A searchable database of
medically documented cases

About the Project

Colorectal cancer

Colorectal Cancer

Epidemiology:

Colorectal cancer (CRC) ranks among the most prevalent and lethal cancers globally, with approximately 152,810 new cases reported annually in the United States alone.¹ Despite significant advances in treatment, CRC remains the second leading cause of cancer-related deaths globally.² Spontaneous remission (SR) in CRC is extremely rare, constituting less than 2% of all reported SR cases linked to malignant neoplasms.³ SR events are usually recognized only when the remission is dramatic and sustained, which makes it difficult to accurately estimate their true prevalence, as less noticeable cases often go unreported.⁴

Clinical Characteristics:

To date, 28 well-documented cases of spontaneous remission involving primary or metastatic CRC have been reported between 1961 and 2025. The ages of affected individuals ranged from 42 to 90 years, with a peak incidence in the 60–80-year group. A modest male predominance (approximately 1.3:1) was observed, consistent with previous reports suggesting a higher SR frequency among men. Rectal cancer–associated SRs were more common in males. Overall, SR tended to occur in older adults, often in those with advanced-stage disease at initial presentation. See table 1 below for further information.

Histological Characteristics:

Patients who experienced spontaneous remission of CRC commonly presented with rectal bleeding, abdominal pain, altered bowel habits, or weight loss. Diagnosis was typically established by colonoscopy followed by histopathological confirmation of adenocarcinoma. In most cases, the disease was advanced or metastatic, frequently involving the liver, lymph nodes, or peritoneum. Remission was generally documented through imaging or histologic evaluation, which demonstrated replacement of tumor tissue with fibrotic or scar-like changes. Nearly all SR cases were associated with prolonged survival or durable remission, in some instances lasting more than a decade, substantially exceeding the expected prognosis for CRC.

Proposed Contributing Mechanisms:

Various potential SR mechanisms in CRC have been proposed. The most frequently reported involve immune-mediated antitumor responses, often triggered by infection, biopsy, or local inflammation. Other suggested contributors include autoimmune activation, ischemia or necrosis resulting from vascular compromise, and psychological or metabolic stress. More recent reports emphasize immune reactivation following biopsy or tumor manipulation, supporting the hypothesis that antigen exposure or immune priming plays a central role in tumor remission. Additional factors hypothesized to influence SR include concomitant viral or bacterial infections, psychological or spiritual influences such as meditation or religious practice, favorable psychosocial changes, underlying genetic predispositions, and interruption of the tumor’s blood supply.

Site and Extent of Remission:

The colon and rectum remain the most common primary sites affected by SR, although remission has also been reported in hepatic, lymphatic, and local recurrence sites. Among documented cases, SR involved metastatic lesions alone in several patients, both primary and metastatic sites in others, and isolated primary tumors in the remainder. Several recent cases (2020–2025) described biopsy-associated remission at the original lesion site. The median follow-up across published reports was approximately 10 years, with most patients surviving five years or longer after remission. Unlike many other malignancies in which SR may precede relapse, most CRC SR cases exhibited durable remission or long-term disease stability.

Table 1: CRC SR Cases and Clinical Characteristics

Author–year

Age/sex

Primary site

Remission site

Proposed mechanisms

Follow-up

Brown et al. 19611

54/F

Sigmoid colon

Not specified

Not reported

16 years

Mayo et al. 19632

63/F

Left colon,

Not specified

Not reported

12 years

Rankin et al. 19653

44/M

Colon

Liver

Not reported

10 years

Margolis et al. 19674

71/M

Colon

Abdomen

Fecal redirection

Not reported

Snyder et al. 19685

62/F

Colon

Not specified

Not reported

14.5 years

Bir et al., 20096

86/F

Colon

Retroperitoneal and aortocaval lymph nodes

Possible autoimmune response (unconfirmed)

Not reported

Sakamoto et al. 20097

80/M

Rectum

Not specified (Lesion in the middle part of the rectum)

Immune-mediated host responses

Not reported

Lee et al. 20118

54/M

colon

The lymphatic system in the colon

Alternative routes of lymphatic drainage

2 year

Nakamura et al. 20139

60/M

Rectum

Not specified (Lesion in the lower rectum)

Immunity activation, inflammation, ischemic change

Not reported

Karakuchi et al. 201910

78/M

Colon

Scar tissue

Cancer cells as antigens

Not reported

Linuma et al. 201911

63/M

Rectum

Anterior rectal wall

Not reported

1 Month

Nishiura et al. 202012

67/F

Colon

Scar-like lesion was observed around the preoperative inking.

