Erlotinib in Pancreatic Cancer: A Major Breakthrough?

OncologyONCOLOGY Vol 21 No 14
Volume 21
Issue 14

Erlotinib (Tarceva) is a human epidermal growth factor receptor type 1/epidermal growth factor receptor (HER1/EGFR) tyrosine kinase inhibitor initially approved by the US Food and Drug Administration for the treatment of patients with locally advanced or metastatic non–small-cell lung cancer after failure of at least one prior chemotherapy regimen. In this report, we present the pivotal study that led to the approval of erlotinib in combination with gemcitabine (Gemzar) in patients with locally advanced/metastatic chemonaive pancreatic cancer patients. The combination demonstrated a statistically significant increase in overall survival accompanied by an increase in toxicity. Physicians and patients now have a new option for the treatment of locally advanced/metastatic adenocarcinoma of the pancreas.


Since the approval of gemcitabine (Gemzar) a decade ago for advanced pancreatic cancer, a number of studies have been conducted-many of them investing enormous time, effort, and patient resources-to evaluate the benefit of combining gemcitabine with other therapeutic agents. The vast majority of these studies have been disappointingly negative, failing to demonstrate any significant prolongation of survival using a gemcitabine-containing combination. Thus, the PA.3 trial conducted by the National Cancer Institute of Canada was a landmark study of sorts in that it was the first phase III trial in advanced pancreatic cancer to show a survival advantage with the addition of a second drug, in this case the oral epidermal growth factor receptor (EGFR) inhibitor erlotinib (Tarceva), to gemcitabine.

When the data were first presented in 2005, many oncologists responded with a fair degree of skepticism: the median survival difference between the two arms was only 2 weeks (6.4 vs 6.0 months, gemcitabine plus erlotinib vs gemcitabine plus placebo, respectively). However, the hazard ratio for survival-reflecting the difference in survival between the two arms over time, rather than at a predefined static time point-was 0.81, suggesting a 19% reduction in the risk of death for patients receiving combination therapy. Nevertheless, these results led to the obvious question: even if something is statistically significant, is it clinically meaningful?


Survival vs Toxicity

One might argue that in a disease with as poor a prognosis as pancreatic cancer, even a very modest benefit in outcomes can be important to patients. However, the necessary corollary to this argument is to evaluate whether any modest increments in longevity are counterbalanced by the greater toxicities caused by study treatment. Looking at the data from PA.3, it is not surprising that patients receiving gemcitabine plus erlotinib did have side effects more frequently than those receiving gemcitabine monotherapy. These included both expected toxicities (rash, diarrhea) as well as several that were less anticipated (stroke, cardiac events, thromboembolic events, and interstitial lung disease, to name a few). Whether these potential adverse events outweigh the modest benefits in survival is obviously a very subjective decision, based on a patient's threshold for accepting risk and the relative merits (s)he may place on quantity vs quality of life.

The ability to make such a decision might be easier were we to have information regarding the likelihood of a patient's responding, or not responding, to a given therapy a priori. This more individualized, "patient-tailored" strategy to decision-making (as opposed to a one-size-fits-all approach) has already borne fruit in a number of other solid tumors, such as lung and breast cancer,[1,2] in which molecular analysis of tumor tissue for expression of single genes, or expression patterns of a combinatorial set of genes, has shown to be a useful tool in guiding selection of therapeutic agents.

By contrast, one of the great obstacles in pancreatic cancer is the difficulty in obtaining adequate tumor material for such detailed interrogation, as the vast majority of patients have inoperable disease at presentation and are usually diagnosed by fine-needle aspiration or cytologic brushings during endoscopic retrograde cholangiopancreatogram (ERCP). This barrier was illustrated quite clearly in the PA.3 trial, in which only a quarter of study patients had tumor samples available for assessment of EGFR status. Although the numbers were clearly too small to make any definitive conclusions, the fact that benefit derived from erlotinib seemed to be independent of EGFR expression is consistent with other studies assessing this class of agents in certain solid tumors.[3]


