Priya GaneshkumarObjectives We evaluated the impact of a standardized, simple audio-visual (AV) training video developed in regional languages on cervical cancer awareness among apparently healthy women and their willingness to undergo regular cervical cancer screening. Materials and Methods This cross-sectional noninterventional multicentric survey was conducted in 69 centers across 14 states in India and one center in UAE among women aged between 18 and 88 years attending clinics for a variety of indications. Using a short questionnaire, cervical cancer awareness and willingness to undergo cervical cancer screening were assessed before and after the AV training. Statistical Analysis In addition to descriptive analysis, improvement in awareness after the AV training was assessed using McNemar's test, and comparison of responses between subgroups was performed using Pearson chi-squared test. Results The survey was completed by 3,188 apparently healthy women (mean age: 36.8 ± 11.3 years). Before AV training, correct answers were given to only 4/6 questions by majority of the participants; most participants were unaware about the main cause of cervical cancer (1,637/3,188, 51.4%), availability of cervical cancer screening tests (1,601/3,188, 50.2%), and cervical cancer vaccines (1,742/3,188, 54.6%). Only 576 women (18.1%) had undergone cervical cancer screening in the past. After the AV training, the proportion of women correctly responding to all six questions improved significantly (p < 0.05), and 84.4% (2691/3188) women showed willingness to undergo periodic cervical cancer screening. Compared to unmarried and professional women, although married women and home-makers had lower awareness scores, the latter subgroups had more often undergone previous cervical cancer screening. Conclusion It is possible to improve cervical cancer awareness among healthy women, and to enhance their willingness to undergo regular cervical cancer screening tests using a simple, six minute-long, standardized AV training material.
{"title":"Audio-Visual Training Improves Awareness and Willingness of Cervical Cancer Screening among Healthy Indian Women: Findings from a Survey.","authors":"Priya Ganeshkumar","doi":"10.1055/s-0042-1751094","DOIUrl":"https://doi.org/10.1055/s-0042-1751094","url":null,"abstract":"<p><p>Priya Ganeshkumar<b>Objectives</b> We evaluated the impact of a standardized, simple audio-visual (AV) training video developed in regional languages on cervical cancer awareness among apparently healthy women and their willingness to undergo regular cervical cancer screening. <b>Materials and Methods</b> This cross-sectional noninterventional multicentric survey was conducted in 69 centers across 14 states in India and one center in UAE among women aged between 18 and 88 years attending clinics for a variety of indications. Using a short questionnaire, cervical cancer awareness and willingness to undergo cervical cancer screening were assessed before and after the AV training. <b>Statistical Analysis</b> In addition to descriptive analysis, improvement in awareness after the AV training was assessed using McNemar's test, and comparison of responses between subgroups was performed using Pearson chi-squared test. <b>Results</b> The survey was completed by 3,188 apparently healthy women (mean age: 36.8 ± 11.3 years). Before AV training, correct answers were given to only 4/6 questions by majority of the participants; most participants were unaware about the main cause of cervical cancer (1,637/3,188, 51.4%), availability of cervical cancer screening tests (1,601/3,188, 50.2%), and cervical cancer vaccines (1,742/3,188, 54.6%). Only 576 women (18.1%) had undergone cervical cancer screening in the past. After the AV training, the proportion of women correctly responding to all six questions improved significantly (p < 0.05), and 84.4% (2691/3188) women showed willingness to undergo periodic cervical cancer screening. Compared to unmarried and professional women, although married women and home-makers had lower awareness scores, the latter subgroups had more often undergone previous cervical cancer screening. <b>Conclusion</b> It is possible to improve cervical cancer awareness among healthy women, and to enhance their willingness to undergo regular cervical cancer screening tests using a simple, six minute-long, standardized AV training material.</p>","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"23-29"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/10/f1/10-1055-s-0042-1751094.PMC9966178.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10813465","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Myint Myint Thinn, Soe Aung, Aye Aung, Nwe Mar Tun
In Myanmar, the cervical cancer burden is still noticeably high, and it is still a leading cause of cancer-related deaths among Myanmar women. According to the GLOBOCAN 2020,1 age-standardized incidence of cervical cancer in Myanmar was 22.6/100,000 women, whereas it was 14.5/100,000 for mortality. It was said to be the first most common female cancer. However, according to executive report of Yangon PBCR,2 age-standardized incidence was 19.5/100,000 in 2018 for Yangon region. Naypyidaw PBCR report of 5 consecutive years from 2013 to 2017 stated that age-standardized rate (ASR) was 14.1/100,000, and it is the eighth leading cause of cancer death in both sexes combined and the fourth in female.3 According to hospital statistics, cervical cancer is the second most common female cancer after breast cancer.4 Myanmar was selected as one of the countries for United Nations Global Joint Program (UNGJP) for cervical cancer prevention and control since 2017. With the technical assistance of UNGJP,Myanmar tries to improve all the three pillars of cervical cancer prevention, that is, primary, secondary, and tertiary preventions, as well as development of palliative care centers and population-based cancer registries. As for primary prevention, human papillomavirus (HPV) vaccination was first introduced in Expanded Programme of Immunization (EPI) program as 13th new vaccine for 9-yearold girls as a single age cohort since 2020. First dose of HPV vaccine was planned to be introduced in 2020 with both school-based and community-based strategies. For secondary prevention, guidelines for screening and treatment of cervical precancer in public health care facilities were published and launched in 2018. In this guideline, hybrid approach based on both HPV DNA and visual inspectionwith acetic acid (VIA) testing is adopted. Since 