Camptothecin Cancer Therapy Guide

Biopharma PEG https://www.biochempeg.com
Camptothecin & Its Derivatives for
Cancer Therapy
Camptothecin (CPT) is a pentacycle quinoline alkaloid that was basically isolated from
woody plant Camptotheca acuminata. Due to their selectivity as topoisomerase I inhibitors
that trap topoisomerase I cleavage complexes, camptothecin and its derivatives are
promising anti-cancer drugs.
Origin of Camptothecin
In 1966, Monreoe E. Wall and Mansukh C. Wani of the National Cancer Institute isolated a
pentacyclic monoterpene alkaloid from woody plant Camptotheca acuminata distributed in
Southwest China.
From 1967 to 1970, researchers found that this pentacyclic monoterpene alkaloid showed
strong antitumor activity in vitro against Hela cells (a cell line of cervical cancer cells),
L1210 cells (mouse lymphocytic leukemia cells) and rodents, and also showed efficacy
against a variety of malignancies such as gastric cancer, rectal cancer and leukemia. This
triggered a wave of scientific research on the plant Camptothecin and Camptothecin-like
compounds, and more and more Camptothecin-like compounds were discovered one
after another. However, for many reasons, the clinical application of camptothecin
has not been effectively advanced.
In 1985, Hsiang and his colleagues discovered that camptothecin and its derivatives
target Topoisomerase I and reversibly bind through the TopoI-DNA cleavable complex,
forming a CPT-Topo I-DNA ternary complex that inhibits DNA replication and transcription,
which in turn leads to cancer cell death. Compared with TopoII inhibitors, Topo I inhibitors
are highly potent and have a broad anti-tumor spectrum, and the specific inhibition of
Topoisomerase I by camptothecin has triggered a new wave of interest.

Figure 1. Pharmacological effects of camptothecin
Development of Camptothecin
Camptothecin has a planar pentacyclic ring structure, that includes
a pyrrolo[3,4-β]-quinoline moiety (rings A, B and C), conjugated pyridone moiety (ring D)
and one chiral center at position 20 within the alpha-hydroxy lactone ring with (S)
configuration (the E-ring).
Figure 2. Strucure of camptothecin

There are three main problems in the development of camptothecin-based drugs.
 ▶ Due to its special structure, camptothecin has poor lipid and water solubility,
thus it has poor druggability and must be modified for water solubility.
 ▶ Modification leads to rapid release of the drug, and excessive blood
concentrations can trigger serious toxic side effects, such as diarrhea, hemorrhagic
cystitis, and severe bone marrow suppression.
 ▶ Structural modifications need to consider the release rate and stability of the
drug to ensure effectiveness with high safety.
In order to acquire low-toxic water-soluble camptothecin derivatives, certain active sites
on their five-ring backbone are usually modified, such as the A, B and E rings, to improve
the water solubility of camptothecin, reduce the toxic side effects and increase the stability
of the lactone ring, where the most studied modification sites are the 7, 9, 10 and 20
carbon positions.
The first camptothecin derivative, 10-Hydroxycamptothecin (HCPT), was developed
independently in China in the 1970s and received widespread attention due to its reliable
clinical efficacy. In the 1990s, a new generation of camptothecin drugs, Topotecan (TPT)
and Irinotecan (CPT-11), were successfully developed, and many similar drugs have been
developed since then.

Figure 3. Chemical structure of (A) camptothecin, and its derivatives: (B) topotecan, (C)
irinotecan, (D) SN-38, (E) belotecan, (F) exatecan, and (G) deruxtecan, source: reference
[4]
Currently, 3 camptothecin-derived topoisomerase I inhibitors were approved
worldwide. In 1996, Irinotecan (CPT-11) was approved by the FDA for the treatment of
small cell and non-small cell lung cancer and cervical and ovarian cancer; in 1996,
Topotecan (TPT) was approved by the FDA for the second-line treatment of small cell
lung cancer and ovarian cancer; and in 2003, Belotecan (CDK-602) was approved in
Korea for the treatment of small cell lung cancer and ovarian cancer (Table 1).

Table 1. Approved camptothecin-derived topoisomerase I inhibitors
Drug Delivery Technology Helps
Camptothecin-derived Drugs
Drug delivery is widely used in the antineoplastic field to improve drug efficacy, reduce
drug toxicity, and improve drug safety. Various technologies have been applied to
overcome the problem of the bioavailability of camptothecin drugs, such as liposomes,
antibody-drug conjugates, dendrimers and micelles, etc.
Liposomes
Irinotecan, a semisynthetic analog of the quinoline-basedalkaloid camptothecin, was first
discovered and synthesized in Japan byYakult Honsha Co, Ltd, in 1983. It initially
demonstrated strong activityagainst a broad variety of experimental tumors. Subsequently,
clinical phaseI studies were initiated. Irinotecan was approved for the treatment of
cervical, lung, and ovarian cancer in Japan in 1994. In the following years, its use was
approved in Europe (1995) and the USA (1996).
Liposomal irinotecan (nal-IRI; Onivyde®; also known as pegylated liposomal irinotecan)
was developed to maximize antitumor efficacy while minimizing drug-related toxicity
compared to conventional (non-liposomal) formulations of this topoisomerase 1 inhibitor.

