Vismodegib (GDC-0449), an orally bioavailable small-molecule inhibitor of Hedgehog signaling, was recently approved by the U.S. Food and Drug Administration for the treatment of basal cell carcinoma that is either metastatic or locally advanced in patients who are not candidates for surgical resection or radiation. Given the absence of previously defined effective drug therapy for this disease, approval was granted primarily on the basis of outcome of a nonrandomized parallel cohort phase II study of 99 patients with advanced basal cell carcinoma, with a primary endpoint of objective response rate. Response rates of 30.3% and 42.9% were observed in metastatic and locally advanced cohorts in this study, respectively, associated with median progression-free survival in both cohorts of 9.5 months. Ongoing clinical investigations include evaluation of the potential efficacy of vismodegib in a variety of diseases and in combination with other agents. The mechanism of action, preclinical and clinical data, and potential utility in other disease contexts are reviewed here. Clin Cancer Res; 18(12); 3218–22. ©2012 AACR.

Vismodegib is the first targeted inhibitor of the Hedgehog signaling pathway to be approved by the U.S. Food and Drug Administration (FDA). It is also the first agent of any class approved for the treatment of metastatic or locally advanced unresectable basal cell carcinoma (BCC). Its rapid path to market was based, in large part, on the strengths of a nonrandomized pivotal phase II study with a primary endpoint of response rate. Data from this study were buttressed by substantial and supportive efficacy, safety, pharmacokinetic, and pharmacodynamic data from other sources. This approval came almost precisely 5 years after the date of the first human administration of vismodegib. The pathway to approval of vismodegib represents an interesting case study in the era of molecularly targeted drug development and shows the willingness of regulatory agencies to consider alternative registration strategies, beyond the traditional randomized phase III study focused on overall survival, in unusual circumstances and in rare disease contexts.

The Hedgehog pathway has been the subject of multiple recent reviews (1) and is outlined schematically in Fig. 1; this CCRDrug Updates article focuses primarily on the clinical development of vismodegib, with brief reference to salient details of this particularly interesting signaling cascade.

Figure 1.

Hedgehog signaling, vismodegib action, and acquired resistance. The Hedgehog pathway is normally regulated through a cascade of primarily inhibitory signals. Any of 3 mammalian Hedgehog (Hh) ligands (Sonic, Indian, or Desert Hedgehog) bind to cell surface PTCH1. Ligand binding to PTCH1 relieves PTCH1 inhibition of the critical activator of Hedgehog signaling, SMO. PTCH1 deficiency, found in the majority of BCC and about 30% of medulloblastoma, is associated with constitutive, ligand-independent activation of SMO. In mammalian cells, derepression of SMO is associated with its translocation from internal vesicles to the cell membrane cilium (not shown). Active SMO signals downstream through an intermediary Sufu, promoting the release of Gli family transcription factors, which can then translocate to the nucleus to affect gene transcription. There are multiple Gli proteins whose functions are somewhat cell type dependent; in general, Gli2 seems to be a particularly strong activator of downstream gene transcription (along with Gli1), while Gli3 is inhibitory in most contexts. Pathway activation and release from Sufu can lead to proteosomal degradation of Gli3 and to preferential nuclear translocation of Gli1 and Gli2, which activate transcription of multiple target genes, including key regulators of the Hedgehog pathway, notably Gli1 and PTCH1. Vismodegib binds to the extracellular domain of SMO, markedly inhibiting downstream signaling, even in the absence of PTCH1. The first documented mechanism of clinical acquired resistance to vismodegib is a secondary mutation in the extracellular domain of SMO, D473H (indicated in the inset as a red circle), which prevents vismodegib binding.

Figure 1.

