Author: Tracey L. Evans, MD
Oral, targeted therapies represent an important advance for patients with metastatic non-small cell lung cancer (NSCLC), but only a minority of patients are eligible for these approaches. It is true, however, that agents such as gefitinib, afatinib, and erlotinib in EGFR-
mutated NSCLC and crizotinib in ALK
-translocated NSCLC are sufficiently efficacious and nontoxic that patients with these subtypes of lung cancer often warrant treatment even when they are in a weakened state.1
This cannot be said of cytotoxic chemotherapy, which, unfortunately, remains the only anticancer treatment option for the vast majority of patients with NSCLC. It is certainly possible that in an individual patient the risks of cytotoxic chemotherapy could exceed the benefits, and treatment with chemotherapy could lead to worse survival and quality of life. This is most likely to be the case in patients who are chemorefractory, whose cancer has progressed following multiple prior lines of chemotherapy, and in the initial treatment of less-robust patients in whom first-line chemotherapy has increased potential for morbidity and mortality.
Unfortunately, NSCLC frequently is a disease of the less robust as well as a disease of the elderly. The median age at diagnosis is 70 years. In an analysis of the national Surveillance, Epidemiology, and End Results (SEER) database from 2008 to 2012, 68.6% of patients diagnosed with lung cancer were 65 years or older, 36.7% were 75 or older, and 9.1% were 84 years or older.2
Approximately one-third to one-half of all patients with lung cancer have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 2 to 4.3
In spite of their overrepresentation within our practices, these subgroups of patients have been underrepresented in the clinical trials that have established the standard-of-care treatment for advanced NSCLC.
Historical Data for Chemotherapy in the Elderly and Patients With Poor PS
The benefit of platinum-based chemotherapy in advanced NSCLC was definitively accepted only 2 decades ago, with the publication of a meta-analysis of platinum-based chemotherapy compared with best supportive care (BSC). ECOG 1594,4
a randomized comparison of 4 platinum-based doublets in advanced NSCLC, solidified the equivalent efficacy of the majority of the current preferred first-line platinum partners: paclitaxel, docetaxel, and gemcitabine. Only pemetrexed5
have been added to the first-line armamentarium since then. However, only 20% of the patients included in the ECOG 1594 trial were 70 years or older.7,8
While the patients 70 years and older did as well as the younger patients, given the relative paucity of older patients relative to the general population, it is reasonable to conclude that these patients represented particularly “fit” elderly patients who may not have been representative of older patients as a group. Other cooperative group trials in advanced NSCLC similarly had representation of elderly patients at less than 30%, and therefore may not be representative of the true elderly population.9-13
Initially, patients with ECOG PS 0-2 were permitted entry into ECOG 1594. However, among the initial 66 patients with ECOG PS 2, there was a high rate of serious adverse events (AEs), and median survival was only 3.9 months. The study eligibility was therefore amended to include only patients with ECOG PS 0 to 1.7,14
Therefore, although ECOG 1594 validated the current standard of care of platinum-based doublets when it was published in 2002, treatment of the general elderly population, as well as treatment of patients with ECOG PS 2 or greater, remained a very much open question. ECOG 4599, the study demonstrating the efficacy of bevacizumab added to chemotherapy, similarly included only patients with ECOG PS 0-1, and only 25% of patients enrolled were 70 years or older.10,15
Because of a lack of initial data supporting the use of first-line, platinum-based doublet chemotherapy in both the elderly and patients with poor-PS NSCLC, these 2 groups are often lumped together as “special populations.” It is important to realize, however, that while there is overlap between these populations, the challenges surrounding the use of chemotherapy in each of these populations are distinctly different, so evaluating these 2 groups separately is warranted. Determination of physiologic age, or an evaluation of life expectancy and functional reserve through a formal geriatric assessment, better correlates with chemotherapy tolerance than chronologic age. Patients with poor PS always demonstrate poor functional reserve, and whether that poor PS is determined by the cancer or other comorbidities may not be relevant to a patient’s ability to tolerate chemotherapy.