Antitumor immune response

Not reported

Matsui et al. 202113

70/M

Rectum

Lower rectum (scar tissue formation)

Not reported

14 months

Yokota et al. 202114

76/F

Transverse colon

Biopsy site

Antitumor immune reaction

Not reported

Yokota et al. 202114

64/F

Cecum

Biopsy site

Antitumor immune reaction

Not reported

Yokota et al. 202114

64/M

Transverse colon

Biopsy site

Antitumor immune reaction

Not reported

Zwart et al. 202315

59/F

Colon

Liver

Immune response

Not reported

Harata et al. 202316

76/F

Transverse colon

Biopsy site

Immune response to biopsy

Not reported

Lee et al. 202417

78/M

Kidney

Not reported

Not reported

Not reported

Ortigão et al. 202418

42/F

Rectum

Rectal stump (scar with fibrosis)

None reported

Not reported

Ohno et al. 202519

83/F

Transverse colon

Biopsy and resection site

Biopsy and stress-induced immune response

Not reported

Nakano et al. 202520

90/M

Ascending colon

Colon and lymph nodes

Not reported

Not reported

Chida et al., 201721

80/M

Transverse colon

Adaptive immune response

Absence of tumors at 5 months

Kihara et al., 201522

64/M

Transverse colon

Scar at resection site

None reported

Complete regression confirmed at 1 year

Shimizu et al., 201023

80/M

Transverse colon

Transverse colon

Tumor dislodgement

6 months

Airewele, 200724

Eye/Brain/Nervous System/Endocrine

Abdelrazeq, 200525

51/M

Colon

Antigen or carcinogen reduction

Five years later

Matsuki, 201826

72/F

Colon

Liver

Immunological mechanism

Matsuki, 201826

72/F

Liver

Liver

Immune response

Shuttleworth, 202327

78/F

Colon

Inflammation and immune response

Shuttleworth, 202327

86/F

Colon

Colon

Inflammation and immune response

Imai, 202028

75/M

Anus

Rectal ulcer

None reported

6 months

Coulier, 201829

76/M

Greater omentum

Greater omentum

Resorptive foreign body reaction

6 months

Andrén & Frieberg et al., 195630

5/F

Polyp

6 months

Andrén & Frieberg et al., 195630

5.5/F

Polyp

18 months

References:

  1. Brown CH. Regression of metastatic lesions: report of two cases. Am Pract (Clin Pediatr). 1961;12:655-656.
  2. Mayo CW. Tumor clinic conference. Cancer Bull. 1963;15:78-79
  3. Rankin, G. B., Brown, C. H., & Crile Jr, G. (1965). Spontaneous regression of hepatic metastases from a carcinoma of the colon: 10-year follow up of a patient with familial polyposis. Annals of surgery162(1), 156.
  4. Margolis J, West D. Spontaneous regression of malignant disease: report of three cases. J Am Geriatr Soc. 1967;15(3):251-253.
  5. Snyder W, Clark RM, Rubini JR. Long-term survival of mother and son with widespread metastatic adenocarcinoma of colon. Cancer. 1968;21(1):129-133.
  6. Bir AS, Fora AA, Levea C, Fakih MG. Spontaneous regression of colorectal cancer metastatic to retroperitoneal lymph nodes. Anticancer Res. 2009;29(2):465-468.
  7. Sakamoto S, Fujisaki J, Nakajima T, et al. Spontaneous complete regression of a rectal cancer. Endoscopy. 2009;41(10):910-912.
  8. Lee JM, Chung WC, Lee KM, Paik CN, Kim YJ, Lee BI, Cho YS, Choi HJ. Spontaneous resolution of multiple lymphangiomas of the colon: a case report. World J Gastroenterol. 2011;17(11):1515-1518. doi:10.3748/wjg.v17.i11.1515
  9. Nakamura F, Sakamoto T, Nakajima T, Saito Y, Taniguchi H, Matsuda T. A case of rectal tumor in which the shape altered with regression in a short period. BMC Gastroenterol. 2013;13:146. doi:10.1186/1471-230X-13-146
  10. Karakuchi N, Shimomura M, Toyota K, Hinoi T, Yamamoto H, Sadamoto S, Mandai K, Egi H, Ohdan H, Takahashi T. Spontaneous regression of transverse colon cancer with high-frequency microsatellite instability: a case report and literature review. World J Surg Oncol. 2019;17(1):19. doi:10.1186/s12957-018-1552-x
  11. Iinuma K, Mizutani K, Kato T, Nakane K, Tanaka H, Nakano M, Matsuo M, Koie T. Spontaneous healing of rectal penetration by SpaceOAR hydrogel insertion during permanent iodine-125 implant brachytherapy: a case report. Mol Clin Oncol. 2019;11(6):580-582. doi:10.3892/mco.2019.1937
  12. Nishiura B, Kumamoto K, Akamoto S, Asano E, Ando Y, Suto H, Kishino T, Oshima M, Fujiwara M, Usuki H, Okano K, Suzuki Y. Spontaneous regression of advanced transverse colon cancer with remaining lymph node metastasis. Surg Case Rep. 2020;6(1):100. doi:10.1186/s40792-020-00858-1
  13. Matsui T, Naitoh E, Furutani K, Katoh T, Kobayashi K, Sekigawa K, Mitsui H. Spontaneous regression of a rectal tonsil presenting as a large submucosal tumor. DEN Open. 2021;2(1):e34. doi:10.1002/deo2.34
  14. Yokota T, Saito Y, Takamaru H, Sekine S, Nakajima T, Yamada M, Sakamoto T, Taniguchi H, Kushima R, Tsukamoto S, Shida D, Kanemitsu Y, Matsuda T. Spontaneous regression of mismatch repair-deficient colon cancer: a case series. Clin Gastroenterol Hepatol. 2021;19(8):1720-1722.e3. doi:10.1016/j.cgh.2020.08.051
  15. Zwart K, Ruigrok D, de Graaf-Bos M, Goldschmeding R, Koopman M, Bol GM. Spontaneous complete regression of colon cancer liver metastases in a lung transplant patient: a case report. Case Rep Transplant. 2023;2023:9643370. doi:10.1155/2023/9643370
  16. Harata S, Takahashi H, Ando N, Kato A, Watanabe K, Yanagita T, Suzuki T, Ushigome H, Shiga K, Ogawa R, Matsuo Y, Mitsui A, Kimura M, Takiguchi S. Spontaneous regression of advanced transverse colon cancer with deficient mismatch repair: a case report. Surg Case Rep. 2023;9(1):64. doi:10.1186/s40792-023-01595-x
  17. Lee S, Jung S, Jeon H, Jang H, Kim HJ, Lee TW, Bae E, Park DJ, Chang SH. Spontaneous regression of minimal change disease in a colon cancer patient: a case report. Biomed Hub. 2024;9(1):62-66. doi:10.1159/000538279
  18. Ortigão R, Souto-Moura M, Jacome M, Libânio D. Spontaneous regression of a rectal cancer. Rev Esp Enferm Dig. 2024;116(9):498-499. doi:10.17235/reed.2023.9486/2023
  19. Ohno S, Iwata Y, Mitsutome S, Kawai S, Neo M, Fukuda M, Wang B, Suetsugu T, Watanabe T, Komori S, Tanaka C, Nagao N, Kawai M. Spontaneous regression of advanced transverse colon cancer: a case report. Surg Case Rep. 2025;11(1):24-0018. doi:10.70352/scrj.cr.24-0018
  20. Nakano Y, Nishikawa G, Degawa K, Moriyoshi K, Kuriyama K, Watanabe Y, Miyamoto S. A case of multiple advanced colon cancers with spontaneous regression of only one lesion after biopsy: a case report and literature review. Clin J Gastroenterol. 2025;18(3):393-398. doi:10.1007/s12328-025-02106-1
  21. Chida, K., Nakanishi, K., Shomura, H., Homma, S., Hattori, A., Kazui, K., & Taketomi, A. (2017). spontaneous regression of transverse colon cancer: a case report. Surgical case reports, 3(1), 65. https://doi.org/10.1186/s40792-017-0341-z
  22. Kihara, K., Fujita, S., Ohshiro, T., Yamamoto, S., & Sekine, S. (2015). spontaneous regression of colon cancer. Japanese journal of clinical oncology, 45(1), 111–114. https://doi.org/10.1093/jjco/hyu170
  23. Shimizu, H., Kochi, M., Kaiga, T., Mihara, Y., Fujii, M., & Takayama, T. (2010). A case of spontaneous regression of advanced colon cancer. Anticancer research, 30(6), 2351–2353.
  24. Airewele, G., Miller, G., McCluggage, C., & Chintagumpala, M. (2007). Lesion regression. Journal of Neurosurgery, 107(1 Suppl), 80-1; author reply 81. doi:10.3171/PED-07/07/080
  25. abdelrazeq, A. S., Lund, J. N., & Leveson, S. H. (2005). spontaneous regression of peritoneal carcinomatosis from a rectal cancer. European journal of gastroenterology & hepatology, 17(12), 1421–1423. https://doi.org/10.1097/00042737-200512000-00025
  26. Matsuki, R., Sugiyama, M., Yoshiike, S., Shibahara, J., Kogure, M., Yokoyama, M., Suzuki, Y., Abe, N., Masaki, T., & Mori, T. (2018). spontaneous regression of colorectal liver metastasis. Clinical journal of gastroenterology, 11(4), 263–267. https://doi.org/10.1007/s12328-018-0849-1
  27. Shuttleworth, P. W., Ullah, S., Scott, M., Sabri, S., & Solkar, M. (2023). Complete Spontaneous Regression of Colorectal Cancer: A Report of Two Cases. Cureus, 15(5), e39128. https://doi.org/10.7759/cureus.39128
  28. Imai, K., Sakamoto, H., Akahane, M., Nakashima, M., Fujimoto, T., & Aoyama, T. (2020). Spontaneous remission of rectal ulcer associated with SpaceOAR® hydrogel insertion in radiotherapy for prostate cancer. IJU case reports, 3(6), 257–260. https://doi.org/10.1002/iju5.12209
  29. Coulier B. (2018). Spontaneous and rapid healing of massive symptomatic postoperative right-sided infarction of the greater omentum. Diagnostic and interventional imaging, 99(5), 339–340. https://doi.org/10.1016/j.diii.2017.12.002
  30. Andrén & Frieberg, 1956. Spontaneous Regression of Polyps of the Colon in Children. Acta Radiologica 46: 1956; 507-510