70% of the eligible population resides in the rural areas, VIA testing is not feasible to apply for those regions with limited human resource. HPV DNA testing with self-collected samples is planned to be used in rural areas. In urban and suburban areas where there are enough health care personnels who can performVIA testing, the primary screening test would be with VIA. HPV testing is aimed to be used for the whole country when enough resources are available. In community setting, screening age is 30 to 49 years, while in hospital setting, up to 65 years are screenedmainlywith cytology and HPV tests if it is readily available. Treatment of the screen-positive women is mainly by the ablative method for both VIA and HPV testing in community settings. Thermal coagulation is the preferred ablative treatment after visual assessment test (VAT) in HPV-based screening. Here, ablation of the whole transformation zone even without obvious lesion after VAT is also offered after thorough counseling for those women from remote areas who prefer less frequent visits. Precancerous lesions which are not eligible for ablative treatment or suspicious of cance
{"title":"Current Status of Cervical Cancer Prevention and Screening in Myanmar.","authors":"Myint Myint Thinn, Soe Aung, Aye Aung, Nwe Mar Tun","doi":"10.1055/s-0043-1764212","DOIUrl":"https://doi.org/10.1055/s-0043-1764212","url":null,"abstract":"In Myanmar, the cervical cancer burden is still noticeably high, and it is still a leading cause of cancer-related deaths among Myanmar women. According to the GLOBOCAN 2020,1 age-standardized incidence of cervical cancer in Myanmar was 22.6/100,000 women, whereas it was 14.5/100,000 for mortality. It was said to be the first most common female cancer. However, according to executive report of Yangon PBCR,2 age-standardized incidence was 19.5/100,000 in 2018 for Yangon region. Naypyidaw PBCR report of 5 consecutive years from 2013 to 2017 stated that age-standardized rate (ASR) was 14.1/100,000, and it is the eighth leading cause of cancer death in both sexes combined and the fourth in female.3 According to hospital statistics, cervical cancer is the second most common female cancer after breast cancer.4 Myanmar was selected as one of the countries for United Nations Global Joint Program (UNGJP) for cervical cancer prevention and control since 2017. With the technical assistance of UNGJP,Myanmar tries to improve all the three pillars of cervical cancer prevention, that is, primary, secondary, and tertiary preventions, as well as development of palliative care centers and population-based cancer registries. As for primary prevention, human papillomavirus (HPV) vaccination was first introduced in Expanded Programme of Immunization (EPI) program as 13th new vaccine for 9-yearold girls as a single age cohort since 2020. First dose of HPV vaccine was planned to be introduced in 2020 with both school-based and community-based strategies. For secondary prevention, guidelines for screening and treatment of cervical precancer in public health care facilities were published and launched in 2018. In this guideline, hybrid approach based on both HPV DNA and visual inspectionwith acetic acid (VIA) testing is adopted. Since 70% of the eligible population resides in the rural areas, VIA testing is not feasible to apply for those regions with limited human resource. HPV DNA testing with self-collected samples is planned to be used in rural areas. In urban and suburban areas where there are enough health care personnels who can performVIA testing, the primary screening test would be with VIA. HPV testing is aimed to be used for the whole country when enough resources are available. In community setting, screening age is 30 to 49 years, while in hospital setting, up to 65 years are screenedmainlywith cytology and HPV tests if it is readily available. Treatment of the screen-positive women is mainly by the ablative method for both VIA and HPV testing in community settings. Thermal coagulation is the preferred ablative treatment after visual assessment test (VAT) in HPV-based screening. Here, ablation of the whole transformation zone even without obvious lesion after VAT is also offered after thorough counseling for those women from remote areas who prefer less frequent visits. Precancerous lesions which are not eligible for ablative treatment or suspicious of cance","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"47-48"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a3/f3/10-1055-s-0043-1764212.PMC9966159.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10813462","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A F M Kamal Uddin, Mostafa Aziz Sumon, Shahana Pervin, Farzana Sharmin
Bangladesh is a densely populated country having a population of 165,158,616asper the census2022.Among them83,347,206 are female and here majority of them (113,063,587) lives in rural area.1 The allocation of health sector budget is 2.34% of gross domestic product and in the year 2018, share of 75.3% of the total health expenditure was from private sector with an annual growth of 0.93%.2 There is no national cancer registry of the country. As per GOLOBOCAN 2020, the age-standardized incidence rate ofcancer ofBangladesh is calculated as 106.2 and the case load of cancer in Bangladesh was 1,56,775 and the cancer death was 1,08,990.3 Cervical cancer is the fourth most common cancer globally among women. In the year 2020, an estimated 6,04,000 new cases and 3,42,000 deaths were recorded. Alarmingly 90% of these new case and deaths occurred worldwide in 2020 were in lowand middle-income countries. The annual number of global new cases of cervical cancer has been projected to increase between 2018 and 2030 from 570,000 to 700,000 and the annual number of deaths projected to increase from 311,000 to 400,000.4 In Bangladesh, cervical cancer is the secondmost common cancer of female (12%).3 The number of new cases was 8,068 (10.6 per 100,000 women) and deaths was 5.214 (7.1 per 100,00 women) in 2018.3 The prediction was that without any intervention a total of 505,703 women in Bangladesh will die from cervical cancer by the year 2070 and the number will rise to 1,042,859 by 2120.5 The Government of Bangladesh (GOB) is giving due emphasis to noncommunicable disease (NCD) to achieve the target of sustainable development goalwhere cervical cancer management is considered as an important component of NCD. Both the government and private sectors are working together to fight against cervical cancer.