Given the concerns about chemotherapy in elderly patients, the first landmark study to look specifically at an elderly patient population included a BSC arm that was compared with single-agent vinorelbine. The Elderly Lung Cancer Vinorelbine Italian Study (ELVIS)13
randomly assigned 161 patients 70 years and older (range, 70-86 years) to either BSC or vinorelbine 30 mg/m2
on days 1 and 8, repeated every 3 weeks until disease progression or a maximum of 6 cycles. Overall survival (OS) was statistically improved for patients taking vinorelbine, with a median survival of 28 weeks versus 21 weeks in the BSC arm (P
= .03). The hazard ratio (HR) was 0.65 (95% CI, 0.45-0.93) in favor of the vinorelbine arm, in which the 1-year survival was 32% versus 14% in the BSC group. In addition, quality-of life-benefits, as determined by the European Organization for Research and Treatment of Cancer (EORTC) core questionnaire (QLQ-C30) and the lung cancer–specific module (QLQ-LC13), were observed in the vinorelbine arm. The ELVIS study therefore established single-agent chemotherapy as a reasonable standard of care in elderly patients with advanced NSCLC. The debate continued, however, as to whether the best approach in elderly patients was single-agent chemotherapy or the same platinum-based doublets used in younger patients. Proponents of the latter strategy argued that age is just a number and that there is no reason to adjust our standard-of-care approach based upon something so arbitrary. Indeed, it is the presence of comorbid conditions that better predicts poor outcomes in NSCLC rather than age.16
Defendants of the single-agent approach rightfully argued, however, that the elderly as a group have more comorbidities, and even those elderly who were deemed sufficiently fit to enroll in cooperative group studies of platinum-based doublet therapy nevertheless experienced increased toxicity compared with younger patients.8,12
Therefore, the only appropriate evidence-based approach established prospectively to demonstrate benefit within the elderly population was single-agent chemotherapy.
At the initiation of this debate, it was not necessarily clear that doublets were superior to modern single agents in any patient with advanced NSCLC. Therefore, this was the question posed by the CALGB 9730 trial.11
Patients with advanced NSCLC were randomly assigned to receive single-agent paclitaxel versus paclitaxel in combination with carboplatin. Survival was indeed better for the platinum-based doublet in the population as a whole (median survival). Twenty-seven percent of the patients enrolled in this study were 70 years or older. This was, however, still not an elderly-specific study. Mixed results were seen in randomized, elderly-specific approaches comparing non– platinum-based doublets versus single agents in the elderly.17,18
Ultimately, the question of whether the elderly are best served by single-agent or doublet chemotherapy was most directly addressed in a study by the French Intergroup.19
A total of 451 treatment-naïve patients aged 70 to 89 years were randomly assigned to either single-agent chemotherapy (vinorelbine or gemcitabine) versus a modified dosing schedule of carboplatin and paclitaxel (carboplatin administered at an area under the curve [AUC] 6 weeks with paclitaxel 90 mg/m2
on days 1, 8, and 15). Toxicity was increased in the doublet cohort, with more neutropenia and asthenia. However, survival was unequivocally improved in the doublet arm, with a median survival of 10.3 months and a 1-year survival of 45% versus, in the single-agent arm, a median survival of 6.2 months and a 1-year survival of 25% (P
<.0001). This survival benefit was realized even in the subgroup of patients older than 80 years (25% of the study population), as well as those with ECOG PS 2 (27% of total group). Therefore, it is now established
that for elderly patients with advanced NSCLC who wish to maximize OS, platinum-based doublet chemotherapy is the standard of care. A more recent comparison of carboplatin with either standard paclitaxel or albumin-bound paclitaxel (nab
-paclitaxel) showed similar efficacy overall, but rather surprisingly showed dramatically improved survival for the subgroup of patients 70 years and older in the nab
-paclitaxel arm (median survival, 19.9 vs 10.4 months; HR, 0.583; P
Elderly-specific trials of nab
-paclitaxel–based therapy are planned.
