Assessment of early-death in gynecologic malignancy in the United States

IF 2.4 3区 医学 Q2 OBSTETRICS & GYNECOLOGY International Journal of Gynecology & Obstetrics Pub Date : 2024-09-02 DOI:10.1002/ijgo.15890
Andrew Vallejo, Matthew W. Lee, Maximilian Klar, Jason D. Wright, Koji Matsuo
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The objective of this study was to describe early death in patients with gynecologic malignancy who received care at the Commission-on-Cancer facilities in the United States.</p><p>This retrospective cohort study examined the National Cancer Database, a nationwide tumor registry collaboratory mechanism between the American Cancer Society and the American College of Surgeons.<span><sup>4</sup></span> Their data-capturing mechanism collects more than 70% of new incident cancer cases in each year in the United States.</p><p>The study population was 12 805 885 patients from 27 gender-stratified malignancy groups diagnosed from 2004 to 2019 who had follow-up of at least 2 months after the diagnosis: (i) 1 173 955 patients with five gynecologic malignancies (uterus [<i>n</i> = 639 591], tubo-ovary [<i>n</i> = 285 452], cervix [<i>n</i> = 156 616], vulva [<i>n</i> = 75 514], and vagina [<i>n</i> = 15 496]); (ii) 7 107 174 female patients with 11 non-gynecologic malignancies (breast, lung, colo-rectum, central nervous system, bladder, kidney, pancreas, liver, lymphoma, leukemia, and myeloma); and (iii) 4 524 756 male patients with 11 non-gynecologic malignancies.</p><p>Early death, defined as mortality within 2 months from the date of cancer diagnosis,<span><sup>1, 2</sup></span> was described based on malignancy type. Sensitivity analyses included race and ethnicity specific evaluations. The University of Southern California institutional review boards deemed this study exempt as it included only publicly available, deidentified data (registration no. UP-23-00221).</p><p>Across the 27 gender-stratified malignancy groups, early-death rates ranged from 0.7% for female breast cancer to 22.7% for male pancreatic cancer with the median early-death rate of 6.4% for female colorectal cancer (ranked 14th of 27 groups; Figure 1). There were six malignancy groups in which the early-death rates exceeded 15%: 22.7% for male pancreatic cancer, 21.8% for female pancreatic cancer, 19.4% for male liver cancer, 18.0% for male lung cancer, 17.4% for female liver cancer, 16.1% for female leukemia, and 15.0% for male leukemia (Figure 1).</p><p>All five gynecologic malignancies had early-death rates of lower than the median of early-death rate rank (6.4% for female colorectal cancer, 14th of 27 groups), including 6.2% for tubo-ovarian cancer (ranked 15th), 2.8% for vaginal cancer (ranked 22nd), 2.0% for cervical cancer (ranked 23rd), 1.5% for uterine cancer (ranked 24th), and 1.1% for vulvar cancer (ranked 26th; Figure 1).</p><p>These statistics were consistent when stratified for race and ethnicity, except for non-Hispanic black patients with tubo-ovarian cancer in which the early-death rate was 8.5% and ranked 10th highest among 27 genders-stratified malignancy groups and higher than other racial and ethnic groups (6.2% for non-Hispanic White [ranked 15th], 4.5% for Hispanic [ranked 15th], 3.5% for Asian [ranked 15th], and 3.4% for Native American [ranked 19th]) (Figures S1–S5).</p><p>The results of current real-world data across the Commission-on-Cancer facilities suggest that patients with gynecologic malignancy had overall lower rates of early death following diagnosis compared with non-gynecologic malignancies, with the exception of non-Hispanic black patients with tubo-ovarian cancer.</p><p>Key limitations included lack of data on cause of death, patient-related factors including comorbidity, performance status, and living-will, tumor-related factors, including extent of malignancy and anti-cancer treatment, and healthcare-related factors, including access to care and hospital quality for cancer care. Together with the results of prior investigations,<span><sup>3</sup></span> further studies to assess early death in this patient group are necessary, including early death as a quality indicator in oncologic care.<span><sup>5</sup></span></p><p>Conceptualization: KM, JDW; data curation: MWL; formal analysis: KM; funding acquisition: KM; investigation: all authors; methodology: KM; project administration: MWL, KM; resources: MK, JDW; software: KM, MWL; supervision: KM, MK, JDW; validation: KM; visualization: KM; writing—original draft: AV, KM; writing—review and editing: all authors.</p><p>Ensign Endowment for Gynecologic Cancer Research (KM). The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.</p><p>All conflicts of interest were unrelated to the work: consultation, Cooper Surgical, AstraZeneca, Immunogen, and KLS Martin (MK); research grant, Merck, royalties, UpToDate, honoraria, American College of Obstetricians and Gynecologists (JDW). 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Abstract

Early death following the diagnosis of malignancy, even if expected, regardless of the etiology from patient-, disease-, and healthcare-related reasons, may pose a grave emotional and psychological impact to the patient's family.1, 2 Prior investigations on early death in gynecologic malignancies were limited, but available data showed a wide range of early-death rates across ovarian, uterine, cervical, vulvar, and vaginal cancers.3 Yet, these statistics of gynecologic cancers in relation to other malignancies were understudied, especially as stratified by gender. The objective of this study was to describe early death in patients with gynecologic malignancy who received care at the Commission-on-Cancer facilities in the United States.