{"title":"Cervical Cancer in Bangladesh.","authors":"A F M Kamal Uddin, Mostafa Aziz Sumon, Shahana Pervin, Farzana Sharmin","doi":"10.1055/s-0043-1764202","DOIUrl":"https://doi.org/10.1055/s-0043-1764202","url":null,"abstract":"Bangladesh is a densely populated country having a population of 165,158,616asper the census2022.Among them83,347,206 are female and here majority of them (113,063,587) lives in rural area.1 The allocation of health sector budget is 2.34% of gross domestic product and in the year 2018, share of 75.3% of the total health expenditure was from private sector with an annual growth of 0.93%.2 There is no national cancer registry of the country. As per GOLOBOCAN 2020, the age-standardized incidence rate ofcancer ofBangladesh is calculated as 106.2 and the case load of cancer in Bangladesh was 1,56,775 and the cancer death was 1,08,990.3 Cervical cancer is the fourth most common cancer globally among women. In the year 2020, an estimated 6,04,000 new cases and 3,42,000 deaths were recorded. Alarmingly 90% of these new case and deaths occurred worldwide in 2020 were in lowand middle-income countries. The annual number of global new cases of cervical cancer has been projected to increase between 2018 and 2030 from 570,000 to 700,000 and the annual number of deaths projected to increase from 311,000 to 400,000.4 In Bangladesh, cervical cancer is the secondmost common cancer of female (12%).3 The number of new cases was 8,068 (10.6 per 100,000 women) and deaths was 5.214 (7.1 per 100,00 women) in 2018.3 The prediction was that without any intervention a total of 505,703 women in Bangladesh will die from cervical cancer by the year 2070 and the number will rise to 1,042,859 by 2120.5 The Government of Bangladesh (GOB) is giving due emphasis to noncommunicable disease (NCD) to achieve the target of sustainable development goalwhere cervical cancer management is considered as an important component of NCD. Both the government and private sectors are working together to fight against cervical cancer.","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"36-38"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/40/a6/10-1055-s-0043-1764202.PMC9966158.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10813466","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In Pakistan, cervical cancer continues to be a challenge. About 68.6millionwomen over the age of 15 are at risk of developing cervical cancer, with the annual number of cases being over 5,000. Of these, more than 3,000 women lose their lives, making cervical cancer the third leading cause of cancerrelated deaths in women of the reproductive age group in Pakistan. In the country, 88% of cervical cancer cases are due to humanpapillomavirus (HPV) serotypes 16 and 18, as reported by the International Agency for Research on Cancer.1 HPV is a nonenveloped DNA virus belonging to the Papillomaviridae family, with over a hundred different serotypes. Of which, 15 to 20 are oncogenic, with 16 and 18 being the most common. HPV is transmitted via sexual activity. It is found that 75% of all sexually active adults are estimated to be positive for at least one HPV serotype. However, most of these infections have spontaneous resolution with only less than 1% progressing to cancer.2 This progression can be reduced by regular screening via pap smears. The developed world has seen a significant decline in cervical cancer mortality since screening through pap smears introduced to the population. Unfortunately, in developing countries like Pakistan, the uptake of pap smears is very limited, estimated at one instance to be as low as 2%.3 In such circumstances, where pap smears are already difficult to conduct and have low uptake, HPV vaccinations become even more crucial for cervical cancer prevention. Two globally licensed HPV vaccines have been introduced in Pakistan: a quadrivalent vaccine Gardasil (marketed by Merck, Pakistan) and a bivalent vaccine Cervarix (marketed by GlaxoSmithKline, Pakistan). Gardasil is protective against the HPV serotypes 6, 11, 16, and 18, providing protection against both cervical cancer and genital warts. On the other hand, Cervarix is effective against serotypes 16 and 18, thereby protecting only against cervical cancer. It is important to note that both these vaccines work prophylactically and do not have any effect on pre-existing infections.2 Despite their introduction in Pakistan, there is a dearth of awareness regarding these vaccines and a low uptake in the general population. One study done in women of the reproductive age group at a tertiary care center in Karachi estimated the awareness of HPV vaccines to be as low as 20% and their uptake to be less than 10%.4
