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Pattern of Reproductive Cancers in India

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Background: Reproductive cancers are those that affect the human organs that are involved in producing offspring. An attempt is made in the present communication to assess the magnitude and pattern of reproductive cancers, including their treatment modalities, in India. The cancer incidence data related to reproductive cancers collected by five population-based urban registries, namely Bangalore, Bhopal, Chennai, Delhi and Mumbai, for the years 2006-08 were utilized. The reproductive cancers among females constituted around 25% of the total and around 9% among males. Among females, the three major contributors were cervix (55.5%), ovary (26.1%) and corpus uteri (12.4%). Similarly among males, the three major contributors were prostate (77.6%), penis (11.6%) and testis (10.5%). For females, the AAR of reproductive cancers varied between 30.5 in the registry of Mumbai to 37.3 in the registry of Delhi. In males, it ranged between 6.5 in the registry of Bhopal to 14.7 in the registry of Delhi. For both males and females, the individual reproductive cancer sites showed increasing trends with age. The leading treatment provided was: radio-therapy in combination with chemo-therapy for cancers of cervix (48.3%) and vagina (43.9%); surgery in combination with chemo-therapy (54.9%) for ovarian cancer; and surgery in combination with radio-therapy for the cancers of the corpus uteri (39.8%). In males, the leading treatment provided was hormone-therapy for prostate cancer (39.6%), surgery for penile cancer (81.3%) and surgery in combination with chemo-therapy for cancer of the testis (57.6%).
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Asian Pacic Journal of Cancer Prevention, Vol 15, 2014 599
DOI:http://dx.doi.org/10.7314/APJCP.2014.15.2.599
Pattern of Reproductive Cancers in India
Asian Pac J Cancer Prev, 15 (2), 599-603
Introduction
Cervix and Ovarian cancers are the two leading sites
of cancer among women in India. Based on the data of
13 Population Based Cancer Registries in India, Cervix
and Ovarian cancer are the second and the fourth most
common cancer in India, NCRP (2013). The cancer of
the Corpus uteri has also shown an emerging trend over
the years Takiar and Vijay (2010). Similarly, among men,
Prostate cancer has shown an emerging trend Takiar and
Vijay (2011). All these sites belong to Reproductive sites
of cancers. Reproductive cancers are those that affect the
human organs that are involved in producing offspring. In
India, while there are studies (Murthy et al., 2005, Takiar
and Srivastav 2008; Yeole, 2008; Nandakumar et al., 2009;
Takiar and Vijay, 2010; 2011) available related to one or
more sites of cancers that are associated with reproductive
cancers, hardly there is any study discussing all the sites
of cancers together related to reproductive cancers. An
attempt is therefore made in the present communication to
assess the magnitude and pattern of reproductive cancers
including their treatment modalities in India.
Materials and Methods
The cancer incidence data related to reproductive
1National Centre for Disease Informatics and Research, Bangalore, India *For correspondence: ramnath_takiar@yahoo.co.in
Abstract
Background: Reproductive cancers are those that affect the human organs that are involved in producing
offspring. An attempt is made in the present communication to assess the magnitude and pattern of reproductive
cancers, including their treatment modalities, in India. The cancer incidence data related to reproductive cancers
collected by ve population-based urban registries, namely Bangalore, Bhopal, Chennai, Delhi and Mumbai, for
the years 2006-08 were utilized. The reproductive cancers among females constituted around 25% of the total
and around 9% among males. Among females, the three major contributors were cervix (55.5%), ovary (26.1%)
and corpus uteri (12.4%). Similarly among males, the three major contributors were prostate (77.6%), penis
(11.6%) and testis (10.5%). For females, the AAR of reproductive cancers varied between 30.5 in the registry
of Mumbai to 37.3 in the registry of Delhi. In males, it ranged between 6.5 in the registry of Bhopal to 14.7 in
the registry of Delhi. For both males and females, the individual reproductive cancer sites showed increasing
trends with age. The leading treatment provided was: radio-therapy in combination with chemo-therapy for
cancers of cervix (48.3%) and vagina (43.9%); surgery in combination with chemo-therapy (54.9%) for ovarian
cancer; and surgery in combination with radio-therapy for the cancers of the corpus uteri (39.8%). In males,
the leading treatment provided was hormone-therapy for prostate cancer (39.6%), surgery for penile cancer
(81.3%) and surgery in combination with chemo-therapy for cancer of the testis (57.6%)
Keywords: Reproductive cancers - cervix - ovary - corpus uteri - prostate - penis - testis
RESEARCH ARTICLE
Pattern of Reproductive Cancers in India
Ramnath Takiar, Sathish Kumar
cancers collected by five urban registries namely
Bangalore, Bhopal, Chennai, Delhi and Mumbai for the
years 2006-08 were utilized. In women, the sites which
are included under reproductive cancers with respective
ICD10 codes are: Vulva (C51), Vagina (C52), Cervical
Uteri (C53), Corpus Uteri (C54), Uterus Unspecied
(C55), Ovary etc. (C56), Other Female genital (C57) and
Cancers of Placenta (C58). In men, it include Penis (C60),
Prostate (C61), Testis (C62) and Other Male Genital (C63)
NCRP 2013.
