol 2012; 24: 889-94.

Trousse D, Barlesi F, Loundou A, Tasei AM, Doddoli C, Giudicelli R, et al. Synchronous multiple primary lung cancer: an increasing clinical occurrence requiring multidisciplinary management. J Thorac Cardiovasc Surg 2007; 133: 1193-200.

Chang Y-L, Wu C-T, Lee Y-C. Surgical treatment of synchronous multiple primary lung cancers: experience of 92 patients. J Thorac Cardiovasc Surg 2007; 134: 630-7.

Nakata M, Sawada S, Yamashita M, Saeki H, Kurita A, Takashima S, et al. Surgical treatments for multiple primary adenocarcinoma of the lung. Ann Thorac Surg 2004; 78: 1194-9.

Mun M, Kohno T. Single-stage surgical treatment of synchronous bilateral multiple lung cancers. Ann Thorac Surg 2007; 83: 1146-51.

Rostad H, Strand T-E, Naalsund A, Norstein J. Resected synchronous primary malignant lung tumors: a population-based study. Ann Thorac Surg 2008; 85: 204-9.

Sherwood J, Dearden S, Ratcliffe M, Walker J. Mutation status concordance between primary lesions and metastatic sites of advanced non-small-cell lung cancer and the impact of mutation testing methodologies: a literature review. J Exp Clin Cancer Res 2015; 34: 92.

Yu HA, Arcila ME, Rekhtman N, Sima CS, Zakowski MF, Pao W, et al. Analysis of mechanisms of acquired resistance to EGFR-TKI therapy in 155 patients with EGFR-mutant lung Cancers. Clin Cancer Res 2013; 19: 2240-7.

Girard L, Zöchbauer-Müller S, Virmani AK, Gazdar AF, Minna JD. Genome-wide allelotyping of lung cancer identifies new regions of allelic loss, differences between small cell lung cancer and non-small cell lung cancer, and loci clustering. Cancer Res 2000; 60: 4894-906.

Warren S. Multiple primary malignant tumors. A survey of the literature and a statistical study. Am J Cancer 1932; 16: 1358-414.

Goldstraw P, Chansky K, Crowley J, Rami-Porta R, Asamura H, Eberhardt WEE, et al. The IASLC lung cancer staging project: proposals for revision of the TNM stage groupings in the forthcoming (eighth) edition of the TNM classification for lung cancer. J Thorac Oncol 2016; 11: 39-51.

Mountain CF. Revisions in the international system for staging lung cancer. Chest 1997; 111: 1710-7.

Rami-Porta R, Giroux DJ, Goldstraw P. The new TNM classification of lung cancer in practice. Breathe 2011; 7348-60.

Loukeri AA, Kampolis CF, Ntokou A, Tsoukalas G, Syrigos K. Metachronous and synchronous primary lung cancers: diagnostic aspects, surgical treatment, and prognosis. Clin Lung Cancer 2015; 16: 15-23.

Roberts PF, Straznicka M, Lara PN, Lau DH, Follette DM, Gandara DR, et al. Resection of multifocal non-small cell lung cancer when the bronchioloalveolar subtype is involved. J Thorac Cardiovasc Surg 2003; 126: 1597-601.

Shimada Y, Saji H, Otani K, Maehara S, Maeda J, Yoshida K, et al. Survival of a surgical series of lung cancer patients with synchronous multiple ground-glass opacities, and the management of their residual lesions. Lung Cancer 2015; 88: 174-80.

Riquet M, Cazes A, Pfeuty K, Ngabou UD, Foucault C, Dujon A, et al. Multiple lung cancers prognosis: what about histology? Ann Thorac Surg 2008; 86: 921-6.

Voltolini L, Rapicetta C, Luzzi L, Ghiribelli C, Paladini P, Granato F, et al. Surgical treatment of synchronous multiple lung cancer located in a different lobe or lung: high survival in node-negative subgroup. Eur J Cardiothoracic Surg 2010; 37: 1198-204.

Fabian T, Bryant AS, Mouhlas AL, Federico JA, Cerfolio RJ. Survival after resection of synchronous non-small cell lung cancer. J Thorac Cardiovasc Surg 2011; 142: 547-53.

Kocaturk CI, Gunluoglu MZ, Cansever L, Demir A, Cinar U, Dincer SI, et al. Survival and prognostic factors in surgically resected synchronous multiple primary lung cancers. Eur J Cardiothoracic Surg 2011; 39: 160-6.

van Rens MTM, Zanen P, de la Rivière AB, Elbers HRJ, van Swieten HA, van den Bosch JMM. Survival after resection of metachronous non-small cell lung cancer in 127 patients. Ann Thorac Surg 2001; 71: 309-13.