Hedgehog signaling, vismodegib action, and acquired resistance. The Hedgehog pathway is normally regulated through a cascade of primarily inhibitory signals. Any of 3 mammalian Hedgehog (Hh) ligands (Sonic, Indian, or Desert Hedgehog) bind to cell surface PTCH1. Ligand binding to PTCH1 relieves PTCH1 inhibition of the critical activator of Hedgehog signaling, SMO. PTCH1 deficiency, found in the majority of BCC and about 30% of medulloblastoma, is associated with constitutive, ligand-independent activation of SMO. In mammalian cells, derepression of SMO is associated with its translocation from internal vesicles to the cell membrane cilium (not shown). Active SMO signals downstream through an intermediary Sufu, promoting the release of Gli family transcription factors, which can then translocate to the nucleus to affect gene transcription. There are multiple Gli proteins whose functions are somewhat cell type dependent; in general, Gli2 seems to be a particularly strong activator of downstream gene transcription (along with Gli1), while Gli3 is inhibitory in most contexts. Pathway activation and release from Sufu can lead to proteosomal degradation of Gli3 and to preferential nuclear translocation of Gli1 and Gli2, which activate transcription of multiple target genes, including key regulators of the Hedgehog pathway, notably Gli1 and PTCH1. Vismodegib binds to the extracellular domain of SMO, markedly inhibiting downstream signaling, even in the absence of PTCH1. The first documented mechanism of clinical acquired resistance to vismodegib is a secondary mutation in the extracellular domain of SMO, D473H (indicated in the inset as a red circle), which prevents vismodegib binding.

Close modal

The Hedgehog pathway was initially identified as a critical developmental regulator of embryonic segment polarity in Drosophila in 1980 (2). This and related developmental work in fly body patterning was recognized by the Nobel Prize in Physiology or Medicine in 1995. Vertebrate homologs of the Drosophila Hedgehog ligand were first reported in 1993, and definition of central components of the mammalian signaling pathway followed in the late 1990s and early 2000s (reviewed in ref. 3). The first definitive linkage of mutation in this pathway to cancer, that is, to development of BCC, was made in 1996 (4, 5).

The first small-molecule inhibitor of the Hedgehog pathway, the naturally occurring compound cyclopamine, was identified in 2000 (6). This discovery, together with rapidly accumulating evidence implicating the Hedgehog pathway in oncogenesis, led to focused efforts by multiple biotechnology and pharmaceutical companies to develop cyclopamine derivatives with improved pharmacologic properties or to develop agents that effectively out-competed cyclopamine for binding to the critical cell-surface activator of Hedgehog signaling, the 7-transmembrane G protein-coupled–like receptor, SMO.

Vismodegib is a member of this second class: structurally unrelated to cyclopamine but able to bind with high affinity and specificity to SMO, leading to potent suppression of Hedgehog signaling in reporter systems and in a preclinical model of Hedgehog-dependent disease (7). An Investigational New Drug application for vismodegib was filed with the FDA in September 2006, leading to launch of a first-in-human phase I clinical trial at 3 U.S. sites in January 2007.

The first-in-human study of vismodegib employed a traditional 3+3 phase I dose-escalation schema in patients with any advanced solid tumor, designed to define a maximally tolerated dose. We modified this initial plan on the basis of 2 interesting early observations: (i) this agent had strikingly unusual pharmacokinetic properties that obviated the need for continued dose escalation (summarized in the following section); and (ii), this agent had remarkable single-agent activity in a patient with widely metastatic BCC treated in the initial dose cohort.

Hedgehog signaling has been implicated in solid tumor biology through several mechanisms, including a paracrine pathway involving signaling between epithelial cancer cells and surrounding mesenchymal stromal cells (reflecting a common mode of Hedgehog signaling in normal embryonic development), and has a role in maintenance of a putative tumor stem cell niche through autocrine signaling in a subset of cancer cells with high tumorigenic potential (reviewed in refs. 1, 8). In addition, there are 2 tumor types in which mutations in key regulatory components of the Hedgehog pathway result in markedly hyperactive, constitutive, ligand-independent signaling: BCC and medulloblastoma.

Advanced and surgically incurable BCC can occur spontaneously or in association with an inherited genetic syndrome affecting the Hedgehog pathway, such as basal cell nevus syndrome (BCNS; discussed below; ref. 9). One patient with advanced BCC was included in each of the 3 dose levels explored in phase I. After BCC responses were seen, the trial was amended to include expansion cohorts focusing on patients with advanced BCC. Of the 68 patients ultimately enrolled on this phase I study, 33 had locally advanced or metastatic BCC, and of these 33 patients with BCC, objective responses were observed in 18 (10). Enrichment of the phase I trial to substantially oversample patients with BCC provided both an important proof of principle about the single-agent efficacy of this novel inhibitor and an immediate framework for the subsequent phase II study supporting registration.