Percentage contribution of reproductive sites
All cancer cases of individual reproductive sites
when added will give the total number of reproductive
cancers. When this number is expressed as percentage
of all cancers, provides an idea about their percentage
contribution to all cancers. In order to decide the major
sites of reproductive cancers, the number of cancer
cases by individual reproductive site is expressed as the
percentage of total number of reproductive cancers. If
‘n’ represents the number of reproductive cancers and
‘x’ represents the number of cases by an individual
reproductive cancer site (S) then (x/n)*100 provides the
percentage contribution of site ‘S’ to total reproductive
cancers.
To form an idea about the burden of the Reproductive
Ramnath Takiar and Sathish Kumar
Asian Pacic Journal of Cancer Prevention, Vol 15, 2014
600
cancers in India, it is necessary to study their Crude Rates.
Crude Rate (CR): The Crude Rate is obtained by the
division of number of cases by the corresponding
estimated population (midyear) for given reproductive
site, sex, area and year (period) and multiplied by 100000.
In terms of formula it is given by: CR=(New cases of cancer
for a given site and year or period/Estimated mid-population of the
same year or period)5100000
Age specic rate (ASR)
Cancer incidence is known to increase with age.
Hence, it is important to assess the Age Specic Rates. It is
obtained by the division of the total number of cancer cases
of a given site by the corresponding estimated midyear
population for given age, sex, period and multiplying by
100000.
ASR=[New cancer cases of a site in the given age group,
sex and year (period)/Estimated mid-population of the same
year (period) for given age group and sex]5100000
Age adjusted rate (AAR)
In order to make the rates comparable between
developed and developing countries, an Age Adjusted
Rate is derived using a common world standard population
proportions as weightings to various age specic rates.
The details of it can be seen in the report NCRP 2010.
The formula for derivation of AAR is given below:
AAR=∑(ai5wi)/∑wi)5100000 for all i=1,2,3,................16.
Where: ai=Age specic rate for ith age group and; wi=World
standard population for ith age group. Note that i=1 refers
to 0-4 age group; i=2 refers to 5-9 age group and so on.
Treatment modalities for Reproductive cancers:
Hospital Based Cancer Registries (HBCR) working under
the co-ordination of National Cancer Registry Programme
(NCRP) are routinely collecting information on treatments
provided to all cancer patients. Same information was
utilized to throw light on the treatment modalities carried
out for reproductive cancers in India.
Results
The ve registries reported 47054 cases of cancers
during the period 2006-08 (NCRP 2010), out of which
12044 (25.6%) cases constituted that of reproductive
cancers. In case of females, the percentage of reproductive
cancers varied from 24.3% in the registry of Mumbai to
28.1% in the registry of Bhopal. While, for males, the
percentage of reproductive cancers varied from 5.4% in
the registry of Bhopal to 9.0% in the registry of Bangalore
(Table 1).
Among reproductive cancers for females, the three
major contributors are: Cervix (55.5%), Ovary (26.1%)
and Corpus uteri (12.4%). Each of the other sites, in
general, contributed less than 3% of the total reproductive
cancer cases (Table 2).
Among reproductive cancers in males, the three major
contributors are: Prostate (77.6%), Penis (11.6%) and
Testis (10.5%). Other male genital cases contributed only
0.3% of the total reproductive cancer cases (Table 3).
For females, the CR of reproductive cancers varied
between 22.0 in the registry of Bhopal to 29.6 in the
registry of Chennai. While, in the case of AAR, it varied
between 30.5 in the registry of Mumbai to 37.3 in the
registry of Delhi. In males, the CR (AAR) ranged between
4.0 (6.5) in the registry of Bhopal to 7.6(14.7) in the
registry of Delhi (Table 4).