Figure 4. Liposomal irinotecan structure
Liposomes are phospholipid bilayers equipped with an internal aqueous pocket and are
used as drug delivery enhancers for hydrophobic and hydrophilic drugs. Liposomes
provide a protective layer that shields the encapsulated drug from structural changes or
chemical degradation. In addition, the covalent adhesion of PEG molecules can be used
to improve the systemic circulation of the drug.
Liposomal drugs are also being developed for belotecan and SN-38
(7-ethyl-10-hydroxycamptothecin), the active metabolite of irinotecan after carboxylase
conversion, which has a much greater activity than irinotecan in inhibiting topoisomerase I.
LE-SN38 (Liposome-Entrapped SN38 ) is a SN-38 liposome developed by Neopharm.
The core technology of this product is the use of tetraglyceride cardiolipin, which can
closely interact with lipophilic drugs and stably embed into the liposomal phospholipid
membrane, greatly improving the stability in vitro and in vivo, and also enabling the poorly
soluble SN-38 to be injected for drug delivery.
Antibody Drug Conjugates (ADCs)
Nanoparticle formulations increase drug solubility and prolong half-life, however, their
tumor targeting efficiency remains suboptimal due to their passive targeting effect.

For ADC, antibody-mediated active targeting provides selectivity and very high affinity due
to specific antibody-antigen binding, which can distinguish tumors from healthy cells
based on antigen expression levels. Thus, ADCs are designed to deliver
topoisomerase I inhibitor specifically to tumor cells without an off-target effect.
(Table 2)
Table 2. Antibody–Camptothecin Conjugates, Source: reference [4]
Sacituzumab govitecan (Trodelvy®, IMMU-132) conjugated hRS7, a humanized
monoclonal antibody targeting Trop-2, to SN-38, the active metabolite of irinotecan, via a
CL2A linker. Among them, hRS7 is a humanized IgG1 monoclonal antibody with high
specificity, high affinity, good stability and long half-life; CL2A linker is a cleavable linker;
SN-38 is a topoisomerase I inhibitor, which is highly stable in blood and effectively avoids
systemic off-target effects.

Figure 5. Structure of Trodelvy. DOI:10.3390/ph13090245
IMMU-132 is designed to undergo hydrolysis in acidic conditions similar to the tumor
microenvironment, allowing for precise and efficient drug delivery release as well as
bystander effects. With the dual action of antibodies and chemotherapeutic drugs, it can
both precisely target and bind tumor cells with high expression of Trop-2 and release
chemotherapeutic drugs to attack tumors without causing serious toxic side effects. On
April 22, 2020, IMMU-132 received accelerated approval from the FDA for use in third-line
and above metastatic triple-negative breast cancer, becoming the first Trop-2 targeted
drug on the market.
Another ADC delivering a camptothecin drug is trastuzumab deruxtecan
(T-DXd; DS-8201), developed by Daiichi Sankyo in collaboration with AstraZeneca.
DS-8201 comprises an anti-HER2 antibody (trastuzumab), a cleavable
tetrapeptide-based linker, and a topoisomerase I inhibitor (deruxtecan，DXd). In the
presence of the linker, DS-8201 is highly stable in the blood with a very low shedding rate,
which does not affect the metabolic rate and ensures stability and homogeneity. The
cleavable linker makes the drug delivery process of DS-8201 simple and more efficient, as
the lysosomal protease recognizes the linker site and releases the drug after entering the
cell. DS-8201 can target delivery of cytotoxic agents into cancer cells, reducing systemic
exposure of cytotoxic agents.
Figure 6. Structure of DS-8201. DOI:10.3390/ph13090245

DS-8201 has several innovative features; a highly potent novel payload with a high
drug-to-antibody ratio, good homogeneity, a tumor-selective cleavable linker, stable
linker-payload in circulation, and a short systemic half-life cytotoxic agent in vivo; the
released cytotoxic payload could exert a bystander effect. In a head-to-head comparison
of DS-8201 and T-DM1 (trastuzumab emtansine), DS-8201 reduced the risk of patient
progression by 72% and reduced the risk of patient death by 45% compared to T-DM1.
On December 20, 2019, the FDA accelerated approval of DS-8201 for the treatment of
unresectable or metastatic HER2-positive breast cancer. On Jan 15, 2021, DS-8201 was
approved in the U.S. for the treatment of patients with previously treated HER2 positive
advanced gastric cancer. In 2022, FDA approved DS-8201 for patients with
HER2-positive metastatic breast cancer, HER2-low metastatic breast cancer and
previously treated HER2-mutant metastatic non-small cell lung cancer.
Dendrimers
Starpharma, an Australian company, has been working with dendrimers for many years
and has developed DEP®, a technology platform for the delivery and encapsulation of
dendrimers. DEP® irinotecan is a dendrimer version of irinotecan, predominantly used for
colorectal cancer. DEP® irinotecan phase 2 program is currently underway.

