A phase II trial of docetaxel and erlotinib as first-line therapy for elderly patients with androgen-independent prostate cancer
© Gross et al; licensee BioMed Central Ltd. 2007
Received: 08 March 2007
Accepted: 27 July 2007
Published: 27 July 2007
Docetaxel is the standard first-line agent for the treatment of androgen-independent prostate cancer (AIPC). The combination of docetaxel with molecularly targeted therapies may offer the potential to increase the efficacy and decrease the toxicity of cytotoxic chemotherapy for prostate cancer. Previous studies demonstrate activation of the human epidermal growth factor receptor (EGFR) in prostate cancer. Erlotinib is a specific inhibitor of the tyrosine-kinase activity of EGFR. The goal of this study is to determine the anti-cancer activity docetaxel combined with erlotinib for the treatment of elderly subjects with AIPC.
This is a multi-institutional Phase II study in patients with histologically confirmed adenocarcinoma of the prostate and age ≥ 65 years. Patients were requred to have progressive disease despite androgen-deprivation therapy as determined by: (1) measurable lesions on cross-sectional imaging; (2) metastatic disease by radionucleotide bone imaging; or (3) elevated prostate specific antigen (PSA). Treatment cycles consisted of docetaxel 60 mg/m2 IV on day 1 and erlotinib 150 mg PO days 1–21. Patients with responding or stable disease after 9 cycles were eligible to continue on erlotinib alone as maintenance therapy.
Characteristics of 22 patients enrolled included: median age 73.5 years (range, 65–80); median Karnofsky Performance Status 90 (range 70–100); median hemoglobin 12.1 g/dl (range, 10.0–14.3); median PSA 218.3 ng/ml (range, 9–5754). A median of 6 treatment cycles were delivered per patient (range 1–17). No objective responses were observed in 8 patients with measurable lesions (0%, 95% CI 0–31%). Bone scan improvement and PSA decline was seen in 1 patient (5%, 95% CI 0.1–25%). Five of 22 patients experienced ≥ 50 % decline in PSA (23%, 95% CI 8–45%). Hematologic toxicity included grade 3 neutropenia in 9 patients and neutropenic fever in 2 patients. Common non-hematologic toxicities (≥ grade 3) included fatigue, anorexia, and diarrhea.
Docetaxel/erlotinib can be delivered safely in elderly patients with AIPC. Anti-cancer disease activity appears generally comparable to docetaxel when used as monotherapy. Hematologic and non-hematologic toxicity may be increased over docetaxel monotherapy. Prospective randomized studies would be required to determine if the toxicity of docetaxel and erlotinib justifies its use in this setting.
Prostate cancer is a significant cause of cancer morbidity and mortality with a projected U.S. incidence of 230,000 cases diagnosed and 27,000 deaths in 2006 . The progression to androgen-independent prostate cancer (AIPC) marks a stage of clinical acceleration to a lethal form of the disease. Mitoxantrone is commonly used for AIPC based on improvement in pain measures with no effect on overall survival [2, 3]. Two large Phase III trials recently demonstrated a survival advantage for docetaxel over mitoxantrone and have led to the widespread use of docetaxel as first-line treatment for AIPC [4, 5].
The human epidermal growth factor receptor (EGFR) tyrosine kinases are part of a network of pathways which are implicated in the development and progression of prostate cancer, in particular as part of the progression to androgen-independent growth [6–10]. Erlotinib is a selective inhibitor of the tyrosine kinase activity of the EGFR. Erlotinib was approved by the US Food and Drug Administration as a first-line therapy (in combination with gemcitabine) for pancreatic cancer and as second or third-line therapy for non-small cell lung cancer (NSCLC) based on improvement in overall survival [11, 12].
The combination of pre-clinical and clinical data linking the HER-kinase axis to AIPC and early clinical data which demonstrated the safety of erlotinib in combination with docetaxel on a three-week schedule led us to perform this clinical study to examine the efficacy of erlotinib with docetaxel in AIPC .