The Age Specic Rates of Reproductive cancer sites
for females, pooled for all selected ve urban registries,
is shown in Table 5. The cervix incidence rate starts
increasing rapidly after the age of 35 years and reaches to
Table 2. Reproductive Cancers Sites and their
Percentage Contribution to Total Reproductive
Cancers-Females
Cancer Site Bangalore Bhopal Chennai Delhi Mumbai Pooled
Cervix uteri 57.2 62.3 59.4 54.5 52.8 55.5
Ovary 21.8 26.0 24.0 28.4 27.3 26.1
Corpus uteri 14.3 9.0 9.7 12.1 13.4 12.4
Uterus unspecied 2.7 0.4 2.0 2.1 2.7 2.3
Vagina 2.1 0.5 3.2 1.2 2.2 2.0
Vulva 1.8 0.5 1.5 1.2 1.3 1.3
Placenta 0.1 1.3 0.2 0.2 0.1 0.2
Other Female genital 0.1 0.0 0.1 0.2 0.2 0.1
Reproductive cancer cases -
Total 1910 546 1996 3364 4228 12044
Table 3. Reproductive Cancers Sites and their
Percentage Contribution to Total Reproductive
Cancers-Males
Cancer Site Bangalore Bhopal Chennai Delhi Mumbai Pooled
Prostate 77.0 75.0 66.4 81.4 78.5 77.6
Penis 13.0 8.3 22.2 9.1 10.0 11.6
Testis 9.8 16.7 11.4 9.5 10.9 10.5
Other Male genital 0.2 0.0 0.0 0.1 0.6 0.3
Reproductive cases
Total 522 108 428 1182 1281 3521
Table 1. Number and Percentage of Reproductive
Cancers by Sex and Selected Urban Registries of India
Cancer Registry Females Males
Reproductive All % of all Reproductive All % of all
Cancer cases cancers cancers Cancer cases cancers cancers
Bangalore 1910 7210 26.5 522 5812 9.0
Bhopal 546 1946 28.1 108 1992 5.4
Chennai 1996 7866 25.4 428 7392 5.8
Delhi 3364 12602 26.7 1182 13708 8.6
Mumbai 4228 17430 24.3 1281 15602 8.2
Pooled 12044 47054 25.6 3521 44506 7.8
*Source: National Cancer Registry Programme (2010): Three-year Report of
Population Based Cancer Registries (2006-2008)
Table 4. Crude Rate (CR) and Age Adjusted Rate (
AAR) per 100000 Person of Reproductive cancers by
Sex and Selected Urban Registries of India
Registry Females Males
CR AAR CR AAR
Bangalore 27.9 36.3 6.9 11.0
Bhopal 22.0 31.2 4.0 6.5
Chennai 29.6 32.9 6.2 7.2
Delhi 25.4 37.3 7.6 14.7
Mumbai 25.3 30.5 6.3 10.7
Range 22.0-29.6 30.5-37.3 4.0-7.6 6.5-14.7
Mean 26.0 33.6 6.2 10.0
SD 2.89 3.03 1.35 3.30
Asian Pacic Journal of Cancer Prevention, Vol 15, 2014 601
DOI:http://dx.doi.org/10.7314/APJCP.2014.15.2.599
Pattern of Reproductive Cancers in India
it peak in the age group of 55-64 years. Similar trend was
also seen in the case of corpus uteri and ovarian cancer.
In general, the Age Specic Rate (ASR) for reproductive
cancers increased rapidly with advancement of every 10
years after the age of 25 years. It starts from 0.9 for the
age group below 25 years to 131.0 in 55+ years age group .
In males the ASR of prostate cancer increases rapidly
particularly after the age of 55 years and reaches to its peak
after the age of 65 years (Table 6). For both males and
females, the Individual reproductive cancer sites showed
the increasing trend with age.
The type of treatment provided to female cancer
patients according to their reproductive cancer sites is
shown in Table 7. The leading treatment provided was
Radio-therapy in combination with Chemo-therapy for the
cancers of Cervix (48.3%) and Vagina (43.9%); Surgery in
combination with Chemo-therapy (54.9%) for the cancer
of Ovary; Surgery in combination with Radio-therapy for
the cancers of Corpus uteri (39.8%) and Uterus unspecied
(36.7%); Surgery for the cancer of Vulva (34.1%) and
Chemo-therapy for the cancer of Placenta (85.7%).
The type of treatment provided to male cancer patients
according to their reproductive cancer sites is shown in
Table 8. The leading treatment provided was Hormone-
therapy for Prostate cancer (39.6%); Surgery for penile
cancer (81.3%); Surgery in combination with Chemo-
therapy for cancer of testis (57.6%).
Discussion
The data has shown that among females, about 25% of
the total cancers constitutes that of reproductive cancers
while among males its percentage is around 8%. In
females, the leading three sites of reproductive cancers
are Cervix, Ovary and Corpus uteri. In males, they are
Prostate, Penis and Testis. These leadings sites contributed
more than 90% of the total reproductive cancers. The data
has shown that the age specic rates in women above 55
years increases to almost 4 folds as compared to that seen
in 35-44 years age group of women. In men, above 55
years age, the rise was found to be 5 to 20 times higher
as compared to that seen in 35-44 years age group. Thus,
like any other cancer, the age specic rates of reproductive
cancers show an increasing trend.
There were an estimated 530000 cases of cervical
cancer and 275000 deaths from the disease in 2008.
