aThe reasons patients with wild-type (wt), indeterminate, or unknown KRAS status were excluded were not captured at the time of exclusion.
bAmendment 5 limited trial eligibility to only patients with KRAS wild-type colorectal cancer in November 2008.
cThis double-biologic treatment group was dropped from the trial and primary analysis based on amendment 6, which was established September 2009.
dThe primary cohort comprises patients whose KRAS wt colorectal cancer was centrally confirmed by the Southwest Oncology Group and who had consented for the use of their specimens.
eReasons for ineligibility in the primary cohort were not captured.
fForty-nine tumor samples lacked sufficient DNA or analyses were incomplete.
Tick marks on the curves denote the last known follow-up time for patients with no death date reported. The hazard ratio and P value are adjusted for prior adjuvant therapy, prior radiotherapy, protocol chemotherapy, and randomization before and after the amendment restricting eligibility to the KRAS wild-type tumor. Hazard ratio and P value for the RAS analysis are adjusted for prior adjuvant therapy, prior radiotherapy, protocol chemotherapy, and randomization before or after the amendment restricting eligibility to KRAS wild type tumor (KRAS is defined as exon 2 codons 12, 13; exon 4, codons 117, 146; exon 3 codons 59, 61 or NRAS: exon 2 codons 12, 13; exon 3 codons 59, 61; exon 4 codons 117, 146).
eFigure 1. Kaplan-Meier Estimates of Progression-Free Survival (PFS) by Treatment
eFigure 2. Forest plots for comparisons of Overall Survival (OS) by Treatment Regimen Overall and within each level of Sex, Race and Chemotherapy. Hazard ratios and 95% Confidence Intervals are provided
eFigure 3. Progression-Free Survival (PFS) by Treatment among patients determined to be wt by expanded RAS analysis (KRAS: exon 2 codons 12, 13; exon 4, codons 117, 146; exon 3 codons 59, 61 or NRAS: exon 2 codons 12, 13; exon 3 codons 59, 61; exon 4 codons 117, 146)
eFigure 4. Overall Survival (OS) by Treatment Biologic among patients on the mFOLFOX6 Chemotherapy Regimen (Oxaliplatin 85 mg/m2 over 120 minutes, leucovorin 400 mg/m2 over 2 hours followed by 5FU 400 mg/m2 bolus then 5FU 2400 mg/m2 by 46-48 hour infusion)
eFigure 5. Overall Survival (OS) by Treatment Biologic among patients on the FOLFIRI Chemotherapy Regimen (Irinotecan 180 mg/m2 over 90 minutes, leucovorin 400 mg/m2 over 2 hours followed by 5FU 400 mg/m2 bolus then 5FU 2400 mg/m2 by 46-48 hour infusion)
eTable 1. Summary of Major Scientific Amendments to CALGB/SWOG 80405
eTable 2. Summary of Treatment Administration on CALGB/SWOG 80405 by Agent and Treatment Arm
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Venook AP, Niedzwiecki D, Lenz H, et al. Effect of First-Line Chemotherapy Combined With Cetuximab or Bevacizumab on Overall Survival in Patients With KRAS Wild-Type Advanced or Metastatic Colorectal Cancer: A Randomized Clinical Trial. JAMA. 2017;317(23):2392–2401. doi:10.1001/jama.2017.7105
Does the addition of cetuximab with a combination chemotherapeutic regimen improve overall survival compared with the addition of bevacizumab with a combination chemotherapeutic regimen as the initial treatment for patients with advanced or metastatic colorectal cancer who have KRAS wild-type tumors?
In this randomized clinical trial involving 1137 patients, there was no significant difference in overall survival among patients treated with either leucovorin, fluorouracil, and oxaliplatin (mFOLFOX6) or leucovorin, fluorouracil, and irinotecan (FOLFIRI) and then randomized to receive cetuximab or bevacizumab.
Neither biologic monoclonal antibody demonstrated significantly greater overall survival for initial treatment of advanced or metastatic colorectal cancer.
Combining biologic monoclonal antibodies with chemotherapeutic cytotoxic drugs provides clinical benefit to patients with advanced or metastatic colorectal cancer, but the optimal choice of the initial biologic therapy in previously untreated patients is unknown.
