The more and the heavier may not always be an answer

The more and the heavier may not always be an answer

Hongryull Pyo1#, Se-Hoon Lee2#, Jhingook Kim3#

1Department of Radiation Oncology, 2Division of Hematology and Oncology, Department of Medicine, 3Department of Thoracic and Cardiovascular Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea

#These authors contributed equally to this work.

Correspondence to: Hongryull Pyo, MD, PhD. Professor, Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81, Irwon-ro, Gangnam-gu, Seoul 06351, Republic of Korea. Email:; Se-Hoon Lee, MD, PhD. Professor, Division of Hematology and Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81, Irwon-ro, Gangnam-gu, Seoul 06351, Republic of Korea. Email:; Jhingook Kim, MD. Professor, Department of Thoracic and Cardiovascular Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81, Irwon-ro, Gangnam-gu, Seoul, 06351, Republic of Korea. Email:

Provenance: This is an invited Editorial commissioned by the Section Editor Dr. Jie Dai (Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University, Shanghai, China).

Comment on: Francis S, Orton A, Stoddard G, et al. Sequencing of Postoperative Radiotherapy and Chemotherapy for Locally Advanced or Incompletely Resected Non-Small-Cell Lung Cancer. J Clin Oncol 2018;36:333-41.

Submitted Mar 29, 2018. Accepted for publication Apr 03, 2018.

doi: 10.21037/jtd.2018.04.127

Non-small cell lung cancer (NSCLC), especially locally advanced NSCLC, is difficult to treat. As patients with locally advanced NSCLC present no evidence of systemic spread, cure is suggested as the treatment goal. However, treatment outcomes are often unsatisfactory. Furthermore, this stage includes heterogeneous combinations of disease, ranging from T4 (invasion to heart, great vessel, or vertebrae) disease to mediastinal nodal invasions (N2 or N3). However, there is no doubt that locally advanced NSCLC should be treated with curative intent, using both local and systemic modalities.

Then, how should we manage patients with locally-advanced NSCLC by means of systemic and local control? As noted above, no definitive answer currently exists. Whether to perform surgery or radiotherapy as the local modality and whether chemotherapy should precede local therapy remain debated. Moreover, locally advanced NSCLC is more difficult to treat than other cancers because the patient’s functions are often impaired by the treatment. Therefore, we need to give special attention not only to short-term treatment-related toxicities but also to long-term systemic effects.

In cases where complete local control is unlikely to be achieved by surgery alone, such as resected locally advanced NSCLC or incompletely resected NSCLC, the optimal way to integrate chemotherapy and radiotherapy for adjuvant treatment remains unknown. Adjuvant chemotherapy has been shown to improve overall survival in several clinical trials (1). Postoperative radiotherapy (PORT) has also gained positive agreement for patients with pN2 disease or incomplete resection (2-4). However, although both therapies have been proven effective respectively, each treatment requires considerable time to deliver. Hence, it is difficult to deliver both treatments within an appropriate period after surgery. Therefore, ideal sequence of postoperative chemotherapy and RT remains controversial.

Postoperative concurrent chemoradiotherapy (CCRT) has been proposed as an alternative approach (5); however, two problems exist with this method. First, postoperative CCRT, after removal of the gross tumor, is associated with high toxicity. As such, the risk of adverse events may outweigh the potential benefits. Especially in patients with lung cancer, systemic performance is mostly affected by lung function. Therefore, treatment-related toxicities should be considered as the first priority. Even in early-stage lung cancer, the diffusion lung capacity for carbon monoxide (DLCO) and respiratory co-morbidities are associated with long-term prognosis (6,7). We should avoid treatments that are likely to significantly impair patient performance. Second, the role of chemotherapy in CCRT is known as a radio-sensitizer rather than as a systemic controller (8). The use of dose-reduced chemotherapy, to obviate the excessive toxicity that is associated with full-dose chemotherapy or radiotherapy, could potentiate the local control effect without impacting the systemic control of systemically overt metastatic lesions.

In the February 2018 issue of the Journal of Clinical Oncology, Francis and coworkers (9) discussed this controversial issue, based on relatively recent practical experiences using the National Cancer Database, between 2006 and 2012. It is very difficult to carry out reliable prospective studies, which require patient recruitment and effective treatment qualities. However, considering that this study used a modern radiotherapeutic-technique, it would be reasonable to modify or maintain treatment strategies based on the results of this study. In patients with complete resected (R0) NSCLC and pN2 disease, results of the propensity matching analysis in this study revealed that the postoperative CCRT was ineffective and associated with worse survival outcomes. Meanwhile, for patients with positive resection margins (mainly R1 resection), there were no statistically significant differences between sequential chemotherapy followed by PORT and CCRT. CCRT is generally associated with higher therapeutic toxicity than individual treatment modalities. Although this study did not demonstrate the risk of CCRT, this therapy should not be applied unless there is a benefit. In other words, after potentially hazardous surgery which regarded as a potentially hazardous procedure, CCRT is considered inappropriate.

Then what is the preferred sequence of chemotherapy and PORT? Some groups suggesting that chemotherapy should be used first argue that systemic control should be the main treatment, because recurrence patterns are mostly systemic. Other groups suggesting radiotherapy should be used first argue that completeness of local control is critically associated with recurrence free survival, and local tumor regrowth eventually causes systemic metastasis. Unfortunately, no studies have provided a clear answer to this question so far. However, from recent findings from liquid biopsy, circulating tumor cells (CTC) and cell-free DNA (cfDNA) are expected to be the potential surrogate markers for treatment decisions (10-12). For example, if CTC or cfDNA are detected after surgery, we can assume that chemotherapy could be performed first. If not, radiotherapy would be the first choice, or no adjuvant treatment needs to be performed.