A significant portion of patients treated with metastatic AIPC are elderly. The median patient age in the recent multi-center trials of first-line chemotherapy for AIPC trials was >65 years [4, 14]. Older patients may not tolerate standard or investigational cytotoxic chemotherapies as well as younger patients . Selection bias may limit extrapolation of results from non-randomized trials as patients treated in specialized referral centers may be younger and with better performance status than the general patient population. Therefore, we restricted our investigation to elderly patients (defined as age ≥ 65 years) to increase the feasibility and relevance of our results to the management of AIPC.
This study was a multi-center, non-randomized phase II study. The primary endpoint was best overall response and response duration for elderly patients with AIPC. Secondary endpoints were changes in PSA levels, safety, and changes in patient reported health-related quality of life measures. At entry, patients were categorized according to extent and type of metastatic disease (bone, visceral/lymph nodes, or both) for later response assessment.
Patients were required to have histologically confirmed adenocarcinoma of the prostate progressed following primary or secondary hormonal manipulations. Disease progression was defined as at least two successive increases in serum PSA (> 20% rise from baseline value) taken at least two weeks apart or documented soft tissue or osseous progression demonstrable on imaging studies. Prior hormonal treatment (flutamide, ketoconazole, diethylstilbesterol) must have been discontinued at least four weeks prior to study treatment (6 weeks for bicalutamide). Other entry criteria included: age ≥ 65 years; Karnofsky Performance Status (KPS) ≥ 70%; castrate levels of testosterone (≤ 50 ng/ml) maintained with medical or surgical castration; no prior treatment with cytotoxic chemotherapy; peripheral neuropathy ≤ grade 1; and appropriate renal, hepatic, and hematologic function consistent with package insert for docetaxel. The Institutional Review Boards at participating institutions approved this protocol and all patients were counseled regarding the benefits, risks, and alternatives to study participation. All patients signed written informed consent forms before any study related procedures were performed.
Treatment consisted of docetaxel 60 mg/m2 IV over 60 minutes every 21 days and erlotinib 150 mg orally daily for 21 days. Patients received dexamethasone 8 mg orally twice daily for 3 days beginning one day prior to the docetaxel infusion. Anti-emetics were administered as per institutional standard of care.
A complete blood count, PSA, AST, ALT, alkaline phospatase, total bilirubin, BUN, creatinine, and electrolytes were obtained at baseline and prior to each cycle of therapy. Patients were evaluated with cross sectional imaging of chest, abdomen, and pelvis and radionucleotide bone scintigraphy at baseline and after every 3 cycles. An electrocardiogram was obtained at screening.
Patients without objective progression of disease (at least stable bone scans and/or stable disease by RECIST criteria) following 9 cycles of docetaxel/erlotinib were allowed to continue on 3 weeks cycles of erlotinib therapy administered alone for up to 8 additional cycles.
For erlotinib, dose reductions to 100 mg, 50 mg, or 25 mg, were required for moderate to severe (≥ grade 3) keratitis, rash, or diarrhea. Dose interruptions of erlotinib for up to two weeks were allowed as clinically indicated for erlotinib-related toxicities. For docetaxel, a 25% dose reduction for hematologic toxicities (neutropenia and thrombocytopenia ≥ grade 3) was allowed. Alternatively, myeloid growth factor support for secondary prophylaxis of neutropenia was permitted without dose modification. Dose interruption followed by a subsequent 25% docetaxel dose reduction was required for liver enzyme abnormalities including total bilirubin > upper limit of normal (ULN), alkaline phosphatase > 5 × ULN, and alanine transferase >5 × ULN. Dose reductions were also required for neuropathy ≥ grade 2 and other toxicities ≥ grade 3. Dose delays were required if stomatitis was present on day 1. If moderate to severe (≥ grade 3) stomatitis occurred during any cycle, then subsequent docetaxel doses were reduced by 25%.
Toxicity and response criteria
The National Cancer Institute Common Toxicity Criteria (version 2.0) was used to evaluate patient toxicity during each cycle. Adverse events were reported to authorities as required by institutional and regulatory guidelines. Every effort was made to administer the regimen at full dose, as tolerated. Standard supportive care measures were employed according to routine local practice.