To determine if the addition of cetuximab vs bevacizumab to the combination of leucovorin, fluorouracil, and oxaliplatin (mFOLFOX6) regimen or the combination of leucovorin, fluorouracil, and irinotecan (FOLFIRI) regimen is superior as first-line therapy in advanced or metastatic KRAS wild-type (wt) colorectal cancer.
Design, Setting, and Participants
Patients (≥18 years) enrolled at community and academic centers throughout the National Clinical Trials Network in the United States and Canada (November 2005-March 2012) with previously untreated advanced or metastatic colorectal cancer whose tumors were KRAS wt chose to take either the mFOLFOX6 regimen or the FOLFIRI regimen as chemotherapy and were randomized to receive either cetuximab (n = 578) or bevacizumab (n = 559). The last date of follow-up was December 15, 2015.
Cetuximab vs bevacizumab combined with either mFOLFOX6 or FOLFIRI chemotherapy regimen chosen by the treating physician and patient.
Main Outcomes and Measures
The primary end point was overall survival. Secondary objectives included progression-free survival and overall response rate, site-reported confirmed or unconfirmed complete or partial response.
Among 1137 patients (median age, 59 years; 440 [39%] women), 1074 (94%) of patients met eligibility criteria. As of December 15, 2015, median follow-up for 263 surviving patients was 47.4 months (range, 0-110.7 months), and 82% of patients (938 of 1137) experienced disease progression. The median overall survival was 30.0 months in the cetuximab-chemotherapy group and 29.0 months in the bevacizumab-chemotherapy group with a stratified hazard ratio (HR) of 0.88 (95% CI, 0.77-1.01; P = .08). The median progression-free survival was 10.5 months in the cetuximab-chemotherapy group and 10.6 months in the bevacizumab-chemotherapy group with a stratified HR of 0.95 (95% CI, 0.84-1.08; P = .45). Response rates were not significantly different, 59.6% vs 55.2% for cetuximab and bevacizumab, respectively (difference, 4.4%, 95% CI, 1.0%-9.0%, P = .13).
Conclusions and Relevance
Among patients with KRAS wt untreated advanced or metastatic colorectal cancer, there was no significant difference in overall survival between the addition of cetuximab vs bevacizumab to chemotherapy as initial biologic treatment.
clinicaltrials.gov identifier: NCT00265850
Colorectal cancer is the second leading cause of cancer death in North America. Fluorouracil became the only cytotoxic drug indicated for colorectal cancer in the 1990s1 when the adoption of continuous infusion of this agent was found to have improved the median overall survival from 12 to 15 months.2 Since then, combination therapies of fluorouracil with leucovorin and either irinotecan (FOLFIRI regimen3) or oxaliplatin (mFOLFOX6 regimen4) were found to further improve survival and have become the main chemotherapeutic treatment options for colorectal cancer. A randomized crossover trial showed that these combination regimens were not statistically different, with patients receiving these agents in any sequence surviving a median 18 to 20 months.5,6
Cetuximab, a chimerized monoclonal antibody to the epidermal growth factor receptor (EGFR), was approved in combination with irinotecan or alone following irinotecan failure for patients with advanced or metastatic colorectal cancer whose tumors expressed EGFR.7 Subsequent evidence indicated that cetuximab activity was unrelated to tumor expression of EGFR.8 Bevacizumab, a humanized murine antihuman vascular endothelial growth factor (VEGF) monoclonal antibody, was then approved for patients with advanced colorectal cancer in combination with fluorouracil-based chemotherapy.9 The addition of cetuximab or bevacizumab to cytotoxic chemotherapeutic combinations proved feasible and appeared to be more active than cytotoxic chemotherapies alone.10 These new options for patients with advanced or metastatic colorectal cancer raised the question of which was the optimal biologic monoclonal antibody-chemotherapy combination.
This trial was conducted to determine if the addition of cetuximab vs bevacizumab to the mFOLFOX6 regimen or the FOLFIRI regimen was superior as first-line therapy in advanced or metastatic KRAS wild-type (wt) colorectal cancer.