{"title":"HPV Vaccination as a Mode of Cervical Cancer Prevention in Pakistan.","authors":"Asma Burney, Ramsha Zafar","doi":"10.1055/s-0043-1764211","DOIUrl":"https://doi.org/10.1055/s-0043-1764211","url":null,"abstract":"In Pakistan, cervical cancer continues to be a challenge. About 68.6millionwomen over the age of 15 are at risk of developing cervical cancer, with the annual number of cases being over 5,000. Of these, more than 3,000 women lose their lives, making cervical cancer the third leading cause of cancerrelated deaths in women of the reproductive age group in Pakistan. In the country, 88% of cervical cancer cases are due to humanpapillomavirus (HPV) serotypes 16 and 18, as reported by the International Agency for Research on Cancer.1 HPV is a nonenveloped DNA virus belonging to the Papillomaviridae family, with over a hundred different serotypes. Of which, 15 to 20 are oncogenic, with 16 and 18 being the most common. HPV is transmitted via sexual activity. It is found that 75% of all sexually active adults are estimated to be positive for at least one HPV serotype. However, most of these infections have spontaneous resolution with only less than 1% progressing to cancer.2 This progression can be reduced by regular screening via pap smears. The developed world has seen a significant decline in cervical cancer mortality since screening through pap smears introduced to the population. Unfortunately, in developing countries like Pakistan, the uptake of pap smears is very limited, estimated at one instance to be as low as 2%.3 In such circumstances, where pap smears are already difficult to conduct and have low uptake, HPV vaccinations become even more crucial for cervical cancer prevention. Two globally licensed HPV vaccines have been introduced in Pakistan: a quadrivalent vaccine Gardasil (marketed by Merck, Pakistan) and a bivalent vaccine Cervarix (marketed by GlaxoSmithKline, Pakistan). Gardasil is protective against the HPV serotypes 6, 11, 16, and 18, providing protection against both cervical cancer and genital warts. On the other hand, Cervarix is effective against serotypes 16 and 18, thereby protecting only against cervical cancer. It is important to note that both these vaccines work prophylactically and do not have any effect on pre-existing infections.2 Despite their introduction in Pakistan, there is a dearth of awareness regarding these vaccines and a low uptake in the general population. One study done in women of the reproductive age group at a tertiary care center in Karachi estimated the awareness of HPV vaccines to be as low as 20% and their uptake to be less than 10%.4","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"51-52"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/07/78/10-1055-s-0043-1764211.PMC9966174.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10813460","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Dinesh Chandra DovalBackground Circulating tumor cells (CTCs) in the peripheral blood may play a major role in the metastatic spread of breast cancer. This study was conducted to assess the role of CTCs to determine the prognosis in terms of survival in metastatic breast cancer patients. Methods This prospective study of 36 patients was conducted at the Hospital from April 2016 to May 2018. Details of each patient related to the demographic profile, tumor type, treatment, and follow-up information were recorded. The number of CTCs in the peripheral blood was measured by Celsee PREP 400 sample processing system and Celsee Analyzer imaging station. Results There was a positive correlation between the number of site of metastasis with number of CTCs ( p -value < 0.001). In the patients with clinical/partial response, a significant reduction in the number of CTCs after 1 month of therapy was observed ( p -value = 0.003). When the number of CTCs at baseline and 6 months were compared with the positron emission tomography response at 6 months, a statistically significant difference in CTCs in patients having partial response after 6 months was observed ( p -value = 0.001). On comparison with the responder groups, a statistically significant reduction in CTCs at baseline and 6 months was observed ( p -value = 0.001). Patients with CTCs less than 5 and more than or equal to 5 after 1 month of treatment had a mean progression-free survival of 11.1 months and 7.5 months ( p -value = 0.04) and a mean overall survival of 11.6 and 9.6 months ( p -value = 0.08), respectively. Conclusion Assessment of CTCs provides a more quantifiable response than radiographic evaluation and at a much earlier time point and is also a better predictor of survival.