Cervical cancer is generally caused by sexually acquired
infection with certain types of HPV; Schiffman M,
Solomon D (2013). Two HPV types (16 and 18), almost
cause 70% of cervical cancers and precancerous cervical
lesions WHO (2013). Sexual activity that increases the
risk for infection for cervical cancer includes: Having
multiple sexual partners or Sexual intercourse at a young
age (WHO 2013, Reproductivecancer.com). Regular
screening via Pap Smears greatly reduces the risk
for developing invasive cervical cancer by detecting
precancerous changes in cervical cells. Women who do
not receive regular Pap smears have a higher risk for
Table 5. Age Specic Rate (ASR) per 100000 person of
Reproductive Cancer sites-Females-Pooled
(2006-2008)
Site of Cancer <25 25-34 35-44 45-54 55-64 65+
Cervix Uteri 0.1 3.2 20.2 48.7 69.8 61.9
Corpus Uteri 0.0 0.4 2.4 8.8 22.6 17.6
Ovary 0.8 2.9 7.4 19.5 31.6 30.3
Other female genitals 0.0 0.4 1.2 3.9 7.5 11.7
Pooled 0.9 6.8 31.2 80.9 131.5 121.5
Table 6. Age Specic Rate (ASR) per 100000 person of
Reproductive cancer sites-Males-Pooled (2006-2008)
Site of Cancer <25 25-34 35-44 45-54 55-64 65+
Prostate 0.0 0.0 0.2 2.3 20.1 101.8
Penis 0.0 0.2 0.7 1.8 3.8 6.6
Other male genitals 0.4 1.3 0.9 0.6 0.8 1.3
Pooled 0.4 1.5 1.8 4.8 24.7 109.7
Table 7. The distribution of Treatment by Different Reproductive Cancer Sites-Females
Treatment Cervix Uteri Ovary Corpus Uteri Vagina Vulva Placenta Uterus unspecied
Radio therapy (R) 39.2 0.5 5.9 39.5 18.8 0.0 6.7
Chemo thearpy (C) 2.3 33.1 3.5 7.8 15.3 85.7 10.0
Surgery (S) 3.3 8.7 32.0 2.4 34.1 2.0 10.0
R+C 48.3 1.1 2.8 43.9 9.4 2.0 0.0
R+S 3.3 0.5 39.8 1.0 3.5 0.0 36.7
C+S 0.6 54.9 5.8 1.5 12.9 6.1 23.3
S+R+C 2.9 0.5 8.6 2.9 4.7 4.1 13.3
Other combinations 0.1 0.7 1.6 1.0 1.3 0.1 0.0
Number 5604 1464 538 205 85 49.0 30
*Based on Pooled HBCR data of Bangalore, Chennai, Mumbai, Thiruvananthapuram, Dibrugarh (2004-06)
Table 8 The Distribution of Treatment by Different
Reproductive Cancer Sites-Males
Treatment Prostate Penis Testis
Radio therapy (R) 10.2 0.9 0.0
Chemo therapy (C) 2.0 4.7 21.2
Harmone therapy (H) 39.6 0.0 0.0
Surgery (S) 8.6 81.3 12.4
R+H 20.1 0.0 0.0
R+S 1.2 4.4 4.7
H+S 3.5 0.0 0.0
S+C 0.0 7.0 57.6
S+R+C 1.8 1.6 2.9
Other combinations 13.0 0.1 1.2
Number 512 316 170
*Based on Pooled HBCR data of Bangalore, Chennai, Mumbai, Thiruvananthapuram,
Dibrugarh (2004-06)
Ramnath Takiar and Sathish Kumar
Asian Pacic Journal of Cancer Prevention, Vol 15, 2014
602
the condition (WHO 2013, Reproductivecancer.com,
Ofce of Population Affairs). The early stages of cervical
cancer may be completely symptom free. The possible
symptoms in early stages may include: Vaginal bleeding;
contact bleeding; moderate pain during sexual intercourse;
vaginal discharge. The symptoms of advanced cervical
cancer may include: loss of appetite; weight loss; fatigue;
pelvic pain; single swollen leg; heavy bleeding from the
vagina (WHO 2013, Reproductivecancer.com, Ofce of
Population Affairs).
Ovarian cancer is the fourth most common cancer
among women in India. Based on the data of Mumbai
PBCR, the AAR of death rate in ovarian cancer was 3.7
as compared to AAR of 3.9 seen in cervix cancer NCRP
(2010). For ovarian cancer, the risk factors are: Family
history of ovarian cancer; Fertility Drugs; Hormone
replacement therapy (HRT) with estrogens only (without
progesterone); Late menopause (after age 52); Never
given birth or delivering first child after the age 30
(Reproductivecancer.com, Ofce of Population Affairs).
The symptoms that are often found to be associated
with ovarian cancer are: Loss of appetite, full feeling,
Unexplained weight gain, Swelling and Pain in the lower
abdomen, Lower back pain, Abnormal vaginal bleeding
and Pain during sex (Reproductivecancer.com, Ofce of
Population Affairs, Can Teen).
For cancer of corpus uteri, the risk factors are:
Exposure to estrogen increases the risk for developing
the disease and estrogen often affects tumor growth.
The following factors increase estrogen exposure: Early
menarche (before the age 12 years), Hormone replacement
therapy (HRT) with estrogens only (without progesterone);
Late menopause (after age 52); Never given birth or
delivering rst child after the age 30 (Reproductivecancer.
com, Can Teen). The symptoms that are often found to
be associated with Abnormal uterine bleeding, abnormal
menstrual periods, Bleeding between normal periods
in premenopausal women, vaginal bleeding and/or
spotting in postmenopausal women, Lower abdominal
pain and Anemia caused by chronic loss of blood
(Reproductivecancer.com, Ofce of Population Affairs,
Can Teen).
In men, Prostate cancer constitutes about 80% of
newly diagnosed reproductive cancer cases. The risk for
developing prostate cancer rises signicantly with age.
It’s AAR increases rapidly after the age of 55 years (20.1)
and reaches to its peak (101.8). It has been found to be
an emerging cancer in India Takiar and Vijay (2011).
A family history of prostate cancer increases the risk
(Reproductivecancer.com, Ofce of Population Affairs,
Can Teen). Other possible risk factors include: Diet
high in saturated fat, Sedentary lifestyle and Smoking.
Early prostate cancer usually causes no symptoms.