Figure 7. Enhanced efficacy of DEP® irinotecan, alone, and in combination with
Lynparza® (olaparib), in human colon cancer model (HT-29). Source:
https://biomelbourne.org/
Micelles
NK012 (Nippon Kayaku, Co.) is a polymeric micelle comprised of PEG and polyglutamate
(PGlu) conjugated covalently with SN-38.
Figure 8. Preparation and characterization of NK012 , Source: reference [5]
In clinical phase II studies, NK012 is being administered every 3 weeks for the treatment
of unresectable, recurrent or metastatic colorectal cancer that has been treated with
cisplatin chemotherapy. NK012 is currently in clinical phase II studies in the United States
for the treatment of recurrent small cell lung cancer and triple-negative breast cancer.
NK012 is also being investigated in combination with 5-fluorouracil or cisplatin for the
treatment of small cell lung cancer in order to improve monotherapy and further enhance
efficacy.
By the way, PEG here is the shell-forming polymer of the polymeric micelles. There
are several reasons for using PEGs. First, it is non-toxic and is one of the few synthetic

polymers that has been approved by the FDA for use in pharmaceutical products. Second,
in an aqueous environment, PEG is highly hydrated and can move quickly, sweeping out
a large exclusion volume. In micelles, PEG forms a dense, brush-like shell that extends
out from the core. These properties serve to limit the interaction of micelles with other
micelles (leading to aggregation) and proteins (opsonin), thus facilitating uptake and
clearance by the mononuclear phagocytic system. Third, PEG can be readily
functionalized to tether ligands for targeted drug delivery. This particular property has led
to a great interest in the delivery of highly potent compounds, such as anticancer agents,
which would benefit greatly in terms of efficacy and safety. All of the above reasons have
contributed to the extensive research on polymeric micelles involving PEGs.
Drug delivery technology is a powerful tool for drug development, and the current
development for camptothecin drugs is mainly focused on irinotecan and SN-38. It is
hoped that with the help of drug delivery technology, more new antitumor drugs can be
developed by overcoming the disadvantages of poor water solubility and inadequate
tissue distribution of more camptothecin drugs.
Biopharma PEG is a professional PEG supplier. We can provide high-purity PEG
linkers from milligram to kilogram scale in GMP and Non-GMP grade for your PEGylated
liposomes, antibody-camptothecin conjugates and micelles development.
References:
[1] Noura Khaiwa, Noor R. Maarouf, Mhd H. Darwish, Dima W.M. Alhamad, Anusha Sebastian,
Mohamad Hamad, Hany A. Omar, Gorka Orive, Taleb H. Al-Tel,, Camptothecin's journey from discovery
to WHO Essential Medicine: Fifty years of promise, European Journal of Medicinal Chemistry, Volume
223, 2021, 113639, ISSN 0223-5234,
[2] Venditto VJ, Simanek EE. Cancer therapies utilizing the camptothecins: a review of the in vivo
literature. Mol Pharm. 2010 Apr 5;7(2):307-49. doi: 10.1021/mp900243b. PMID: 20108971; PMCID:
PMC3733266.

[3] Fujita K, Kubota Y, Ishida H, Sasaki Y. Irinotecan, a key chemotherapeutic drug for metastatic
colorectal cancer. World J Gastroenterol. 2015 Nov 21;21(43):12234-48. doi: 10.3748/wjg.v21.i43.12234.
PMID: 26604633; PMCID: PMC4649109.
[4] Han S, Lim KS, Blackburn BJ, et al. The Potential of Topoisomerase Inhibitor-Based Antibody-Drug
Conjugates. Pharmaceutics. 2022;14(8):1707. Published 2022 Aug 16.
doi:10.3390/pharmaceutics14081707
[5] Lu Y, Park K. Polymeric micelles and alternative nanonized delivery vehicles for poorly soluble drugs.
Int J Pharm. 2013 Aug 30;453(1):198-214. doi: 10.1016/j.ijpharm.2012.08.042. Epub 2012 Aug 25. PMID:
22944304; PMCID: PMC3760723.
Related Articles:
The Rise of the TROP2-Directed ADCs for Solid Tumors
The Bystander Effect of ADCs
HER2 Targeted Therapies In Breast Cancer
Enhertu (Trastuzumab Deruxtecan): Magic ADC Drug

Camptothecin Cancer Therapy Guide

Recomendados

Recomendados

Más contenido relacionado

Similar a Camptothecin Cancer Therapy Guide

Similar a Camptothecin Cancer Therapy Guide (20)

Más de DoriaFang

Más de DoriaFang (20)

Último

Último (20)

Camptothecin Cancer Therapy Guide