It remains less clear whether the addition of bevacizumab to cytotoxic chemotherapy improves outcomes for elderly patients. Patients 70 years and older made up 25% of the ECOG 4599 study10
(carboplatin/paclitaxel/bevacizumab vs carboplatin/ paclitaxel). Within the 70-years-and-older subgroup, there was no improvement in OS, and the older patients suffered more grade 3/4 toxicity. In an analysis that combined the carboplatin/paclitaxel/bevacizumab-treated patients from ECOG 4599 with the same arm from the PointBreak study (randomized comparison of carboplatin/paclitaxel/bevacizumab vs carboplatin/pemetrexed/bevacizumab), it did appear that the addition of bevacizumab to chemotherapy improved survival relative to carboplatin/paclitaxel for all age groups except those patients 75 years and older.21
However, in an analysis of the SEER database, patients age 65 years and older receiving carboplatin/ paclitaxel/bevacizumab fared no better than patients receiving only carboplatin and paclitaxel.22
In conclusion, first-line, platinum-based, cytotoxic chemotherapy should be offered to patients with advanced NSCLC and no actionable mutations regardless of age if maximizing OS is consistent with the patient’s goals. It is less clear from the data whether bevacizumab offers benefit, but it is reasonable to offer it to elderly patients who do not have contraindications to the taking bevacizumab.
Patients With PS 2
While the elderly have been underrepresented in many clinical trials, patients with poor PS have typically been excluded from clinical trials. It is fair to say that there is no evidence supporting the use of cytotoxic chemotherapy in patients with PS 3 or greater. Erlotinib has been used in patients with PS 3, and in the second- and third-line setting, erlotinib has been shown to be better than BSC in terms of progression-free survival (PFS) and OS in molecularly unselected patients.23
In a study of molecularly unselected patients felt to be unfit for first-line cytotoxic chemotherapy due to poor PS (≥2) and/or multiple comorbidities,24
erlotinib demonstrated improved PFS but not OS in the population as a whole. However, patients taking erlotinib who developed a rash did have an OS advantage relative to those receiving placebo.
Due to the generally poor outcomes of patients with poor PS treated with chemotherapy, the tendency has been to either not give chemotherapy at all or to give less toxic single-agent chemotherapy. It nevertheless stands to reason that if the patient’s poor PS is caused by the cancer, treating the cancer more aggressively may lead to improved outcomes. The previously mentioned CALGB 9730 study comparing carboplatin/ paclitaxel with single-agent paclitaxel in the first-line treatment of advanced NSCLC did permit enrollment of patients with PS 2.11
Only 99 such patients were enrolled, and as a group, these patients fared considerably worse than the those with PS 0-1. However, as with the group as a whole, the patients receiving doublet therapy did significantly better than those receiving single-agent paclitaxel. In fact, 9% of the patients with PS 2 in the doublet arm survived 2 years, while none of the patients with PS 2 treated with single-agent paclitaxel survived 2 years.
Once again, however, CALGB 9730 was not a study specific for patients with PS 2, so it could be argued that such a study is required. Fortunately, one now exists. In a study performed almost exclusively in Brazil, 205 patients with ECOG PS 2 with treatment-naïve, advanced NSCLC (later amended to include only nonsquamous histology) were assigned to either single-agent pemetrexed or the combination of pemetrexed plus carboplatin.25
The response rates (10.3% vs 23.8%; P
= .032) and PFS (2.8 vs 5.8 months; HR, 0.46; P
<.001) were significantly better in the combination arm. Most important, however, the OS was also significantly better; patients taking the combination had a median OS of 9.3 months versus 5.3 months for the patients treated with single-agent pemetrexed (HR, 0.62; P
= .001). One-year survival rates were 40.1% versus 21.9%, respectively. Not surprisingly, anemia and neutropenia were more frequently observed in the combination arm. It can therefore be concluded that for patients with PS 2 who are interested in maximizing OS and who are willing to undergo cytotoxic chemotherapy, carboplatin-based doublet therapy is indicated and is superior to single-agent therapy.
In summary, for patients with ECOG PS 2 who are diagnosed with advanced NSCLC and who do not have an actionable mutation, platinum-based doublet chemotherapy should be offered to those wishing to maximize OS.