{"title":"Role of Circulating Tumor Cells in Determining Prognosis in Metastatic Breast Cancer.","authors":"Sonia Dhaka, Rupal Tripathi, Dinesh Chandra Doval, Anurag Mehta, Udip Maheshwari, Venkata Pradeep Babu Koyyala, Jatinderpal Singh","doi":"10.1055/s-0042-1753477","DOIUrl":"https://doi.org/10.1055/s-0042-1753477","url":null,"abstract":"<p><p>Dinesh Chandra Doval<b>Background</b> Circulating tumor cells (CTCs) in the peripheral blood may play a major role in the metastatic spread of breast cancer. This study was conducted to assess the role of CTCs to determine the prognosis in terms of survival in metastatic breast cancer patients. <b>Methods</b> This prospective study of 36 patients was conducted at the Hospital from April 2016 to May 2018. Details of each patient related to the demographic profile, tumor type, treatment, and follow-up information were recorded. The number of CTCs in the peripheral blood was measured by Celsee PREP 400 sample processing system and Celsee Analyzer imaging station. <b>Results</b> There was a positive correlation between the number of site of metastasis with number of CTCs ( <i>p</i> -value < 0.001). In the patients with clinical/partial response, a significant reduction in the number of CTCs after 1 month of therapy was observed ( <i>p</i> -value = 0.003). When the number of CTCs at baseline and 6 months were compared with the positron emission tomography response at 6 months, a statistically significant difference in CTCs in patients having partial response after 6 months was observed ( <i>p</i> -value = 0.001). On comparison with the responder groups, a statistically significant reduction in CTCs at baseline and 6 months was observed ( <i>p</i> -value = 0.001). Patients with CTCs less than 5 and more than or equal to 5 after 1 month of treatment had a mean progression-free survival of 11.1 months and 7.5 months ( <i>p</i> -value = 0.04) and a mean overall survival of 11.6 and 9.6 months ( <i>p</i> -value = 0.08), respectively. <b>Conclusion</b> Assessment of CTCs provides a more quantifiable response than radiographic evaluation and at a much earlier time point and is also a better predictor of survival.</p>","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"62-67"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7b/23/10-1055-s-0042-1753477.PMC9966169.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10813468","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cervical cancer screening is still an opportunistic mode of procedure. Conventional pap smear was the first method used for long, then the visual method introduced in practice. However, it has been limited to the mid-level paramedics with lesser priority in facility level. Specialist service providers put more effort on newer methods like liquid-based cytology and human papillomavirus (HPV) DNA testing but without feasible and affordable system in place. Cervical cancer prevention and control program is in place from the Department of Health Services but still the implementation part is poor. Systematic approach is being followed if the screening is a part of research or thesis from academia. Screening and treatment of invasive lesions are not linked yet in practice because of poor implementation of public– private partnership considering a huge magnitude of service from private sector.
{"title":"Cervical Cancer Screening and HPV Vaccination in Nepal.","authors":"Gehanath Baral","doi":"10.1055/s-0043-1764155","DOIUrl":"https://doi.org/10.1055/s-0043-1764155","url":null,"abstract":"Cervical cancer screening is still an opportunistic mode of procedure. Conventional pap smear was the first method used for long, then the visual method introduced in practice. However, it has been limited to the mid-level paramedics with lesser priority in facility level. Specialist service providers put more effort on newer methods like liquid-based cytology and human papillomavirus (HPV) DNA testing but without feasible and affordable system in place. Cervical cancer prevention and control program is in place from the Department of Health Services but still the implementation part is poor. Systematic approach is being followed if the screening is a part of research or thesis from academia. Screening and treatment of invasive lesions are not linked yet in practice because of poor implementation of public– private partnership considering a huge magnitude of service from private sector.","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"53-54"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/60/74/10-1055-s-0043-1764155.PMC9966170.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9138067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
[This corrects the article DOI: 10.1055/s-0043-1764155.].