The Cancer and Leukemia B and Southwest Oncology Group 80405 trial was designed in collaboration with the National Cancer Institute (NCI) and was started in September 2005 to compare various combinations of chemotherapies and biologic therapies as first-line treatment of advanced and metastatic colorectal cancer: (1) chemotherapies plus cetuximab; (2) chemotherapies plus bevacizumab; and (3) chemotherapies plus cetuximab and bevacizumab (The study protocol is available in Supplement 1). Within 3 years, the lack of efficacy of EGFR antibodies in KRAS-mutant tumors11 and failures of the dual antibody and chemotherapy combination treatments12,13 resulted in a pivotal amendment restricting eligibility to patients with confirmed KRAS wt tumors and then later to closure of the dual antibody group. After 10 years and additional amendments a revised 2-group trial (cetuximab vs bevacizumab with chemotherapy regimens) completed patient enrollment and follow-up (see eTable 1 in Supplement 2).
In 2010, the Cancer and Leukemia B group became a part of the Alliance for Clinical Trials in Oncology (Alliance). This cooperative research group performed critical aspects of the present study: (1) captured the clinical data; (2) performed all statistical analyses; (3) provided data and safety monitoring for toxicity and for preplanned interim efficacy analyses. The Southwest Oncology Group partner for the present study oversaw specimen biobanking and the distribution of samples to laboratory investigators.
Institutional review board approval was required at all participating centers and all participating patients provided written informed consent. Patients were enrolled at centers across the National Cancer Trials Network in the United States and Canada. Eligible patients had pathology-documented untreated locally advanced or metastatic colorectal cancer, although measurable disease (tumor that could be quantified) was not require. Patients had to be candidates for either mFOLFOX6 or FOLFIRI regimens without known central nervous system metastases or grade II or greater peripheral neuropathy. In addition, hypertension had to be well controlled (blood pressure <160/90 mm Hg with treatment) and there could be no concurrent congestive heart failure. Therapeutic anticoagulation was permitted as long as the patient was therapeutic on a stable dose of anticoagulant. Patients with a significant bleeding event within 6 months of enrollment or a gastrointestinal perforation within 12 months of enrollment were excluded unless the perforated bowel segment had been resected. Up to 6 months of prior adjuvant treatment had to have concluded at least 12 months before recurrence. Prior radiotherapy to 5040 cGy was allowed but could not have encompassed more than 25% of bone marrow. Patients were excluded if they had undergone major surgery within the last 4 weeks or minor surgery within the last 2 weeks.
National Cancer Institute trials are required to capture and report data on race/ethnicity. Data for patient covariates were captured in the NCI-standardized format and entered at the time of patient registration usually by a clinical research associate at the treating institution. Race/ethnicity was determined by self-report.
Patients were 18 years or older with an Eastern Cooperative Oncology Group performance status of 0 to 1 and normal hepatic, renal, and hematologic laboratory values. Initially, enrolled patients could consent to the biomarker companion study (Cancer and Leukemia Group B 150506) and submit a specimen for EGFR status evaluation. In November 2008, KRAS wt (codons 12 and 13) became an eligibility criterion. In September 2009, the combined treatment group of both cetuximab and bevacizumab with chemotherapeutic regimen was discontinued. Patients in that treatment group were removed from the study, received treatment at the discretion of their physician, and were followed up per protocol. Patients enrolled and consented to the companion study whose tumor was KRAS wt and who received single antibody treatment were included in the primary cohort. Patients with KRAS mutant tumors were excluded from analysis but were given the option to continue taking the study treatment.
Following the amendment restricting eligibility to patients with KRAS wt tumors, patients consented to be tested for KRAS and agreed to submit 2 archival paraffin-embedded tumor tissue sections and 1 histology reference slide or 1 paraffin-embedded tumor block to the Southwest Oncology Group Solid Tumor Specimen Repository. Patients with KRAS wt tumors were offered registration and randomization whereas patients with mutant KRAS tumors were ineligible. In July 2010, eligibility could be determined by testing for KRAS mutation in any Clinical Laboratory Improvement Amendments–certified laboratory, although specimen submission was mandated to confirm KRAS status by central review. Only patients with confirmed KRAS wt were included in this primary analysis. Following completion of the study, a subset of specimens were analyzed for expanded RAS status (see eMethods in Supplement 2 for KRAS and expanded RAS assays.)