However there are some symptoms and they are: frequent
urination, increased urination at night, difculty starting
and maintaining a steady stream of urine, blood in
the urine, and painful urination, problems with sexual
function(Reproductivecancer.com, Ofce of Population
Affairs, Can Teen).
The main risk factor for testicular cancer is a problem
called undescended testicle(s) and accounts for 10% of the
cases. A family history of prostate cancer increases the risk.
Other possible risk factors include: HIV infection, Cancer
of the other testicle, Body Size(Reproductivecancer.com,
Can Teen). Symptoms may include one or more of the
following: a lump in one testis or a hardening of one of
the testicles, pain and tenderness in the testicles, loss of
sexual activity, build-up of uid in the scrotum, a dull ache
in the lower abdomen or groin, an increase, or signicant
decrease, in the size of one testis, blood in semen(Ofce
of Population Affairs, Can Teen). Possible signs of penile
cancer include sores, discharge, and bleeding. The risk
factors include: Being age 60 or older. Having phimosis
(a condition in which the foreskin of the penis cannot be
pulled back over the glans), Having poor personal hygiene,
Having many sexual partners, Using tobacco products (
Ofce of Population Affairs).
For cancer patients in PBCRs, the detailed information
on treatment is not available. Therefore, the HBCR data
(2009) was utilized to throw light on treatment details.
The treatment depends on the type of cancer. Reproductive
cancers are often treated with Chemotherapy (medicine
to kill cancer cells), Hormone therapy (medicine to
block hormones that are related to cancer growth) or
Radiation. Depending on the type of cancer, one or more
treatments may be used together. Radiotherapy alone or
in combination with Chemo-therapy was the preferred
choice of treatment in the cancers of Cervix uteri and
Vagina. Surgery alone or surgery in combination with
Radio-therapy was the preferred choice of treatment
in the cancers of Corpus uteri and in cancers of Uterus
unspecied. In the case of cancers of Ovary or Placenta,
the preferred choice of treatment was essentially Chemo-
therapy or Chemo-therapy in combination with Surgery.
In case of men, for Prostate cancer, the preferred choice
of treatment was mainly Hormone therapy while it was
Surgery for Penile cancer. In case of Cancer of Testis,
Chemo-therapy or Chemo-therapy in combination with
Surgery was the main course of treatment.
Survival rates are important for prognosis, for example
whether a type of cancer has a good or bad prognosis
can be determined from its survival rate. Cervix cancer
is considered as one of the major leading sites among
females. Survival studies carried out in India (IARC,
2011) have shown that the 5 years absolute % survival for
Cervix cancer is around 42% while for Ovarian cancer it is
relatively less and is around 23%. Among males, Prostate
cancer has the least absolute % survival of 24% while
Penile cancer (43.6%) and Testicular cancer (53.0%) have
relatively higher 5 years absolute % survivals.
It is to remember that an early diagnosis leading to
an early treatment can increase the chances of survival
signicantly among the Reproductive cancer cases. The
success of early detection and cancer treatment may be
measured by improvement in survival from cancer.
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... Testicular cancers represent 10.5% of all male reproductive cancers in India. 9 Various studies have been done to access the incidence of neoplastic and non-neoplastic testicular lesions. Our study was also an attempt to do so. ...
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Testicular tumors are relatively rare and comprise 1% of all male cancers worldwide with peak prevalence in the age group 15-35 years. Testicular lesions have a varied histomorphological spectrum and are largely categorized as non-neoplastic and neoplastic lesions. To study the incidence of testicular lesions, to study the histomorphological spectrum of testicular lesions including non-neoplastic as well as neoplastic lesions and to determine age-wise distribution, laterality and clinical presentation in testicular lesions. The present study is an observational study, carried out in the Pathology Department of Indira Gandhi Medical college, a tertiary care hospital in the northern India, over a duration of two years i.e from June 2020 to May 2022. A total of 52 radical orchidectomy and testicular biopsies were studied for gross and microscopic findings. 45 orchidectomy specimens and 7 testicular biopsies were studied. Out of these, 42 cases were non neoplastic and 10 were neoplastic. Maximum number of patients presented in the 2 & 4 decade of life. Undescended testis was the most common non-neoplastic lesion (17/42;40.47%), followed by testicular torsion (12/42;28.57%). Seminoma was the most common neoplastic lesions (50%), followed by Mixed Germ Cell Tumors (20%) and Non-Hodgkin lymphoma (20%) and a single case of yolk sac tumor (10%). Clinically, most of the patients presented with scrotal swelling (58.53%). Right testis was involved more commonly (32/52;61.53%). Testicular cancers represent 10.5% of all male reproductive cancers in India. Germ cell tumors accounted for highest percentage of cases with a commonest subtype of seminoma followed by mixed germ cell tumors. Histopathologic examination can help in accurately diagnosing and determining the prognosis of these rare tumor and tumor like lesions of testis.
... Our findings are confined to a sample of relatively illiterate women in both areas, thus limiting their applicability to the Kurnool district. The study findings A study done by Takiar and Kumar [5] showed that 55.5% had a cervix, the present study noticed 32% cervical cancers among the 81 patients enrolled in the department of radiotherapy. A study done by Nagaraju et al. (2014) [6] who showed that breast cancer found in 21%, which is nearly similar findings (22%) reported in the present study. ...