Three dose levels were explored in phase I: 150 mg, 270 mg, and 540 mg orally daily (11). Allometric scaling of preclinical animal models suggested estimates of vismodegib half-life in humans as short as 13.6 hours (12), and, in fact, the original phase I study design allowed for consideration of twice-daily dosing. However, single-dose administration followed by 7-day washout in patients revealed minimal decline in plasma drug concentrations between days 2 and 8, suggesting an exceptionally long terminal half-life (13). Vismodegib is highly protein bound, and total drug levels closely parallel blood levels of alpha 1-acid glycoprotein (13). With continuous daily dosing, steady state plasma concentrations averaging 22 μmol/L were achieved within 7 to 14 days, independent of dose: Indistinguishable levels of vismodegib were observed in all 3 dose cohorts (11). On the basis of the observed similar steady state plasma concentrations among initial dose cohorts and the clear signal of biologic efficacy, no further dose escalation was explored. The lowest daily dose level tested, 150 mg, was suggested as the recommended phase II dose.

A subsequent detailed pharmacokinetic study explored the question of whether intermittent dosing could maintain similarly stable and high vismodegib concentrations following an 11-day “loading” period of 150 mg daily (14). However, compared with continuous daily dosing, 3-times-weekly and once-weekly maintenance schedules of vismodegib were associated with 50% and 80% decreases in plasma levels of unbound drug, respectively, below threshold levels most effective in preclinical models, reinforcing the recommended phase II dose and schedule of 150 mg orally daily.

On the basis of the observed responses in patients with advanced BCC treated on the phase I protocol and the lack of any standard-of-care therapies in this patient population, a multicenter phase II study was launched to document objective response rate in patients with advanced BCC (15). The phase II study enrolled patients with advanced BCC in 2 cohorts: one with Response Evaluation Criteria in Solid Tumors (RECIST)–measurable metastatic BCC (n = 33), and the other with locally advanced BCC considered inoperable or surgically inappropriate (n = 63). For the latter cohort, a composite endpoint for objective response that included measurable diameter and ulceration of visible tumors as well as RECIST criteria for localized, but deeply invasive, tumors was employed. For both cohorts, responses were assessed by centralized independent review.

The primary results of this study largely confirm, and extend, the data obtained in phase I. Objective responses were observed in 30% of patients in metastatic BCC and in 43% of those with locally advanced disease (15). Thirteen patients with locally advanced disease (21%) experienced complete responses. The overall disease control rate (response plus disease stability) for the entire study population was more than 86%. The response rates observed in both cohorts significantly exceeded the predefined criteria for study success and supported the approval of vismodegib in the BCC disease categories defined in this study. However, the long-term durability of these promising effects remains a concern: Median duration of response in both cohorts was 7.6 months, and median progression-free survival 9.5 months (see below, “Acquired Resistance”).

BCNS is caused by germline-inactivating mutation of 1 copy of the PTCH1 gene, encoding the primary inhibitory regulator of the Hedgehog pathway (Fig. 1). Inactivation of the second allele leads to tumorigenesis. Patients with BCNS commonly develop hundreds to thousands of BCCs over the course of their adult lives (9). A recent small, but innovative, study of 41 patients with BCNS with substantial disease burden evaluated the effect of vismodegib compared with placebo in a 2:1 randomization, with a primary endpoint of reduction in new surgically eligible BCCs (16). Vismodegib significantly reduced the rate of new tumor formation, from 29 to 2.3 tumors per patient per year (P < 0.001). In addition, consistent with the larger phase II study above, responses in existing lesions were observed, including some complete regressions. These data suggest that vismodegib may have a role as a cancer-preventive agent, although this study does not definitively distinguish between prevention of tumor initiation and delay in the appearance of clinically significant disease.

The Hedgehog pathway, although playing essential roles in embryonic development, is minimally active in most adult tissues. Nonetheless, adverse events are experienced by patients on vismodegib, particularly with prolonged administration. Several of the most common toxicities seem to be class effects, seen consistently in early-phase clinical studies of structurally diverse SMO inhibitors. Final reports of phase I studies of other SMO antagonists are not yet available, but several have been publicly presented (17–19). Taken together, these data suggest muscle spasms, alopecia, dysgeusia, nausea, and fatigue as common toxicities across the class.

In the phase II BCC registration study of vismodegib, muscle spasms or cramps were experienced by 68% of subjects; alopecia, 64%; dysgeusia, 51%; weight loss, 46%; and fatigue, 36%. Between 20% and 30% of patients experienced nausea, decreased appetite, or diarrhea. For all of these adverse effects, a large majority reported only grade 1 to 2 (mild to moderate) toxicity. Severe toxicity was rare and without evident consistency or pattern: Only 4 .severe adverse events were considered to be possibly related to vismodegib, including 1 patient each with cholestasis, pulmonary embolus, dehydration and/or syncope, and cardiac failure with pneumonia. No deaths on study were attributable to vismodegib.