The choice of either the mFOLFOX6 or FOLFIRI chemotherapeutic regimen was made by the patient and physician prior to trial enrollment and randomization. From November 2005 to September 2009 patients were randomized 1:1:1 to receive cetuximab, bevacizumab, or both of these biologic treatments in combination with either the mFOLFOX6 or FOLFIRI regimen. Thereafter, patients were randomized 1:1 to cetuximab or bevacizumab biologic treatment. At randomization, the primary physician indicated whether the treatment goal was palliative or potentially curative. Randomization was stratified by (1) chemotherapeutic regimen administered (mFOLFOX6; FOLFIRI), (2) receipt of prior adjuvant chemotherapy, and (3) prior pelvic radiation. Patients were stratified for statistical analysis by the time of enrollment either before or after the KRAS amendment. Treatment assignments were generated according to randomly permuted blocks within strata. A fixed-block size of 9 was used prior to the study amendment that stopped enrollment into the double-biologic group. Afterward, a block size of 6 was used.
Cetuximab or bevacizumab was administered prior to cytotoxic chemotherapies: 400 mg/m2 of cetuximab was infused intravenously over 120 minutes on day 1, then 250 mg/m2 over 60 minutes every week, and 5 mg/kg of bevacizumab was infused over 90 minutes in week one. Assuming no adverse reactions, subsequent infusions were administered over 30 to 60 minutes every other week.
The FOLFIRI regimen was administered as 180 mg/m2 of irinotecan over 90 minutes and 400 mg/m2 of leucovorin over 2 hours followed by a 400-mg/m2 bolus of fluorouracil, then a 2400-mg/m2 bolus of fluorouracil by a 46- to 48-hour infusion repeated every 2 weeks. The mFOLFOX6 regimen was administered as 85 mg/m2 of oxaliplatin over 120 minutes and 400 mg/m2 of leucovorin over 2 hours followed by a 400-mg/m2 bolus of fluorouracil then a 2400-mg/m2 bolus of fluorouracil by a 46- to 48-hour infusion repeated every 2 weeks.
Patients received routine supportive care at the discretion of the treating physician. Standard-dose adjustment criteria were applied to both mFOLFOX6 and FOLFIRI regimens. Treatment for the acneiform skin reaction was at the discretion of the treating physician. Patients experiencing oxaliplatin or other infusion reactions were not rechallenged with treatment. Adverse events were assessed using the NCI Common Toxicity Criteria version 3.0.
The primary end point of overall survival was defined as time of study entry until death. Patients without reported deaths were censored at their last known follow-up. Secondary end points included response rate (site-reported confirmed or unconfirmed complete or partial response by RECIST [Response Evaluation Criteria in Solid Tumors]) and progression-free survival measured from study entry until first documented progression or death. For the progression-free survival end point, patients alive without documented tumor progression were censored for progression at the most recent disease assessment. An additional secondary end point was 60-day mortality assessed as the proportion of patients dying due to any cause within 60 days of beginning protocol therapy. The incidence of arterial thrombotic events in each treatment group was monitored throughout the trial. Patients were evaluated every 8 weeks for response by conventional cross-sectional imaging using the RECIST v1.0 criteria.14 Patients maintained their study treatment until disease progression, unacceptable toxic effects, a gap of more than 28 days between treatments, or decision to discontinue treatment. Disease assessment was done by the treating investigator and was not blinded.
The primary statistical analyses were 2-sided tests of superiority comparing cetuximab vs bevacizumab with regard to the primary and main secondary outcomes among patients whose tumors were determined to be KRAS wt (exon 2, codons 12,13) by Southwest Oncology Group review using intention-to-treat analyses. Sample-size calculations considered a median overall survival of 22.0 months with bevacizumab based on Hurwitz et al9 and a clinically meaningful difference of 5 to 6 months in median overall survival. The trial was designed to target a hazard ratio (HR) of 0.80 (an improvement from 22 to 27.5 months) with 90% power (2-sided α = .05). Based on these factors, 1142 patients and 849 primary outcome events were needed.