Chapter
Penile cancers have a heterogeneous distribution worldwide, ranging from age-standardised incidence of >2 per 100,000 in Africa, South America and South Asia to incidence of <0.5 per 100,000 in the Middle East and East Asia [1]. Penile cancer (PC) is an extremely uncommon disease with an incidence as low as 0.29/100,000 in the United States [2].The World Health Organization (WHO) estimated a total of 36,068 new cases in 2020 with an incidence of 0.8 per 100,000 men worldwide [3]. Penile squamous cell carcinoma (PSCC) is the fourth least common cancer by incidence and is classified under “rare tumour” as per the definition by the National Cancer Institute [4]. The incidence is higher in certain African and South American countries such as Uganda with an incidence of 4.4 per 100,000 and Paraguay with an incidence of 4.2 per 100,000 [2]. This heterogeneity is attributed to various risk factors such as socioeconomic status, history of penile injuries and inflammation, tobacco smoking, hygiene, genetic predisposition, the prevalence of practice of circumcision and human papillomavirus (HPV) infection [5, 6].
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The chapter provides a snapshot of one of the important innate immune receptors, surfactant protein-D (SP-D), as a promising molecule for cancer therapy that targets multiple pathways for its action.
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The Indian Society for the Study of Reproduction and Fertility (ISSRF) published a Special Issue of the Newsletter titled "A Kaleidoscopic View of Advances in Reproductive Health Research as India Turns 75" to commemorate the 75th Anniversary of Indian Independence (Azadi ka Amrit Mahotsav).
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Mangifera indica L. is a popular and widely available plant. Mangifera zeylanica Hook.f. is a plant endemic to Sri Lanka. Both plants bare edible fruits and possess medicinal properties. In the present study, potential anticancer effects of M. zeylanica and M. indica leaves were investigated in lung cancer cells. Hexane, chloroform, ethyl acetate, and methanol extracts of leaves from both plants were obtained using sequential extraction. Chloroform extract of M. zeylanica leaves (MZC) and ethyl acetate extract of M. indica leaves (MIEA) inhibited the proliferation, migration, and colony formation. These extracts showed low cytotoxicity in MRC-5 normal lung fibroblast cells. Furthermore, DNA fragmentation analysis and ethidium bromide/acridine orange (AO/EB) staining showed that MZC and MIEA can induce apoptosis. Gene expression analysis by real-time PCR identified that MZC and MIEA can regulate the expression of apoptosis-associated genes p53, Bax, and survivin. In addition, treatment of both MZC and MIEA decreased histone deacetylase (HDAC) activity, indicating the HDAC inhibitory potentials of leaf extracts. Liquid chromatography-mass spectrometry (LC-MS) identified the presence of mangiferin, 6-geranylnaringenin, nodakenin, and pyrogallol in both leaf extracts as major phytochemicals. Overall, our findings indicate that M. zeylanica and M. indica leaf extracts exert anticancer activity by decreasing the proliferation of non-small lung cancer cells possibly through the inhibition of the activity of HDACs, a major class of enzymes implicated in epigenetic modifications. This investigation provides a rationale to isolate compounds with anticancer and HDAC inhibitory potentials from M. zeylanica and M. indica leaves.
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There has been a transition of diseases among the Indian masses seen over the last two decades. Of late, noncommunicable diseases and diseases due to environmental factors have increased manifold. Among them, cancer is a concern with every passing day across regions of India. Among them, reproductive cancers are conditions that occur in the reproductive organs contributing to the increased burden of diseases. These are cancers in the breast, cervix, uterus, vulva, endometrium and ovaries, which affect across demographics and geographies of India. Reproductive cancers can also be found in men, like prostate cancer, testicular cancer, and penile cancer. Reproductive cancers have a significant impact on the lives of men and women worldwide. Given the seriousness of the problem, this review discusses the various determinants of reproductive cancer care in India. Further, this review examines the access to cancer care among Indian men and women. The paper gathered existing evidence through a literature search about facts, figures, and narratives of reproductive cancer in India. According to the basic objective, a literature review was done to assess various factors affecting reproductive cancer in the Indian population. The issues of reproductive cancer were assessed at different levels like socio-cultural, concerns of cancer and access to cancer care. The search sites like PubMed, Scopus, Web of Science, and Journal Storage (JSTOR) were used to unravel the issues of reproductive cancer among men and women. The article brings out many concerns about the control of reproductive cancer in India. In India, the screening, diagnosis, and modern cancer care procedures are insufficient, especially reproductive cancer care. There is also a lack of access to reproductive cancer care in most parts of the country, especially in the rural areas. The infrastructure, workforce, and supply chain of medications for cancer care are very worrisome, which needs to be augmented for primary cancer care. Overall, the public health system has to be augmented by considering the systems thinking approach by including all the stakeholders. The complex issues need simplified solutions. Hence, there is a need for training and capacity building to enhance reproductive cancer care among individuals, families, and communities at large.