K-ras Mutational Status

Besides intratumoral EGFR expression, analysis of the mutational status of the K-ras oncogene represents another possibility that could help decide whether or not to use erlotinib in pancreatic cancer, given the mounting evidence that mutated K-ras predicts for lack of sensitivity to EGFR inhibitors.[4,5] Investigators of the PA.3 trial did examine, post hoc, K-ras mutational status as a predictor for treatment benefit in the subset of study patients in whom tumor tissue was available (n = 117).[6] While a trend toward greater benefit of erlotinib for overall survival was observed in the 21% of evaluable patients with wild-type K-ras (hazard ratio = 0.66), this finding was not statistically significant (P = .34). Again, however, this perhaps reflected inadequate sample size rather than indicating a truly negative result. Going forward, study designs in pancreatic cancer may very well mandate acquisition of tumor material prior to initiation of treatment-the technical challenges of doing so notwithstanding-so that these kinds of analyses can be performed with greater power. Such an approach may in the future lead to more rational selection of therapy for any given individual based on his or her unique tumor characteristics.



In the end, does the US Food and Drug Administration approval of erlotinib for use in combination with gemcitabine in patients with advanced pancreatic cancer establish a new standard of care? Certainly, it is a small positive step in the right direction for a disease in which negative phase III studies had been becoming the norm. Moreover, the approval provides an important proof of concept regarding the use of newer "targeted" therapies in pancreatic cancer.

Other combination regimens, including gemcitabine plus capecitabine and gemcitabine plus a platinum analog, have also demonstrated some measure of benefit (including survival) in phase III studies and meta-analyses,[7-9] and may be equally appropriate alternatives to consider for select patients, particularly those with good performance status. Thus, until the day when we are able to more rationally select which agents should be used for any given patient with advanced pancreatic cancer, gemcitabine plus erlotinib can be considered as one of several acceptable choices-with the obvious caveat that the best option still, whenever possible, is participation in well-designed clinical trials that hopefully will provide further breakthroughs and insight into this challenging disease.


-Andrew H. Ko, MD


Dr. Ko has received clinical research support from Genentech, Eli Lilly, ImClone, Sanofi-Aventis, and AstraZeneca and is a member of the speakers bureau for Roche.


1. Olaussen KA, Dunant A, Fouret P, et al: DNA repair by ERCC1 in non-small-cell lung cancer and cisplatin-based adjuvant chemotherapy. N Engl J Med 355:983-991, 2006.

2. Paik S, Tang G, Shak S, et al: Gene expression and benefit of chemotherapy in women with node-negative, estrogen receptor-positive breast cancer. J Clin Oncol 24:3726-3734, 2006.

3. Tsao MS, Sakurada A, Cutz JC, et al: Erlotinib in lung cancer-molecular and clinical predictors of outcome. N Engl J Med 353:133-144, 2005.

4. Eberhard DA, Johnson BE, Amler LC, et al: Mutations in the epidermal growth factor receptor and in KRAS are predictive and prognostic indicators in patients with non-small-cell lung cancer treated with chemotherapy alone and in combination with erlotinib. J Clin Oncol 23:5900-5909, 2005.

5. Khambata-Ford S, Garrett CR, Meropol NJ, et al: Expression of epiregulin and amphiregulin and K-ras mutation status predict disease control in metastatic colorectal cancer patients treated with cetuximab. J Clin Oncol 25:3230-3237, 2007.

6. Moore MJ, Santos GdC, Kamel-Reid S, et al: The relationship of K-ras mutations and EGFR gene copy number to outcome in patients treated with Erlotinib on National Cancer Institute of Canada Clinical Trials Group trial study PA.3 (abstract 4521). J Clin Oncol 25(18S):202s, 2007.

7. Cunningham D, Chau I, Stocken D, et al: Phase III randomised comparison of gemcitabine (GEM) versus gemcitabine plus capecitabine (GEM-CAP) in patients with advanced pancreatic cancer (abstract PS11). Eur J Cancer 3(suppl):4, 2005.

8. Herrmann R, Bodoky G, Ruhstaller T, et al: Gemcitabine plus capecitabine compared with gemcitabine alone in advanced pancreatic cancer: A randomized, multicenter, phase III trial of the Swiss Group for Clinical Cancer Research and the Central European Cooperative Oncology Group. J Clin Oncol 25:2212-2217, 2007.

9. Louvet C, Hincke A, Labianca R, et al: Increased survival using platinum analog combined with gemcitabine as compared to gemcitabine single agent in advanced pancreatic cancer (APC): Pooled analysis of two randomised trials, the GERCOR/GISCAD Intergroup Study and a German Multicenter Study (abstract 4003). J Clin Oncol 24(18S):179s, 2006.

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