Although the toxicities of vismodegib are generally mild, the chronic and persistent nature of these toxicities can limit patient willingness to stay on therapy. At the time of data cutoff for the definitive phase II study, 30% of patients with metastatic and 45% of patients with locally advanced BCC had discontinued vismodegib for reasons other than disease progression or death (15); similarly, in the BCNS prevention study, 54% of patients on vismodegib discontinued therapy because of adverse events (16).

Somatic mutations leading to constitutive activation of Hedgehog signaling and consequent dependence on the pathway are found in about a third of medulloblastoma cases. The phase I study of vismodegib included a single patient with widely metastatic PTCH1-mutant medulloblastoma, who experienced rapid tumor regression in all sites of disease (20). This dramatic improvement, however, was short lived, followed by multifocal disease progression. Recurrent disease in this individual was associated with an acquired tumor-specific mutation in SMO that inhibited vismodegib binding to the protein (Fig. 1, inset; ref. 21).

BCC is a more indolent cancer than medulloblastoma, and the responses observed have been more durable. Nonetheless, the 9.5-month median progression-free survival observed in both patients with locally advanced and with metastatic BCC treated with vismodegib speaks to the need for continued research to define the mechanisms of acquired resistance and to develop combinatorial strategies to improve the long-term prognosis of patients with this disease. A secondary SMO mutation has been identified in a progressive lesion from a patient with BCC on vismodegib, suggesting that similar mechanisms of acquired resistance may apply to both BCC and medulloblastoma (unpublished data).

Although BCC is the most common human malignancy, affecting more than 2 million individuals in the United States annually, it is almost always surgically curable: Metastatic BCC is a rare disease. Medulloblastoma, although the most common brain cancer in children, is also not a major cause of cancer mortality. There has been great interest in exploring the potential utility of vismodegib, and other SMO inhibitors, in patients with other diseases.

To date, no definitive clinical responses to SMO inhibitors have been reported in diseases other than BCC and medulloblastoma. On the basis of extensive preclinical data implicating Hedgehog signaling in tumor–stroma interactions and in maintenance of tumor progenitor cell populations, several studies have been initiated combining vismodegib with standard cytotoxic therapies or other targeted agents for a wide range of malignancies. Results of most of these studies are not yet available. An initial 199-patient randomized phase II study evaluating first-line cytotoxic therapies for colorectal cancer with vismodegib or placebo was disappointing, with no statistically significant differences in outcome between arms, and a hazard ratio for progression-free survival showing a trend in favor of the control arm (22). Overall survival data for this study are not yet available.

Recent preclinical data strongly support a role for Hedgehog signaling in maintenance of tumorigenic capacity in small cell lung cancer (23). We recently completed accrual to a randomized phase II study evaluating standard first-line chemotherapy for extensive-stage small cell lung cancer alone, with vismodegib, or with another targeted agent (cixitumumab, targeting insulin-like growth factor I receptor), with continuation of the investigational agents as maintenance therapy, through the Eastern Cooperative Oncology Group. Outcome data from this study are not yet available.

Vismodegib is a potent, selective, orally bioavailable Hedgehog antagonist. Its approval represents the latest in a series of success stories in rapid deployment of molecularly targeted anticancer agents, based on a strategy of focusing early-phase clinical development on molecularly defined subsets of patients. Vismodegib shows remarkable activity against BCC, with recent studies supporting both therapeutic and preventive efficacy. Factors contributing to its exceptionally rapid progress from first-in-human testing to regulatory approval include an acceptable toxicity profile, early recognition of achievement of a biologically effective concentration in the first dose cohort explored, and an early-phase development plan that focused on a disease strongly dependent on the pathway being targeted, and for which there was a clear unmet need.

Several questions and challenges remain. Although categorized as mild to moderate, cumulative toxicity of this agent over time has led to discontinuation of therapy in a substantial fraction of patients. Chronic adverse effects will limit the potential utility of vismodegib as a preventive agent in any but the highest risk settings. Strategies to ameliorate some of the common toxicities of vismodegib will be important and may improve the quality of life of patients receiving this, and similar, agents.