At entry, patients were classified by disease site according to the presence of measurable lesions by RECIST criteria or non-measurable lesions (by bone scan only) . Patients were evaluated after 3 cycles with bone scans and/or cross sectional imaging as clinically indicated. For patients with measurable disease, response was assessed by standardized RECIST criteria . For patients with bone-only disease, response was assessed by a combination of an improvement in non-measurable lesions (on bone scan) and a reduction in PSA levels (≥ 50%) sustained for at least 21 days. Patients with at least stable disease were continued on therapy. Additional response evaluations were performed after cycles 6, 9, 13, and at study completion (following cycle 17 or at early termination).
Serial measurements of PSA were obtained at baseline and before every cycle. Criteria for response for declines in PSA were based on the guidelines from the PSA working group .
Patient reported quality of life outcomes were measured with the FACT-P questionnaire at baseline (day 1 prior to study treatment) and before every treatment cycle. Patients were also asked to complete the FACT-P at the early termination visit, if applicable.
The primary outcome variable was response for each patient as classified by measurable or non-measurable disease. Secondary end points included toxicity, patient reported quality of life, and survival. The study was powered to both estimate the true percent of responders with a tolerance of +/- 23%, based on an exact 95% confidence interval, and to test the null hypothesis of a 5% response versus >5% response with 90% power with a significance level of 0.05. Confidence intervals for the proportion responders were computed using exact binominal confidence intervals. Changes in mean FACT-P scores from baseline to cycle 3 and baseline to end-of-study visit were computed with two-sided Student's t-tests. The Kaplan-Meier curve and mean survival were calculated with S-Plus (version 5; Insightful).
Baseline patient characteristics
Alkaline phosphatase (U/l)
Duration of androgen deprivation (months)
Secondary hormonal manipulations
Prostatectomy and radiation
Androgen-deprivation therapy alone
Sites of Disease
Study treatment delivered
A total of 121 cycles of docetaxel with erlotinib were administered to 22 patients. The median number of treatment cycles delivered per patient was 6 (range 1–17). During combination treatment, there were 10 dose reductions and 12 dose delays of docetaxel and 3 dose reduction and 3 dose delays of ≥ 7 days of erlotinib due to adverse events. The average dose intensity of docetaxel was 17.8 mg/m2/week (standard deviation [SD], 3.6). The treatment plan specified erlotinib monotherapy after completion of 9 cycles of docetaxel/erlotinib combination treatment with stable disease or better response. Six patients remained on study after cycle 9 to receive a total of 23 cycles of erlotinib monotherapy. There were no dose reductions or delays for erlotinib monotherapy.
Reasons for withdrawal from the study included disease progression in 8 patients, toxicity in 6 patients, and investigator discretion in 6 patients. Two patients completed study drug treatment (after 17 cycles) with stable disease.
Response and overall survival
Best overall response by criteria.
% (95% CI)
Treatment Related Toxicity
Liver enzyme elevation (AST)
Liver enzyme elevation (ALT)
Patient reported quality of life measures
Patients were asked to complete the FACT-P questionnaire before treatment at cycle 1 (baseline), cycle 3, and at the end-of-study visit (occurring variably before cycles 3 through 17). The mean ± SD FACT-P scores observed at baseline, cycle 3, and end-of-study were112 ± 11 (22 patients); 112 ± 14 (18 patients), 106 ± 17 (20 patients), respectively. No significant differences were observed in pair-wise comparisons between mean FACT-P at baseline and cycle 3 and baseline and end-of-study (p > 0.05).
The development of specific inhibitors of the HER-kinase axis represents an important advance in oncology. In many pre-clinical models, inhibitors of HER-kinase pathway are found to be additive or synergistic when combined with cytotoxic agents. This study demonstrates that docetaxel (60 mg/m2 every 21 days) with erlotinib 150 mg daily is active and well-tolerated therapy for elderly patients with AIPC.
