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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1243365 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type0 M! c" C0 Y9 c3 d# a2 M6 C
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
2 j3 i5 c, g' @: C0 n  F+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan # O. s% A  \) m9 T2 R
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
) ~% J" h# {" Q: o- b- Y4 g; g3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
# G1 y2 l9 C1 E, l" Z( o7 j4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan # u1 S2 h# [+ M' E. U* W
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ) p2 v9 |* {+ r/ g" I/ O/ r: R
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
' K9 A8 J5 P5 U. J7Kinki University School of Medicine, Osaka 589-8511, Japan 0 ?! O6 N; f3 D4 ?# M* _" I  B
8Izumi Municipal Hospital, Osaka 594-0071, Japan ' l3 o7 K* a7 |. m6 |3 d: n
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
4 Q# f+ a0 G7 S6 |! x* cCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp - Y# [2 B; O( ~
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. 9 t- r% Q9 g* d" N+ o3 P

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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+ S1 o) ]3 f4 i, SAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 1 T& t: m6 b- Z2 B- t* w
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  , t! z! V3 m! Z% n: v% k$ l+ v. ~
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Published online on: Thursday, December 1, 2011 ) R2 j4 m, `6 o# i" f1 A: m3 w

9 X, t' N4 q6 E3 `& d' |Doi: 10.3892/ol.2011.507 % x- h! K3 @0 a* l
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Pages: 405-410
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Abstract:3 r3 h6 R1 X/ {) u, e8 k
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
0 R) ?) K2 [4 n# }& ~8 S4 mF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 6 s. k% ^/ z. V6 T
+ Author Affiliations9 M* G6 @  j' v5 g$ w
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
! C& I3 U& r5 R6 B2 A3 F; X2Department of Thoracic Surgery, Kyoto University, Kyoto ( ^* Y; \$ Z; _# U" ~
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
  i. e  D! L) M/ s& c&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
8 Y/ ~* n2 i# t+ |- R# y$ ?Received September 3, 2010.
3 R  ?$ Q1 _" {1 X, N! iRevision received November 11, 2010. : E' [) f: j" i, [3 U
Accepted November 17, 2010.
6 q; w4 {, O# o* X( V& _' E$ [Abstract
2 u7 o" D+ }  }7 a- m5 RBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. / `& k& e( e6 u- }# L1 X4 e
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. % r8 q& N( F+ A9 t* |9 _, L
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
) I3 B- r4 H; g' B3 |Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ! w  d" u) v4 F# y% o. S+ l6 M
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
+ Y7 K8 n& ^: b2 W今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
6 C9 h) b+ s& k. K8 Ohttp://clinicaltrials.gov/ct2/show/NCT01523587+ \5 `7 S& j' p0 ?' G7 j% m2 @- |4 h
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC6 {& ~1 C0 O+ K4 t. x  n; `
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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% P' z8 a+ z; |$ p' E从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。) X- a4 @1 J$ V0 ~3 H. h$ j' q0 `1 P
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 * f& w- P. X0 \* N1 e  g/ n- \8 Z
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
9 L4 l7 s- t7 z至今为止,未出 ...

' R% ?& l+ `$ l没有副作用是第一追求,效果显著是第二追求。9 [6 Y' E0 m0 Q7 Q7 r9 S* c! o
不错。

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