This retrospective cohort study examined the National Cancer Database, a nationwide tumor registry collaboratory mechanism between the American Cancer Society and the American College of Surgeons.4 Their data-capturing mechanism collects more than 70% of new incident cancer cases in each year in the United States.

The study population was 12 805 885 patients from 27 gender-stratified malignancy groups diagnosed from 2004 to 2019 who had follow-up of at least 2 months after the diagnosis: (i) 1 173 955 patients with five gynecologic malignancies (uterus [n = 639 591], tubo-ovary [n = 285 452], cervix [n = 156 616], vulva [n = 75 514], and vagina [n = 15 496]); (ii) 7 107 174 female patients with 11 non-gynecologic malignancies (breast, lung, colo-rectum, central nervous system, bladder, kidney, pancreas, liver, lymphoma, leukemia, and myeloma); and (iii) 4 524 756 male patients with 11 non-gynecologic malignancies.

Early death, defined as mortality within 2 months from the date of cancer diagnosis,1, 2 was described based on malignancy type. Sensitivity analyses included race and ethnicity specific evaluations. The University of Southern California institutional review boards deemed this study exempt as it included only publicly available, deidentified data (registration no. UP-23-00221).

Across the 27 gender-stratified malignancy groups, early-death rates ranged from 0.7% for female breast cancer to 22.7% for male pancreatic cancer with the median early-death rate of 6.4% for female colorectal cancer (ranked 14th of 27 groups; Figure 1). There were six malignancy groups in which the early-death rates exceeded 15%: 22.7% for male pancreatic cancer, 21.8% for female pancreatic cancer, 19.4% for male liver cancer, 18.0% for male lung cancer, 17.4% for female liver cancer, 16.1% for female leukemia, and 15.0% for male leukemia (Figure 1).

All five gynecologic malignancies had early-death rates of lower than the median of early-death rate rank (6.4% for female colorectal cancer, 14th of 27 groups), including 6.2% for tubo-ovarian cancer (ranked 15th), 2.8% for vaginal cancer (ranked 22nd), 2.0% for cervical cancer (ranked 23rd), 1.5% for uterine cancer (ranked 24th), and 1.1% for vulvar cancer (ranked 26th; Figure 1).

These statistics were consistent when stratified for race and ethnicity, except for non-Hispanic black patients with tubo-ovarian cancer in which the early-death rate was 8.5% and ranked 10th highest among 27 genders-stratified malignancy groups and higher than other racial and ethnic groups (6.2% for non-Hispanic White [ranked 15th], 4.5% for Hispanic [ranked 15th], 3.5% for Asian [ranked 15th], and 3.4% for Native American [ranked 19th]) (Figures S1–S5).

The results of current real-world data across the Commission-on-Cancer facilities suggest that patients with gynecologic malignancy had overall lower rates of early death following diagnosis compared with non-gynecologic malignancies, with the exception of non-Hispanic black patients with tubo-ovarian cancer.

Key limitations included lack of data on cause of death, patient-related factors including comorbidity, performance status, and living-will, tumor-related factors, including extent of malignancy and anti-cancer treatment, and healthcare-related factors, including access to care and hospital quality for cancer care. Together with the results of prior investigations,3 further studies to assess early death in this patient group are necessary, including early death as a quality indicator in oncologic care.5

Conceptualization: KM, JDW; data curation: MWL; formal analysis: KM; funding acquisition: KM; investigation: all authors; methodology: KM; project administration: MWL, KM; resources: MK, JDW; software: KM, MWL; supervision: KM, MK, JDW; validation: KM; visualization: KM; writing—original draft: AV, KM; writing—review and editing: all authors.

Ensign Endowment for Gynecologic Cancer Research (KM). The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

All conflicts of interest were unrelated to the work: consultation, Cooper Surgical, AstraZeneca, Immunogen, and KLS Martin (MK); research grant, Merck, royalties, UpToDate, honoraria, American College of Obstetricians and Gynecologists (JDW). The remaining authors have no conflicts of interest.