In patients with macroscopically positive resection margins, there is no convincing evidence that CCRT is more beneficial than sequential approaches. Re-operation and the completion of local control is most desirable in this setting; however, such procedures are almost impossible to accomplish in clinical practice. Although there is no definite answer, on the basis of personal experience from surgical treatments for stage IIIa (N2) disease (13,14), macroscopically positive surgical margins should be regarded as non-surgical, and CCRT is more appropriate, whenever possible. Considering that sufficient chemotherapy or radiotherapy doses cannot be delivered immediately after surgery, reckless surgery where complete resection is unlikely should be avoided.

This study could not establish firm treatment guidelines for locally advanced lung cancer. However, regardless of the direction and degree of improvement, real-world clinical experience is very important, and generation of a national data system has contributed greatly to this improvement. It would also be very useful if national data from the US, Europe, and Asia are globally compiled and analyzed together. Moreover, if we know recurrence dynamics and patterns, which represent treatment failure mechanisms, we will acquire deeper insight into the proper ways to overcome the limitations of current therapies.


Authors appreciate Drs. Byung Jo Park, Junghee Lee and Jinseon Lee for their valuable contribution in the scientific discussion and manuscript preparation.


Conflicts of Interest: The authors have no conflicts of interest to declare.


  1. Pignon JP, Tribodet H, Scagliotti GV, et al. Lung Adjuvant Cisplatin Evaluation: A Pooled Analysis by the LACE Collaborative Group. J Clin Oncol 2008;26:3552-9. [Crossref] [PubMed]
  2. Robinson CG, Patel AP, Bradley JD, et al. Postoperative radiotherapy for pathologic N2 non-small-cell lung cancer treated with adjuvant chemotherapy: a review of the National Cancer Data Base. J Clin Oncol 2015;33:870-6. [Crossref] [PubMed]
  3. Mikell JL, Gillespie TW, Hall WA, et al. Postoperative radiotherapy is associated with better survival in non-small cell lung cancer with involved N2 lymph nodes: results of an analysis of the National Cancer Data Base. J Thorac Oncol 2015;10:462-71. [Crossref] [PubMed]
  4. Wang EH, Corso CD, Rutter CE, et al. Postoperative Radiation Therapy Is Associated With Improved Overall Survival in Incompletely Resected Stage II and III Non-Small-Cell Lung Cancer. J Clin Oncol 2015;33:2727-34. [Crossref] [PubMed]
  5. Shen WY, Ji J, Zuo YS, et al. Comparison of efficacy for postoperative chemotherapy and concurrent radiochemotherapy in patients with IIIA-pN2 non-small cell lung cancer: An early closed randomized controlled trial. Radiother Oncol 2014;110:120-5. [Crossref] [PubMed]
  6. Park B, Lee G, Kim HK, et al. A retrospective comparative analysis of elderly and younger patients undergoing pulmonary resection for stage I non-small cell lung cancer. World J Surg Oncol 2016;14:13. [Crossref] [PubMed]
  7. Eguchi T, Bains S, Lee MC, et al. Impact of Increasing Age on Cause-Specific Mortality and Morbidity in Patients With Stage I Non-Small-Cell Lung Cancer: A Competing Risks Analysis. J Clin Oncol 2017;35:281-90. [Crossref] [PubMed]
  8. Seiwert TY, Salama JK, Vokes EE. The concurrent chemoradiation paradigm—general principles. Nat Clin Pract Oncol 2007;4:86-100. [Crossref] [PubMed]
  9. Francis S, Orton A, Stoddard G, et al. Sequencing of Postoperative Radiotherapy and Chemotherapy for Locally Advanced or Incompletely Resected Non-Small-Cell Lung Cancer. J Clin Oncol 2018;36:333-41. [Crossref] [PubMed]
  10. Krebs MG, Sloane R, Priest L, et al. Evaluation and Prognostic Significance of Circulating Tumor Cells in Patients With Non-Small-Cell Lung Cancer. J Clin Oncol 2011;29:1556-63. [Crossref] [PubMed]
  11. Naito T, Tanaka F, Ono A, et al. Prognostic Impact of Circulating Tumor Cells in Patients with Small Cell Lung Cancer. J Thorac Oncol 2012;7:512-9. [Crossref] [PubMed]
  12. Tie J, Wang Y, Tomasetti C, et al. Circulating tumor DNA analysis detects minimal residual disease and predicts recurrence in patients with stage II colon cancer. Sci Transl Med 2016;8:346ra92. [Crossref] [PubMed]
  13. Kim HK, Cho JH, Choi YS, et al. Outcomes of neoadjuvant concurrent chemoradiotherapy followed by surgery for non-small-cell lung cancer with N2 disease. Lung Cancer 2016;96:56-62. [Crossref] [PubMed]
  14. Lee J, Kim HK, Park BJ, et al. Recurrence dynamics after trimodality therapy (Neoadjuvant concurrent chemoradiotherapy and surgery) in patients with stage IIIA (N2) lung cancer. Lung Cancer 2018;115:89-96. [Crossref] [PubMed]
Cite this article as: Pyo H, Lee SH, Kim J. The more and the heavier may not always be an answer. J Thorac Dis 2018;10(Suppl 17):S1953-S1955. doi: 10.21037/jtd.2018.04.127