Tanvetyanon T, Robinson L, Sommers KE, Haura E, Kim J, Altiok S, et al. Relationship between tumor size and survival among patients with resection of multiple synchronous lung cancers. J Thorac Oncol 2010; 5: 1018-24.

Finley DJ, Yoshizawa A, Travis W, Zhou Q, Seshan VE, Bains MS, et al. Predictors of outcomes after surgical treatment of synchronous primary lung cancers. J Thorac Oncol 2010; 5: 197-205.

Okada M, Yamagishi H, Satake S, Matsuoka H, Miyamoto Y, Yoshimura M, et al. Survival related to lymph node involvement in lung cancer after sleeve lobectomy compared with pneumonectomy. J Thorac Cardiovasc Surg 2000; 119: 814-9.

Rea F, Zuin A, Callegaro D, Bortolotti L, Guanella G, Sartori F. Surgical results for multiple primary lung cancers. Eur J Cardio-Thoracic Surg 2001; 20: 489-95.

Armato SG, Roberts RY, Kocherginsky M, Aberle DR, Kazerooni EA, Macmahon H, et al. Assessment of radiologist performance in the detection of lung nodules: dependence on the definition of “truth”. Acad Radiol 2009; 16: 28-38.

Detterbeck FC, Lewis SZ, Diekemper R, Addrizzo-Harris D, Alberts WM. Executive summary: diagnosis and management of lung cancer,3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013; 143: 7-37.

Kozower BD, Larner JM, Detterbeck FC, Jones DR. Special treatment issues in non-small cell lung cancer: Diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013; 143: e369S99S.

Sugimura H, Nichols FC, Yang P, Allen MS, Cassivi SD, Deschamps C, et al. Survival after recurrent nonsmall-cell lung cancer after complete pulmonary resection. Ann Thorac Surg 2007; 83: 409-18.

Johnson BE, Cortazar P, Chute JP. Second lung cancers in patients successfully treated for lung cancer. Semin Oncol 1997; 24: 492-9.

Pairolero PC, Williams DE, Bergstralh EJ, Piehler JM, Bernatz PE, Payne WS. Postsurgical stage I bronchogenic carcinoma: morbid implications of recurrent disease. Ann Thorac Surg 1984; 38: 331-8.

Martini N, Bains MS, Burt ME, Zakowski MF, McCormack P, Rusch VW, et al. Incidence of local recurrence and second primary tumors in resected stage I lung cancer. J Thorac Cardiovasc Surg 1995; 109: 120-9.

Hung JJ, Hsu WH, Hsieh CC, Huang BS, Huang MH, Liu JS, et al. Post-recurrence survival in completely resected stage I non-small cell lung cancer with local recurrence. Thorax 2009; 64: 192-6.

Watanabe Y, Shimizu J, Oda M, Tatsuzawa Y, Hayashi Y, Iwa T. Second surgical intervention for recurrent and second primary bronchogenic carcinomas. Scand J Thorac Cardiovasc Surg 1992; 26: 73-8.

Dartevelle P, Khalife J. Surgical approach to local recurrence and the second primary lesion. In: Delarue NC, Eschapasse H, editors. International trends in general thoracic surgery. Vol 1. Philadelphia: Saunders 1985; 156-63.

Regnard JF, Icard P, Magdeleinat P, Jauffret B, Fares E, Levasseur P. Completion pneumonectomy: experience in eighty patients. J Thorac Cardiovasc Surg 1999; 117: 1095-101.

Zimmermann FB, Molls M, Jeremic B. Treatment of recurrent disease in lung cancer. Semin Surg Oncol 2003; 21: 22-7.

Yano T, Hara N, Ichinose Y, Asoh H, Yokoyama H, Ohta M, et al. Local recurrence after complete resection for non-small-cell carcinoma of the lung: significance of local control by radiation treatment. J Thorac Cardiovasc Surg 1994; 107: 8-12.

Yoshino I, Yohena T, Kitajima M, Ushijima C, Nishioka K, Ichinose Y, et al. Survival of non-small cell lung cancer patients with postoperative recurrence at distant organs. Ann Thorac Cardiovasc Surg 2001; 7: 204-9.

Downloads

Published

2023-04-19

How to Cite

Kocatürk, C. İbrahim. (2023). Synchronous, Metachronous or Metastases?. European Journal of Therapeutics, 24(S1), S44-S51. https://doi.org/10.5152/EurJTher.2018.1010

Issue

Section

Original Articles