This trial was designed and executed before the results of randomized trials of erlotinib or geftinib (a related EGFR-tyrosine kinase inhibitor) with cytotoxic chemotherapy for other solid tumors became available. In non-small cell lung cancer, four large randomized trials of erlotinib or geftinib with first-line cytotoxic chemotherapy demonstrated no additive anticancer effect of the combination [18–21]. Subsequently, erlotinib was shown to increase overall survival over supportive care for patients previously treated with cytotoxic chemotherapy . In pancreatic cancer, a recent trial showed a small, but statistically significant, improvement in overall survival with erlotinib added to gemcitabine versus gemcitabine alone in the first-line setting . These data suggest that, in some settings, EGFR-tyrosine kinase inhibitors may produce a modest increase in anti-cancer efficacy when added to cytotoxic chemotherapy. However, additional data are needed to better understand patient selection and sequencing for these agents.
The toxicity of docetaxel with erlotinib needs to be considered in the context of published data for docetaxel and erlotinib used as monotherapy in comparable patient populations. Rash and diarrhea are the main dose-limiting toxicities of erlotinib and both were commonly observe in this trial, though generally mild . Otherwise, the non-hematologic toxicities of docetaxel with erlotinib appear comparable to docetaxel montherapy as reported in the TAX-327 trial . However, the frequency of dose-modifications and patient withdrawals in this study raises concerns. In the present study, the median number of cycles delivered per patient was 6 (of 9 cycles intended) compared to 9.5 (of 10 cycles intended) in TAX 327 . Further, it is notable that 4 patients withdrew before the first scheduled evaluation (at cycle 3) due to toxicity or patient/physician preference. These dose reductions and delays occurred despite a lower intended dose intensity of docetaxel at 60 mg/m2 every 21 days compared to 75 mg/m2 every 21 days in TAX-327. These data may raise concerns regarding the ability to deliver sufficient doses of docetaxel to affect the overall survival advantage associated with docetaxel-based therapy for AIPC.
The key results of this trial should also be considered in the context of the docetaxel monotherapy arm in TAX-327 . We observed a PSA decline of ≥ 50% in 23% (95% CI 8–45%) which just overlaps with the PSA decline rate of 45% (95% CI 40–51%) observed in TAX-327. The absence of objective responses in 8 patients with measurable disease (0%, 95% CI: 0–31%) in our trial is not surprising considering an objective response rate of 12% (95% CI 7–19%) in TAX-327. Perhaps most significantly, the median overall survival of 24.6 months compares favorably with a median survival of 18.9 months observed in TAX-327 despite a generally older patient population (mean age 74 years in this report versus 68 years in TAX-327) and decreased intended dose intensity of docetaxel (20 mg/m2/week in this report versus 25 mg/m2/week in TAX-327).
In summary, we found docetaxel with erlotinib to be a relatively well-tolerated regimen in this elderly patient population. Our data suggests that the overall survival of patients treated with docetaxel and erlotinib appears comparable docetaxel monotherapy despite an apparent increase in toxicity. A randomized study would be needed to determine if the toxicity of the docetaxel and erlotinib results in a demonstrable benefit in terms of overall survival.
This study was supported by NIH Prostate SPORE P50 CA92131 to DBA. Phase One Foundation to MEG and DBA. We thank David Elashoff for statistical support.