Interim analyses were conducted every 6 months after 15% of the expected number of overall survival outcome events were observed. The 2-sided Lan-DeMets analogue of O’Brien-Fleming boundaries was used to test the null hypothesis at each interim analysis according to the stratified log-rank test. Boundaries were truncated at 2.58; based on the actual boundaries used in the analyses, the 2-sided adjusted significance level at the final analysis was .06. A progression-free survival HR of 0.76 was detectable with 85% power based on a log-rank test (526 events; 2-sided α = .05). The Kaplan-Meier method was used to estimate overall and progression-free survival. The stratified log-rank test was used to compare overall survival between the biologics. No adjustments were made for multiple comparisons in the analysis of secondary end points. Thus, these analyses should be considered exploratory. Proportional hazards modeling was used to estimate HRs and associated 95% confidence intervals and to test interactions of sex, race (white vs nonwhite), and chemotherapy by treatment. Because white patients comprised 82% of the study sample, levels of race were collapsed to white vs nonwhite race for data analysis. Ethnicity was not considered other than descriptively. Hazard ratio estimates were adjusted for prior adjuvant therapy, prior radiotherapy, protocol chemotherapy, and randomization before and after the study was amended. Due to the large number of enrollment sites, this variable was not considered in the analysis. Subset analyses were conducted in the expanded RAS, mFOLFOX6, and FOLFIRI subgroups. In addition, κ statistics were used to estimate agreement between institutional and central review of KRAS status.
Power was approximately 0.92 to detect a difference of 0.1 in the magnitude of response between treatment groups at the final analysis (2-sided α = .05). Within each treatment group, the hypothesis that the arterial thrombotic event rate was 0.5 or less was tested against the alternative, 0.08 or higher; 90% power was achieved to test this hypothesis (n = 571; 1-sided α = .05). The lower 90% confidence bound estimate for the κ statistic was used to estimate assay agreement with 0.75 as a benchmark. Analyses are based on clinical data and patient follow-up as of December 15, 2015. Data collection and statistical analyses were conducted by the Alliance Statistics and Data Center (SAS v9.2, SAS Institute Inc; R 3.1.1, http://www.r-project.org). Data quality was reviewed and audited by the Alliance Statistics and Data Center and by the study chairperson following Alliance policies.
From September 2005 to March 2012, 3058 patients were preregistered or registered, and 2334 patients were randomized to 1 of 3 treatment groups at 396 study sites. Of these, 1137 patients with confirmed KRAS wt tumors received bevacizumab (n = 559) or cetuximab (n = 578). The 804 patients randomized after and the 333 patients registered before the KRAS amendment was implemented comprise the final primary analysis cohort (Figure 1). Data were released by the Alliance Data and Safety Monitoring Board in January 2014 after the 11th interim analysis concluded with high probability that neither treatment group could meet the preplanned goal of a 5.5-month superior overall survival compared with the other. Results are reported for (1) the primary 2-group comparison between cetuximab and bevacizumab; (2) the comparison of cetuximab vs bevacizumab in an expanded RAS subset described above; and (3) the chemotherapy subgroups.
Patient and tumor characteristics are presented in Table 1. The treatment groups were well-balanced for age, sex, race, performance status, and site of primary tumor. Cure was the intent for 17.1% (99 of 578) of patients in the cetuximab group vs 13.2% (74 of 559) in the bevacizumab group. Ninety-six percent (1096 of 1137) of randomized patients with confirmed KRAS wt tumors started protocol therapy; 15 patients (1.1%) reported that they “withdrew prior to beginning protocol therapy” for an off-treatment reason: 7, bevacizumab; 8 ,cetuximab (Figure 1). See treatment administration and dose modification summary for details (eTable 2 in Supplement 2).
All randomized patients with confirmed KRAS wt tumors were evaluated. Among 235 patients enrolled with KRAS wt status by local assessment, 228 were confirmed by the Southwest Oncology Group (0.97; 95% CI, 0.94-0.99); the κ estimate for 239 patients with complete data was 0.52 with a 90% lower confidence bound estimate of 0.32. Of 1137 patients, 874 (76.9%) patients died. Median follow-up for surviving patients (n = 263) was 47.4 months (range, 0.0-110.7 months). Eighty-two percent of patients (938 of 1137) experienced disease progression. No significant differences were observed for either overall survival or progression-free survival in the primary analysis cohort. Median overall survival was 30.0 months in the cetuximab-chemotherapy group and 29.0 months in the bevacizumab-chemotherapy group (stratified HR, 0.88; 95% CI, 0.77-1.01; P = .08). Median progression-free survival was 10.5 months in the chemotherapy-cetuximab group and 10.6 months in the chemotherapy-bevacizumab (stratified HR, 0.95; 95% CI, 0.84-1.08; P = .45; Figure 2 and eFigure 3 in Supplement 1). Response rates were 55.2% (309 of 559) in the bevacizumab group and 59.6% (345 of 578) in the cetuximab group (difference, 4.4%; 95% CI, 1.0%-9.0%; χ2P = .13).