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美国妇科恶性肿瘤早期死亡评估。
恶性肿瘤诊断后的早期死亡,即使是预期的,无论病因来自患者、疾病和卫生保健相关的原因,都可能对患者家属造成严重的情感和心理影响。1,2先前对妇科恶性肿瘤早期死亡的调查有限,但现有数据显示,卵巢癌、子宫癌、宫颈癌、外阴癌和阴道癌的早期死亡率范围很广然而,这些妇科癌症与其他恶性肿瘤的相关统计数据还没有得到充分的研究,特别是按性别分层的研究。本研究的目的是描述在美国癌症委员会机构接受治疗的妇科恶性肿瘤患者的早期死亡。这项回顾性队列研究检查了国家癌症数据库,这是美国癌症协会和美国外科医师学会之间的一个全国性肿瘤登记合作机制。4他们的数据捕获机制收集了美国每年70%以上的新发癌症病例。研究人群为2004 - 2019年诊断的27个性别分层恶性肿瘤组的12 805 885例患者,诊断后随访至少2个月:(i) 1 173 955例妇科恶性肿瘤(子宫[n = 639 591]、输卵管-卵巢[n = 285 452]、宫颈[n = 156 616]、外阴[n = 75 514]、阴道[n = 15 496]);(ii)患有11种非妇科恶性肿瘤(乳腺、肺、结肠直肠、中枢神经系统、膀胱、肾脏、胰腺、肝脏、淋巴瘤、白血病和骨髓瘤)的女性患者107174例;(3)男性11种非妇科恶性肿瘤患者4 524 756例。早期死亡,定义为自癌症诊断之日起2个月内的死亡,1,2是根据恶性类型来描述的。敏感性分析包括种族和民族特定评估。南加州大学的机构审查委员会认为这项研究是免税的,因为它只包括公开可用的、未识别的数据(注册号码:- 23 - 00221)。在27个按性别分层的恶性肿瘤组中,早期死亡率从女性乳腺癌的0.7%到男性胰腺癌的22.7%不等,女性结直肠癌的中位早期死亡率为6.4%(27个组中排名第14位;图1)早期死亡率超过15%的恶性肿瘤组有6组:男性胰腺癌为22.7%,女性胰腺癌为21.8%,男性肝癌为19.4%,男性肺癌为18.0%,女性肝癌为17.4%,女性白血病为16.1%,男性白血病为15.0%(图1)。5种妇科恶性肿瘤的早期死亡率均低于早期死亡率排名中位数(女性结直肠癌为6.4%,在27组中排名第14),其中输卵管卵巢癌为6.2%(排名第15),阴道癌为2.8%(排名第22)。宫颈癌2.0%(第23位)、子宫癌1.5%(第24位)、外阴癌1.1%(第26位);图1)这些统计数据在种族和民族分层时是一致的,除了非西班牙裔黑人卵巢癌患者,其早期死亡率为8.5%,在27个性别分层的恶性肿瘤群体中排名第10,高于其他种族和民族群体(非西班牙裔白人6.2%[排名第15],西班牙裔4.5%[排名第15],亚洲人3.5%[排名第15],美洲原住民3.4%[排名第19])(图S1-S5)。目前癌症委员会机构的真实数据结果表明,除了非西班牙裔黑人输卵管卵巢癌患者外,妇科恶性肿瘤患者在诊断后的早期死亡率总体低于非妇科恶性肿瘤。主要限制包括缺乏死亡原因、患者相关因素(包括合并症、身体状况和生前遗嘱)、肿瘤相关因素(包括恶性肿瘤和抗癌治疗的程度)以及医疗保健相关因素(包括获得护理和癌症护理的医院质量)的数据。结合先前的调查结果,有必要进行进一步的研究来评估该患者组的早期死亡,包括将早期死亡作为肿瘤护理的质量指标。5概念化:KM、JDW;数据管理:MWL;形式分析:KM;资金获取:KM;调查对象:所有作者;方法:公里;项目管理:MWL、KM;资源:MK, JDW;软件:KM、MWL;监督:KM, MK, JDW;验证:公里;可视化:公里;写作-原稿:AV、KM;写作-评审和编辑:所有作者。妇科癌症研究少尉基金。资助者在研究的设计和实施中没有任何作用;收集、管理、分析和解释数据;审稿:手稿的准备、审查或批准;并决定投稿发表。 所有利益冲突均与工作无关:咨询、库珀外科、阿斯利康、免疫原和KLS马丁(MK);研究经费,默克,版税,更新日期,酬金,美国妇产科学院(JDW)。其余作者没有利益冲突。
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来源期刊
CiteScore
5.80
自引率
2.60%
发文量
493
审稿时长
3-6 weeks
期刊介绍: The International Journal of Gynecology & Obstetrics publishes articles on all aspects of basic and clinical research in the fields of obstetrics and gynecology and related subjects, with emphasis on matters of worldwide interest.
期刊最新文献
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