- Jemal A, Siegel R, Ward E, Murray T, Xu J, Smigal C, Thun MJ: Cancer statistics, 2006. CA Cancer J Clin. 2006, 56 (2): 106-130.View ArticlePubMedGoogle Scholar
- Tannock IF, Osoba D, Stockler MR, Ernst DS, Neville AJ, Moore MJ, Armitage GR, Wilson JJ, Venner PM, Coppin CM, Murphy KC: Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points. J Clin Oncol. 1996, 14 (6): 1756-1764.PubMedGoogle Scholar
- Kantoff PW, Halabi S, Conaway M, Picus J, Kirshner J, Hars V, Trump D, Winer EP, Vogelzang NJ: Hydrocortisone with or without mitoxantrone in men with hormone- refractory prostate cancer: results of the cancer and leukemia group B 9182 study. J Clin Oncol. 1999, 17 (8): 2506-2513.PubMedGoogle Scholar
- Tannock IF, de Wit R, Berry WR, Horti J, Pluzanska A, Chi KN, Oudard S, Theodore C, James ND, Turesson I, Rosenthal MA, Eisenberger MA: Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer. N Engl J Med. 2004, 351 (15): 1502-1512. 10.1056/NEJMoa040720.View ArticlePubMedGoogle Scholar
- Petrylak DP, Tangen CM, Hussain MH, Lara PN, Jones JA, Taplin ME, Burch PA, Berry D, Moinpour C, Kohli M, Benson MC, Small EJ, Raghavan D, Crawford ED: Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer. N Engl J Med. 2004, 351 (15): 1513-1520. 10.1056/NEJMoa041318.View ArticlePubMedGoogle Scholar
- Agus DB, Akita RW, Fox WD, Lofgren JA, Higgins B, Maiese K, Scher HI, Sliwkowski MX: A potential role for activated HER-2 in prostate cancer. Semin Oncol. 2000, 27 (6 Suppl 11): 76-83; discussion 92-100..PubMedGoogle Scholar
- Gross ME, Jo S, Agus DB: Update on HER-Kinase-Directed Therapy in Prostate Cancer. Clin Adv Hematol Oncol. 2004, 2 (1): 53-64.PubMedGoogle Scholar
- Arteaga CL: The epidermal growth factor receptor: from mutant oncogene in nonhuman cancers to therapeutic target in human neoplasia. J Clin Oncol. 2001, 19 (18 Suppl): 32S-40S.PubMedGoogle Scholar
- Craft N, Shostak Y, Carey M, Sawyers CL: A mechanism for hormone-independent prostate cancer through modulation of androgen receptor signaling by the HER-2/neu tyrosine kinase. Nat Med. 1999, 5 (3): 280-285. 10.1038/6495.View ArticlePubMedGoogle Scholar
- Signoretti S, Montironi R, Manola J, Altimari A, Tam C, Bubley G, Balk S, Thomas G, Kaplan I, Hlatky L, Hahnfeldt P, Kantoff P, Loda M: Her-2-neu expression and progression toward androgen independence in human prostate cancer. J Natl Cancer Inst. 2000, 92 (23): 1918-1925. 10.1093/jnci/92.23.1918.View ArticlePubMedGoogle Scholar
- Moore MJ, Goldstein D, Hamm J, Figer A, Hecht J, Gallinger S, Au H, Ding K, Christy-Bittel J, W. P: Erlotinib plus gemcitabine compared to gemcitabine alone in patients with advanced pancreatic cancer. A phase III trial of the National Cancer Institute of Canada Clinical Trials Group [NCIC-CTG] . Proc Am Soc Clin Oncol. 2005, 23 (16S): Abstract 1-Google Scholar
- Shepherd FA, Rodrigues Pereira J, Ciuleanu T, Tan EH, Hirsh V, Thongprasert S, Campos D, Maoleekoonpiroj S, Smylie M, Martins R, van Kooten M, Dediu M, Findlay B, Tu D, Johnston D, Bezjak A, Clark G, Santabarbara P, Seymour L: Erlotinib in previously treated non-small-cell lung cancer. N Engl J Med. 2005, 353 (2): 123-132. 10.1056/NEJMoa050753.View ArticlePubMedGoogle Scholar
- Forouzesh B, Hidalgo M, Takimoto C, de Bono JS, Forero L, al. E: Phase I, pharmacokinetic (PK), and biological studies of the epidermal growth factor-tyrosine kinase (EGFR-TK) inhibitor OSI-774 in combination with docetaxel . Proc Am Soc Clin Oncol. 2002, 21: Abstract 81-Google Scholar