The median response duration of 7.6 months in patients with advanced BCC responding to vismodegib underscores the need to consider strategies to treat, or prevent the emergence of, vismodegib-resistant disease. Essentially all Hedgehog inhibitors in clinical development bind the extracellular domain of SMO, and cross-resistance is likely. Notably in this context, although clearly anecdotal, we observed no responses in 7 patients with advanced BCC who had previously progressed on vismodegib when treated with IPI-926, a similarly active SMO inhibitor (19). Agents targeting other critical nodes of the Hedgehog pathway, beyond SMO, are being actively pursued.

Medulloblastoma has peak incidence at age 5, a period of active bone growth and morphogenesis. Exposure of young animals to Hedgehog inhibition has been associated with permanent defects in skeletal development (24). Trials are ongoing to assess the feasibility and efficacy of administration of vismodegib in prepubescent children with this important disease.

Finally, despite multiple lines of preclinical evidence suggesting potential roles for Hedgehog signaling in common lethal cancers, early signals from studies combining SMO inhibitors with chemotherapy, or following chemotherapy as maintenance, have not yet shown clear evidence of benefit. Multiple such trials are in progress or recently completed, and results are eagerly awaited.

Treating advanced BCC may prove to be the hedgehog's “One Big Thing” (25), even better would be if it turns out to address many things.

C.M. Rudin has previously been a consultant for Genentech.

Burroughs Wellcome Clinical Scientist Award in Translational Research and the Flight Attendant Medical Research Institute Center of Excellence.