The combination of chemotherapy and surgery rendered 140 patients disease free; median overall survival for the bevacizumab group was 62.2 months (95% CI, 49.4 months to not reached) and 64.7 months for the cetuximab group (95% CI, 51.6 months to not reached). Fifty-eight patients remained alive and disease free on the last data survey.
Unplanned subgroup analyses were conducted for the expanded RAS, sex, race, and chemotherapy subsets. The results for overall survival (HR, 0.88; 95% CI, 0.72-1.08) and progression-free survival (HR, 1.03; 95% CI, 0.86-1.24) in the expanded RAS wt cohort were similar to those in the full cohort (Figure 2 and eFigure 3 in Supplement 2). Baseline characteristics were comparable between patients with and without expanded RAS results. No significant interactions were observed for sex (HR for interaction, 0.92; 95% CI, 0.70-1.21) or race (HR for interaction, 1.04; 95% CI, 0.71-1.51) by biologic. A difference in overall survival was observed with mFOLFOX6 in favor of cetuximab (HR, 0.83; 95% CI, 0.71-0.98; eFigure 4 in Supplement 2) but not with FOLFIRI, for which the HR for overall survival was 1.04 (CI 95%, 0.79-1.35). The chemotherapy by biologic interaction HR for overall survival was 1.27 (95% CI, 0.94-1.73; P for interaction, .11; eFigures 4 and 5 in Supplement 2).
Among 1137 patients, 1092 patients (96%) reported at least 1 adverse event: 584 patients (53%) experienced grade 3 or higher and 153 (14%) experienced grade 4 or higher adverse events. Thirty-one patients died while receiving the protocol therapy: 16, bevacizumab; 15, cetuximab. The deaths of 8 patients in the bevacizumab group and 7 in the cetuximab group could possibly be related to the protocol treatment. Adverse events reported in at least 10% of patients were not different across groups (Table 2). Toxic effects that were lower than grade 3 were distinct with acneiform rash predominating for cetuximab and hypertension predominating for bevacizumab. The rate of arterial thrombotic events was not statistically higher than 5% on either regimen. No significant difference in 60-day mortality was observed (1.4% [8 of 555] for bevacizumab; 2.0% [12 of 571] for cetuximab (Fisher exact test, P = .50).
In this clinical trial involving patients with advanced or metastatic KRAS wt colorectal cancer, there was no significant difference in overall survival with treatment using cetuximab vs bevacizumab added to the mFOLFOX6 or FOLFIRI chemotherapeutic regimens as first-line treatments. These findings persisted following exclusion of patients with any RAS mutations.