[这更正了文章DOI: 10.1055/s-0043-1764155.]。
{"title":"Erratum: Cervical Cancer Screening and HPV Vaccination in Nepal.","authors":"Gehanath Baral, Rajendra Baral","doi":"10.1055/s-0043-1764405","DOIUrl":"https://doi.org/10.1055/s-0043-1764405","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1055/s-0043-1764155.].</p>","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"e1"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cc/80/10-1055-s-0043-1764405.PMC10017259.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9146321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Elroy Saldanha, Sanjay M Desai, Dhruv G Patel, Vinod Dhakad, Bonny Joseph, Sandeep Ghosh, Varun Prakash, Harsha Deepti, Ashma Monteiro
Sanjay M. DesaiObjectives Epithelial ovarian cancer (EOC) is a heterogeneous, essentially peritoneal disease. Standard treatment consists of staging, cytoreductive surgery (CRS), and adjuvant chemotherapy. In this study, we intended to assess the effectiveness of single-dose intraperitoneal (IP) chemotherapy in optimally debulked advanced EOC patients. Materials and Methods A prospective randomized study of 87 patients with advanced EOC was done from January 2017 to May 2021 in a tertiary care center. Patients who underwent primary and interval cytoreduction received a single dose of IP chemotherapy for 24 hours after being divided into four groups: group A, IP cisplatin; group B, IP paclitaxel; group C, IP paclitaxel and cisplatin; and group D, saline. Pre- and postperitoneal IP cytology was assessed along with possible complications. Statistical Analysis Logistic regression analysis was used to assess for intergroup significance in cytology and complications. Kaplan-Meir analysis was done to assess disease-free survival (DFS). Results Of 87 patients, 17.2% of patients had FIGO stage IIIA, 47.2% had IIIB, and 35.6% had IIIC. Also, 22 (25.3%) patients were in group A (cisplatin), 22 (25.3%) patients in group B (paclitaxel), 23 (26.4%) in group C (cisplatin and paclitaxel), and 20 (23%) in group D (saline). Cytology samples taken during staging laparotomy were positive, and 48 hours post-IP chemotherapy, 2 (9%) of 22 samples in cisplatin group and 14 (70%) of 20 samples in saline group were positive; all of the post-IP samples in groups B and C were negative. No major morbidity was noted. In our study, DFS in saline group was 15 months, while in IP chemotherapy group it was 28 months and was statistically significant based log-rank test. However, there was no significant difference in DFS between different IP chemotherapy groups. Conclusion Complete or optimal CRS in advanced EOC does have a possibility of microscopic peritoneal residue. Adjuvant locoregional strategies should be considered to prolong DFS. Single-dose normothermic IP chemotherapy can be offered to the patients with minimal morbidity, and its prognostic benefits are comparable to hyperthermic IP chemotherapy. Future clinical trials are required to validate these protocols.
{"title":"NIPEC with Single-Dose Intraperitoneal Cisplatin and Paclitaxel in Stage III Epithelial Ovarian Cancer.","authors":"Elroy Saldanha, Sanjay M Desai, Dhruv G Patel, Vinod Dhakad, Bonny Joseph, Sandeep Ghosh, Varun Prakash, Harsha Deepti, Ashma Monteiro","doi":"10.1055/s-0042-1751098","DOIUrl":"https://doi.org/10.1055/s-0042-1751098","url":null,"abstract":"<p><p>Sanjay M. Desai<b>Objectives</b> Epithelial ovarian cancer (EOC) is a heterogeneous, essentially peritoneal disease. Standard treatment consists of staging, cytoreductive surgery (CRS), and adjuvant chemotherapy. In this study, we intended to assess the effectiveness of single-dose intraperitoneal (IP) chemotherapy in optimally debulked advanced EOC patients. <b>Materials and Methods</b> A prospective randomized study of 87 patients with advanced EOC was done from January 2017 to May 2021 in a tertiary care center. Patients who underwent primary and interval cytoreduction received a single dose of IP chemotherapy for 24 hours after being divided into four groups: group A, IP cisplatin; group B, IP paclitaxel; group C, IP paclitaxel and cisplatin; and group D, saline. Pre- and postperitoneal IP cytology was assessed along with possible complications. <b>Statistical Analysis</b> Logistic regression analysis was used to assess for intergroup significance in cytology and complications. Kaplan-Meir analysis was done to assess disease-free survival (DFS). <b>Results</b> Of 87 patients, 17.2% of patients had FIGO stage IIIA, 47.2% had IIIB, and 35.6% had IIIC. Also, 22 (25.3%) patients were in group A (cisplatin), 22 (25.3%) patients in group B (paclitaxel), 23 (26.4%) in group C (cisplatin and paclitaxel), and 20 (23%) in group D (saline). Cytology samples taken during staging laparotomy were positive, and 48 hours post-IP chemotherapy, 2 (9%) of 22 samples in cisplatin group and 14 (70%) of 20 samples in saline group were positive; all of the post-IP samples in groups B and C were negative. No major morbidity was noted. In our study, DFS in saline group was 15 months, while in IP chemotherapy group it was 28 months and was statistically significant based log-rank test. However, there was no significant difference in DFS between different IP chemotherapy groups. <b>Conclusion</b> Complete or optimal CRS in advanced EOC does have a possibility of microscopic peritoneal residue. Adjuvant locoregional strategies should be considered to prolong DFS. Single-dose normothermic IP chemotherapy can be offered to the patients with minimal morbidity, and its prognostic benefits are comparable to hyperthermic IP chemotherapy. Future clinical trials are required to validate these protocols.</p>","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"74-80"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/95/c9/10-1055-s-0042-1751098.PMC9970754.