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Introduction: The male genital system consists of the prostate, seminal vesicle, testes, epididymis, vas deferens, bulbourethral gland, ejaculatory duct, penis and scrotum. Male genital cancers are histologically diverse. They are difficult to detect and treat because of their anatomic locations, biological characters and complications. Aim: To study the histopathological spectrum of tumours of the male genital system according to World Health Organisation (WHO) classification. Materials and Methods: The present study is a hospital based descriptive study conducted in the Department of Pathology, Guru Gobind Singh Medical College and Hospital, Faridkot, Punjab, India, during February 2019 to August 2020 which included 128 cases. All biopsies, specimens and review blocks and slides of male genital tract tumours were processed and slides were stained with Haematoxylin and Eosin (H&E) stain. Serum tumour markers and immunohistochemical stains were used. The clinical information including symptoms related to the male genital system, histopathological findings and diagnosis were recorded on the predesigned proforma. Other necessary information was collected from the requisition form received along with the biopsy material. The association between categorical variables was explored using Pearson’s Chi-square test. A p-value
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Changes in cancer pattern are often studied with regard to rank of leading sites, variation in age adjusted rates of sites over the time or with the help of time trends. However, these methods do not quantify the changes in relation to overall changes that occurred in the total cancer cases over the period of time. An alternative approach is therefore necessary, particularly to identify emerging new cancers. The cancer incidence data of various sites for men, over the periods 1988-90 and 2003-05 in India, for five urban registries namely Bangalore, Bhopal, Chennai, Delhi and Mumbai, functioning under the network of National Cancer Registry Programme (ICMR), formed the sources of data for the present analysis. Changes in incidence cases by various cancer sites for men are assessed by calculating the differences in incidence cases over the two period of time. Based on the contribution of each site to total change, the ten most leading sites are identified separately for each registry. The relative changes in the sites with time are taken to identify the most emerging new cancer cases over the period of time. The pooled cancer cases for men among five urban registries increased from 30042 cases in 1988-90 to 46946 cases in 2003-05 registering an increase of about 55.8%. The lowest percentage of increase is observed in the registry of Mumbai (25.6%) and the maximum in Bhopal (96.4%). Based on the pooled figures of five urban registries, the lung cancer contributed the maximum % change (9.7%), followed by cancer of prostate (9.2%), mouth (7.5%), tongue (5.9%) and NHL (5.9%). Based on the pooled figures and the relative changes, the emerging new cancers are prostate (140%), liver (112%) and mouth (95%). The % change by sites and the emerging new cancers varied between the registries.
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The changes in the cancer pattern are often studied with the help of changes in the rank of leading sites, changes in the Age Adjusted Rates of the sites over the time or with the help of time trends. However, these methods do not quantify the changes in relation to overall changes that occurred in the total cancer cases over the period of time. An alternative approach was therefore used to assess the changes in cancer pattern in relation to overall changes in time and also an attempt was made to identify the most emerging new cancers in India. The cancer incidence data of various sites for women, over the periods 1988-90 and 2003-05 in India, for five urban registries namely Bangalore, Bhopal, Chennai, Delhi and Mumbai, functioning under the network of National Cancer Registry Programme (ICMR), formed the sources of data for the present analysis. The changes in incidence cases by various cancer sites for women were assessed by calculating the differences in incidence cases over the two period of time. Based on the contribution of each site to total change, the ten most leading sites were identified separately for each registry. The relative changes in the sites with time were taken to identify the most emerging new cancer cases over the period of time. The pooled cancer cases for women among five urban registries increased from 29447 cases in 1988-90 to 48472 cases in 2003-05 registering an increased of about 63.3%. The lowest percentage of increase was observed in the registry of Chennai (41.5%) and the maximum in Bhopal (102.0%). Based on the pooled figures, the breast cancer contributed to the maximum % change (38%), followed by ovarian (8.0%), gallbladder (5.1%), corpus uteri (4.9%) and cervix uteri (4.1%). Based on the pooled data and relative changes, the emerging new cancers were corpus uteri (187%), gallbladder (162.1%) and lung cancer (136.1%). The % change by sites and the emerging new cancers varied between the registries.
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The Indian Council of Medical Research initiated a network of cancer registries under the National Cancer Registry Programme (NCRP) in 1981 and data collection commenced in these registries from January 1982. The results on incidence rates provided by the Population Based Cancer Registries (PBCRs) have shown the variation in patterns of cancer in general and that of cancer cervix in particular. Cancer of the cervix has been the most important cancer in women in India, over past two decades. All the urban Population Based Cancer Registries at Bangalore, Bhopal, Chennai, Delhi and Mumbai have shown a statistically significant decrease in incidence rates of this site of cancer. Since over 70 per cent of the Indian population resides in the rural areas, cancer cervix still constitutes the number one cancer in either sex. Based on the data of the PBCRs, the estimated number of new cancers during 2007 in India was 90.708. The relative five year survival reported some time earlier averaged 48.7 per cent.