When planning this randomized clinical trial, a 22-months’ median survival was expected for the combination of bevacizumab and the chemotherapeutic regimen, yet survival was at least 29 months in both groups. Better chemotherapeutic regimens, patient selection, and changing multidisciplinary management likely contributed to these outcomes as did the exclusion of patients with KRAS mutations. This eligibility change increased the proportion of study patients who might benefit from cetuximab but also improved the prognosis for the entire group by eliminating patients with negatively prognostic RAS mutations. Also, patients in this study likely had lower tumor burden compared with patients who participated in earlier studies as a result of better imaging at diagnosis as well as the coincidental detection of small cancers when patients undergo diagnostic imaging for other indications. The majority of patients also had access to both cetuximab and bevacizumab at progression because each biologic therapy was commercially available. Patients who received any subsequent treatment could have changed chemotherapy and either crossed over to or continued with bevacizumab beyond tumor progression.15 Twelve percent of patients were rendered temporarily disease free (41% remained without evidence of cancer at a median of 5.5 years’ follow-up) with surgery of all sites of disease. This also contributed to the survival results. In addition, some patients may have benefitted from subsequent experimental or off-label treatments,
These results differ from 2 smaller but contemporary studies that asked a similar question. First, the FIRE-3 trial (n=592) led by the Arbeitsgemeinschaft Internistische Onkologie cooperative group (AIO)16 also compared cetuximab and bevacizumab but differed from the present study in that the chemotherapy was limited to FOLFIRI and the primary outcome was investigator-adjudicated response rate. This trial found no significant difference in response rate (62% vs 58%, P = .18) between cetuximab and bevacizumab biologic therapies. However, overall survival favored cetuximab by 3.7 months (28.7 vs 25.0 months) and was even more favorable with expanded RAS analysis (33.1 vs 25.6 months; P = .011). Second, the PEAK (Panitumumab Efficacy in Combination With mFOLFOX6 Against Bevacizumab Plus mFOLOFOX6 in mCRC Subjects With Wild-Type KRAS Tumors) trial17 enrolled 285 patients but compared panitumumab (a fully humanized anti-EGFR antibody) to bevacizumab in combination with FOLFOX. The primary outcome of progression-free survival was not statistically different between the panitumumab and bevacizumab treatment groups (10.9 vs 10.1 months, P = .35). However, there was a significant difference in overall survival between panitumumab and bevacizumab (34.2 vs 24.3 months; P = .009).
Neither of these studies mandated subsequent treatment choices (although FIRE-3 had recommended specific second-line treatments per protocol). Furthermore, the variances in management preferences across the world can have important effects on overall survival. The FIRE-3 investigators made an effort to document subsequent treatments and postulated that patients receiving first-line cetuximab treatment would have better overall survival because of a biological advantage when an EGFR inhibitor is followed by bevacizumab.18 However, a poorer overall survival for patients receiving bevacizumab in FIRE-3 compared with this study accounts for most of the survival difference (expanded RAS, chemotherapy + bevacizumab, overall survival for 80405 was 31.2 months; for FIRE-3,25.6 months). The use of bevacizumab beyond progression after FOLFIRI and bevacizumab18 in patients in the FIRE-3 study (11% of the 68% of patients who received any second-line treatment) is infrequent compared with its routine use in the United States. This is speculative, however, because the collection of subsequent treatment details across hundreds of sites in North America is extremely difficult and the details of such data would be open to questioning no matter the resources put into such an effort. Therefore, the sequencing theory promulgated by FIRE-3 investigators is not addressed.
This study has several limitations. First, the imbalance in choice of mFOLFOX6 vs FOLFIRI regimens limits the ability to statistically compare the cytotoxic chemotherapy regimens and any possible interaction with the antibodies. Second, this study only mandated first-line treatment with patients who at any time went more than 28 days without treatment being removed from study. Because treatment holidays were used more commonly during the course of the study and because collection of the details of treatment drugs and schedules, dosing and complications has been challenging, it is difficult to infer the effects of subsequent management decisions. Third, one element not included in the on-study information was primary cancer site (eg, right vs left colon). This information was collected post hoc through chart review and has been suggested to influence outcome as a biologic surrogate.19
Among patients with KRAS wt untreated advanced or metastatic colorectal cancer, there was no significant difference in overall survival between the addition of cetuximab vs bevacizumab to chemotherapy as initial biologic treatment.
Corresponding Author: Alan Venook, MD, University of California, San Francisco, 1450 Third St, HD 376, San Francisco, CA 94158 (email@example.com).
Accepted for Publication: May 25, 2017.
Author Contributions: Drs Venook and Niedzwiecki had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. In addition, Dr Niedzwiecki (Alliance Statistics and Data Center, Duke University Medical Center) and Mr Fruth (Alliance Statistics and Data Center, Mayo Clinic Cancer Center) conducted and are responsible for the statistical analyses.
Concept and design: Venook, Niedzwiecki, Lenz, Schrag, Goldberg, Schilsky, Bertagnolli, El-Khoueiry, Benson, Mayer, Blanke.
Acquisition, analysis, or interpretation of data: Venook, Niedzwiecki, Lenz, Innocenti, Fruth, Meyerhardt, Schrag, Greene, O'Neil, Atkins, Berry, Polite, O'Reilly, Goldberg, Hochster, Schilsky, El-Khoueiry, Watson, Benson, Mulkerin, Blanke.