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9368931","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Navneet KaurBackground Fatigue is one of the commonest sequelae of breast cancer treatment that adversely impacts quality of life (QOL) of breast cancer survivors (BCSs). However, very limited data are available about cancer-related fatigue in Indian patients. Hence, this study was planned with the objectives to study (1) prevalence of fatigue in short-, intermediate-, and long-term follow-up; (2) severity and characteristics of fatigue; (3) impact of fatigue on QOL; and (4) correlation of fatigue with other survivorship issues. Materials and Methods The study was conducted on ( n = 230) BCSs who had completed their primary treatment (surgery, radiotherapy, and chemotherapy) and were coming for follow-up. The prevalence of fatigue was noted from a screening tool, which comprised of 14 commonly reported survivorship issues. Assessment of fatigue was done by using survivorship fatigue assessment tool-1 score and QOL was assessed by functional assessment of cancer therapy-breast (FACT-B) questionnaires. To understand how fatigue evolved over time, survivors were divided into three groups according to the time elapsed since initial treatment: Group 1: <2 years ( n = 105); Group 2: 2-5 years ( n = 70); Group 3: >5 years ( n = 55). Statistical Analysis Data was analyzed by using simple descriptive statistics, one way analysis of variance followed by Tukey's test for comparison of quantitative data among the three groups, and Pearson correlation coefficients for association of fatigue with other survivorship issues. Results Clinically significant fatigue (≥4) was noted in 38% of BCSs. However, high overall prevalence of fatigue (60%) was seen, which persisted in long-term survivors (51%) as well. Severity of fatigue was mostly mild (37.7%) to moderate (47.1%). Fatigue scores were significantly higher in short-term survivors ( 5.01 ± 2.06) than intermediate- (4.03 ± 1.42) and long-term BCSs (3.57 ± 1.37). The mean score on FACT-B was 90.07 ± 10.17 in survivors with fatigue and 104.73 ± 7.13 in those without fatigue ( p = 0.000). Significant correlation of fatigue was seen with other survivorship issues like limb swelling, chronic pain, premature menopause, and its related symptoms and emotional distress. Conclusion Fatigue is highly prevalent in BCSs. Survivorship care programs should include appropriate measures to evaluate and address fatigue.
{"title":"Prevalence, Characteristics, and Correlates of Fatigue in Indian Breast Cancer Survivors: A Cross-Sectional Study.","authors":"Navneet Kaur, Puneet Prasan Mahapatra, Sagar Chakraborty","doi":"10.1055/s-0042-1749319","DOIUrl":"https://doi.org/10.1055/s-0042-1749319","url":null,"abstract":"<p><p>Navneet Kaur<b>Background</b> Fatigue is one of the commonest sequelae of breast cancer treatment that adversely impacts quality of life (QOL) of breast cancer survivors (BCSs). However, very limited data are available about cancer-related fatigue in Indian patients. Hence, this study was planned with the objectives to study (1) prevalence of fatigue in short-, intermediate-, and long-term follow-up; (2) severity and characteristics of fatigue; (3) impact of fatigue on QOL; and (4) correlation of fatigue with other survivorship issues. <b>Materials and Methods</b> The study was conducted on ( <i>n</i> = 230) BCSs who had completed their primary treatment (surgery, radiotherapy, and chemotherapy) and were coming for follow-up. The prevalence of fatigue was noted from a screening tool, which comprised of 14 commonly reported survivorship issues. Assessment of fatigue was done by using survivorship fatigue assessment tool-1 score and QOL was assessed by functional assessment of cancer therapy-breast (FACT-B) questionnaires. To understand how fatigue evolved over time, survivors were divided into three groups according to the time elapsed since initial treatment: Group 1: <2 years ( <i>n</i> = 105); Group 2: 2-5 years ( <i>n</i> = 70); Group 3: >5 years ( <i>n</i> = 55). <b>Statistical Analysis</b> Data was analyzed by using simple descriptive statistics, one way analysis of variance followed by Tukey's test for comparison of quantitative data among the three groups, and Pearson correlation coefficients for association of fatigue with other survivorship issues. <b>Results</b> Clinically significant fatigue (≥4) was noted in 38% of BCSs. However, high overall prevalence of fatigue (60%) was seen, which persisted in long-term survivors (51%) as well. Severity of fatigue was mostly mild (37.7%) to moderate (47.1%). Fatigue scores were significantly higher in short-term survivors <b>(</b> 5.01 ± 2.06) than intermediate- (4.03 ± 1.42) and long-term BCSs (3.57 ± 1.37). The mean score on FACT-B was 90.07 ± 10.17 in survivors with fatigue and 104.73 ± 7.13 in those without fatigue ( <i>p</i> = 0.000). Significant correlation of fatigue was seen with other survivorship issues like limb swelling, chronic pain, premature menopause, and its related symptoms and emotional distress. <b>Conclusion</b> Fatigue is highly prevalent in BCSs. Survivorship care programs should include appropriate measures to evaluate and address fatigue.</p>","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"55-61"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/bf/c1/10-1055-s-0042-1749319.PMC9966180.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10805961","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sara Rehman, Bushra Rehman, Anis Ur Rehman, Islah Ud Din, Aamer Iftikhar, Ainy Javaid, Muhammad Asad Parvaiz