In a way, the treatment recommendations for elderly patients and patients with ECOG PS 2 are simple. The most appropriate treatments for advanced NSCLC are exactly the same as for anyone else. Platinum-based doublet chemotherapy as first-line treatment for patients without actionable mutations is standard of care. That, however, is where the simplicity ends, because what is true of these so-called “special populations” is true of the treatment for all patients with advanced lung cancer: the treatment must be consistent with the patient’s individualized wishes and goals. In addition, immune checkpoint inhibitors display a side effect profile very different from that of traditional cytotoxic chemotherapy. Therefore, with the demonstrated efficacy of these agents in advanced NSCLC,26,27
we will once again need to sort out which patients may or may not be appropriate for treatment.
Tracey L. Evans, MD, is from the Abramson Cancer Center of the University of Pennsylvania.
Dr Evans is a board member of Wissahickon Hospice (nonprofit), and has served as a consultant or on a paid advisory board and received honoraria from Celgene Corporation, Eli Lilly and Company, and Genentech.
Address correspondence to:
Tracey L. Evans, MD, 2 Perelman West, 3400 Civic Center Blvd, Philadelphia, PA 19104; email email@example.com.
Inoue A, Kobayashi K, Usui K, et al. First-line gefitinib for patients with advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutations without indication for chemotherapy. J Clin Oncol. 2009;27(9):1394-1400.
Howlader N, Noone AM, Krapcho M, et al (eds). SEER Cancer Statistics Review, 1975-2012. April 2015. Bethesda, MD: National Cancer Institute. http://seer.cancer.gov/ csr/1975_2012/. Accessed June 22, 2015.
Lilenbaum R, Zukin M, Pereira JR, et al. A randomized phase III trial of single-agent pemetrexed (P) versus carboplatin and pemetrexed (CP) in patients with advanced non-small cell lung cancer (NSCLC) and performance status (PS) of 2. Presented at: the 2012 American Society of Clinical Oncology Annual Meeting; June 1-5, 2012; Chicago, IL. Abstract 7506.
Non-small Cell Lung Cancer Collaborative Group. Chemotherapy in non-small cell lung cancer: a meta-analysis using updated data on individual patients from 52 randomised clinical trials. BMJ. 1995;311(7010):899-909.
Scagliotti GV, Parikh P, von Pawel J, et al. Phase III study comparing cisplatin plus gemcitabine with cisplatin plus pemetrexed in chemotherapy-naive patients with advanced-stage non-small-cell lung cancer. J Clin Oncol. 2008;26(21):3543-3551.
Socinski MA, Langer CJ, Okamoto I, et al. Safety and efficacy of weekly nab®-paclitaxel in combination with carboplatin as first-line therapy in elderly patients with advanced non-small-cell lung cancer. Ann Oncol. 2013;24(2):314-321.
Schiller JH, Harrington D, Belani CP, et al. Comparison of four chemotherapy regimens for advanced non-small-cell lung cancer. N Engl J Med. 2002;346(2):92-98.
Langer CJ, Vangel M, Schiller JH. Age-specific subanalysis of ECOG 1594: fit elderly patients (70-80 yrs) with NSCLC do as well as younger pts (<70 years). Proc Am Soc Clin Oncol. 2003;22: 639.
Blanchard EM, Moon J, Hesketh PJ, et al. Comparison of platinum-based chemotherapy in patients older and younger than 70 years: an analysis of Southwest Oncology Group Trials 9308 and 9509. J Thorac Oncol. 2012;6(1):115-120.
Ramalingam SS, Dahlberg SE, Langer CJ, et al. Outcomes for elderly, advanced-stage non small-cell lung cancer patients treated with bevacizumab in combination with carboplatin and paclitaxel: analysis of Eastern Cooperative Oncology Group Trial 4599. J Clin Oncol. 2008;26(1):60-65.
Lilenbaum RC, Herndon JE, 2nd, List MA, et al. Single-agent versus combination chemotherapy in advanced non-small-cell lung cancer: the Cancer and Leukemia Group B (study 9730). J Clin Oncol. 2005;23(1):190-196.