Drafting of the manuscript: Venook, Niedzwiecki, Lenz, Innocenti, Fruth, Schrag, O'Neil, Bertagnolli, El-Khoueiry.
Critical revision of the manuscript for important intellectual content: Venook, Niedzwiecki, Lenz, Innocenti, Fruth, Meyerhardt, Schrag, Greene, O'Neil, Atkins, Berry, Polite, O'Reilly, Goldberg, Hochster, Schilsky, El-Khoueiry, Watson, Benson, Mulkerin, Mayer, Blanke.
Statistical analysis: Niedzwiecki, Fruth, Schrag.
Obtained funding: Schrag, Berry, Schilsky, Bertagnolli, Mayer.
Administrative, technical, or material support: Lenz, Innocenti, Schrag, Greene, Atkins, Berry, Polite, O'Reilly, Goldberg, Hochster, Schilsky, Bertagnolli, Mayer, Blanke.
Supervision: Venook, Lenz, Schrag, O'Neil, Goldberg, Hochster, Bertagnolli, Blanke.
Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Venook reports receiving grants from University of California, San Francisco, Genentech/Roche, and Bristol-Myers Squibb. Dr Lenz reported receiving support for clinical trials and for serving on the advisory boards and speakers bureaus for Genentech/Roche and Merck KG and for clinical trial support from Bristol-Myers Squibb. Dr Meyerhardt reports receiving personal fees from Genentech. Dr O'Neil reports receiving personal fees from Genentech, Lilly, and Bristol-Myers Squibb. Dr Berry reports serving on the advisory boards of Lilly, Amgen, Shire, and Celgene. Dr Polite reports receiving personal fees from Astra Zeneca and GLG Consulting and grant support from Merck. Dr Goldberg reports receiving personal fees from Lilly and Merck KGA. Dr Hochster reports receiving personal fees from Roche/Genentech, Bristol-Myers Squibb, Bayer, Amgen, Lilly, and Merck. Dr Schilsky reports receiving grant support from Bristol-Myers Squibb Co. Dr El-Khoueiry reports receiving grants from National Cancer Institute-CTEP; serving as a consultant for and on the advisory boards of Bristol-Myers Squibb, Bayer, Roche Genentech, Astra Zeneca, and Celgene; and serving on the speakers bureau of Merrimack. Dr Benson reports receiving personal fees and nonfinancial support from Bayer Health Care, Lilly, Taiho Pharmaceuticals, Novartis, Dava Oncology, Genentech, Emron, and the National Comprehensive Cancer Network; personal fees from Bristol-Myers Squibb, Celgene, Exelixis, Boston Biomedical Oncology, Coherus, EMD Serono, Guerbet, HalioDx, Helsinn, Lexicon Pharmaceuticals, Oncosil Medical, Opsana, and Pfizer; and nonfinancial support from Association of Community Cancer Centers, ECOG-ACRIN Cancer Research Group, and National Patient Advocate Foundation. Dr Mulkerin reports receiving institutional research grant support from the NCI cooperative group funding. No other disclosures were reported.
Funding/Support: Research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health by grants U10CA180821 and U10CA180882 (to the Alliance for Clinical Trials in Oncology), U10CA180790 (Mayo Clinic), U10CA180791 (Memorial Sloan-Kettering), U10CA180795 (Indiana University), U10CA180799 (University of Wisconsin), U10CA180830 (USC Norris Cancer Hospital), U10CA180836 (University of Chicago), U10CA180838 (University of North Carolina), U10CA180850 (Ohio State University), U10CA180867 (Dana-Farber Cancer Institute), and U10CA180888 (Southwest Oncology Group). The trial was also supported in part by Eli Lilly andCompany, Genentech, Pfizer Inc, and Sanofi.
Role of the Funder/Sponsor: The NCI, Eli Lilly and Company, Genentech, and Pfizer participated in the protocol development and review and approval of the final manuscript. Eli Lilly provided the cetuximab.
Disclaimer: The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Dr Schrag, a JAMA Associate Editor, had no involvement in the review of the manuscript or decision to accept for publication.
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