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The Indian Council of Medical Research (ICMR) started a National Cancer Registry Programme (NCRP) in the year 1982 with the main objective of generating reliable data on the magnitude and pattern of cancer in India. There are about 20 Population Based Cancer Registries (PBCR) which are currently functioning under the network of NCRP. The present paper aims to provide the time trends in the incidence of breast and cervix cancer among females of India. The incidence data collected by Bangalore, Barshi, Bhopal, Chennai, Delhi and Mumbai over the period 1990 to 2003 formed the sources of data. In the year 1990, cervix was the leading site of cancer followed by breast cancer in the registries of Bangalore (23.0% vs 15.9%), Bhopal (23.2% vs 21.4%), Chennai (28.9% vs 17.7%) and Delhi (21.6% vs 20.3%), while in Mumbai breast was the leading site of cancer (24.1% vs 16.0%). By the years 2000-3, the scenario had changed and breast had overtaken as the leading site of cancer in all the registries except in Barshi (16.9% vs 36.8%). The time trend analysis for these sites suggested a significant decreasing trend in the case of cervix in Bangalore and Delhi registries, while the registries of Bhopal, Chennai and Mumbai did not show any significant changes. However, in the case of breast cancer, a significant increasing trend was observed in Bhopal, Chennai and Delhi registries with Bangalore and Mumbai registries demonstrating no such significant changes. Histopathologic confirmation for both malignancies was found to be more than 80% in these registries. It is concluded that in India the cervix cancer rates are decreasing while breast cancer is on the increase.
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Cancer of the uterine cervix is the second most common cancer among women in the world after breast cancer. It is the most common cancer among Indian women. The present communication reports the trends in the incidence rate of cervical cancer for the Indian population. The data published in Cancer Incidence in Five Continents for various Indian registries for different periods and/or publication by the individual registry served as the source material. During the years 1990-1997, the age-adjusted incidence rates (AAR) for cervical cancer varied from 10.9 to 65.4 amongst various registries. The highest incidence was noted in the Ambillikai registry. The age-specific incidence rates (ASIR) for cervical cancer revealed that the disease increases from 35 years and reaches a peak between the ages 55 to 64 years. The trend analysis by period showed a decreasing trend in the incidence rate of cervical cancer in all the registries. However, the decrease was very small. The mean annual percentage decrease in the AAR ranged from 0.9 to 2.6% amongst various registries. Analysis of the data by ASIR revealed that the mean annual percentage decrease was higher for women in earlier age groups in most of the registries. For women beyond 64 years, the disease incidence showed an increasing trend or minimal decrease. It was also noted that most of the cervical cancer cases were detected with regional spread of the disease and a very small proportion were diagnosed at a localized stage. In India, an organized mass-screening programme with Pap smear for early detection of cervical cancer is not in practice. The data suggest an urgent need for initiation of community screening and educational programmes for the control and prevention of cervical cancer.
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A healthy 35-year-old woman wants to discuss cervical-cancer screening. She reports no symptoms and has a negative screening history except for an "abnormal Pap" about 10 years previously that did not require treatment. She has two children, is currently taking oral contraceptives, and does not smoke. She is interested in human papillomavirus (HPV) testing because of an article she read in a magazine, which suggested that "testing with HPV and Pap is better than just Pap alone." What would you advise?
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Epidemiological and experimental studies have clearly shown that high-risk HPV infection is the main etiologic factor for cervical cancer. Recent studies have indicated that the E6 and E7 gene products play a critical role in cervical carcinogenesis. The E6 and E7 products interfere with the p53 and pRB functions, respectively, and deregulate the cell cycle. The HPV DNA is integrated into the host's chromosomes with disruption of the E2 gene. This disruption promotes the expression of E6 and E7, leading to the accumulation of DNA damage and the development of cervical cancer. The study of the immune response against HPV has been hampered by the lack of a cell culture system for the virus. A breakthrough was made by the discovery that a major capsid protein L1 self-assembles into virus-like particles (VLP) when expressed in eukaryotic systems. Clinical trials of VLP-based vaccines are in progress, and DNA vaccines for the HPV surface protein genes are under development. The E7 and E6 oncoproteins are attractive targets for cancer immunotherapy because their expression is required to maintain the oncogenicity of cervical cancer cells. Cancer immunotherapy for cervical cancer with vaccinations of E7 peptides or dendritic cell-based immunotherapy is moving toward clinical trials.
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Trends in prostate cancer in five population-based cancer Registries (Mumbai, Chennai, Bangalore, Delhi & Bhopal) in India were studied over a period of two decades using a model that fitting the data as the logarithm of Y=ABx which represents a Linear Regression model. This approach showed increasing trends in the age adjusted incidence rates throughout the entire period of observation for most of the registries, especially in Chennai and Bhopal and to the least extent in Mumbai. Particularly in Asia we face a future major increase in the rates of prostate cancer. Collaborative action now is a high priority to allow the preparations necessary for effective control of prostate cancer.
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Trends in breast, cervix uteri, corpus uteri and ovarian cancers in six population based cancer registries (Mumbai, Bangalore, Chennai, Delhi, Bhopal, and Barshi) were evaluated over a period of the last two decades. For studying trends we used a model that fits this data is the logarithm of Y=ABx which represents a Linear Regression model. This approach showed a decreasing trend for cancer of the cervix and increasing trends for cancers of breast, ovary and corpus uteri throughout the entire period of observation in most of the registries. The four cancers, breast, cervix, corpus uteri and ovary, constitute more than 50% of total cancers in women. As all these cancers are increasing, to understand their etiology in depth, analytic epidemiology studies should be planned in a near future on a priority basis.