- Petrylak DP, Tangen C, Hussain M, Lara PN, Jones J, Talpin ME, Burch P, Greene G, Small E, Crawford ED: SWOG 99-16: Randomized phase III trial of docetaxel (D)/estramustine (E) versus mitoxantrone(M)/prednisone(p) in men with androgen-independent prostate cancer (AIPCA). Proc ASCO. 2004, 23: 2 (abstract 3)-Google Scholar
- Chen H, Cantor A, Meyer J, Beth Corcoran M, Grendys E, Cavanaugh D, Antonek S, Camarata A, Haley W, Balducci L, Extermann M: Can older cancer patients tolerate chemotherapy? A prospective pilot study. Cancer. 2003, 97 (4): 1107-1114. 10.1002/cncr.11110.View ArticlePubMedGoogle Scholar
- Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, Verweij J, Van Glabbeke M, van Oosterom AT, Christian MC, Gwyther SG: New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000, 92 (3): 205-216. 10.1093/jnci/92.3.205.View ArticlePubMedGoogle Scholar
- Bubley GJ, Carducci M, Dahut W, Dawson N, Daliani D, Eisenberger M, Figg WD, Freidlin B, Halabi S, Hudes G, Hussain M, Kaplan R, Myers C, Oh W, Petrylak DP, Reed E, Roth B, Sartor O, Scher H, Simons J, Sinibaldi V, Small EJ, Smith MR, Trump DL, Wilding G, et al: Eligibility and response guidelines for phase II clinical trials in androgen-independent prostate cancer: recommendations from the Prostate-Specific Antigen Working Group. J Clin Oncol. 1999, 17 (11): 3461-3467.PubMedGoogle Scholar
- Giaccone G, Herbst RS, Manegold C, Scagliotti G, Rosell R, Miller V, Natale RB, Schiller JH, Von Pawel J, Pluzanska A, Gatzemeier U, Grous J, Ochs JS, Averbuch SD, Wolf MK, Rennie P, Fandi A, Johnson DH: Gefitinib in combination with gemcitabine and cisplatin in advanced non-small-cell lung cancer: a phase III trial--INTACT 1. J Clin Oncol. 2004, 22 (5): 777-784. 10.1200/JCO.2004.08.001.View ArticlePubMedGoogle Scholar
- Herbst RS, Giaccone G, Schiller JH, Natale RB, Miller V, Manegold C, Scagliotti G, Rosell R, Oliff I, Reeves JA, Wolf MK, Krebs AD, Averbuch SD, Ochs JS, Grous J, Fandi A, Johnson DH: Gefitinib in combination with paclitaxel and carboplatin in advanced non-small-cell lung cancer: a phase III trial--INTACT 2. J Clin Oncol. 2004, 22 (5): 785-794. 10.1200/JCO.2004.07.215.View ArticlePubMedGoogle Scholar
- Herbst RS, Prager D, Hermann R, Fehrenbacher L, Johnson BE, Sandler A, Kris MG, Tran HT, Klein P, Li X, Ramies D, Johnson DH, Miller VA: TRIBUTE: a phase III trial of erlotinib hydrochloride (OSI-774) combined with carboplatin and paclitaxel chemotherapy in advanced non-small-cell lung cancer. J Clin Oncol. 2005, 23 (25): 5892-5899. 10.1200/JCO.2005.02.840.View ArticlePubMedGoogle Scholar
- Gatzemeier U, Pluzanska A, Szczesna A, Kaukel E, Roubec J, Brennscheidt U, De Rosa F, Mueller B, Von Pawel J: Results of a phase III trial of erlotinib (OSI-774) combined with cisplatin and gemcitabine (GC) chemotherapy in advanced non-small cell lung cancer (NSCLC). Proc Am Soc Clin Oncol. 2004, 22 (14S): Abstract 7010-Google Scholar
- Malik SN, Siu LL, Rowinsky EK, deGraffenried L, Hammond LA, Rizzo J, Bacus S, Brattain MG, Kreisberg JI, Hidalgo M: Pharmacodynamic evaluation of the epidermal growth factor receptor inhibitor OSI-774 in human epidermis of cancer patients. Clin Cancer Res. 2003, 9 (7): 2478-2486.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/7/142/prepub
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