1.
Ng
JM
,
Curran
T
. 
The Hedgehog's tale: developing strategies for targeting cancer
.
Nat Rev Cancer
2011
;
11
:
493
501
.
2.
Nüsslein-Volhard
C
,
Wieschaus
E
. 
Mutations affecting segment number and polarity in Drosophila
.
Nature
1980
;
287
:
795
801
.
3.
Ingham
PW
,
McMahon
AP
. 
Hedgehog signaling in animal development: paradigms and principles
.
Genes Dev
2001
;
15
:
3059
87
.
4.
Hahn
H
,
Wicking
C
,
Zaphiropoulous
PG
,
Gailani
MR
,
Shanley
S
,
Chidambaram
A
, et al
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome
.
Cell
1996
;
85
:
841
51
.
5.
Johnson
RL
,
Rothman
AL
,
Xie
J
,
Goodrich
LV
,
Bare
JW
,
Bonifas
JM
, et al
Human homolog of patched, a candidate gene for the basal cell nevus syndrome
.
Science
1996
;
272
:
1668
71
.
6.
Taipale
J
,
Chen
JK
,
Cooper
MK
,
Wang
B
,
Mann
RK
,
Milenkovic
L
, et al
Effects of oncogenic mutations in Smoothened and Patched can be reversed by cyclopamine
.
Nature
2000
;
406
:
1005
9
.
7.
Robarge
KD
,
Brunton
SA
,
Castanedo
GM
,
Cui
Y
,
Dina
MS
,
Goldsmith
R
, et al
GDC-0449-a potent inhibitor of the hedgehog pathway
.
Bioorg Med Chem Lett
2009
;
19
:
5576
81
.
8.
Merchant
AA
,
Matsui
W
. 
Targeting Hedgehog—a cancer stem cell pathway
.
Clin Cancer Res
2010
;
16
:
3130
40
.
9.
Epstein
EH
. 
Basal cell carcinomas: attack of the hedgehog
.
Nat Rev Cancer
2008
;
8
:
743
54
.
10.
Von Hoff
DD
,
LoRusso
PM
,
Rudin
CM
,
Reddy
JC
,
Yauch
RL
,
Tibes
R
, et al
Inhibition of the hedgehog pathway in advanced basal-cell carcinoma
.
N Engl J Med
2009
;
361
:
1164
72
.
11.
LoRusso
PM
,
Rudin
CM
,
Reddy
JC
,
Tibes
R
,
Weiss
GJ
,
Borad
MJ
, et al
Phase I trial of hedgehog pathway inhibitor vismodegib (GDC-0449) in patients with refractory, locally advanced or metastatic solid tumors
.
Clin Cancer Res
2011
;
17
:
2502
11
.
12.
Wong
H
,
Chen
JZ
,
Chou
B
,
Halladay
JS
,
Kenny
JR
,
La
H
, et al
Preclinical assessment of the absorption, distribution, metabolism and excretion of GDC-0449 (2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonyl)benzamide), an orally bioavailable systemic Hedgehog signalling pathway inhibitor
.
Xenobiotica
2009
;
39
:
850
61
.
13.
Graham
RA
,
Lum
BL
,
Cheeti
S
,
Jin
JY
,
Jorga
K
,
Von Hoff
DD
, et al
Pharmacokinetics of hedgehog pathway inhibitor vismodegib (GDC-0449) in patients with locally advanced or metastatic solid tumors: the role of alpha-1-acid glycoprotein binding
.
Clin Cancer Res
2011
;
17
:
2512
20
.
14.
Lorusso
PM
,
Jimeno
A
,
Dy
G
,
Adjei
A
,
Berlin
J
,
Leichman
L
, et al
Pharmacokinetic dose-scheduling study of hedgehog pathway inhibitor vismodegib (GDC-0449) in patients with locally advanced or metastatic solid tumors
.
Clin Cancer Res
2011
;
17
:
5774
82
.
15.
Sekulic
A
,
Migden
MR
,
Oro
AE
,
Dirix
L
,
Lewis
KD
,
Hainsworth
JD
, et al
Efficacy and safety of vismodegib in advanced basal-cell carcinoma
.
N Engl J Med
2012
;
366
:
2171
9
.
16.
Tang
JY
,
Mackay-Wiggan
JM
,
Aszterbaum
M
,
Yauch
RL
,
Lindgren
J
,
Chang
K
, et al
Inhibiting the hedgehog pathway in patients with the basal-cell nevus syndrome
.
N Engl J Med
2012
;
366
:
2180
8
.
17.
Rodon Ahnert
J
,
Baselga
J
,
Tawbi
HA
,
Shou
Y
,
Granvil
C
,
Dey
J
, et al
A phase I dose-escalation study of LDE225, a smoothened (Smo) antagonist, in patients with advanced solid tumors
.
J Clin Oncol
2010
;
28
:
2500
.
18.
Siu
LL
,
Papadopoulos
K
,
Alberts
SR
,
Kirchoff-Ross
R
,
Vakkalagadda
B
,
Lang
L
, et al
A first-in-human, phase I study of an oral hedgehog pathway antagonist, BMS-833923 (XL139), in subjects with advanced or metastatic solid tumors
.
J Clin Oncol
2010
;
29
:
2501
.
19.
Rudin
CM
,
Jimeno
A
,
Miller
WH
,
Eigl
BJ
,
Gettinger
SN
,
Chang
ALS
, et al
A phase I study of IPI-926, a novel hedgehog pathway inhibitor, in patients with advanced or metastatic solid tumors
.
J Clin Oncol
2011
;
29
:
3014
.
20.
Rudin
CM
,
Hann
CL
,
Laterra
J
,
Yauch
RL
,
Callahan
CA
,
Fu
L
, et al
Treatment of medulloblastoma with hedgehog pathway inhibitor GDC-0449
.
N Engl J Med
2009
;
361
:
1173
8
.
21.
Yauch
RL
,
Dijkgraaf
GJ
,
Alicke
B
,
Januario
T
,
Ahn
CP
,
Holcomb
T
, et al
Smoothened mutation confers resistance to a Hedgehog pathway inhibitor in medulloblastoma
.
Science
2009
;
326
:
572
4
.
22.
Berlin
J
,
Bendell
J
,
Hart
LL
,
Firdaus
I
,
Gore
I
,
Hermann
RC
, et al
A phase 2, randomized, double-blind, placebo-controlled study of Hedgehog pathway inhibitor GDC-0449 in patients with previously untreated metastastic colorectal cancer
.
Ann Oncol
2010
;
21
:
LBA21
.
23.
Park
KS
,
Martelotto
LG
,
Peifer
M
,
Sos
ML
,
Karnezis
AN
,
Mahjoub
MR
, et al
A crucial requirement for Hedgehog signaling in small cell lung cancer
.
Nat Med
2011
;
17
:
1504
8
.
24.
Kimura
H
,
Ng
JM
,
Curran
T
. 
Transient inhibition of the Hedgehog pathway in young mice causes permanent defects in bone structure
.
Cancer Cell
2008
;
13
:
249
60
.
25.
Attributed to Achilochus
.
(The fox knows many things, but the hedgehog knows one big thing). Circa 650 BCE
.