Sara RehmanObjectives The purpose of this study was to determine the diagnostic accuracy of breast magnetic resonance imaging (MRI) in classifying incidental satellite masses in biopsy-proven breast cancer patients as benign or malignant masses and assessing its impact on surgical management of these patients. We also analyzed the incidence of MRI-detected lesions, which were thereafter assessed with second look ultrasound (US). Materials and Methods A retrospective study was performed on breast cancer patients presenting from August 01, 2016 to July 31, 2019, with satellite masses seen on base line MRI. Satellite masses were classified as benign and malignant based on MRI features of shape, margin, T2-weighted imaging signals, internal enhancement pattern, enhancement kinetic curves, and diffusion restriction. This was compared with results of histopathological examination. The number of MRI-detected lesions, location of the satellite mass, and type of surgery were also documented. Results Out of 400 breast cancer patients undergoing MRI breast, 115 patients had multiple masses. Histopathological diagnosis was available for 73 patients; and a total of 93 satellite masses were evaluated. There was evidence of additional masses on second look ultrasound in 21 patients. Of 72 masses classified as malignant on MRI, 58 showed malignant pathological outcome; while out of 21 masses characterized as benign on MRI, 18 turned out to be benign on histopathology. A statistically significant association was found between MRI features and pathological outcome of satellite masses ( p = 0.001). The sensitivity, specificity, positive and negative predictive values, and accuracy were 95%, 56%, 80.56%, 85.7% and 81.7%, respectively. Based on these findings, modified radical mastectomy (MRM)/mastectomy was done for 42 patients, 5 patients underwent lumpectomy limited to a single tumor, extended resection done for 14 patients, 5 underwent bilateral breast conservation surgery (BCS), BCS for contralateral breast done for 4 patients undergoing ipsilateral MRM/mastectomy, and bilateral MRM/mastectomies were performed for 2 patients. One patient was lost to follow up. Conclusion Breast MRI is the most sensitive modality for the assessment of breast cancer and plays an essential role in the detection of additional tumor foci. These findings can modify the surgical approach in these patients. However, considering the low specificity, biopsy of satellite masses is imperative to determine the most appropriate surgical plan.
{"title":"MRI Features of Synchronous Masses in Known Breast Cancer Patients in Predicting Benign Versus Malignant Lesions: A Case Based Review at Tertiary Care Cancer Hospital.","authors":"Sara Rehman, Bushra Rehman, Anis Ur Rehman, Islah Ud Din, Aamer Iftikhar, Ainy Javaid, Muhammad Asad Parvaiz","doi":"10.1055/s-0042-1755468","DOIUrl":"https://doi.org/10.1055/s-0042-1755468","url":null,"abstract":"<p><p>Sara Rehman<b>Objectives</b> The purpose of this study was to determine the diagnostic accuracy of breast magnetic resonance imaging (MRI) in classifying incidental satellite masses in biopsy-proven breast cancer patients as benign or malignant masses and assessing its impact on surgical management of these patients. We also analyzed the incidence of MRI-detected lesions, which were thereafter assessed with second look ultrasound (US). <b>Materials and Methods</b> A retrospective study was performed on breast cancer patients presenting from August 01, 2016 to July 31, 2019, with satellite masses seen on base line MRI. Satellite masses were classified as benign and malignant based on MRI features of shape, margin, T2-weighted imaging signals, internal enhancement pattern, enhancement kinetic curves, and diffusion restriction. This was compared with results of histopathological examination. The number of MRI-detected lesions, location of the satellite mass, and type of surgery were also documented. <b>Results</b> Out of 400 breast cancer patients undergoing MRI breast, 115 patients had multiple masses. Histopathological diagnosis was available for 73 patients; and a total of 93 satellite masses were evaluated. There was evidence of additional masses on second look ultrasound in 21 patients. Of 72 masses classified as malignant on MRI, 58 showed malignant pathological outcome; while out of 21 masses characterized as benign on MRI, 18 turned out to be benign on histopathology. A statistically significant association was found between MRI features and pathological outcome of satellite masses ( <i>p</i> = 0.001). The sensitivity, specificity, positive and negative predictive values, and accuracy were 95%, 56%, 80.56%, 85.7% and 81.7%, respectively. Based on these findings, modified radical mastectomy (MRM)/mastectomy was done for 42 patients, 5 patients underwent lumpectomy limited to a single tumor, extended resection done for 14 patients, 5 underwent bilateral breast conservation surgery (BCS), BCS for contralateral breast done for 4 patients undergoing ipsilateral MRM/mastectomy, and bilateral MRM/mastectomies were performed for 2 patients. One patient was lost to follow up. <b>Conclusion</b> Breast MRI is the most sensitive modality for the assessment of breast cancer and plays an essential role in the detection of additional tumor foci. These findings can modify the surgical approach in these patients. However, considering the low specificity, biopsy of satellite masses is imperative to determine the most appropriate surgical plan.</p>","PeriodicalId":22053,"journal":{"name":"South Asian Journal of Cancer","volume":"12 1","pages":"68-73"},"PeriodicalIF":0.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/00/d9/10-1055-s-0042-1755468.PMC9966179.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10813459","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}