Langer CJ, Manola J, Bernardo P, et al. Cisplatin-based therapy for elderly patients with advanced non-small-cell lung cancer: implications of Eastern Cooperative Oncology Group 5592, a randomized trial. J Natl Cancer Inst. 2002;94(3):173-181.
The Elderly Lung Cancer Vinorelbine Italian Study Group. Effects of vinorelbine on quality of life and survival of elderly patients with advanced non-small-cell lung cancer. J Natl Cancer Inst. 1999;91(1):66-72.
Sweeney CJ, Zhu J, Sandler AB, et al. Outcome of patients with a performance status of 2 in Eastern Cooperative Oncology Group Study E1594: a phase II trial in patients with metastatic nonsmall cell lung carcinoma. Cancer. 2001;92(10):2639-2647.
Sandler A, Gray R, Perry MC, et al. Paclitaxel-carboplatin alone or with bevacizumab for non-small-cell lung cancer. N Engl J Med. 2006;355(24):2542-2550.
Asmis TR, Ding K, Seymour L, et al. Age and comorbidity as independent prognostic factors in the treatment of non small-cell lung cancer: a review of National Cancer Institute of Canada Clinical Trials Group trials. J Clin Oncol. 2008;26(1):54-59.
Gridelli C, Perrone F, Gallo C, et al. Chemotherapy for elderly patients with advanced non-small-cell lung cancer: the Multicenter Italian Lung Cancer in the Elderly Study (MILES) phase III randomized trial. J Natl Cancer Inst. 2003;95(5):362-372.
Frasci G, Lorusso V, Panza N, et al. Gemcitabine plus vinorelbine yields better survival outcome than vinorelbine alone in elderly patients with advanced non-small cell lung cancer: a Southern Italy Cooperative Oncology Group (SICOG) phase III trial. Lung Cancer. 2001;34(suppl 4):S65-S69.
Quoix E, Zalcman G, Oster JP, et al. Carboplatin and weekly paclitaxel doublet chemotherapy compared with monotherapy in elderly patients with advanced non-small-cell lung cancer: IFCT-0501 randomised, phase 3 trial. Lancet. 2011;378(9796):1079-1088.
Socinski MA, Bondarenko I, Karaseva NA, et al. Weekly nab-paclitaxel in combination with carboplatin versus solvent-based paclitaxel plus carboplatin as first-line therapy in patients with advanced non-small-cell lung cancer: final results of a phase III trial. J Clin Oncol. 2012;30(17):2055-2062.
Langer CJ, Socinski MA, Patel JD, et al. Isolating the role of bevacizumab in elderly patients with previously untreated nonsquamous non-small cell lung cancer: secondary analyses of the ECOG 4599 and PointBreak trials [published online January 24, 2015]. Am J Clin Oncol.
Zhu J, Sharma DB, Gray SW, et al. Carboplatin and paclitaxel with vs without bevacizumab in older patients with advanced non-small cell lung cancer. JAMA. 2012;307(15):1593-1601.
Shepherd FA, Rodrigues Pereira J, Ciuleanu T, et al. Erlotinib in previously treated non-small-cell lung cancer. N Engl J Med. 2005;353(2):123-132.
Lee SM, Khan I, Upadhyay S, et al. First-line erlotinib in patients with advanced non-small-cell lung cancer unsuitable for chemotherapy (TOPICAL): a double-blind, placebo-controlled, phase 3 trial. Lancet Oncol. 2012;13(11):1161-1170.
Zukin M, Barrios CH, Pereira JR, et al. Randomized phase III trial of single-agent pemetrexed versus carboplatin and pemetrexed in patients with advanced non-small-cell lung cancer and Eastern Cooperative Oncology Group performance status of 2. J Clin Oncol. 2013;31(23):2849-2853.
Garon EB, Rizvi NA, Hui R, et al. Pembrolizumab for the treatment of non-small-cell lung cancer [published online April 19, 2015]. N Engl J Med.
Gettinger SN, Horn L, Gandhi L, et al. Overall survival and long-term safety of nivolumab (anti-programmed death 1 antibody, BMS-936558, ONO-4538) in patients with previously treated advanced non-small-cell lung cancer [published online April 20, 2015]. J Clin Oncol.